method for the control of soy cyst nematode (heterodera glycines) by infesting a nematode resistant

专利摘要:
USE OF ACTIVE INGREDIENTS TO CONTROL NEMATOIDS IN NEMATOID-RESISTANT CROPS The present invention relates generally to the use of fluopyram and compositions comprising fluopyram to control nematodes in resistant nematode cultures and / or increasing culture yield and particularly useful methods to control nematodes and / or increasing crop productivity in those crops and to methods particularly useful for controlling nematodes and / or increasing crop yield.
公开号:BR112013006611B1
申请号:R112013006611-3
申请日:2011-09-21
公开日:2021-01-19
发明作者:Wolfram Andersch；Kevin Bugg；Bill Striegel；Steven Riniker；Nalini Desai；Candace Poutre
申请人:Bayer Intellectual Property Gmbh；
IPC主号:

专利说明:

Field of invention
The present invention generally relates to the use of N- {[3-chloro-5- (trifluoromethyl) - 2-pyridinyl] -ethyl} -2,6-dichlorobenzamide (fluopyram) to control nematodes in nematode-resistant cultures and methods particularly useful for controlling nematodes and / or increasing the yield of these cultures. Description of the present technology
Fluopiram is defined as the compound of formula (I)
as well as the N-oxides of its compounds.
Fluopiram is a broad spectrum fungicide with penetrating and translaminating properties for foliar, drip, wetting and seed treatment applications in a wide range of different cultures against many economically important plant diseases. It is very effective in preventive applications against powdery mildew, gray mold and white mold species. It is effective against many plant diseases. Fluopiram showed activity in spore germination, elongation of the germ tube and mycelial growth tests. At the biochemical level, fluopiram inhibits mitochondrial respiration, blocking electron transport in the succinate dehydrogenase respiratory chain (SDH inhibitor - complex II).
Fluopyram and its manufacturing process from known and commercially available compounds are described in patent document EP-A-1 389 614 and WO 2004/016088.
A general description of the nematicidal activity of pyridylethylbenzamide derivatives is found in WO-A 2008/126922.
Nematodes are tiny multicellular animals, wormlike, adapted to live in water. The number of nematode species is estimated at half a million. An important part of soil fauna, nematodes live in a maze of interconnected channels, called pores, which are formed by soil processes. They move in the water films that stick to the soil particles. Plant parasitic nematodes are mostly those that feed on roots, and are found in association with most plants. Some are endoparasites, living and feeding inside the tissue of the roots, tubers, shoots, seeds, etc. Others are ectoparasites, feeding externally through plant walls. A single endoparasitic nematode can kill a plant or reduce its productivity. Root-fed endoparasites include such economically important pests, such as gall nematodes (Meloidogyne species), reniform nematodes (Rotylenchulus species), cyst nematodes (Heterodera species), and root lesion nematodes (Pratylenchus species) ). Direct feeding by nematodes can dramatically decrease a plant's absorption of nutrients and water. Nematodes have the greatest impact on crop productivity when they attack the roots of seedlings right after seed germination. Nematode feeding also creates open wounds that provide input for a wide variety of pathogenic plants, fungi and bacteria. These microbial infections are often economically more harmful than the direct effects of nematode feeding.
Generally, nematode resistance is characterized by the death of host plant cells at or near the parasitic nematode feeding site. Particular resistance genes and nematode interaction influence the time and location of the resistance response. Williamson et al. (Trends in Genetics, vol. 22, No.7, July 2006) describe the nature and mechanisms of interactions of plants and nematodes in relation to resistance in plants.
Nematode resistant plants can be related to three main approaches that are targets for nematodes, nematode interface - harvest and plant response. Insecticidal or nematicidal proteins, interruption of expression of the essential nematode gene by interfering RNA, interruption of sensory function by interfering RNA, peptides or planibodies or nematicidal metabolites are examples of nematode targets; disruption of nematode pathogenicity factors in terms of migration and invasion or induction at the site regarding food and maintenance by interference RNA, peptides or antibodies, camouflage or repellent plants, or the conversion of host plants to non-host plants are examples for the interface of the nematode culture as the plant resistance gene or activation of the hypersensitivity reaction by the invasion of nematodes; induced cell death or other site incompatibility through specific site feed promoters or conversion of cultures to tolerance are examples of plant response.
Although nematode-resistant plants are described as being resistant to specific nematodes, there are still some interactions between the nematode and the crop that, due to the different defense reactions of the plant, can lead to a partially impaired plant. An example of these defense reactions is the hypersensitivity response. One consequence can result in deficiency of the roots and loss of vigor of the affected plants.
Current nematode control focuses primarily on preventing nematode attack on the plant. Once the plant is parasitized, it is practically impossible to kill the nematode without also destroying the plant. Therefore, it would be advantageous to provide improved nematode control compounds and methods of treating nematode resistant plants to prevent or reduce nematode damage.
A large part of the damage to crop plants, which is caused by pests, occurs earlier, when the seed is attacked during storage and then the seed is introduced into the soil, during and immediately after plant germination. This phase is particularly critical since the roots and buds of the growing plant are particularly sensitive and even a small damage can lead to the death of the entire plant. Thus, it is desirable to develop methods to protect the seed and the germinating plant that grants the additional application of crop protection agents, after sowing or after the emergence of the plants. In addition, it is desirable to optimize the amount of active compound used in such a way as to provide maximum protection for the seed and the germination plant against attack by parasites, but without damaging the plant itself by the active compound used. In particular, seed treatment methods must also take into account the intrinsic insecticidal properties of transgenic plants, in order to ensure optimum protection of the plant's seed and also germination with a minimum of crop protection agents to be employed . SUMMARY OF THE INVENTION
The present invention now provides advantageous uses of fluopyram to control nematodes that infest resistant nematode cultures and / or increase productivity.
Accordingly, the present invention also relates to the use of compositions comprising: fluopyram to control nematodes by infesting nematode resistant cultures and / or increasing productivity.
Accordingly, the present invention also relates to the use of compositions comprising: fluopyram to control nematodes that infest insect-resistant cultures.
Accordingly, the present invention also relates to the use of compositions comprising: A) fluopyram and B) at least one agrochemically active compound, to control nematodes by infesting nematode resistant cultures and / or increasing productivity. Accordingly, the present invention also relates to the use of compositions comprising: A) and fluopyram B) at least one agrochemically active compound, to control nematodes that infest insect resistant cultures.
In a preferred embodiment, the invention also relates to the use of compositions comprising: A) fluopyram B) the biological control agent Bacillus firmus CNCM I-1582, in particular spores (US Patent 6,406,690) to control nematodes that infest cultures resistant to nematodes and / or increasing yield.
In a preferred embodiment, the invention also relates to the use of compositions comprising: A) fluopyram B) the biological control agent Bacillus firmus CNCM I-1582, in particular spores (US Patent 6,406,690) to control nematodes that infest resistant cultures to insects.
An exemplary method of the present invention comprises applying fluopyrams of the invention to either the soil or a plant (e.g., seeds or leaf pathway) to control nematode damage and / or increase crop yield.
The present invention is designed for compositions and methods for regulating pest resistance or tolerance in plants or plant cells. By "resistance" is meant that pests (for example, insects or nematodes) are killed after ingestion or other contact with parts of plants. "Tolerance" means a decrease or reduction in movement, feeding, reproduction, or other functions of the pest. Methods for measuring pesticidal activity are well known in the art. See, for example, Czapla and Lang (1990) J. Econ. Entomol. 83: 2480-2485; Andrews et al. (1988) Biochem. J. 252: 199-206; Marrone et al. (1985) J. of Economic Entomology 78: 290-293, and U.S. Patent 5,743,477, all of which are incorporated herein by reference in their entirety.
In conjunction with the present invention "controlling" denotes a preventive or curative reduction of infestation by insects or nematodes, compared to that of untreated cultures, more preferably the infestation is essentially repelled, more preferably the infestation is completely suppressed.
By "pesticide effective amount" is meant an amount of pesticide that is capable of causing the death of at least one of the pests, or visibly reducing the growth of the pests, food, or normal physiological development. This amount will vary depending on factors such as, for example, the specific target pests to be controlled, the specific environment, location, plant, crop or agricultural site to be treated, the environmental conditions, and the method, rate, concentration, stability and amount of application of the effective polypeptide pesticidal composition.
The present invention also relates to a method for the protection of germinating seeds and plants, or plants against attack by parasites, through the selective application of pesticidal agents to the seed of a transgenic plant. Pesticidal agents include chemical control agents or biological compositions applied to the seed of the transgenic plant, where the agent is intended to provide protection to the plant or its seed against damage caused by one or more plant pests. In addition, the invention relates to seeds that have been treated with a pesticidal agent, as described in this document. Application of a pesticidal agent to the seed of a transgenic plant results in better resistance or tolerance to one or more plant pests and / or improved yield or vigor compared to a transgenic plant, grown from an untreated seed. agent as described herein as a pesticide, or from a plant of the same species as the referenced transgenic plant that was grown from a seed treated with an agent, as described herein as a pesticide, but which does not have the transgene (either of which may be referred to here as a "control" of the plant).
In some modalities, the treatment of the seed with these agents, not only protects the seed itself, but also the resulting plants after emergence against pests. In this way, immediate treatment of the crop at the time of sowing or shortly thereafter can be used. DESCRIPTION OF PREFERRED EMBODIMENTS
The methods according to the present invention have been found to provide a higher degree of plant vigor and yield in environments infested with nematodes and fungi than would be expected from the application of a biological or chemical control agent, or the presence of a insect gene or nematode control alone. At least, some of the insect control agents within the scope of the present invention have been shown to provide increased root mass even in the absence of insect pressure that increasing the improved root mass leads to the establishment of beneficial bacteria in the rhizosphere, which , in turn, reduces general losses in the vigor of the crop and the yields caused by parasitic nematodes of plants or fungi. Along with the physical combination of these components, while treating plants and plant material, in a preferred embodiment of the present invention, the compositions of the present invention have been formulated to provide a stable environment for living biological control agents, such as spores, colonization bacteria at the root. Various additives can be added to each of the compositions of the invention, depending on the properties desired for the final composition which has the necessary physical and chemical stability to produce a commercially viable product.
Nematode-resistant plants
Fluopiram is particularly useful in controlling plant parasitic nematodes in plants that carry one or more of the genes listed in Table 1. Fluopyram in combination with at least one agrochemical active compound is particularly useful in controlling plant parasitic nematodes in plants that carry a or more of the genes listed in Table 1. Fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 is particularly useful in controlling plant parasitic nematodes in plants that carry one or more of the genes listed in Table 1. Information on the nucleotide and amino acid sequence for each of these genes is represented by the SEQ ID NOs indicated in columns 4 and 5 of Table 1, in relation to the United States patent application of the series listed in column 2 of Table 1.


Fluopiram is particularly useful in controlling plant parasitic nematodes in plants that carry one or more of the genes listed in Table 1. Fluopyram in combination with at least one agrochemical active compound is particularly useful in controlling plant parasitic nematodes in plants that carry a or more of the genes listed in Table 1. Fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 is particularly useful in the control of plant parasitic nematodes in plants that carry one or more of the genes listed in Table 1
Fluopiram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopyram in combination with at least one agrochemically active compound is particularly useful in the control of plant parasitic nematodes in plants that carry one or more of the genes, such as described in the following documents: WO2009 / 027539A2, WO2009 / 027313A2, WO2008 / 152008A2, WO2008 / 110522A1, WO2008 / 095972A1, WO2008 / 095970A1, WO2008 / 095969A1, WO2008 / 095919A1, WO2008 / 095916A200, WO2008 / 095916A1, WO2008 / 095916A1, / 095889A1, WO2008 / 095886A1, WO2008 / 077892A1, WO2008 / 071726A2, WO2006 / 020821A2, WO2005 / 082932A2, WO2009 / 048847A1, WO2007 / 095469A2, WO2005 / 012340A1, WO200 / 7,47 / 7,4, 7,4, 7,4 , 10 / 782,020, 12 / 032,479, 10 / 783,417, 10 / 782,096, 11 / 657,964, 12 / 192,904, 11 / 396,808, 12 / 166,253, 12 / 166,239, 12 / 166,224, 12 / 166,124, 12 / 166,209, 11 / 762,886, 12 / 364,335, 11 / 763,947, 12 / 252,453, 12 / 209,354, 12 / 491,396 or 12 / 497,221. Fluopyram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopyram in combination with at least one agrochemically active compound is particularly useful in the control of plant parasitic nematodes in plants that carry one or more of the following Hs1pro- 1, Mi-1, Mi-1.2, Hero A, Gpa2, Gro1-4, Rhg1, Rhg4, Mi-3, Mi-9, Cre1, Cre3, Ma, Hsa-1Og, Me3, Rmc1, CLAVATA3-like peptides (for SYV46).
A preferred embodiment comprises the nematode resistant plant, as described above treated with Fluopiram.
A preferred embodiment comprises the nematode resistant plant, as described above treated with fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582.
A preferred embodiment comprises the nematode resistant plant, as described above treated with fluopyram in combination with at least one agrochemically active compound.
In various embodiments, the compositions and methods of the present invention comprise the treatment of a transgenic plant comprising one or more of the genes listed in Table 1 with fluopyram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or with fluopyram in combination with at least one agrochemically active compound. In particular modalities, fluopy or fluopy in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopy in combination with at least one agrochemically active compound is applied to the seed of the transgenic plant that comprises one or more of the genes listed in Table 1, including biologically active variants and fragments thereof.
An exemplary method of the present invention comprises the application of fluopyram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopyram in combination with at least one agrochemical active compound of the invention, the propagation material (for example, seeds ) of plants to combat nematode damage and / or increase crop productivity.
Another exemplary method of the present invention comprises the application of fluopyram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopyram in combination with at least one agrochemically active compound either to the soil or to a plant (for example, via leaf) to combat nematode damage and / or increase crop productivity.
In several modalities, the biological control agent is the fluopyram nematicide, and the nematode-resistant culture comprises a transgenic plant comprising Axmi031 or Axn2 (Table 1).
The nucleotides and amino acids of SEQ ID NOs listed in Table 1 are exemplary sequences and are not intended to limit the scope of the invention. The present invention encompasses plants and plant parts, including plant and seed cells, comprising one or more of the genes listed in column 1 of Table 1. In some embodiments, the present invention encompasses plants and plant parts, including plant and seed cells, which comprise one or more nucleotide sequences listed in column 4 of Table 1. In some embodiments, the present invention encompasses plants and parts of plants, including plant and seed cells, comprising a or more nucleotide sequences that encode one or more of the polypeptides indicated in column 5 of Table 1.
In yet another embodiment, the present invention encompasses plants and parts of plants, including plant and seed cells, comprising one or more nucleotide sequences encoding a biologically active variant or a fragment of the amino acid sequence (s) listed in column 5 of Table 1.
A fragment of a nucleotide sequence that encodes a biologically active portion of a pesticidal protein of the present invention will encode at least about 15, 25, 30, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, 400, 450 contiguous amino acids, or even the total number of amino acids present in a full-length pesticidal protein listed here in Table 2. Such biologically active portions can be prepared by recombinant techniques and evaluated for pesticidal activity. Methods for measuring pesticidal activity are well known in the art. See, for example, Czapla and Lang (1990) J. Econ. Entomol. 83: 2480-2485; Andrews et al. (1988) Biochem. J. 252: 199-206; Marrone et al. (1985) J. of Economic Entomology 78: 290-293; and U.S. Patent No. 5,743,477, all of which are incorporated herein by reference in their entirety.
In some embodiments, the fragment is a fragment of proteolytic cleavage. For example, the proteolytic cleavage fragment can have an N-terminal or a C-terminal truncation of at least about 100 amino acids, about 120, about 130, about 140, about 150, or about 160 amino acids in relation to the amino acid sequence listed in Table 2. In some embodiments, the fragments covered here result from the removal of the C-terminal crystallization domain, for example, through proteolysis or by inserting a stop codon into the coding sequence .
The preferred pesticidal proteins of the present invention are encoded by a nucleotide sequence sufficiently identical to the nucleotide sequence (s) listed in Table 2, or are pesticidal proteins that are sufficiently identical to the amino acid sequence (s) listed in Table 2. By " sufficiently identical "means an amino acid or nucleotide sequence that has at least about 60% sequence identity or 65%, or about 70% sequence identity of 75%, about 80% sequence identity or 85%, about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more of sequence identity compared to a reference sequence, using one of the alignment programs described here using conventional parameters. One skilled in the art will recognize that these values can be properly adjusted to determine the corresponding identity of the proteins encoded by two nucleotide sequences, taking into account codon degeneration, amino acid similarity, positioning of the reading frame, and the like.
To determine the percent identity of two amino acid sequences or two nucleic acids, the sequences are aligned for optimal comparison purposes. The percentage of identity between the two strings is a function of the number of identical positions shared by the strings (that is, the percentage of identity = number of identical positions / total number of positions (for example, overlapping positions) x 100). In one embodiment, the two strings are of the same length. In another embodiment, the percentage of identity is calculated using the entire reference sequence (for example, a sequence listed in Table 2). The percentage of identity between two sequences can be determined using techniques similar to those described below, whether or not they allow openings. When calculating the identity percentage, typically exact matches are counted. The opening, that is, a position in which the alignment of a residue is present in one sequence, but not in the other, is considered to be a position of non-identical residues.
The determination of the percentage of identity between two sequences can be carried out using a mathematical algorithm. A non-limiting example of a mathematical algorithm used to compare two sequences is the algorithm by Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87: 2264, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90: 5873-5877. Such an algorithm is incorporated in the BLASTN and BLASTX programs by Altschul et al. (1990) J. Mol. Biol. 215: 403. BLAST nucleotide searches can be performed with the BLASTN program, score = 100, word length = 12, to obtain homologous nucleotide sequences of pesticide as nucleic acid molecules of the present invention. Searches for BLAST proteins can be performed with the BLASTX program, punctuation = 50, word length = 3, to obtain sequences of amino acids homologous to pesticide protein molecules of the present invention. To obtain spaced alignments for comparison purposes, BLAST gapped (BLAST 2.0) can be used as described in Altschul et al. (1997) Nucleic Acids Res. 25: 3389. Alternatively, PSI-Blast can be used to perform a repeated search that detects distant relationships between molecules. See Altschul et al. (1997) supra. When using BLAST, BLAST gapped and PSI-Blast programs, the default parameters of the respective programs (for example, BLASTX and BLASTN) can be used. Alignment can also be carried out manually, by inspection.
Another non-limiting example of a mathematical algorithm used for sequence comparison is the ClustalW algorithm (Higgins et al. (1994) Nucleic Acids Res. 22: 46734680). ClustalW compares the sequences and aligns the entire amino acid or DNA sequence and therefore can provide data on the conservation of the entire amino acid sequence sequence. The ClustalW algorithm used in several commercially available DNA / amino acid analysis software packages, such as the Vector NTI Program Suite module (Invitrogen Corporation, Carlsbad, CA). After aligning the amino acid sequences with ClustalW, the percentage of amino acid identity can be assessed. A non-limiting example of a software program useful for ClustalW alignment analysis is GENEDOC ™. GENEDOC ™ (Karl Nicholas) allows the evaluation of similarity and identity of the amino acid (or DNA) between multiple proteins. Another non-limiting example of a mathematical algorithm used for sequence comparison is the algorithm by Myers and Miller (1988) CABIOS 4: 11-17. This algorithm is incorporated into the ALIGN program (version 2.0) which is part of the GCG Wisconsin Genetics software package, Version 10 (available from Accelrys, Inc., 9685 Scranton Road., San Diego, CA, USA). When using the ALIGN program to compare amino acid sequences, a PAM120 residue table, a gap length loss of 12 and a gap loss of 4 can be used.
Unless otherwise indicated GAP, version 10, which uses the algorithm of Needleman and Wunsch (1970) J. Mol. Biol. Biol. 48 (3): 443-453, will be used to determine the identity or similarity of sequence using the following parameters:% identity and% similarity of nucleotide sequence using Weight GAP of Weight 50 and of length 3 and the scoring matrix nwsgapdna.cmp,% identity or% similarity for an amino acid sequence using the GAP weight of 8 and weight of length 2 and the BLOSUM62 scoring program. Equivalent programs can also be used. By "equivalent program" is meant any sequence comparison program that, for any two sequences in question, generates an alignment with identical results of nucleotide residues and a percentage of identical sequence identity when compared to the corresponding alignment generated by the GAP version 10.
"Variants" of the amino acid sequences shown in Table 2 include the sequences that encode the pesticidal proteins described here, but which differ conservatively because of the degeneracy of the genetic code, as well as those that are sufficiently identical, as discussed above. Variants that occur in naturally allelic forms can be identified with the use of well-known molecular biology techniques, such as polymerase chain reaction (PCR) and hybridization techniques, as described below. Variant nucleotide sequences include synthetically derived nucleotide sequences that have been generated, for example, using site-directed mutagenesis, but which still encode the pesticidal proteins disclosed in the present invention, as discussed below.
Those skilled in the art will further appreciate that changes can be introduced by mutating the nucleotide sequences of the present invention leading to changes in the amino acid sequence of the encoded pesticidal proteins, without altering the biological activity of the proteins. In this way, variants of isolated nucleic acid molecules can be created by introducing one or more nucleotide substitutions, additions or deletions within the corresponding nucleotide sequence described here, such that one or more amino acid substitutions, additions or deletions are introduced into the encoded protein. Mutations can be introduced using standard techniques, such as directed mutagenesis and PCR-mediated mutagenesis. Such variant nucleotide sequences are also encompassed by the present invention.
For example, conservative amino acid substitutions can be made on one or more predicted non-essential amino acid residues. An "non-essential" amino acid residue is a residue that can be altered from the wild-type sequence of a pesticidal protein without altering biological activity, whereas an "essential" amino acid residue is necessary for biological activity. A "conservative amino acid substitution" is one in which the amino acid residue is replaced by an amino acid residue with a similar side chain. Families of amino acid residues having similar side chains have been defined in the prior art. These families include amino acids with basic side chains (for example, lysine, arginine, histidine), acidic side chains (for example, aspartic acid, glutamic acid), uncharged polar side chains (for example, glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), non-polar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and side chains aromatic (eg tyrosine, phenylalanine, tryptophan, histidine).
Amino acid substitutions can be made in non-conserved regions that retain function. In general, such substitutions would not be made for conserved amino acid residues, or for amino acid residues residing in a conserved motif, where these residues are essential for protein activity. Examples of residues that are conserved and that may be essential for protein activity include, for example, residues that are identical among all proteins contained in an alignment of similar toxins or related to the sequences of the present invention (for example, residues which are identical in a homologous protein alignment). Examples of residues that are conserved but that can allow conservative amino acid substitutions and still maintain activity include, for example, residues that have only conservative substitutions among all proteins contained in an alignment of similar toxins or related to the sequences of the present invention. (for example, residues that have only conservative substitutions among all proteins contained in the alignment of homologous proteins). However, one skilled in the art will understand that functional variants may have minor conserved or non-conservative changes in conserved waste.
Alternatively, variant nucleotide sequences can be made by introducing random mutations throughout all or part of the coding sequence, such as by saturation mutagenesis, and the resulting mutants can be screened for the ability to impart pesticidal activity to identify mutants that retain activity. Following mutagenesis, the encoded protein can be expressed recombinantly and the activity of the protein can be determined using conventional assay techniques.
Using methods such as PCR, hybridization and the corresponding pesticide sequences, as can be identified, such sequences have substantial identity with the sequences of the invention. See, for example, Sambrook and Russell (2001) Molecular Cloning: A Laboratory Manual. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY) and Innis, et al. (1990) PCR Protocols: A Guide to Methods and Applications (Academic Press, NY).
Variant nucleotide and amino acid sequences of the present invention also encompass sequences derived from mutagenic and recombinant gene processes, such as DNA shuffling. With such a procedure, one or more different regions of the coding pesticidal protein can be used to create a new pesticidal protein that has the desired properties. In this way, the recombinant polynucleotide libraries are generated from a population of related sequence polynucleotides that comprise regions of sequences that have substantial sequence identity and can be homologously recombined in vitro or in vivo. For example, using this approach, the sequence motifs encoding a domain of interest can be shuffled between the pesticidal gene of the present invention and other known pesticidal genes to obtain a new gene encoding a protein with an improved property of interest, such as increased insecticidal activity. Strategies for such DNA rearrangement are known in the art. See, for example, Stemmer (1994) Proc. Natl. Acad. Sci. USA 91: 10747-10751; Stemmer (1994) Nature 370: 389-391; Crameri et al. (1997) Nature Biotech. 15: 436-438; Moore et al. (1997) J. Mol. Biol. 272: 336-347; Zhang et al. (1997) Proc. Natl. Acad. Sci. USA 94: 4504-4509; Crameri et al. (1998) Nature 391: 288-291; and U.S. Patent Nos. 5,605,793 and 5,837,458.
Domain exchange or shuffling is another mechanism for generating altered pesticide proteins. Domains can be switched between pesticidal proteins, resulting in hybrid or chimeric toxins with better pesticidal activity or target spectrum. Methods for generating recombinant proteins and testing them for pesticidal activity are well known in the art (see, for example, Naimov et al (2001) Appl Environ Microbiol 67: 5328-5330, De Maagd et al (1996) Appl Environ Microbiol 62: 1537-1543; Ge et al (1991) J. Biol Chem 266: 17954-17958, Schnepf et al (1990) J. Biol Chem 265: 20923-20930; rang et al. 91999) Appl. Environ. Microbiol. 65: 2918-2925).
Variants and fragments of the proteins covered by the present invention are biologically active, which means that they continue to possess the desired biological activity of the native protein, that is, pesticidal activity. By "retains activity" it means that the variant will have at least about 30%, at least about 50%, at least about 70%, or at least about 80% of the pesticidal activity of the native protein. Methods for measuring pesticidal activity are well known in the art. See, for example, Czapla and Lang (1990) J. Econ. Entomol. 83: 2480-2485; Andrews et al. (1988) Biochem. J. 252: 199206; Marrone et al. (1985) J. of Economic Entomology 78: 290-293, and U.S. Patent No. 5,743,477, all of which are incorporated herein by reference in their entirety.
In the present context, agrochemically active compounds are to be understood as meaning all substances that are or can normally be used for the treatment of plants. Fungicides, bactericides, insecticides, acaricides, nematicides, molluscicides, phytotoxicity protectors, plant growth regulators and plant nutrients, as well as biological control agents can be mentioned as being preferred. Mixing partners
The agrochemically active compound described in B), are the following fungicidal active ingredients, which can be mentioned are: (1) Ergosterol biosynthesis inhibitors, for example, (1.1) aldimorf (1704-28-5), (1.2) azaconazole (60207-31-0), (1.3) bitertanol (55179-31-2), (1.4) bromuconazole (11625548-2), (1.5) cyproconazole (113096-99-4), (1.6) diclobutrazole (75736- 33-3), (1.7) diphenoconazole (119446-68-3), (1.8) diniconazole (83657-24-3), (1.9) diniconazole-M (8365718-5), (1.10) dodemorf (1593-77- 7), (1.11) dodemorf acetate (31717-87-0), (1.12) epoxiconazole (106325-08-0), (1.13) etaconazole (60207-93-4), (1.14) fenarimol (60168-889) , (1.15) fenbuconazole (114369-43-6), (1.16) fenhexamid (126833-17-8), (1.17) fenpropidin (67306-00-7), (1.18) fenpropimorf (67306-03-0), ( 1.19) fluquinconazole (136426-54-5), (1.20) flurprimidol (56425-91-3), (1.21) flusilazole (85509-19-9), (1.22) flutriafol (76674-21-0), (1.23) furconazole (112839-33-5), (1.24) furconazole-cis (112839-3 2-4), (1.25) hexaconazole (79983-71-4), (1.26) imazalil (60534-80-7), (1.27) imazalil sulfate (58594-72-2), (1.28) imibenconazole (86598- 92-7), (1.29) ipconazole (125225-28-7), (1.30) metconazole (12511623-6), (1.31) miclobutanil (88671-89-0), (1.32) naphthifine (65472-88-0) , (1.33) nuarimol (6328471-9), (1.34) oxpoconazole (174212-12-5), (1.35) paclobutrazol (76738-62-0), (1.36) pefurazoate (101903-30-4), (1.37) penconazole (66246-88-6), (1.38) piperalin (3478-94-2), (1.39) prochloraz (67747-09-5), (1.40) propiconazole (60207-90-1), (1.41) protioconazole ( 178928-70-6), (1.42) pyributicarb (88678-67-5), (1.43) pyrifenox (88283-41-4), (1.44) quinconazole (103970-75-8), (1.45) simeconazole (149508- 90-7), (1.46) spiroxamine (118134-30-8), (1.47) tebuconazole (107534-96-3), (1.48) terbinafine (91161-71-6), (1.49) tetraconazole (112281-77- 3), (1.50) triadimefon (43121-43-3), (1.51) triadimenol (89482-177), (1.52) tridemorf (81412-43-3), (1.53) triflumizole (68694-11-1), ( 1.54) triforin (266 44-46-2), (1.55) triticonazole (131983-72-7), (1.56) uniconazole (83657-22-1), (1.57) uniconazole-p (83657-17-4), (1.58) viniconazole ( 77174-66-4), (1.59) voriconazole (137234-62-9), (1.60) 1- (4-chlorophenyl) -2- (1H-1,2,4-triazol-1-yl) cycloheptanol (129586 -32-9), (1.61) methyl 1- (2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) -1H-imidazole-5-carboxylate (110323-95-0), ( 1.62) N '- {5- (difluoromethyl) -2-methyl-4- [3- (trimethylsilyl) propoxy] phenyl} -N-ethyl-N-methylimidoformamide, (1.63) N-ethyl-N-methyl-N' - {2-methyl-5- (trifluoromethyl) -4- [3- (trimethylsilyl) propoxy] phenyl} imidoformamide and (1.64) O- [1- (4-methoxyphenoxy) -3,3-dimethylbutan-2-yl] 1H-imidazole-1-carbothioate (111226-71-2). (2) Respiratory chain inhibitors in complex I or II, for example, (2.1) bixafen (581809-46-3), (2.2) boscalid (188425-85-6), (2.3) carboxin (5234-68-4 ), (2.4) diflumetorim (130339-07-0), (2.5) fenfuram (24691-80-3), (2.6) fluopyram (658066-35-4), (2.7) flutolanil (66332-96-5), (2.8) fluxpyroxad (907204-31-3), (2.9) furametpyr (123572-88-3), (2.10) furmeciclox (60568-05-0), (2.11) isopirazam (syn-epimeric racemate mixture 1RS, 4SR , 9RS and anti-epimeric racemate 1RS, 4SR, 9SR) (881685-58-1), (2.12) isopirazam (anti-epimeric racemate 1RS, 4SR, 9SR), (2.13) isopirazam (anti-epimeric enantiomer 1R, 4S, 9S), (2.14) isopyrazam (1S, 4R, 9R anti-epimeric enantiomer), (2.15) isopyrazam (1RS, 4SR, 9RS epimeric syn racemate), (2.16) 1R, 4S, 9R epimeric syn racemate), ( 2.17) isopyrazam (1S, 4R, 9S epimeric syn racemate), (2.18) mepronil (55814-410), (2.19) oxycarboxine (5259-88-1), (2.20) penflufen (494793-67-8), (2.21 ) pentiopirad (183675-82-3), (2.22) silkxane (874967-67-6), (2.23) tifluzamide (130000-40-7), (2.24) 1- methyl-N- [2- (1,1,2,2-tetrafluoroethoxy) phenyl] -3- (trifluoromethyl) -1H-pyrazole-4-carboxamide, ( 2.25) 3- (difluoromethyl) -1-methyl-N- [2- (1,1,2,2-tetrafluoroethoxy) phenyl] -1H-pyrazole-4-carboxamide, (2.26) 3- (difluoromethyl) -N- [4-fluoro-2- (1,1,2,3,3,3-hexafluoropropoxy) phenyl] -1-methyl-1H-pyrazole-4-carboxamide, (2.27) N- [1- (2,4- dichlorophenyl) -1-methoxypropan-2-yl] -3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide (1092400-95-7) (WO 2008148570), (2.28) 5,8-difluoro- N- [2- (2-fluoro- 4 - {[4- (trifluoromethyl) pyridin-2-yl] oxy} phenyl) ethyl] quinazolin-4-amine (1210070-84-0) (WO2010025451), (2.29) N- [9- (dichloromethylene) -1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.30 ) N - [(1S, 4R) -9- (dichloromethylene) - 1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromethyl) -1-methyl-1H-pyrazole -4- carboxamide and (2.31) N - [(1R, 4S) -9- (dichloromethylene) -1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromethyl) - 1-methyl-1H-pyraz ole-4-carboxamide. (3) Respiratory chain inhibitors in complex III, for example, (3.1) ametoctradine (865318-97-4), (3.2) amisulbrom (348635-87-0), (3.3) azoxystrobin (131860-33-8), (3.4) ciazofamid (120116-88-3), (3.5) coumetoxistrobin (850881-30-0), (3.6) coumoxystrobin (850881-70-8), (3.7) dimoxystrobin (141600-52-4), (3.8 ) enestroburin (238410-11-2) (WO 2004/058723), (3.9) famoxadone (131807-57-3) (WO 2004/058723), (3.10) fenamidone (161326-34-7) (WO 2004/058723) ), (3.11) phenoxystrobin (918162-02-4), (3.12) fluoxastrobin (361377-29-9) (WO 2004/058723), (3.13) kresoxim-methyl (143390-89-0) (WO 2004/058723 ), (3.14) metominostrobin (133408-50-1) (WO 2004/058723), (3.15) orisastrobin (189892-691) (WO 2004/058723), (3.16) picoxystrobin (117428-22-5) (WO 2004 / 058723), (3.17) pyraclostrobin (175013-18-0) (WO 2004/058723), (3.18) pirametostrobin (915410-70-7) (WO 2004/058723), (3.19) piraoxystrobin (862588-11-2 ) (WO 2004/058723), (3.20) piribencarb (799247-52-2) (WO 2004/058723), (3.21) triclo piricarb (902760-40-1), (3.22) trifloxystrobin (141517-21-7) (WO 2004/058723), (3.23) (2E) -2- (2 - {[6- (3-chloro-2- methylphenoxy) - 5-fluoropyrimidin-4-yl] oxy} phenyl) -2- (methoxyimino) -N-methylethylamide (WO 2004/058723), (3.24) (2E) -2- (methoxyimino) -N-methyl-2 - (2 - {[({(1E) -1- [3- (trifluoromethyl) phenyl] ethylidene} amino) oxy] methyl} phenyl) ethanamide (WO 2004/058723), (3.25) (2E) -2- ( methoxyimino) -N-methyl-2- {2 - [(E) - ({1- [3- (trifluoromethyl) phenyl] ethoxy} imino) methyl] phenyl} ethanamide (158169-73-4), (3.26) ( 2E) -2- {2- [({[(1E) -1- (3 - {[(E) -1-fluoro-2-phenylethyl] oxy} phenyl) ethylidene] amino} oxy) methyl] phenyl} - 2- (methoxyimino) -N-methylethylamide (326896-28-0), (3.27) (2E) -2- {2 - [({[(2E, 3E) -4- (2,6-dichlorophenyl) but- 3-en-2-ylidene] amino} oxy) methyl] phenyl} -2- (methoxyimino) -N-methylethylamide, (3.28) 2-chloro-N- (1,1,3-trimethyl-2,3-dihydro -1H-inden-4-yl) pyridine-3-carboxamide (119899-14-8), (3.29) 5-methoxy-2-methyl-4- (2 - {[({(1E) -1- [3 - (trifluoromethyl) phenyl] ethylidene} amino) oxy] methyl} phenyl) - 2,4-dihydro-3H-1,2,4-triazole-3-o na, (3.30) methyl (2E) -2- {2 - [({cyclopropyl [(4-methoxyphenyl) imino] methyl} sulfanyl) methyl] phenyl} -3-methoxyprop-2-enoate (149601-03-6) , (3.31) N- (3-ethyl-3,5,5-trimethylcyclohexyl) -3- (formylamino) -2-hydroxybenzamide (226551-21-9), (3.32) 2- {2 - [(2,5 - dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide (173662-97-0) and (3.33) (2R) -2- {2 - [(2,5-dimethylphenoxy) methyl] phenyl} -2- methoxy-N-methylacetamide (394657-24-0). (4) Inhibitors of cell division and mitosis, for example (4.1) benomyl (17804-35-2), (4.2) carbendazim (10605-21-7), (4.3) chlorphenazole (3574-96-7), (4.4 ) dietofencarb (87130-20-9), (4.5) etaboxam (162650-77-3), (4.6) fluopicolide (239110-15-7), (4.7) fuberidazole (3878-191), (4.8) pencicuron (66063 -05-6), (4.9) thiabendazole (148-79-8), (4.10) thiophanate-methyl (2356405-8), (4.11) thiophanate (23564-06-9), (4.12) zoxamide (156052-68 -5), (4.13) 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6-trifluorophenyl) [1,2,4] triazolo [1,5-a] pyrimidine (214706-53-3) and (4.14) 3-chloro-5- (6-chloropyridin-3-yl) -6-methyl-4- (2,4,6-trifluorophenyl) pyridazine (1002756-87-7) . (5) Compounds capable of having an action in several places, such as (5.1) bordeaux mixture (8011-63-0), (5.2) captafol (2425-06-1), (5.3) captan (133-06- 2) (WO 02/12172), (5.4) chlorothalonil (1897-45-6), (5.5) copper hydroxide (20427-59-2), (5.6) copper naphthenate (1338-02-9), ( 5.7) copper oxide (1317-39-1), (5.8) copper oxychloride (1332-40-7), (5.9) copper sulfate (2+) (7758-98-7), (5.10) diclofluanid ( 1085-98-9), (5.11) ditianon (3347-22-6), (5.12) dodine (2439-10-3), (5.13) free base dodine, (5.14) ferbam (14484-64-1) , (5.15) fluorofolpet (719-96-0), (5.16) folpet (133-07-3), (5.17) guazatin (108173-90-6), (5.18) guazatin acetate, (5.19) iminoctadine (13516 -27-3), (5.20) iminoctadine albesylate (169202-06-6), (5.21) iminoctadine triacetate (57520-17-9), (5.22) mancobre (53988-93-5), (5.23) mancozeb (8018-01-7), (5.24) maneb (12427-38-2), (5.25) meth (9006-42-2), (5.26) meth zinc (9006-42-2), (5.27) oxin- copper (10380-28-6), (5.28) propamidine (104- 32-5), (5.29) propineb (12071-83-9), (5.30) sulfur and sulfur preparations including calcium polysulfide (7704-34-9), (5.31) strip (137-26-8), ( 5.32) tolylfluanid (731-27-1), (5.33) zineb (12122-67-7) and (5.34) ziram (137-30-4). (6) Compounds capable of inducing a host defense, for example, (6.1) acibenzolar-S-methyl (135158-54-2), (6.2) isothianyl (224049-04-1), (6.3) probenazole (27605 -761) and (6.4) thiadinyl (223580-51-6). (7) Amino acid inhibitors and / or protein biosynthesis, for example, (7.1) andoprim (23951-85-1), (7.2) blasticidin-S (2079-00-7), (7.3) ciprodinil (121552- 61-2), (7.4) kasugamycin (6980-18-3), (7.5) kasugamycin hydrate hydrochloride (19408-46-9), (7.6) mepanipyrim (110235-47-7), (7.7) pyrimethanil ( 53112-28-0) and (7.8) 3- (5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl) quinoline (861647-32-7) (WO2005070917). (8) Inhibitors of ATP production, for example, (8.1) fentin acetate (900-958), (8.2) fentin chloride (639-58-7), (8.3) fentin hydroxide (76-87- 9) and (8.4) siltiofam (175217-20-6). (9) Inhibitors of cell wall synthesis, for example (9.1) bentiavalicarb (17740668-7), (9.2) dimetomorf (110488-70-5), (9.3) flumorf (211867-47-9), (9.4) iprovalicarb (14092317-7), (9.5) mandipropamid (374726-62-2), (9.6) polyoxins (11113-80-7), (9.7) polyoxorin (22976-86-9), (9.8) validamicin A (37248- 47-8) and (9.9) valiphenalate (283159-94-4; 283159-90-0). (10) Inhibitors of membrane lipid synthesis and, for example, (10.1) biphenyl (92-52-4), (10.2) chloroneb (2675-77-6), (10.3) dichloran (99-30-9) , (10.4) edifenfos (17109-49-8), (10.5) etridiazole (2593-15-9), (10.6) iodocarb (55406-53-6), (10.7) iprobenfos (26087-47-8), ( 10.8) isoprothiolane (50512-35-1), (10.9) propamocarb (25606-41-1), (10.10) propamocarb hydrochloride (25606-41-1), (10.11) protiocarb (19622-08-3), ( 10.12) pyrazophos (13457-18-6), (10.13) quintozene (82-68-8), (10.14) tecnazene (117-18-0) and (10.15) tolclofos-methyl (5701804-9). (11) Inhibitors of melanin biosynthesis, for example (11.1) carpropamid (104030-54-8), (11.2) diclocimet (139920-32-4), (11.3) phenoxanil (115852-48-7), (11.4) ) phthalide (27355-22-2), (11.5) pyrokylone (57369-32-1), (11.6) tricyclazole (41814-78-2) and (11.7) 2,2,2-trifluoroethyl {3-methyl-1 - [(4-methylbenzoyl) amino] butan-2-yl} carbamate (851524-22-6) (WO2005042474). (12) Nucleic acid synthesis inhibitors, for example, (12.1) benalaxyl (71626-114), (12.2) benalaxyl-M (kiralaxyl) (98243-83-5), (12.3) bupirimate (41483-43-6 ), (12.4) clozilacon (67932-85-8), (12.5) dimethyrimol (5221-53-4), (12.6) ethirimol (23947-60-6), (12.7) furalaxil (57646-30-7), (12.8) himexazole (10004-44-1), (12.9) metalaxyl (57837-19-1), (12.10) metalaxyl-M (mefenoxam) (70630-17-0), (12.11) ofurace (58810-48- 3), (12.12) oxadixyl (77732-09-3) and (12.13) oxolinic acid (14698-29-4). (13) Signal transduction inhibitors, for example, (13.1) clozolinate (84332-86-5), (13.2) fenpiclonil (74738-17-3), (13.3) fludioxonil (131341-86-1), (13.4 ) iprodione (36734-19-7), (13.5) procimidone (32809-16-8), (13.6) quinoxifen (124495-18-7) and (13.7) vinclozolin (50471-44-8). (14) Compounds capable of acting as a decoupler, for example (14.1) binapacril (485-31-4), (14.2) dinocap (131-72-6), (14.3) ferimzone (89269-64-7), ( 14.4) fluazinam (79622-59-6) and (14.5) meptildinocap (131-72-6). (15) Other compounds, for example (15.1) bentiazole (21564-17-0), (15.2) betoxazin (163269-30-5), (15.3) capsimicin (70694-08-5), (15.4) carvone (99 -49-0), (15.5) quinometionat (2439-01-2), (15.6) pyrophenone (clazafenone) (688046-61-9), (15.7) cufraneb (11096-18-7), (15.8) ciflufenamid ( 180409-60-3), (15.9) cymoxanil (57966-95-7), (15.10) cyprosulfamide (221667-31-8), (15.11) dazomet (533-74-4), (15.12) debacarb (62732- 91-6), (15.13) dichlorophen (97-23-4), (15.14) diclomezin (62865-36-5), (15.15) difenzoquat (4986687-7), (15.16) difenzoquat methyl sulfate (43222-48- 6), (15.17) diphenylamine (122-39-4), (15.18) ecomato, (15.19) fenpyrazamine (473798-59-3), (15.20) flumetover (154025-04-4), (15.21) fluoroimide (41205 -21-4), (15.22) flusulfamide (106917-52-6), (15.23) flutianyl (30490025-2), (15.24) phosethyl aluminum (39148-24-8), (15.25) phosethyl calcium, ( 15.26) phosethyl-sodium (3914816-8), (15.27) hexachlorobenzene (118-74-1), (15.28) irumamycin (81604-73-1), (15.29) metasulfocarb (66952 -49-6), (15.30) methyl isothiocyanate (556-61-6), (15.31) metrafenone (220899-03-6), (15.32) mildiomycin (67527-71-3), (15.33) natamycin (7681 -93-8), (15.34) nickel dimethyldithiocarbamate (15521-65-0), (15.35) nitrotal-isopropyl (10552-74-6), (15.36) octylinone (26530-20-1), (15.37) oxamocarb (917242-12-7), (15.38) oxyphenol (34407-87-9), (15.39) pentachlorophenol and salts (87-86-5), (15.40) phenothrin, (15.41) phosphoric acid and its salts (13598- 36-2), (15.42) propamocarb-phosethylate, (15.43) propanosine-sodium (88498-02-6), (15.44) proquinazid (189278-12-4), (15.45) pirimorf (868390-90-3), (15.45e) (2E) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one (1231776 -28-5), (15.45z) (2Z) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en -1-one (1231776-29-6), (15.46) pyrrolnitrine (1018-71-9) (EP-A 1 559 320), (15.47) tebufloquina (376645-78-2), (15.48) keyboard software (76280 -91-6), (15.49) tolnifanide (304911-98-6), (15.50) triazoxide (72459 -58-6), (15.51) triclamide (70193-21-4), (15.52) zarilamid (84527-51-5), (15.53) (3S, 6S, 7R, 8R) -8- benzyl-3- [ ({3 - [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl} carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl 2-methylpropanoate (517875-34 -2) (WO2003035617), (15.54) 1- (4- {4 - [(5R) -5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] - 1,3-thiazol-2-yl} piperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone (1003319-79-6) (WO 2008013622) , (15.55) 1- (4- {4- [(5S) -5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazole- 2-yl} piperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone (1003319-80-9) (WO 2008013622), (15.56) 1- (4- {4- [5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazol-2-yl} piperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone (1003318-67-9) (WO 2008013622), (15.57) 1- (4-methoxyphenoxy) -3,3- dimethylbutan-2-yl 1H-imidazole-1-carboxylate (111227-17-9), (15.58) 2,3,5,6-tetrachloro-4- (methylsulfonyl) pyridine (13108-52-6), (1 5.59) 2,3-dibutyl-6-chlorothieno [2,3-d] pyrimidin-4 (3H) -one (221451-58-7), (15.60) 2,6-dimethyl-1H, 5H- [1, 4] dithino [2,3-c: 5,6-c '] dipyrrole- 1,3,5,7 (2H, 6H) -tetrone, (15.61) 2- [5-methyl-3- (trifluoromethyl) - 1H-pyrazol-1-yl] -1- (4- {4 - [(5R) -5-phenyl-4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazol-2 -yl} piperidin-1-yl) ethanone (1003316-53-7) (WO 2008013622), (15.62) 2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] -1- ( 4- {4 - [(5S) -5-phenyl-4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazol-2-yl} piperidin-1-yl) ethanone (1003316 -54-8) (WO 2008013622), (15.63) 2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] -1- {4- [4- (5-phenyl-4, 5-dihydro-1,2-oxazol-3-yl) -1,3-thiazol-2-yl] piperidin-1-yl} ethanone (1003316-51-5) (WO 2008013622), (15.64) 2-butoxy -6-iodo-3-propyl-4H-chromen-4-one, (15.65) 2-chloro-5- [2-chloro-1- (2,6-difluoro-4-methoxyphenyl) -4-methyl-1H -imidazol-5-yl] pyridine, (15.66) 2-phenylphenol and salts (90-43-7), (15.67) 3- (4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin -1-yl) quinoline (861647-85-0) (WO2005070917), (15.68) 3,4,5-tric loropyridine-2,6-dicarbonitrile (17824-85-0), (15.69) 3- [5- (4-chlorophenyl) -2,3-dimethyl-1,2-oxazolidin-3-yl] pyridine, (15.70) 3-chloro-5- (4-chlorophenyl) -4- (2,6-difluorophenyl) -6-methylpyridazine, (15.71) 4- (4-chlorophenyl) -5- (2,6-difluorophenyl) -3,6 - dimethylpyridazine, (15.72) 5-amino-1,3,4-thiadiazole-2-thiol, (15.73) 5-chloro-N'-phenyl-N '- (prop-2- in-1-yl) thiophene- 2-sulfonohydrazide (134-31-6), (15.74) 5-fluoro-2 - [(4-fluorobenzyl) oxy] pyrimidin-4-amine (1174376-11-4) (WO2009094442), (15.75) 5-fluoro -2 - [(4-methylbenzyl) oxy] pyrimidin-4-amine (1174376-25-0) (WO2009094442), (15.76) 5-methyl-6-octyl [1,2,4] triazole [1,5- a] pyrimidin-7-amine, (15.77) ethyl (2Z) -3-amino-2-cyano-3-phenylprop-2-enoate, (15.78) N '- (4 - {[3- (4-chlorobenzyl) -1,2,4-thiadiazol-5-yl] oxy} -2,5-dimethylphenyl) -N-ethyl-N-methylimidoformamide, (15.79) N- (4-chlorobenzyl) -3- [3-methoxy-4 - (prop-2-in-1-yloxy) phenyl] propanamide, (15.80) N - [(4-chlorophenyl) (cyano) methyl] -3- [3-methoxy-4- (prop-2-in-1 -yloxy) phenyl] propanamide, (15.81) N - [(5-bromo-3-chloropyr ridin-2-yl) methyl] -2,4-dichloropyridine-3-carboxamide, (15.82) N- [1- (5-bromo-3-chloropyridin-2-yl) ethyl] -2,4-dichloropyridine-3 -carboxamide, (15.83) N- [1- (5-bromo-3-chloropyridin-2-yl) ethyl] -2-fluoro-4-iodopyridine-3-carboxamide, (15.84) N - {(E) - [ (cyclopropylmethoxy) imino] [6- (difluoromethoxy) -2,3-difluorophenyl] methyl} -2-phenylacetamide (221201-92-9), (15.85) N - {(Z) - [(cyclopropylmethoxy) imino] [6 - (difluoromethoxy) -2,3-difluorophenyl] methyl} -2-phenylacetamide (221201-92-9), (15.86) N '- {4 - [(3-tert-butyl-4-cyano-1,2- thiazol-5-yl) oxy] -2-chloro-5-methylphenyl} -N- ethyl-N-methylimidoformamide, (15.87) N-methyl-2- (1 - {[5-methyl-3- (trifluoromethyl) - 1H-pyrazol-1-yl] acetyl} piperidin-4-yl) -N- (1,2,3,4-tetrahydronaphthalen-1-yl) -1,3-thiazole-4-carboxamide (922514-49-6 ) (WO 2007014290), (15.88) N-methyl-2- (1 - {[5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] acetyl} piperidin-4-yl) -N- [ (1R) -1,2,3,4-tetrahydronaphthalen-1-yl] -1,3-thiazole-4-carboxamide (922514-07-6) (WO 2007014290), (15.89) N-methyl-2- ( 1 - {[5-methyl-3- (trifluoromethyl) - 1H-pyrazol-1-yl] acetyl} piperidin-4-yl) -N - [(1S) -1,2,3,4-tetrahydronaphthalen-1-yl] -1,3-thiazole-4-carboxamide (922514 -48-5) (WO 2007014290), (15.90) pentyl {6 - [({[(1-methyl-1H-tetrazol-5-yl) (phenyl) methylidene] amino} oxy) methyl] pyridin-2-yl } carbamate, (15.91) phenazine-1-carboxylic acid, (15.92) quinolin-8-ol (134-31-6), (15.93) quinolin-8-ol sulfate (2: 1) (134-31-6 ) and (15.94) tert-butyl {6- [({[(1-methyl-1H-tetrazol-5-yl) (phenyl) methylene] amino} oxy) methyl] pyridin-2-yl} carbamate. (16) Other compounds, for example (16.1) 1-methyl-3- (trifluoromethyl) -N- [2'- (trifluoromethyl) biphenyl-2-yl] -1H-pyrazole-4-carboxamide, (16.2) N- (4'-chlorobiphenyl-2-yl) -3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (16.3) N- (2 ', 4'-dichlorobiphenyl-2-yl) -3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (16.4) 3- (difluoromethyl) -1-methyl-N- [4'- (trifluoromethyl) biphenyl-2-yl] -1H-pyrazole-4 -carboxamide, (16.5) N- (2 ', 5'-difluorobiphenyl-2-yl) -1- methyl-3- (trifluoromethyl) -1H-pyrazole-4-carboxamide, (16.6) 3- (difluoromethyl) -1 -methyl-N- [4 '- (prop- 1-in-1-yl) biphenyl-2-yl] -1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.7) 5- fluoro-1,3-dimethyl-N- [4 '- (prop-1-in-1-yl) biphenyl-2-yl] -1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.8) 2-chloro-N- [4 '- (prop-1-in-1-yl) biphenyl-2-yl] pyridine-3-carboxamide (known from WO 2004/058723), (16.9) 3 - (difluoromethyl) -N- [4 '- (3,3-dimethylbut-1-in-1-yl) biphenyl-2-yl] -1-methyl-1H-pyrazole-4-carboxamide (known after WO 2004/058723), (16.10) N- [4 '- (3,3-dimethylbut-1-in-1-yl) biphenyl-2-yl] -5-fluoro-1,3-dimethyl-1H - pyrazole-4-carboxamide (known from WO 2004/058723), (16.11) 3- (difluoromethyl) -N- (4'-ethynylbiphenyl-2-yl) -1-methyl-1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.12) N- (4'-ethynylbiphenyl-2-yl) -5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.13) 2-chloro-N- (4'-ethynylbiphenyl-2-yl) pyridine-3-carboxamide (known from WO 2004/058723), (16.14) 2-chloro-N- [ 4 '- (3,3-dimethylbut-1- in-1-yl) biphenyl-2-yl] pyridine-3-carboxamide (known from WO 2004/058723), (16.15) 4- (difluoromethyl) -2 -methyl-N- [4 '- (trifluoromethyl) biphenyl-2-yl] -1,3-thiazole-5-carboxamide (known from WO 2004/058723), (16.16) 5-fluoro-N- [4 '- (3-hydroxy-3-methylbut-1-in-1-yl) biphenyl-2-yl] - 1,3-dimethyl-1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.17) 2-chloro-N- [4 '- (3-hydroxy-3-methylbut-1-in-1-yl) biphenyl-2-yl] pyridine-3-carboxamide (known from WO 2004/058723), (16.18) 3- (difluoromethyl) -N- [4 '- (3-methoxy-3-methylbut-1-in-1-yl) biphenyl- 2-yl] - 1-methyl-1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.19) 5-fluoro- N- [4 '- (3-methoxy-3-methylbut-1 -in-1-yl) biphenyl-2-yl] -1,3-dimethyl-1H-pyrazole-4-carboxamide (known from WO 2004/058723), (16.20) 2-chloro-N- [4 ' - (3-methoxy-3-methylbut-1-in-1-yl) biphenyl-2-yl] pyridine-3-carboxamide (known from WO 2004/058723), (16.21) (5-bromo-2- methoxy-4-methylpyridin-3-yl) (2,3,4-trimethoxy-6-methylphenyl) methanone (known from EP-A 1 559 320), (16.22) N- [2- (4 - {[ 3- (4-chlorophenyl) prop-2-in-1-yl] oxy} -3-methoxyphenyl) ethyl] -N2- (methylsulfonyl) valinamide (220706-93-4), (16.23) 4-oxo-4- [(2-phenylethyl) amino] butanoic acid and (16.24) but-3-in-1-yl {6 - [({[(Z) - (1-methyl-1H-tetrazol-5-yl) (phenyl) methylene] amino} oxy) methyl] pyridin-2-yl} carbamate, N- [9- (dichloromethylene) -1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromet il) -1-methyl-1H-pyrazole-4-carboxamide and 3-difluoromethyl -1-methyl-1H-pyrazole-4-carboxylic acid [2- (2,4-dichlorophenyl) -2-methoxy-1-methyl- ethyl] -amide.
Where all mixing partners referred to as classes (1) to (16) can, if their functional groups allow this, optionally, form salts with appropriate bases or acids;
Being bactericidal, which can be mentioned as follows: bronopol, diclorfen, nitrapirin, nickel dimethyldithylcarbamate, kasugamycin, octyline, furanecarboxylic acid, oxytetracycline, probenazole, streptomycin, tec-loftalam, copper sulfate and other copper preparations.
Being insecticides, acaricides and nematicides, which can be mentioned as follows: (1) Acetylcholinesterase (AChE) inhibitors, eg carbamates, eg alanicarb, aldicarb, aldoxicarb, alixicarb, aminocarb, bendiocarb, benfuracarb, snuff , butacarb, butocarboxim, butoxicarboxim, carbaril, carbofuran, carbosulfan, cloetocarb, dimethilan, ethiofencarb, fenobucarb, fenothiocarb, formetanato, furatiocarb, isoprocarb, metam-sodium, metiocarb, metomil, metolcarbicarb, propolcarbocar, oxol , trimetacarb, XMC, and xylylcarb; or organophosphates, e.g. acephate, azametiphos, azinphos (-methyl, -ethyl), bromophos-ethyl, bromphenvinfos (-methyl), butathiophes, cadusaphos, carbofenotion, chlorethoxyphos, chlorfenvinphos, chlormefos, chlorpyrifos (-methyl / -ethyl), coumaphos, cyphaphos, cyphaphos, cyphaphos, cyphaphos, cyphaephians, chlorfenvinfos, demeton-S-methyl, demeton-S-methylsulfon, dialiphos, diazinon, diclofention, dichlorvos / DDVP, dicrotofos, dimetoate, dimethilvinfos, dioxabenzofos, disulfoton, EPN, etion, etoprofos, etrimfos, fenifos, fenifos, fam, fention, flupirazofos, fonofos, formotion, fosmetilan, fostiazato, heptenofos, iodofenfos, iprobenfos, isazofos, isofenfos, isopropil, O-salicylato, isoxation, malation, mecarbam, metacrifos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos, metamidofos methyl, paration (-methyl / -ethyl), fentoate, phorate, fosalone, fosmet, fosfamidon, fosfocarb, foxim, pirimiphos (-methyl / -ethyl), profenofos, propafos, propetamfos, protiofos, protoato, piraclofos, piridafention, piridation, quinalfos, sebufos, sulfotep, sulprofos , tebupirimfos, temefos, terbufos, tetrachlorvinfos, tiometon, triazofos, triclorfon, vamidotion, and imiciafos. (2) GABA-linked chlorine channel antagonists, for example organochlorines, eg camfeclor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane, and methoxychlor; or fiproles (phenylpyrazoles), e.g. acetoprole, etiprole, fipronil, pirafluprole, pyriprole, and vaniliprole. (3) Voltage-dependent sodium channel modulators / sodium channel blockers, for example pyrethroids, eg acrinatrin, aletrin (d-cis-trans, d-trans), beta-cifluthrin, bifentrin, bioaletrin, bioaletrin S-cyclopentyl isomer, bioethanometrin, biopermetrin, bioresmetrin, clovaportrin, cis-cyipermetrin, cis-resmetrin, cis-permetrin, clocithrin, cycloprotrin, ciflutrin, cihalotrin, cypermethrin (alpha-, beta-, teta-, zeta-, zeta-, zeta-, zeta-, zeta-, zeta-, zeta-, zeta-, zeta-) deltametrin, empentrin (isomer 1R), esfenvalerate, etofenprox, fenflutrin, fenpropatrin, fenpiritrin, fenvalerate, flubrocitrinate, flucitrinate, flufenprox, flumetrin, fluvalinate, fubfenprox, gamma-cihalotrin, im-cihalotrin, ci-trotrotrin, ci-trotrin trans-, fenotrin (trans isomer1R), praletrin, proflutrin, protrifenbut, piresmethrin, resmetrin, RU 15525, silafluofen, tau- fluvalinate, teflutrin, teraletrin, tetrametrin (isomer1R), tralometrin, pyrethrin, pyrethrin, trans eflusilana t; DDT; or methoxychlor. (4) Nicotinergic acetylcholine receptor agonists / antagonists, for example, for example, chloronicotinyl acetamiprid, clothianidin, dinotefuran, imidacloprid, imidaclotiz, nitenpiram, nitiazine, thiacloprid, thiamethoxam, AKD-1022; or nicotine, bensultap, cartap, tiosultap-sodium, and thiocilam. (5) Allosteric modulators of acetylcholine receptors (agonists), such as, for example, spinosyns, for example, spinosad and espinetoram. (6) Chlorine channel activators, for example, mectins / macrolides, eg, abamectin, emamectin, emamectin benzoate, ivermectin, lepimectin, and milbemectin; or juvenile hormone analogues, eg, hydroprene, kinoprene, methoprene, epophenonane, triprene, phenoxycarb, pyriproxifen, and diophenolan. (7) Active ingredients with unknown or non-specific mechanisms of action, for example, gasifying agents, eg, methyl bromide, chloropicrin and sulfuryl fluoride; selective insecticides, e.g. cryolite, pimetrozine, pyrifluquinazon and flonicamid; or mite growth inhibitors, e.g. clofentezine, hexithiazox, ethoxazole. (8) Oxidative phosphorylation inhibitors, ATP disruptors, for example, diafentiuron; organotine compounds, eg, azocyclotine, cyhexatin and fenbutatin oxide; or propargite, tetradifon. (9) Decouplers of oxidative phosphorylation acting by interrupting the H proton gradient, for example, chlorfenapyr, binapacril, dinobuton, dinocap and DNOC. (10) Microbial disruptors of the insect gut membrane, for example, strains of Bacillus thuringiensis. (11) Chitin biosynthesis inhibitors, for example benzoylureas, eg, bistrifluron, chlorfluazuron, diflubenzuron, fluazuron, flucicloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, trifururon, trifururon, penflururon, trifururon, penflururon, trifururon, penflururon, trifururon, penifururon, trifururon, trifururon, penifururon, trifururon, penifururon, trifururon. (12) Buprofezin. (13) Seedling disrupters, for example, cyromazine. (14) Ecdysone agonists / disruptors, for example diacylhydrazines, for example, chromafenozide, halofenozide, methoxyfenozide, tebufenozide, and Fufenozide (JS118); or azadiraquitine. (15) Octopaminergic agonists, for example, amitraz. (16) site III electron transport inhibitors / site II electron transport inhibitors, for example, hydramethylnon; acequinocil; fluacripyrim; or ciflumetofen and cienopirafen. (17) Electron transport inhibitors, for example site I electron transport inhibitors, from the METI acaricide group, eg, fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpirad, tolfenpirad, and rotenone; or voltage-dependent sodium channel blockers, e.g. indoxacarb and metaflumizone. (18) Fatty acid biosynthesis inhibitors, for example, derivatives of tetronic acid, for example, spirodiclofen and spiromesifen; or tetramic acid derivatives, eg, spirotetramat. (19) Neuronal inhibitors with a mechanism of action, eg. biphenazate. (20) Ryanodine receptor effectors, for example, diamides, e.g. flubendiamide, (R), (S) -3-chloro-N1- {2-methyl-4- [1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl] phenyl} -N2- (1-methyl -2-methylsulfonylethyl) phthalamide, chlorantraniliprole (Rinaxipir), or Ciantraniliprole (Ciazipir). (21) Other active ingredients with a mechanism of action, for example, amidoflumet, benclothiaz, benzoxide, bromopropylate, buprofezin, quinometionat, clordimeform, chlorobenzylate, clothiazoben, cycloprene, dicofol, dicyclilyl, phenoxacrim, fentrifinil, flenzen, flenzen japonilure, methoxyzazone, petroleum, potassium oleate, pyridalil, sulfluramid, tetrasul, triaratene or verbutine; or one of the following active compounds 4 - {[(6-bromopyrid-3-yl) methyl] (2-fluoroethyl) amino} furan-2 (5H) -one, 4 - {[(6-fluoropyrid-3-yl) methyl] (2,2-difluoroethyl) amino} furan-2 (5H) - one, 4 - {[(2-chloro-1,3-thiazol-5-yl) methyl] (2-fluoroethyl) amino} furan- 2 (5H) -one, 4 - {[(6-chloropyrid-3-yl) methyl] (2-fluoroethyl) amino} furan-2 (5H) -one, 4 - {[(6-chloropyrid-3-yl ) methyl] (2,2-difluoroethyl) amino} furan-2 (5H) -one (all known from WO 2007/115644), 4 - {[(5,6-dichloropyrid-3-yl) methyl] ( 2-fluoroethyl) amino} furan-2 (5H) -one (known from WO 2007/115646), 4 - {[(6-chloro-5-fluoropyrid-3-yl) methyl] (methyl) amino} furan -2 (5H) -one, 4 - {[(6-chloro-5-fluoropyrid-3-yl) methyl] (cyclopropyl) amino} furan-2 (5H) -one (both from WO 2007/115643) , 4 - {[(6-chloropyrid-3-yl) methyl] (cyclopropyl) amino} furan-2 (5H) -one, 4 - {[(6-chloropyrid-3-yl) methyl] (methyl) amino} furan-2 (5H) - one (both from EP-A-0 539 588), [(6-chloropyridin-3-yl) methyl] (methyl) oxido-À4-sulfanilidene cyanamide, [1- (6- chloropyridin-3 -yl) ethyl] (methyl) oxido-À4-sulfanilidene cyanamide (both from WO 2007/149134) and their diastereomers (A) and (B)
(also known from WO 2007/149134), [(6-trifluoromethylpyridin-3-yl) methyl] (methyl) oxide-À4-sulfanylidene cyanamide (known from WO 2007/095229), or [1- (6 - trifluoromethylpyridin-3-yl) ethyl] (methyl) oxide-À4-sulfanilidene cyanamide (known from WO 2007/149134) and its diastereomers (c) and (D), namely sulfoxaflor (also known from WO 2007 / 149134)

Being molluscicides, which can be mentioned are metaldehyde and metiocarb.
Protective agents that can be mentioned are: (1) Derivatives of heterocyclic carboxylic acids, for example dichlorophenylpyrazolin-3-carboxylic acid derivatives, e.g. 1- (2,4-dichlorophenyl) -5- (ethoxycarbonyl) - 5-methyl-4,5-dihydro-1H-pyrazole-3-carboxylic acid, diethyl 1- (2,4-dichlorophenyl) -4,5- dihydro-5-methyl-1H-pyrazole-3,5-dicarboxylate ("mefenpir-diethyl"), and similar compounds known from WO 91/07874; for example dichlorophenylpyrazole carboxylic acid derivatives, e.g. ethyl 1- (2,4-dichlorophenyl) -5-methyl-1H-pyrazole-3-carboxylate, ethyl 1- (2,4-dichlorophenyl) -5-isopropyl-1H-pyrazole-3-carboxylate, ethyl 5-tert -butyl-1- (2,4-dichlorophenyl) -1H-pyrazole-3-carboxylate and similar compounds known from EP-A 0 333 131 and EP-A 0 269 806; for example, 1,5-diphenylpyrazole-3 carboxylic acid derivatives, e.g. ethyl 1- (2,4-dichlorophenyl) -5-phenyl-1H-pyrazole-3-carboxylate, methyl 1- (2-chlorophenyl) -5-phenyl-1H-pyrazole-3-carboxylate, and similar compounds known from EP-A 0 268 554; for example triazolecarboxylic acid derivatives, e.g. fenclorazole, fenclorazole-ethyl, and similar compounds known from EP-A 0 174 562 and EP-A 0 346 620; for example 2-isoxazoline-3-carboxylic acid derivatives, e.g. ethyl 5- (2,4-dichlorobenzyl) -4,5-dihydro-1,2-oxazole-3-carboxylate, ethyl 5-phenyl-4,5-dihodro-1,2-oxazole-3-carboxylate and similar compounds known from WO 91/08202, or 5,5-diphenyl-4,5-dihydro-1,2-oxazole-3-carboxylic acid, ethyl 5,5-diphenyl-4,5-dihydro-1,2- oxazole-3-carboxylate (“isoxadifen-ethyl”), propyl 5,5-diphenyl-4,5-dihydro-1,2-oxazole-3-carboxylate, ethyl 5- (4-fluorophenyl) -5-phenyl-4 , 5-dihydro-1,2-oxazole-3-carboxylate known from WO 95/07897. (2) Derivatives of 8-quinolinol, for example derivatives of (quinolin-8-yloxy) acetic acid, e.g. heptan-2-yl [(5-chloroquinolin-8-yl) oxy] acetate (“cloquintocet-mexil”), 4-methylpentan-2-yl [(5-chloroquinolin-8-yl) oxy] acetate, 4- ( allyloxy) butyl [(5-chloroquinolin-8-yl) oxy] acetate, 1- (allyloxy) propan-2-yl [(5-chloroquinolin-8-yl) oxy] acetate, ethyl [(5-chloroquinolin-8- il) oxy] acetate, methyl [(5-chloroquinolin-8-yl) oxy] acetate, ally [(5-chloroquinolin-8-i) oxy] acetate, 2 - {[ropylidenoamino] oxy} ethyl [(5-chloroquinolinolin -8-yl) oxy] acetate, 2-oxopropyl [(5-chloroquinolin-8-yl) oxy] acetate, and similar compounds known from EP-A 0 086 750, EP-A 0 094 349, EP-A 0 191 736 or EP-A 0 492 366, as well as [(5-chloroquinolin-8-yl) oxy] acetic acid, its hydrates and salts, e.g. the lithium, sodium, potassium, calcium, magnesium, aluminum, iron, ammonia, quartz ammonia, sulfonium or phosphonium salts as known from WO 02/34048; for example derivatives of [(5-chloroquinolin-8-yl) oxy] malonic acid, eg diethyl [(5-chloroquinolin-8-yl) oxy] malonate, dially [(5-chloroquinolin-8-yl) oxy ] malonate, ethyl methyl [(5-chloroquinolin-8-yl) oxy] malonate, and similar compounds known from EP-A 0 582 198. (3) Dichloroacetamides, which are often used as pre-emergence protective agents ( active soil protectors), eg “Dichlormid” (N, N-diallyl-2,2-dichloroacetamide), “R-29148” (3dichloroacetyl-2,2,5-trimethyl-1,3-oxazolidine) and “R-28725” (3-dichloroacetyl- 2,2, -dimethyl- 1,3-oxazolidine) both from Stauffer, “benoxacor” (4-dichloroacetyl-3,4-dihydro-3-methyl-2H-1,4-benzoxazine), “PPG-1292” (N-allyl-N - [(1,3-dioxolan-2-yl) -methyl] -dichloroacetamide) from PPG Industries, “DKA-24” (N-allyl-N - [(allyaminocarbonyl) methyl] -dichloroacetamide) from Sagro-Chem, “AD- 67” or “MON 4660” (3-dichloroacetyl-1-oxa-3-aza-spiro [4,5] dean) from Nitrokemia and Monsanto, “TI-35” (1-dichloroacetyl -azepano) of TRI-Chemical RT, “diclonon” (dicyclonon) or “BAS145138” or “LAB145138” (3-dichloroacetyl-2,5,5-trimethyl-1,3-diazabicyclo [4.3.0] nonana) , "Furilazole" or "MON 13900" [(RS) -3-dichloroacetyl-5- (2-furyl) -2,2-dimethyloxazolidine], as well as its (R) isomer. (4) Acylsulfonamides, for example, N-acylsulfonamide of the formula (II)
and its salts (known from WO 97/45016), wherein R1 represents (C1-C6) alkyl, which is unsubstituted or mono- to tri-substituted by substituents selected from the group consisting of halogen, alkyl ( C1-C4), alkoxy (C1-C6) and haloalkoxy (C1-C4) alkylthio; R2 represents halogen, (C1-C4) alkyl, (C1-C4) alkoxy, CF3; m is 1 or 2; or for example 4- (benzoylsulfamoyl) benzamides of the formula (III)
and its salts (known from WO 99/16744), wherein R3, R4 independently of one represents hydrogen, (C1-C6) alkyl, (C3-C6) alkenyl, (C3-C6) alkynyl, (C3-C6) cycloalkyl, R5 represents halogen, (C1-C4) alkyl, (C1-C4) haloalkyl or (C1-C4) alkoxy n is 1 or 2, in particular compounds of the formula (III), where R3 = cyclopropyl, R4 = hydrogen and R5n = 2-OMe, (“cyprosulfamide”), R3 = cyclopropyl, R4 = hydrogen and R5n = 5-Cl-2-OMe, R3 = ethyl, R4 = hydrogen and R5n = 2-OMe, R3 = isopropyl, R4 = hydrogen and R5n = 5-Cl-2-OMe, R3 = isopropyl, R4 = hydrogen and R5n = 2-OMe. or for example benzoylsulfamoylphenylureas of the formula (IV)
(known from EP-A 0 365 484), wherein R6, R7 independently of each other represents hydrogen, (C1-C8) alkyl, (C3-C6) alkenyl, (C3-C6) alkynyl, R8 represents halogen, ( C1-C4) alkyl, (C1-C4) alkoxy, CF3 n is 1 or 2; in particular 1- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3-methyl urea, 1- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3,3-dimethyl urea, 1- [4- ( N-4,5-dimethylbenzoylsulfamoyl) phenyl] -3-methyl urea. (5) Hydroxy aromatic compounds and aromatic-aliphatic carboxylic acid derivatives, e.g. ethyl 3,4,5-triacetoxybenzoate, 4-hydroxy-3,5-dimethoxybenzoic acid, 3,5-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid, 4-fluoro-2-hydroxybenzoic acid, 2-hydroxycinnamic acid, 2, 4-dichlorokinamic acid (cf. WO 2004/084631, WO 2005/015994, WO 2005/016001). (6) 1,2-Dihydroquinoxalin-2-ones, e.g. 1-methyl-3- (2-thienyl) -1,2-dihydroquinoxalin-2-one, 1-methyl-3- (2-thienyl) -1,2-dihydrochinoxalin-2-thione, 1- (2-aminoethyl ) -3- (2-thienyl) -1,2-dihydroquinoxalin-2-one hydrochloride, 1- (2-methylsulfonylaminoethyl) -3- (2-thienyl) -1,2-dihydroquinoxalin-2-one (cf. WO 2005/112630). (7) Diphenylmethoxyacetic acid derivatives, e.g. methyl (diphenylmethoxy) acetate (CAS-Reg. No. 41858-19-9), ethyl (diphenylmethoxy) acetate or (diphenylmethoxy) acetic acid (cf. WO 98/38856). (8) Compounds of the formula (V)
or its salts (known from WO 98/27049), wherein R9 represents halogen, (C1-C4) alkyl, (C1-C4) haloalkyl, (C1-C4) alkoxy, (C1-C4) haloalkoxy, R10represents hydrogen or (C1-C4) alkyl, R10 represents hydrogen, in each case unsubstituted or mono- to tri-substituted (C1-C8) alkyl, (C2-C4) alkenyl, (C2-C4) alkynyl, or aryl, where the substituents are selected from the group consisting of halogen and (C1-C8) alkoxy, s is 0, 1 or 2. (9) 3- (5-Tetrazolylcarbonyl) -2-quinolones, e.g. 1,2-dihydro-4-hydroxy-1-ethyl-3- (5-tetrazolylcarbonyl) -2-quinolone (CAS-Reg. No. 219479-18-2), 1,2-dihydro-4-hydroxy-1 -methyl-3- (5-tetrazolyl-carbonyl) -2-quinolone (CAS-Reg. No. 95855-00-8) (cf. WO 99/00020). (10) Compounds of the formula (VI-a) and (VI-b)
(known from WO 2007/023719 and WO 2007/023764), where R12 represents halogen, (C1-C4) alkyl, methoxy, nitro, cyano, CF3, OCF3, Y, Z independently represents O or S, t is 0, 1, 2, 3 or 4, R13 represents (C1-C16) alkyl, (C2-C6) alkenyl, aryl, benzyl, halogenobenzyl, R14 represents hydrogen or (C1-C6) alkyl. (11) oxyimino compounds, known as seed treatment agents, e.g. “Oxabetrinyl” [(Z) -1,3-dioxolan-2-ylmethoxyimino (phenyl) acetonitrile], “fluxophenim” [1- (4-chlorophenyl) -2,2,2-trifluoro-1-ethanone-O- ( 1,3-dioxolan-2-ylmethyl) -oxime], and “ciometrinil” or “CGA-43089” [(Z) -cyanomethoxyimino (phenyl) acetonitrile], all known as a seed protection agent for the treatment of sorghum against metolachlor damage. (12) Isothiocromanones, e.g. methyl [(3-oxo-1H-2-benzothiopyran-4 (3H) -ilidene) methoxy] acetate (CAS-Reg. No. 205121-04-6) and similar compounds known from WO 98/13361. (13) Compounds in the group consisting of “naphthalic anhydride” (1,8- naphthalinodicarboxylic acid anhydride), which is known as a phytoprotectant for the treatment of corn (maize) seeds against damage caused by the thiocarbamate herbicides, “fenclorim” (4, 6-dichloro-2-phenylpyrimidine), which is known as a phytoprotective treatment of sown rice seeds against damage by pretilachlor, “flurazole” (benzyl-2-chloro-4-trifluoromethyl-1,3-thiazol-5-carboxylate), which is known as a phytoprotective for treating sorghum seeds against damage by metolachlor and alachlor, “CL 304415” (CAS-Reg. No. 31541-57-8), (4-carboxy-3,4-dihydro-2H- 1- benzopyran-4-acetic acid) from American Cyanamid, which is known as a phytoprotector for corn (corn) against damage caused by imidazolinones, “MG 191” (CAS-Reg. No. 96420-72-3) (2- dichloromethyl -2-methyl-1,3-dioxolana) from Nitrokemia, known as a phytotoxicity protector for corn (maize), “MG-838” (CAS-Reg. No. 133993-74-5), (2-propenyl 1 -oxa-4 -azaspiro [4.5] decane-4-carbodithioate) from Nitrokemia, “Disulfoton” (O, O-diethyl-S-2-ethylethyl phosphorodithioate), “dietolate” (O, O-diethyl-O-phenylphosphorothioate), “mefenate” (4-chlorophenyl-methylcarbamate). (14) Compounds, which in addition to herbicidal activity also exhibit protective activity in crops such as rice, eg. “Dimepiperate” or “MY-93” (S-1-methyl-1-phenylethyl-piperidin-1-carbothioate), which is known as a phytotoxicity protector for rice against damage caused by molinate, “daimuron” or “SK 23 ”[1- (1-methyl-1-phenylethyl) -3-p-tolyl-urea], which is known as a phytotoxicity protector for rice against damage caused by imazosulfuron,“ cumiluron ”=“ JC-940 ”[3 - (2-chlorophenylmethyl) -1- (1-methyl-1-phenyl-ethyl) urea] (cf. JP-A 60-087254), which is known as a phytotoxicity protector for rice against damage from some herbicides, " methoxyphenon "or“ NK 049 ”(3,3'-dimethyl-4-methoxy-benzophenone), which is known as a phytotoxicity protector for rice against damage to some herbicides,“ CSB ”[1-bromo-4- (chloromethylsulfonyl ) benzene] from Kumiai (CAS-Reg. No. 54091-06-4), which is known as a phytotoxicity protector for rice against damage from some herbicides. (15) Compounds, which are mainly used as herbicides, but which also have a phytoprotective activity in some cultures, eg. (2,4-dichlorophenoxy) acetic acid (2,4-D), (4-chlorophenoxy) acetic acid, (R, S) -2- (4-chlor-o-tolyloxy) propionic acid (mecoprop), 4- (2,4-dichlorophenoxy) butyric acid (2,4-DB), (4-chloro-o-tolyloxy) acetic acid (MCPA), 4- (4-chloro-o-tolyloxy) butyric acid, 4- (4 -chlorophenoxy) butyric acid, 3,6-dichloro-2-methoxybenzoic acid (dicamba), 1- (ethoxycarbonyl) ethyl-3,6-dichloro-2-methoxybenzoate (lactidichloro-ethyl).
The plant growth regulators that can be mentioned are chlorocholine and etefon chloride.
Examples of plant nutrients that can be mentioned are usual inorganic or organic fertilizers for supplying plants with macro and / or micronutrients.
In a preferred embodiment, the present invention relates to the use of a composition comprising A) fluopyram and B) one or more of the following insecticides: Chlornicotinil, preferably Imidacloprid, Clotianidin, Tiacloprid and Tiametoxam Pyrethroids, preferably Lambda-Cihalotrin, β-Ciflutrin, Teflutrin, Transflutrin, Deltametrin Carbamates, preferably Metiocarb, Tiodicarb and Aldicarb Organophosphates, preferably Fenamiphos, Fostiazato, Etoprofos.
Anthranilamides, preferably Rinaxipir, Cizazipir Macrolides, preferably Abamectin, Espinosad, Espinetoram Fiproles, preferably Fipronil and Ethiprole Additional nematicides, preferably Oxamil Ketoenol, preferably Spirotetramato, Espirodiclofen and Espiromesifen 4 - [(2,2-difluoro) 2-furyl ) -one - 2-chloro-5-Ethylpyridin (1: 1), Sulfoxaflor, Flonicamid, flupiradifurone Fumigants, and biological control agents, preferably Pasteuria. Nematodes
Fluopiram or fluopyram in combination with the biological control agent Bacillus firmus CNCM I-1582 or fluopyram in combination with at least one agrochemically active compound is particularly useful in the control of plant parasites, nematodes in nematode-resistant plants where nematodes are among the nematodes. following species:
Aphelenchoides spp., Bursaphelenchus spp., Ditylenchus spp., Globodera spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus spp., Trichodorus spp., Tylenchulus spp. , Tylenchorhynchus spp., Scutellonema spp., Paratrichodorus spp., Meloinema spp., Paraphelenchus spp., Aglenchus spp., Belonolaimus spp., Nacobbus spp, Rotylenchulus spp., Rotylenchus spp. ., Hoplolaimus spp., Punctodera spp., Criconemella spp., Quinisulcius spp., Hemicycliophora spp., Anguina spp., Subanguina spp., Hemicriconemoides spp., Psilenchus spp., Pseudohalenchus spp., Criconemoides spp.
Aglenchus agricola, Anguina tritici, Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Cacopaurus pestis, Criconemella curvata, Criconemella onoensis, Criconemellama rata, Criconemellaxata, Criconemellaxata, Criconemellaxata, Criconemellaxata, in general, Criconemoides ferniae, Criconemoides onoense, Criconemoides ornatum and Criconemoides spp. in general, Ditylenchus destructor, Ditylenchus dipsaci, Ditylenchus myceliophagus and Ditylenchus spp. groups, Dolichodorus Heterocephalus, Globodera pallida (= Heterodera pallida), Globodera rostochiensis, Globodera solanacearum, Globodera tabacum, virginiae Globodera, Helicotylenchus digonicus, Helicotylenchus dihystera, Helicotylenchus érythrine, Helicotylenchus multicinctus, Helicotylenchus nannus, and pseudorobustus Helicotylenchus Helicotylenchus spp. in general, Hemicriconemoides, Hemicycliophora arenaria, Hemicycliophora nudata, Hemicycliophora parvana, Heterodera avenae, Heterodera cruciferae, Heterodera glycines, Heterodera oryzae, Heterodera schachtii, Heterodera zeae and Heterodera zeae and Heterodera zeap and Heterodera zeap and Heterodera zeap and Heterodera zeae and Heterodera zeae and Heterodera zeap and Heterodera zeap. in general, Hoplolaimus aegyptii, Hoplolaimus californicus, Hoplolaimus columbus, Hoplolaimus galeatus, Hoplolaimus indicus, Hoplolaimus magnistylus, Hoplolaimus pararobustus, Longidorus africanus, Longidorus breviannulatus, Longidorus elongatus, Longidorus and Longidus laevicus and Longidorus laevicus, Longidorus and Longorus and Longidus laevicus, Longidorus and Longorus and Longorus and Longorus and Longorus and Longorus and Longorus. in general, Meloidogyne acronea, Meloidogyne arenaria, Meloidogyne arenaria thamesi, Meloidogyne artiella, Meloidogyne chitwoodi, Meloidogyne coffeicola, Meloidogyne ethiopica, Meloidogyne exigua, Meloidogyne graminicola, Meloidogyne acrogne, Meloidogyne graminisavan, Meloidogyne araminaria, Meloidogyne Meloidogyne kikuyensis, Meloidogyne naasi, Meloidogyne paranaensis, Meloidogyne thamesi and Meloidogyne spp. in general, Meloinema spp., Nacobbus aberrans,
Neotylenchus vigissi, Paraphelenchus pseudoparietinus, Paratrichodorus allius, Paratrichodorus lobatus, Paratrichodorus minor, Paratrichodorus nanus, Paratrichodorus porosus, Paratrichodorus teres and Paratrichodorus spp. in general, Paratylenchus hamatus, Paratylenchus minutus, Paratylenchus projectus and Paratylenchus spp. groups, agilis Pratylenchus, Pratylenchus alleni, andinus Pratylenchus, Pratylenchus brachyurus, cerealis Pratylenchus, Pratylenchus coffeae, crenatus Pratylenchus, Pratylenchus delattrei, giibbicaudatus Pratylenchus, Pratylenchus goodeyi, hamatus Pratylenchus, hexincisus Pratylenchus, Pratylenchus loosi, neglectus, Pratylenchus, penetrans Pratylenchus, Pratylenchus pratensis , Pratylenchus scribneri, Pratylenchus teres, Pratylenchus thornei, Pratylenchus vulnus, Pratylenchus zeae and Pratylenchus spp. in general, Pseudohalenchus minutus, Psilenchus magnidens, Psilenchus tumidus, Punctodera chalcoensis, Quinisulcius acutus, Radopholus citrophilus, Radopholus similis, Rotylenchulus borealis, Rotylenchulus parvus, Rotylenchulus reniformis and Rotylenchusp and Rotylenchusp. in general, Rotylenchus laurentinus, Rotylenchus macrodoratus, Rotylenchus robustus, Rotylenchus uniformis and Rotylenchus spp. in general, Scutellonema brachyurum, Scutellonema bradys, Scutellonema clathricaudatum and Scutellonema spp. in general, Subanguina radiciola, Tetylenchus nicotianae, Trichodorus cylindricus, Trichodorus minor, Trichodorus primitivus, Trichodorus proximus, Trichodorus similis, Trichodorus sparsus and Trichodorus spp. in general, Tylenchorhynchus agri, Tylenchorhynchus brassicae, Tylenchorhynchus clarus, Tylenchorhynchus claytoni, Tylenchorhynchus digitatus, Tylenchorhynchus ebriensis, Tylenchorhynchus maximus, Tylenchorhynusus tylenchorhynchus nudus, Tylenchorhynchus nudus and Tylenchorhynchus nudus, Tylenchorhynchus nudus. in general, Tylenchulus semipenetrans, Xiphinema americanum, Xiphinema brevicolle, Xiphinema dimorphicaudatum, Xiphinema index and Xiphinema spp. Definition of plant parts
According to the invention, all plants and parts of plants can be treated. “Plants” means all plants and plant populations, such as desirable and undesirable wild plants, cultivars and plant varieties (whether or not protected by plant variety or plant breeder rights). Cultivars and plant varieties can be plants obtained by conventional propagation and breeding methods that can be assisted or complemented by one or more biotechnological methods, such as through the use of double haploids, protoplast fusion, random and directed mutagenesis, markers molecular or genetic or by methods of bioengineering and genetic engineering. “Plant parts” means all plant parts and organs above and below ground, such as bud, leaf, flower, and root, whereby leaves, for example, needles, stems, branches, flowers, fruiting bodies , fruits and seeds, as well as roots, tubers, corms and rhizomes are listed. Cultures and vegetative and generative propagation material, for example, cuttings, corms, tubers, rhizomes, stolons and seeds also belong to parts of the plant.
As already mentioned above, it is possible to treat all plants and their parts according to the invention. In one embodiment, species of wild plants and plant cultivars, or those obtained through conventional biological breeding, such as crossing or fusing protoplasts, and their parts, are treated. In another modality, transgenic plants and plant varieties obtained by genetic engineering, possibly in combination with conventional methods (Genetically Modified Organisms), and their parts, are treated. The term "parts" or "parts of plants" has been explained above. GMOs
The plants of plant cultivars found in each case commercially available or in use can be treated according to the invention. Plant cultivars must be understood in the sense of plants with new properties ("traits") that can be obtained through conventional hybridization methods, through mutagenesis or by recombinant DNA techniques. This can be varieties, bio and genotypes.
The transgenic plants or plant cultivars (that is, those obtained by genetic engineering) that can be treated according to the invention include all plants that, in relation to genetic modification, received the genetic material that transmitted particularly advantageous characteristics useful for them plants. Examples of such properties are better plant growth, greater tolerance to high or low temperatures, greater tolerance to drought or water or to the salt content in the soil, greater flowering performance, easier harvesting, accelerated maturation, higher harvest yields, better quality and / or greater nutritional value of the harvested products, better storage stability and / or the processability of the harvested products. Following and particularly emphasized examples of such properties are a better defense of plants against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria and / or viruses, and also the increased tolerance of plants to certain active herbicidal compounds. . Special emphasis is placed on vegetables, potatoes, corn, soybeans, cotton and bananas.
The treatment method according to the invention can be used in the treatment of genetically modified organisms (GMOs), e.g. plants or seeds. Genetically modified plants (or transgenic plants) are plants with a heterologous gene that has been stably integrated into the genome. The expression "heterologous gene" essentially means a gene that is supplied or assembled outside the plant and, when introduced into the nuclear, chloroplastic or mitochondrial genome, gives the transformed plant new or improved agronomic properties or other properties by expression of a protein or polypeptide of interest, either by down-regulation or by silencing another gene (s) that are present in the plant (using, for example, antisense technology, co-suppression technology or RNA interference technology - RNAi). A heterologous gene that is located in the genome is also called a transgene. A transgene that is defined by its particular position in the plant's genome is called a transgenic transformation or event.
Depending on the species of plants or plant cultivars, their location and growing conditions (soils, climate, vegetation period, diet), the treatment according to the invention, can also result in superadditive ("synergistic") effects. Thus, for example, reduced application rates and / or an increase in the activity spectrum and / or an increase in the activity of the active compounds and compositions that can be used according to the invention, better plant growth, greater tolerance at high or low temperatures, greater tolerance to drought or water or salt content in the soil, greater flowering performance, facilitating harvesting, accelerated ripening, greater harvest yields, larger fruits, greater plant height, green leaf color, flowering precocious, higher quality and / or superior nutritional value of the harvested products, higher concentration of sugar within the fruits, better storage and / or processing stability of the harvested products are possible, which surpass the truly expected effects.
At certain application rates, combinations of active compounds according to the invention can also have a strengthening effect on plants. Therefore, they are also suitable for mobilizing the plant's defense system against the attack of unwanted microorganisms. This may, if appropriate, be one of the reasons for the greater activity of the combinations according to the invention, for example, against fungi. Plant strengthening substances (resistance inducers) should be understood as meaning, in the present context, substances or combinations of substances that are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with undesirable microorganisms, the treated plants exhibit a significant degree of resistance to these microorganisms. In the present case, undesirable microorganisms must be understood as phytopathogenic fungi, bacteria and viruses. Thus, the substances according to the invention can be used to protect plants against attack by the mentioned pathogens within a certain period of time after treatment. The period of time in which protection is carried out generally extends from 1 to 10 days, preferably from 1 to 7 days, after the treatment of the plants with the active compounds.
The plants and varieties of plants that are preferably treated according to the invention include all plants that have the genetic material that give particularly advantageous traits, useful for these plants (both obtained through cultivation and / or biotechnological means).
The plants and varieties of plants that are also preferably treated according to the invention are resistant to one or more biotic stresses, that is, the said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, fungi, phytopathogenic bacteria, viruses and / or viroids.
The plants and varieties of plants that can be treated equally according to the invention are those plants that are resistant to one or more abiotic stress. Abiotic stress conditions may include, for example, drought, exposure to cold, exposure to heat, osmotic stress, flooding, increased soil salinity, increased mineral exposure, exposure to ozone, exposure to high light, limited availability of nutrients nitrogen, limited availability of phosphoric nutrients, escape from the shade.
The plants and varieties of plants that can be treated equally according to the invention, are those plants characterized by improved production characteristics. The increased yield in such plants may be the result of, for example, better plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, efficiency photosynthesis, increased germination and accelerated maturation. Yield can also be affected by improved plant architecture (under stress and non-stress conditions), including, but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, the number and distance of internodes, root growth, seed size, fruit size, pod size, ear or pod number, number of seeds per pod or ear, seed mass, improved seed filling, reduced seed dispersal, reduced pod dehiscence and resistance to housing. Productive characteristics also include the composition of seeds, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction of anti-nutritional compounds, improved processability and better storage stability.
Plants that can be treated according to the invention are hybrid plants that already express the characteristic of heterosis or hybrid vigor that results in a higher yield, usually vigor, health and resistance to biotic and abiotic stresses). Such plants are usually made by crossing a pure sterile male parent line (the female parent) with another pure male fertile parent line (the male parent). Hybrid seed is usually harvested from male sterile plants and sold to producers. Sterile male plants can sometimes (eg maize) be produced by stripping, that is, the mechanical removal of male reproductive organs (or male flowers), but, more typically, male sterility is the result of genetic determinants in the plant genome. In that case, and, especially when the seed is the desired product to be harvested from hybrid plants, it is generally useful to ensure that male fertility in hybrid plants is completely restored. This can be achieved by ensuring that relatives have appropriate male fertility genes that are capable of restoring male fertility in hybrid plants that contain the genetic determinants responsible for male sterility. Genetic determinants for male sterility can be located in the cytoplasm. Examples of cytoplasmic male sterility (CMS), for example, have been described in Brassica species (W0 92/05251, WO 95/09910, WO 98/27806, WO 05/002324, WO 06/021972 and in US 6,229,072). However, the genetic determinants for male sterility can also be located in the nuclear genome. Sterile male plants can also be obtained by plant biotechnology methods, such as genetic engineering. A particularly useful means of obtaining plants with male sterility is described in WO 89/10396, in which, for example, a ribonuclease such as barnase is selectively expressed in the tapetum cells in the stamens. Fertility can be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar (e.g. WO. 91/02069).
Plants or plant cultivars (obtained through plant biotechnology methods, such as genetic engineering) that can be treated according to the invention are plants resistant to herbicides, that is, plants that have become tolerant to one or more of certain herbicides. Such plants can be obtained either by genetic transformation, or by selecting plants that contain a mutation that confer tolerance to such herbicides.
Herbicide-resistant plants are, for example, glyphosate-tolerant plants, that is, plants that have become tolerant to the glyphosate herbicide or its salts. Plants can become tolerant to glyphosate by different means. For example, glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshiquimato-3-phosphate synthase (EPSPS). Examples of such EPSPS genes are the AroA (CT7 mutant) gene from the bacterium Salmonella typhimurium (Comai et al., 1983, Science 221, 370-371), the CP4 gene from the bacterium Agrobacterium sp. (Barry et al., 1992, Curr. Topics Plant Physiol. 7, 139-145), the genes encoding a Petunia EPSPS (Shah et al., 1986, Science 233, 478-481), tomato EPSPS (Gasser et al., 1988, J. Biol. Chem. 263, 4280-4289), or an EPSPS from Eleusina (WO 01/66704). It can also be a mutated EPSPS as described in, for example, EP 0837944, WO 00/66746, WO 00/66747 or WO02 / 26995. Glyphosate-tolerant plants can be obtained by expression of a gene encoding a glyphosate oxido-reductase enzyme, as described in U.S. Patent 5,776,760 and 5,463,175. Glyphosate tolerant plants can be obtained by expression of a gene encoding a glyphosate acetyl transferase enzyme as described in for example WO 02/36782, WO 03/092360, WO 05/012515 and WO 07/024782. Glyphosate-tolerant plants can also be obtained by selecting naturally occurring plants containing mutations of the aforementioned genes, as described in, for example, WO 01/024615 or WO 03/013226. Plants that express EPSPS genes that confer glyphosate tolerance are described in e.g. US patent applications Nos. 11 / 517,991, 10 / 739,610, 12 / 139,408, 12 / 352,532, 11 / 312,866, 11 / 315,678, 12 / 421,292, 11 / 400,598, 11 / 651,752, 11 / 681,285, 11 / 605,824, 12 / 468,205, 11 / 760,570, 11 / 762,526, 11 / 769,327, 11 / 769,255, 11/943801 or 12 / 362,774. Plants that comprise other genes that confer glyphosate tolerance, such as decarboxylase genes, are described in e.g. US patent applications US 11 / 588,811, 11 / 185,342, 12 / 364,724, 11 / 185,560 or 12 / 423,926.
Other herbicide-resistant plants are plants, for example, that become tolerant to herbicides that inhibit the enzyme glutamine synthase, such as bialaphos, phosphinothricin or glufosinate. Such plants can be obtained by the expression of a detoxifying enzyme of the herbicide or a mutant of the enzyme glutamine synthetase which is resistant to inhibition, e.g. described in US patent applications US 11 / 760,602. Such an effective detoxifying enzyme is an enzyme that encodes a phosphinothricin acetyltransferase (such as bar or pat protein from Streptomyces species). Plants that express an exogenous phosphinothricin acetyltransferase are, for example, described in US patent applications. 5,561,236; 5,648,477; 5,646,024; 5,273,894; 5,637,489; 5,276,268; 5,739,082; 5,908,810 and 7,112,665.
Other herbicide-tolerant plants are also plants that become herbicide-tolerant by inhibiting the enzyme hydroxyphenylpyruvatodioxigenase (HPPD). Hydroxyphenylpyruvatodioxigenases HPPD are enzymes that catalyze the reaction in which parahydroxyphenylpyruvate- (HPP) is transformed into homogentisate. Plants tolerant to HPPD inhibitors can be transformed with a gene encoding a naturally occurring HPPD-resistant enzyme, or a gene encoding a mutant or chimeric HPPD enzyme, as described in WO 96/38567, WO 99/24585, and WO 99/24586, WO 2009/144079, WO 2002/046387, or US 6,768,044. Tolerance to HPPD inhibitors can also be obtained by transforming plants with genes that encode certain enzymes that allow the formation of homogentisate despite the inhibition of the native HPPD enzyme by the HPPD inhibitor. Such plants and genes are described in WO 99/34008 and WO 02/36787. Plant tolerance to HPPD inhibitors can also be improved by transforming plants with a gene that encodes an enzyme showing prefenate dehydrogenase (PDH) activity, in addition to a gene that encodes an HPPD-tolerant enzyme, as described in WO 2004 / 024928. In addition, plants may be more tolerant of HPPD-inhibiting herbicides by adding a gene in their genome that encodes an enzyme capable of metabolizing or degrading HPPD-inhibitors, such as the CYP450 enzymes shown in WO 2007/103567 and WO 2008 / 150473.
In addition, plants resistant to additional herbicides are plants that become tolerant to inhibitors of the enzyme acetolactate synthase (ALS). Known ALS inhibitors include, for example, sulfonylurea, imidazolinone, triazolopyrimidines, priimidinioxy (thio) benzoates, and / or sulfonylaminocarbonyltriazolinone herbicides. Different mutations in the ALS enzyme (also known as acetohydroxy acid synthetase, AHAS) are known to confer tolerance to different herbicides and groups of herbicides, as described for example in Tranel and Wright (2002, Weed Science 50: 700-712), but also , in US patent No. 5,605,011, 5,378,824, 5,141,870, and 5,013,659. The production of sulfonylurea tolerant plants and imidazolinone tolerant plants is described in US patents US Nos. 5,605,011; 5,013,659; 5,141,870; 5,767,361; 5,731,180; 5,304,732; 4,761,373; 5,331,107; 5,928,937; and 5,378,824; and international publication WO 96/33270. Other imidazolinone tolerant plants are also described in, for example, WO 2004/040012, WO 2004/106529, WO 2005/020673, WO 2005/093093, WO 2006/007373, WO 2006/015376, WO 2006/024351, and WO 2006/060634. Other sulfonylurea-tolerant plants, imidazolinones are also described in, for example, WO 07/024782 and US patent application No. 61/288958.
Other plants tolerant to imidazolinones and / or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide, or mutation cultivation, as described, for example, for soybeans in US patent US 5,084,082, for rice in WO 97/41218, for sweet beet in US patent US 5,773,702 and WO 99/057965, for lettuce in US patent 5,198,599, or for sunflower in WO 01/065922.
Plants or plant cultivars (obtained through plant biotechnology methods, such as genetic engineering) that can also be treated according to the invention are insect resistant transgenic plants, that is plants that have become resistant to insect attack specific targets. Such plants can be obtained through genetic transformation, or by selecting plants that contain a mutation conferring resistance to such insects.
A "insect resistant transgenic plant", as used herein, includes any plant that contains at least one transgene that comprises a coding sequence that encodes: 1) an insecticidal crystalline protein from Bacillus thuringiensis or an insecticidal part thereof, such as proteins crystal-forming insecticides listed by Crickmore et al. (1998, Microbiology and Molecular Biology Analysis, 62: 807-813), updated by Crickmore et al. (2005) in Bacillus thuringiensis toxin nomenclature, online at: http://www.lifesci.sussex.ac.uk/Home/Neil_Crickmore/Bt/), or insecticidal portions thereof, eg proteins of the Cry protein classes Cry1Ab, Cry1Ac, Cry1B, Cry1C, Cry1D, Cry1F, Cry2Ab, Cry3Aa, or Cry3Bb or insecticidal portions thereof (eg EP 1999141 and WO 2007/107302), or proteins encoded by these synthetic genes as eg. described in US patent application No. 12 / 249,016; or 2) a crystal-forming protein from Bacillus thuringiensis or a part of it that is insecticidal, in the presence of a second crystalline protein from Bacillus thuringiensis from others or a part of it, such as the binary toxin made up of Cry34 Cry35 and crystalline proteins (Moellenbeck et al. 2001, Nat. Biotechnol. 19: 668-72; Schnepf et al. 2006, Applied Environm. Microbiol. 71, 1765-1774) or binary toxin consisting of the Cry1A or Cry1F proteins and the Cry2Aa proteins or Cry2Ab or Cry2Ae (US Patent Appl. No. 12 / 214,022 and EP 08010791.5); or 3) hybrid insecticidal protein comprising parts of different insecticidal crystal-forming proteins from Bacillus thuringiensis, such as a hybrid of proteins from 1) above or a hybrid of proteins from 2) above, eg, the Cry1A.105 protein produced by MON89034 corn event (WO 2007/027777); or 4) a protein of any one from 1) to 3) above where some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain greater insecticidal activity for a target insect species, and / or to enlarge the range of target insect species affected, and / or because of changes introduced in the coding DNA during cloning or transformation, such as the Cry3Bb1 protein in MON863 or MON88017 corn events, or the Cry3A protein in the MIR604 corn event , or 5) an insecticidal protein secreted from Bacillus thuringiensis or Bacillus cereus, or an insecticidal portion thereof, such as vegetative insecticidal proteins (VIP), listed at: http://www.lifesci.sussex.ac.uk/home / Neil Crickmore / Bt / vip.html, eg proteins from the VIP3Aa protein class; or 6) a protein secreted from Bacillus thuringiensis or Bacillus cereus, which is an insecticide, in the presence of a second protein secreted from Bacillus thuringiensis or B. cereus, such as the binary toxin made up of the VIP1A and VIP2A proteins (WO 94/21795), or 7) an insecticidal hybrid protein comprising parts of different proteins secreted from Bacillus thuringiensis or Bacillus cereus, as a hybrid of the proteins in 1) above or a hybrid of the proteins in 2) above, or 8) a protein of any of 5) to 7) above where some, particularly 1 to 10 amino acids have been replaced by another amino acid to obtain greater insecticidal activity for a target insect species, and / or to expand the range of species of affected target insects, and / or because of changes introduced in the coding DNA during cloning or transformation (while still encoding an insecticidal protein), such as the VIP3Aa protein in the event of cotton COT102; or 9) a protein secreted from Bacillus thuringiensis or Bacillus cereus, which is an insecticide, in the presence of a crystalline protein from Bacillus thuringiensis, such as the binary toxin consisting of VIP3 and Cry1A or Cry1F (US patent application No. 61 / 126083 and 61/195019), or the binary toxin consisting of the VIP3 protein and the Cry2Aa Cry2Ab or Cry2Ae proteins (US patent application US 12 / 214,022 and EP 080107915). 10) a protein of 9) above in which some, particularly 1 to 10 amino acids have been replaced by another amino acid to obtain greater insecticidal activity for a target insect species, and / or to expand the range of affected target insect species , and / or because of changes made to the encoding DNA during cloning or transformation (while still encoding an insecticidal protein)
Of course, a transgenic insect-resistant plant, as used herein, also includes all plants that comprise a combination of genes that encode the proteins of any of the previous classes 1 to 10. In one embodiment, an insect-resistant plant contains more of a transgene that encodes a protein from any of the previous classes 1 to 10, to expand the range of affected target insect species when using different proteins targeting different target insect species, or to delay the development of insect resistance to plants using different insecticidal proteins for the same target insect species, but which has a different mode of action, such as binding to different binding receptors on the insect.
A "plant resistant to transgenic insects", as used herein, further includes any plant that contains at least one transgene comprising a production sequence by expression of a double-stranded RNA that after ingestion by a plant insect pest inhibits the insect pest growth, as described e.g. in WO 2007/080126, WO 2006/129204, WO 2007/074405, WO 2007/080127 and WO 2007/035650.
Plants or plant cultivars (obtained through plant biotechnology methods, such as genetic engineering) that can also be treated according to the invention are tolerant to abiotic stress. Such plants can be obtained through genetic transformation, or by selecting plants that contain a mutation providing resistance to such stress. Particularly useful stress-tolerant plants include: 1) plants that contain a transgene capable of reducing the expression and / or activity of the poly (ADP-ribose) polymerase (PARP) gene in plant cells or plants as described in WO 00/04173, WO / 2006/045633, EP 04.077.984,5 or EP 06.009.836,5. 2) plants containing a transgene with an increased stress tolerance capable of reducing the expression and / or activity of the PARG coding genes of plants or plant cells, as described ex. in WO 2004/090140. 3) plants that contain a transgene with increased stress tolerance encoding a functional plant enzyme from the biosynthetic reuse route of nicotinamide adenine dinucleotide, including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid adenyltransferase, nicotinamide dinotinamide, nicotinamide dinotinamide for example. described. in EP 040776247, WO 2006/133827, PCT / EP07 / 002433, EP 1999263, or WO 2007/107326.
Plants or plant cultivars (obtained by methods of plant biotechnology, such as genetic engineering), which in the same way can be treated according to the invention, have an altered quantity, quality and / or storage stability of the harvested product and / or altered properties of the specific ingredients of the harvested product, such as: 1) transgenic plants that synthesize a modified starch whose physico-chemical characteristics, in particular the amylose content or the amylose-amylopectin rate, the degree of branching, the mean the length of the chain, the distribution of the side chain, the viscosity behavior, the gelling force, the grain size of the starch and / or the grain morphology of the starch, is changed compared to the starch synthesized in the wild type of the plant cells or plants, so that this modified starch is more suitable for certain applications. Said transgenic plants that synthesize a modified starch are disclosed, for example, in EP 0571427, WO 95/04826, EP 0719338, WO 96/15248, WO 96/19581, WO 96/27674, WO 97/11188, WO 97/26362 , WO 97/32985, WO 97/42328, WO 97/44472, WO 97/45545, WO 98/27212, WO 98/40503, WO99 / 58688, WO 99/58690, WO 99/58654, WO 00/08184, WO 00/08185, WO 00/08175, WO 00/28052, WO 00/77229, WO 01/12782, WO 01/12826, WO 02/101059, WO 03/071860, WO 2004/056999, WO 2005/030942, WO 2005/030941, WO 2005/095632, WO 2005/095617, WO 2005/095619, WO 2005/095618, WO 2005/123927, WO 2006/018319, WO 2006/103107, WO 2006/108702, WO 2007/009823, WO 00/22140, WO 2006/063862, WO 2006/072603, WO 02/034923, EP 06090134.5, EP 06090228.5, EP 06090227.7, EP 07090007.1, EP 07090009.7, WO 01/14569, WO 02/79410, WO 03/33540, WO WO 2004/078983, WO 01/19975, WO 95/26407, WO 96/34968, WO 98/20145, WO 99/12950, WO 99/66050, WO 99/53072, US 6,734,341, WO 00/11192, WO 98 / 22604, WO 98/32326, WO 01/98509, WO 01/98509, WO 2005/002359, US 5,824,790, US 6,013,861, WO 94/04693, WO 94/09144, WO 94/11520, WO 95/35026, WO 97/20936 2) Transgenic plants that synthesize polymers of carbohydrate other than starch or that synthesize polymers of carbohydrate other than starch with altered properties compared to wild type plants without genetic modification. Examples are plants that produce polyfructose, especially of the inulin or levan type, as disclosed in EP 0663956, WO 96/01904, WO 96/21023, WO 98/39460, and WO 99/24593, the plants producing alpha-1, 4 - glucans as disclosed in WO 95/31553, US 2002031826, US 6,284,479, US 5,712,107, WO 97/47806, WO 97/47807, WO 97/47808 and WO 00/14249, alpha-1 producing plants, 6 branched alpha-1,4-glucans, as disclosed in WO 00/73422, the plants that produce alternan, as disclosed in e.g. WO 00/47727, WO 00/73422, EP 060773017, US 5908975 and EP 0728213, 3) Transgenic plants that produce hyaluronan, as for example described in WO 2006/032538, WO 2007/039314, WO 2007/039315, WO 2007 / 039316, JP 2006304779, and WO 2005/012529. 4) transgenic plants or hybrid plants, such as onions with characteristics such as "high soluble solids", "low pungency" (LP) and / or 'long storage' (LS), as described in the Patent of the USA Appl. No. 12/020, 360 and 61/054, 026.
Plants or plant cultivars (which are obtained by methods of plant biotechnology, such as genetic engineering), which in the same way can be treated according to the invention, are plants, such as cotton plants, with altered fiber characteristics . Such plants can be obtained by genetic transformation, or by selecting plants containing a mutation conferring such altered characteristics of the fiber and includes: a) plants, such as cotton plants, which contain an altered form of the cellulose synthase genes, as described in WO 98/00549 b) plants, such as cotton plants, which contain an altered form of homologous nucleic acids rsw2 or rsw3, as described in WO 2004/053219 c) plants, such as cotton plants with increased expression of sucrose phosphate synthase, such as described in WO 01/17333 d) plants, such as cotton plants with the increased expression of sucrose synthase, such as described in WO 02/45485 e) plants, such as cotton plants, in which the Plasmododemal connection time at the base of the fiber cell is altered, for example, through selective regulation of the fiber by β-1,3-glucanase as described in WO 2005/017157, or as described in EP 08.075.514,3 or p US Patent Order No. 61/128, 938 f) plants, such as cotton plants that have fibers with altered reactivity, for example, through the expression of the N-acetylglucosaminatransferase gene including the nodC and chitin synthase genes, as described in WO 2006/136351
Plants or plant cultivars (which can be obtained by plant biotechnology methods, such as genetic engineering) that can also be treated according to the invention, are plants such as rapeseed or Brassica-related plants, with altered profile characteristics of the oil. Such plants can be obtained by genetic transformation or by selecting plants containing a mutation, which confers such altered oil characteristics, and includes: a) plants, such as rapeseed plants, which produce the oil having a high oleic acid content such as as for example described in US patents US 5,969,169, US 5,840,946 or US 6,323,392 or US 6,063,947 b) plants, such as rapeseed plants, that produce the oil having a low oleic acid content, as described in US patents US 6,270,828, US 6,169,190, or US 5,965,755 c) plants, such as rapeseed plants, that produce the oil having the low level of saturated fatty acids, such as e.g. described in US patent No. 5,434,283 or US patent application No. 12/668303
Plants or plant cultivars (which can be obtained by plant biotechnology methods, such as genetic engineering) which can also be treated according to the invention are plants, such as potatoes, which are resistant to the virus, e.g. against potato Y viruses (event SY230 and SY233 from Tecnoplant, Argentina), which are resistant to diseases, e.g. against late potato rust (eg RB gene), which show a reduction in cold-induced sweetening (carrying the Nt-Inhh, IIR-INV gene) or which have a small phenotype (Gene A-20-oxidase).
Plants or plant cultivars (which can be obtained by plant biotechnology methods, such as genetic engineering) that can also be treated according to the invention are plants, such as rapeseed or Brassica plants related to the fractionation characteristics of plants. altered seeds. Such plants can be obtained through genetic transformation, or by plant selection contain a mutation conferring such fractionation characteristics of the altered seeds and include plants, such as rapeseed plants with reduced or delayed seed fractionation as described in US Patent Appl . No. 61 / 135,230, and EP 08075648.9, WO09 / 068313 and WO10 / 006732.
The particularly useful transgenic plants that can be treated according to the invention are plants that contain transformation events or combination of transformation events, which are the subject of unregulated state requests in the United States of America for Animal and Plant Health Inspection Service (APHIS) of the United States Department of Agriculture (USDA) if such requests are granted or are still pending. At any time this information is readily available from APHIS (4700 River Road Riverdale, MD 20737, USA), for example, on its website (URL http://www.aphis.usda.gov/brs/not_reg. html). On the filing date of this request, unregulated petitions to the state that were pending with APHIS, or granted by APHIS were listed in table B, which contains the following information: - Petition: the petition identification number. Technical descriptions of the transformation events can be found in the individual petition documents that are obtained from APHIS, for example, on the APHIS website, by reference to this petition number. These descriptions are hereby incorporated by reference. - Extension of the Petition: reference to a previous petition for which an extension is requested. - Institution: the name of the entity that submits the petition. - Regulated article: the plant species involved. - Transgenic phenotype: the characteristic given to plants by transformation. - Transformation event or lineage: the name of the event or events (sometimes also called lineages or lineages) for which unregulated status is requested. - APHIS documents: several documents published by APHIS in relation to the petition and which can be requested with APHIS. Formulations
Suitable extenders and / or surfactants that can be contained in the compositions according to the invention are all formulation aids, which can normally be used in plant treatment compositions.
In the compositions according to the invention, the proportion of fluopyram to a compound of the agrochemically active group (B) can vary within a relatively wide range. In general, between 0.02 and 2.0 parts by weight, preferably between 0.05 and 1.0 parts by weight, fluopiram is used in parts by weight of the agrochemically active compound.
When the active compounds of formula (I) that can be used according to the invention are used, application rates can vary within a certain range, depending on the type of application. In seed treatment, the application rates of the active compound of formula (I) are generally comprised between 10 and 10,000 mg per kilogram of seed, preferably between 10 mg and 300 per kilogram of seed. When used in solid formulations, the application rates of the active compound of formula (I) are generally comprised between 20 and 800 mg per kilogram of formulation, preferably between 30 and 700 mg per kilogram of formulation.
According to the invention, the carrier is to be understood as meaning a natural or synthetic, organic or inorganic substance that is mixed or combined with the active compounds for better applicability, in particular for application to plants or parts of plants or seeds. The vehicle, which can be solid or liquid, is generally inert and must be suitable for use in agriculture.
Suitable solid carriers are as follows: for example, ammonia salts, ground natural minerals, such as kaolin, clays, talc, chalk, quartz, atapulgite, montmorillonite or diatomaceous earth, and synthetic soil minerals, such as finely divided silica , aluminum and natural or synthetic silicates, resins, waxes, solid fertilizers, water, alcohols, especially butanol, organic solvents, mineral oils and vegetable oils, and derivatives thereof. It is also possible to use mixtures of such vehicles. Solid vehicles suitable for granules are: for example, gravel and fractionated natural minerals, such as calcite, marble, pumice, sepiolite, dolomite, as well as synthetic granules of inorganic and organic flours, and also granules of organic materials, such as such as sawdust, coconut husks, corn cobs and tobacco stalks. Suitable emulsifiers and / or foaming agents are: for example, nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene ethers of fatty alcohols, for example, alkylaryl polyglycol ethers, alkylsulfonates, sulphates alkyl, arylsulfonates, and also protein hydrolysates. Suitable dispersants are: for example, lignosulfite and methylcellulose waste solutions.
Liquefied gaseous extenders or suitable vehicles are liquids that are gaseous at room temperature and under atmospheric pressure, aerosol propellants for example, such as butane, propane, nitrogen and carbon dioxide.
Tachycants, such as carboxymethylcellulose and natural and synthetic polymers in the form of powders, granules and latex, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, or else natural phospholipids, such as cephalins and lecithins and synthetic phospholipids can be used in the formulations. Other possible additives are mineral and vegetable oils.
If the diluent used is water, it is also possible, for example, to use organic solvents as auxiliary solvents. Liquid solvents are essentially: Aromatic compounds such as xylene, toluene or alkylnaphthalenes, Chlorinated aromatic compounds or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example, mineral oil fractions, mineral and vegetable oils, alcohols, such as butanol or glycol, as well as ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethyl and dimethylformamide sulfoxide, and also water.
The compositions according to the present invention can comprise other additional components, such as, for example, surfactants. Suitable surfactants are emulsifiers, dispersants or wetting agents with ionic or nonionic properties, or mixtures of these surfactants. Examples of these are salts of polyacrylic acid, salts of lignosulfonic acid, salts of phenolsulfonic acid or naphthalenesulfonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (preferably alkylphenols or arylphenols), salts of sulfosucinic esters, derivatives of taurine (preferably alkyl taurates), phosphoric esters of alcohols or polyethoxylated phenols, fatty esters of polyols, and derivatives of compounds containing sulfates, sulfonates and phosphates. The presence of a surfactant is necessary if one of the active compounds and / or one of the inert carriers is insoluble in water and where the application takes place in water. The proportion of surfactants is between 5 and 40 weight percent of the composition according to the invention.
It is possible to use dyes such as inorganic pigments, for example, iron oxide, titanium oxide, Prussian blue and organic dyes, such as alizarin dyes, azo dyes and phthalocyanine metal dyes, and trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
If appropriate, other additional components may also be present, protective colloids, for example, binders, adhesives, thickeners, thixotropic substances, penetrating agents, stabilizers, sequestering agents, complexing agents. In general, the active compounds can be combined with any solid or liquid additive normally used for formulation purposes.
In general, the compositions according to the invention comprise between 0.05 and 99 percent by weight of the combination of active compound according to the invention, preferably between 10 and 70 percent by weight, particularly preferably between 20 and 50 percent by weight, more preferably 25 percent by weight.
The combinations or compositions of active compounds according to the invention can be used as such or, depending on their respective physical and / or chemical characteristics, in the form of their formulations or the use of the same preparations, such as aerosols, capsule suspensions , cold-mist concentrates, hot-mist concentrates, encapsulated granules, fine granules, drainable concentrates for seed treatment, ready-to-use solutions, dustable powders, emulsifiable concentrates, oil-in-water emulsions, water-in-emulsions oil, macrogranules, microgranules, dispersible oil powders, oil-miscible fluid concentrates, oil-miscible fluids, foams, pastes, pesticide-coated seeds, suspension concentrates, suspoemulsion concentrates, soluble concentrates, suspensions, wetting powders, soluble powders , water-soluble powders and granules, granules or tablets, water-soluble powders for seed treatment, wetting powders, natural and synthetic products impregnated with the active substance compound, as well as microencapsulations in polymeric substances and in seed coating materials, as well as cold - misty ULV and hot - misty formulations.
The mentioned formulations can be prepared in a manner known per se, for example by mixing the active compounds or combinations of active compounds with at least one additive. Suitable additives are all the usual formulation aids, such as, for example, organic solvents, thinners, solvents or thinners, solid vehicles and fillers, surfactants (for example, adjuvants, emulsifiers, dispersants, protective colloids, wetting agents and viscosity agents), dispersants and / or binding agents or fixatives, preservatives, dyes and pigments, defoaming agents, organic and inorganic thickeners, water repellents, suitable drying agents and UV stabilizers, gibberellins and also water and other auxiliary processes . Depending on the type of formulation to be prepared, in each case, additional processing steps, such as, for example, milling, dry milling or granulation may be necessary.
Organic diluents that may be present are all polar and non-polar organic solvents that are normally used for such purposes. Preferred are ketones, such as methyl isobutyl ketone and cyclohexanone, on the other hand amides, such as dimethylformamide and alkanecarboxamides, such as N, N-dimethyldecanamide and N, N-dimethyloctanamide, in addition cyclic compounds, such as N-methyl pyrrolidone , N- octylpyrrolidone, N-dodecylpyrrolidone, N octylcaprolactam-, N-dodecylcaprolactam and butyrolactone, in addition to strongly polar solvents, such as dimethyl sulfoxide, aromatic hydrocarbons, in addition, such as xylene, Solvesso ™, mineral oils, such as solution white alcohol, petroleum, alkylbenzenes and spindle oil, on the other hand esters, such as propylene glycol monomethyl ether acetate, dibutyl adipate, hexyl acetate, heptyl acetate, tri-n-butyl citrate and di-n phthalate -butyl, and, in addition, alcohols, such as, for example, benzyl alcohol and 1-methoxy-2-propanol.
Solid vehicles suitable for granules are: for example, gravel and fractionated natural minerals, such as calcite, marble, pumice, sepiolite, dolomite, as well as synthetic granules of inorganic and organic flours, and also granules of organic materials, such as sawdust, coconut husks, corn cobs and tobacco stalks.
Suitable surfactants (adjuvants, emulsifiers, dispersants, protective colloids, wetting agents and viscosity agents) are common ionic and non-ionic substances. Examples that can be mentioned are ethoxylated nonylphenols, straight or branched chain polyalkylene glycol ethers, products of alkylphenol reactions with ethylene oxide and / or propylene oxide, products of fatty amine reactions with ethylene oxide and / or propylene oxide, on the other hand, fatty acid esters, alkyl sulphates, alkyl ether sulphates, alkyl ether phosphates, aryl sulphates, ethoxylated arylalkylphenols, such as, for example, tristyrylphenol ethoxylates, in addition arylalkylphenylisol ethoxylates and propoxylates and also ethoxylates of sulfated or phosphated arylalkylphenol or ethoxy- and propoxylates. Mention may also be made of natural and synthetic water-soluble polymers, such as lignosulfonates, gelatin, gum arabic, phospholipids, starch, hydrophobically modified starch and cellulose derivatives and cellulose esters, in particular and, in addition, cellulose ethers , polyvinyl alcohol, polyvinyl acetate, polyvinylpyrrolidone, polyacrylic acid, polymethacrylic acid and copolymers of (meth) acrylic acid and esters of (meth) acrylic acid, and on the other hand also alkali metal copolymers with neutralized methacrylic acid and hydroxide methacrylic ether and condensates of naphthalenesulfonic acid salts optionally substituted with formaldehyde.
Suitable solid fillers and carrier agents are all substances commonly used for this purpose in crop protection compositions. Inorganic particles, such as carbonates, silicates, sulfates and oxides having an average particle size of 0.005 to 20 μm, in particular preferably 0.02-10 μm, can be mentioned as being preferred. Examples that can be mentioned are: ammonium sulfate, ammonium phosphate, urea, calcium carbonate, calcium sulfate, magnesium sulfate, magnesium oxide, aluminum oxide, silicon dioxide, finely divided silicic acid, silica gels, natural and synthetic silicates and aluminum silicates and products of plant origin such as cereal flour, wood powder and cellulose powder.
Suitable dyes that can be present in the seed treatment formulations to be used according to the invention, include all the usual dyes for such purposes. Both water-soluble pigments and dyes that are soluble in water can be used. Examples that can be mentioned include the dyes known under the designations Rhodamine B, Pigment CI Red 112 and Solvent CI Red 1. The dyes used can be inorganic pigments, for example, iron oxide, titanium oxide, Prussian blue and dyes organic, such as alizarin, azo dyes and phthalocyanine metal dyes, and trace nutrients, such as iron, manganese, boron, copper, cobalt, molybdenum and zinc salts.
Suitable wetting agents, which may be present in seed treatment formulations to be used according to the invention include all substances that promote moistening and are usual in the formulation of agrochemically active compounds. Preference is given to using alkylnaphthalenesulfonates, such as diisopropyl- or diisobutylnaphthalenesulfonates.
Suitable dispersants and / or emulsifiers that may be present in seed treatment formulations to be used in accordance with the present invention include all nonionic, anionic and cationic dispersing agents that are usual in the formulation of agrochemically active compounds. Preference is given to the use of nonionic or anionic dispersants or mixtures of nonionic or anionic dispersing agents. Particularly suitable nonionic dispersants are blocks of ethylene oxide / propylene oxide polymers, polyglycol alkylphenol ethers, as well as polyglycol ethers and their phosphated or sulphated tristryrylphenol derivatives. Particularly suitable anionic dispersants are lignosulfonates, polyacrylic acid salts and arylsulfonate / formaldehyde condensates.
Defoamers that may be present in seed treatment formulations to be used in accordance with the present invention include all foam-inhibiting compounds that are usual in the formulation of agrochemically active compounds. Preference is given to the use of silicone antifoam agents, magnesium stearate, silicone emulsions, long-chain alcohols, fatty acids and their salts and also organofluorinated compounds and mixtures thereof.
Preservatives that can be present in seed treatment formulations to be used according to the invention include all compounds that can be used for such purposes in agrochemical compositions. As an example, mention may be made of dichlorophen and hemiformal benzyl alcohol.
Secondary taquifiers that may be present in seed treatment formulations to be used according to the invention include all compounds that can be used for such purposes in agrochemical compositions. Preference is given to cellulose derivatives, acrylic acid derivatives, polysaccharides, such as xanthan gum or Veegum, modified clays, phyllosilicates, such as atapulgite and bentonite, and also finely divided silicic acids.
Suitable adhesives that may be present in seed treatment formulations to be used according to the invention include all the usual binding agents that can be used in seed treatment. Polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and Tylose can be mentioned as being preferred.
Suitable gibberellins that may be present in the seed treatment formulations to be used according to the invention are preferably gibberellins A1, A3 (= gibberellic acid), A4 and A7; Particular preference is given to the use of gibberellic acid. Gibberellins are known (cf. R. Wegler "Chemie der Planzenschutz and Schadlingsbekampfungsmittel" [Chemistry of Crop Protection Agents and Pesticides], vol. 2, Springer Verlag, 1970, pp 401-412).
The formulations generally comprise between 0.1 and 95% by weight of active compound, preferably between 0.5 and 90%.
The combinations of active compounds according to the invention can be present in commercial formulations as well as in the forms of use prepared from these formulations in mixture with other active compounds, such as insecticides, attractants, sterilizers, bactericides, acaricides, nematicides, fungicides, regulators growth or herbicides. Mixing with fertilizers is also possible.
The treatment according to the invention of plants and plant parts with combinations of active compounds or compositions is carried out directly or by action on their environment, habitat or storage space through usual treatment methods, for example, by immersion , spraying, atomization, watering, evaporation, dusting, fogging, transmission, foaming, painting, spreading, watering (drenching), drip irrigation and, in the case of propagating material, in particular in the case of seeds, on the other hand, as a dry seed treatment powder, a seed treatment solution, a water-soluble powder for suspension treatment, by fouling, by coating with one or more coating layers, etc. Preference is given for application by immersion, spraying, atomization, watering, evaporation, dusting, fogging, transmission, foaming, painting, spreading, watering (drenching) and drip irrigation.
The application of the formulations is carried out according to the usual agricultural practice in a way adapted to the application forms. Usual applications are, for example, dilution in water and spraying the spray application of the resulting solution, after dilution with the application of direct oil without dilution, seed coating, or the application of support granulate in the soil.
The active compound content of the application forms prepared from commercial formulations can vary within wide scales. The concentration of active compound in the application forms can be from 0.0000001 to 95% by weight of active compound, preferably between 0.0001 and 2% by weight.
The compositions according to the present invention not only comprise ready-to-use compositions that can be applied with an apparatus suitable for the plant or the seed, but also commercial concentrates that must be diluted with water before use. Application methods
The treatment according to the invention of plants and parts of plants with Fluopiram or compositions is carried out directly or by action on their environment, habitat or storage space through usual treatment methods, for example, by immersion, spraying, atomization , watering, stem injection, furrow application, evaporation, dusting, fogging, transmission, foaming, painting, spreading, watering (drenching), drip irrigation and, in the case of propagating material, in particular in In the case of seeds, on the other hand, as a powder for dry seed treatment, a solution for seed treatment, a water-soluble powder for suspension treatment, for fouling, for coating with one or more layers, etc. In addition, it is possible to apply the active compounds by the ultra-low volume method, or to inject the preparation of the active compound or the active compound itself into the soil.
Generally, fluopyram is applied at a rate of 10 g to 20 kg per ha, preferably 50 g to 10 kg per ha, more preferably from 100 kg to 5 g per hectare.
The invention further comprises a method for treating seeds. The invention, moreover, relates to seed treated according to one of the methods described in the previous paragraph.
Fluopiram or compositions comprising fluopiram according to the invention are especially suitable for the treatment of seeds. A large part of the damage caused to crop plants by harmful organisms is triggered by an infection of the seed during storage or after sowing, as well as during and after the germination of the plants. This stage is particularly critical since the roots and buds of the growing plant are particularly sensitive, and even minor damage can result in the death of the plant. Consequently, there is a great interest in protecting seeds and plants from germination using appropriate compositions.
The control of nematodes by treating plant seeds has been known for a long time and is the subject of continuous improvement. However, seed treatment presents a number of problems that cannot always be satisfactorily solved. Thus, it is desirable to develop methods to protect the seed and the germinating plant which consists of the additional application of crop protection agents, after sowing or after the emergence of the plants, or which, at least, considerably reduces the additional application. In addition, it is desirable to optimize the amount of active compound used in such a way as to provide maximum protection for the seed and the germination plant against attack by nematodes, but without damaging the plant itself by the active compound used. In particular, seed treatment methods must also take into account the intrinsic nematicidal properties of transgenic plants, in order to guarantee optimum protection of the seeds and the germination plant, with a minimum of crop protection agents to be employed .
Accordingly, the present invention also relates, in particular, to a method of protecting seeds and germinating plants from attack by nematodes by treating the seed with fluopyram or a composition comprising fluopyram according to the invention. The invention also relates to the use of the compositions according to the invention for the treatment of the seed to protect the seed and the germinating plant against nematodes. In addition, the invention relates to seeds treated with a composition according to the invention for protection against nematodes.
The control of nematodes that damage post-emergence plants is carried out primarily by treating the soil and the above-ground parts of plants with crop protection compositions. Due to concerns about the possible impact of the composition on crop protection on the environment and the health of humans and animals, efforts are being made to reduce the amount of active compounds applied.
One of the advantages of the present invention is that, because of the particular systemic properties of Fluopiram or a composition comprising fluopiram according to the invention, the treatment of the seed with Fluopiram or these compositions not only protect the seed itself, but also the resulting plants after emergence, against nematodes. In this way, immediate treatment of the crop at the time of sowing, or shortly thereafter, can be used.
Fluopyram or compositions comprising fluopyram according to the invention are suitable for the protection of vegetable seeds, in particular, tomato and cucurbits, potatoes, corn, soybeans, cotton, tobacco, coffee, fruits, in particular, citrus fruits, pineapples and bananas, and grapes.
As also described below, the treatment of transgenic seed with Fluopiram or compositions according to the invention is of particular importance. This refers to plant seeds that contain at least one heterologous gene, which allows for the expression of a polypeptide or protein with insecticidal properties. The heterologous gene in transgenic seeds may originate, for example, from microorganisms of the species Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. Preferably, this heterologous gene originates from Bacillus sp. The gene product has activity against the European corn borer and / or the western corn rootworm. Particularly preferably, the heterologous gene originates from Bacillus thuringiensis.
In the context of the present invention, Fluopyram or a composition comprising fluopyram according to the invention are applied by itself or in a formulation suitable for the seed. Preferably, the seed is treated in a state in which it is sufficiently stable so that the treatment does not cause any harm. In general, seed treatment can occur at any time between harvest and sowing. Normally, the seed used is separated from the plant and free of ears, husks, stems, coatings, hair or the flesh of the fruits. Thus, it is possible to use, for example, the seed that has been harvested, cleaned and dried to a moisture content of less than 15% by weight. Alternatively, it is also possible to use seeds that, after drying, were treated, for example, with water and then dried again.
When treating the seed, care must be taken generally that the amount of Fluopiram or a composition comprising fluopiram according to the invention applied to the seed and / or the amount of other additives is chosen in such a way that the germination of the seed is not adversely affected, or that the resulting plant is not damaged. This must be taken into account, in particular in the case of active compounds that can have phytotoxic effects at certain rates of application.
Fluopyram or a composition comprising fluopyram according to the invention can be applied directly, that is, without comprising additional components and without having been diluted. In general, it is preferable to apply the compositions to the seed in the form of an appropriate formulation. Suitable formulations and methods for seed treatment are known to a person skilled in the art and are described, for example, in the following documents: US 4,272,417 A, US 4245432 A, US 4808430 A, US 5876739 A, US 2003/0176428 A1, WO 2002/080675 A1, WO 2002/028186 A2.
Fluopyram or a composition comprising fluopyram that can be used according to the invention can be converted into common seed coating formulations, such as solutions, emulsions, suspensions, powders, foams, pastes or other seed coating materials, as well as formulations ULV too.
These formulations are prepared in a known manner by mixing the active compounds or combinations of active compounds with usual additives, such as, for example, usual diluents and also solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, thickeners secondary, adhesives, gibberellins and also water.
Dyes that may be present in seed treatment formulations that can be used in accordance with the present invention include all the usual dyes for such purposes. Both pigments, with little water solubility, and dye, which are soluble in water, can be used. Examples that can be mentioned include the dyes known under the designations of Rhodamine B, Pigment CI Red 112, and Solvent C.I.Red1.
Suitable wetting agents, which can be present in seed treatment formulations that can be used according to the invention include all substances that promote wetting and are usual in the formulation of agrochemical active substances. Preferably, it is possible to use alkylnaphthalene sulfonates, such as diisopropyl- or diisobutylnaphthalene sulfonates.
Suitable dispersants and / or emulsifiers that may be present in seed treatment formulations that can be used in accordance with the present invention include all nonionic, anionic and cationic dispersing agents that are usual in the formulation of agrochemical active substances. Preferably, it is possible to use nonionic or anionic dispersants or mixtures of nonionic or anionic dispersing agents. Particularly suitable nonionic dispersants are blocks of ethylene oxide-propylene oxide polymers, polyglycol alkylphenol ethers, and tristyrylphenol polyglycol ethers and their phosphate or sulfate derivatives. Particularly suitable anionic dispersants are polyacrylic lignosulfonates, salts, and arylsulfonate-formaldehyde condensates.
Defoamers that may be present in seed treatment formulations to be used in accordance with the present invention include all foam-inhibiting compounds that are usual in the formulation of agrochemically active compounds. Preference is given to the use of silicone antifoam agents, magnesium stearate, silicone emulsions, long-chain alcohols, fatty acids and their salts and also organofluorinated compounds and mixtures thereof.
Preservatives that can be present in seed treatment formulations to be used according to the invention include all compounds that can be used for such purposes in agrochemical compositions. As an example, mention may be made of dichlorophen and hemiformal benzyl alcohol.
Secondary thickeners that may be present in seed treatment formulations to be used according to the invention include all compounds that can be used for such purposes in agrochemical compositions. Preference is given to cellulose derivatives, acrylic acid derivatives, polysaccharides, such as xanthan gum or Veegum, modified clays, phyllosilicates, such as atapulgite and bentonite, and also finely divided silicic acids.
Suitable adhesives that may be present in seed treatment formulations to be used according to the invention include all the usual binding agents that can be used in seed treatment. Polyvinylpyrrolidone, polyvinyl alcohol acetate, and Tylose can be mentioned as being preferred.
Suitable gibberellins that may be present in seed treatment formulations to be used according to the invention are preferably gibberellins A1, A3 (= gibberellic acid), A4 and A7; Particular preference is given to the use of gibberellic acid. Gibberellins are known (cf. R. Wegler "Chemie der Planzenschutz and Schadlingsbekampfungsmittel" [Chemistry of Crop Protection Agents and Pesticides], vol. 2, Springer Verlag, 1970, pp 401-412).
Seed treatment formulations that can be used according to the invention can be used directly or after dilution with water, before treating the seed of any of a wide variety of types. Seed treatment formulations, which can be used according to the invention or their diluted preparations can also be used to coat seeds of transgenic plants. In this context, synergistic effects can also arise, in interaction with substances formed by expression.
Mixing equipment suitable for treating seeds with seed coating formulations, which can be used according to the invention or the preparations prepared therefrom by adding water includes all mixing equipment, which can normally be used for the coating. The specific procedure adopted when coating comprises introducing the seed to a mixer, adding the desired amount of special formulation for seed treatment, either alone or with a dilution in previous water, and mixing until the formulation is evenly distributed over the seed. Optionally, a drying operation is carried out later.
The nematicidal compositions according to the invention can be used for curative control or protection of nematodes. Therefore, the invention also relates to methods of cure and protection to control nematodes using fluopyram and compositions containing fluopyram according to the invention, which are applied to seeds, plants or parts of plants, fruit or the soil on which plants grow. Preference is given to application on the plant or parts of the plant, the fruits or the soil.
The compositions according to the invention for controlling nematodes in crop protection comprise an active but non-phytotoxic amount of the compounds according to the invention. "Active, but non-phytotoxic amount" means an amount of the composition according to the invention, which is sufficient to completely control or kill plant diseases caused by nematodes, which rise at the same time, show no symptoms of notable phytotoxicity. These rates of general application may vary over a broader range, where the rate depends on several factors, eg. the nematodes, the plant or culture, the climatic conditions and the ingredients of the composition according to the invention.
The fact that the active compounds, in the concentrations necessary for the control of plant diseases, are well tolerated by the plants allows the treatment of the aerial part of the plants, the vegetative propagation material and seeds, and the soil.
In an exemplary seed treatment method, an aqueous composition comprising fluopyram can be applied at a rate to provide a scale of 0.5 g to 10 kg, preferably from 0.8 g to 5 kg, more preferably from 1 g to 1 kg per Fluopiram 100 kg (dt) of seeds.
In an exemplary method of seed treatment, an aqueous composition comprising the biological control agent, in particular, spores of Bacillus firmus CNCM I-1582 can be applied at a rate that provides a scale of 0.1 g to 20 g, preferably 1-10 g, in particular preferably 2.5 g to 7.5 g., And more preferably about 5 g of spores of Bacillus firmus CNCM I-1582, per hectare or 100,000 grains of seed. The scales above refer to a spore formulation or suspension containing 1011 spores / g.
In various embodiments, the biological control agent is added to the seed at a rate of about 1 x 105 to 1 x 108 colony forming units (cfu) per seed, including about 1 x 105 cfu / seed, or about 1 x 106cfu / seed, or about 1 x 107cfu / seed, or about 1 x 108cfu / seed, including about 1 x 105a 1 x 107cfu / per seed, about 1 x 105a 1 x 106cfu / per seed, about 1 x 106a 1 x 108cfu / per seed, about 1 x 106a 1 x 107cfu / per seed and about 1 x 107a 1 x 108cfu / per seed.
The general concepts of the present invention are described in the following examples, which should not be considered as limiting. Experimental examples Example 1.
Two tests were planted with Jack (a variety of SCN resistant soybeans with PI 88788 resistance) and two genetically modified Jack varieties (AXN2 and AXMI031) known to produce a nematicidal protein. The seed was treated with a color / coating base or the same base with more than two different fluopyram rates (experiment 1 using 0.075 mg fluopyram / seed and experiment 2 using 0.15 mg fluopyram / seed). The SCN used to inoculate two tests were collected from an innate colony (OP50), with the ability to overcome PI 88788 resistance.
The tests were conducted as non-randomized blocks with a minimum of 10 repetitions. The seeds were planted in individual 4 "pots with coarse sand clay and inoculated with about 20,000 young OP50s in 10 equal inoculations starting at planting and approximately every three days. The plants were kept in a germination chamber. The blocks were rotated approximately every three days to minimize the potential influence of environmental variance, two months after planting, the plants were harvested and the cysts were collected and counted to assess the efficacy of the nematicide and characteristics, either individually or in combination with each other.
With the base treatment (color / coating), halfway through the design a reduction in height was recorded with both genetically modified varieties compared to unprocessed plants.
Fluopiram (AR83685) was not shown to provide a positive growth response, which was also seen in Jack's non-transgenic plants in this experiment. However, fluopyram increased the average plant height in both genetically modified varieties, in both experiments, while it had no effect on non-transgenic control plants. Thus, despite not being linked to any particular theory or mechanism, it appears that the application of fluopiram to the transgenic plants Axn2 and Axmi031 overcame the growth inhibitory effects resulting from the presence of the transgene. There were no effects to promote the growth of non-transgenic control plants, nor in untreated transgenic plants.
In both experiments (0.075 mg fluopyram / seed and 0.15 mg fluopyram / seed) the average number of cysts collected from Jack plants with the base (color / coating) of the treatment was relatively consistent (1310 and 1190 cysts). When comparing these averages with those of the AXMI031 plants (also with treatment with a base), the percentage reductions were also very consistent (92% and 88%). As for plants (AXN2 again with base treatment), the individual results in the second experiment were highly variable and, in the end, the overall percentage reduction (compared to Jack) was significantly higher (43%) compared with the first experiment (20%). See Figure 1.
In the first experiment, fluopyram (0.075 mg / seed) reduced NCS populations by 26% compared to non-transgenic Jack plants. When the rate of chemistry was doubled in the second experiment (0.15 mg fluopyram / seed), the reduction almost doubled, as well (43%). Considering that this is an experimental nematicide, the limiting factor was not likely SCN immune to the effects of the chemical, but more likely its distribution within the rhizosphere and the number of SCN which was exposed to a lethal concentration.
Based on the assumption that the percentage of control attributable to fluopyram would be expected to be lower with the transgenic seed, due to a potential overlap (eg, less available nematodes for targeting the fluopyram). However, the control achieved through the characteristics (20/43% - AXN2, 92/88% - AXMI31) did not diminish the effects of fluopyram. Fluopiram provided an approximate 20% reduction in the low rate and an approximate 40% reduction in the high rate for both Axmi031 and Axn2. Thus, fluopiram resulted in a consistent level of nematode control, despite the significantly lower nematode pressure that results from the presence of the transgene (Figure 2).

权利要求:
Claims (6)
[0001]
1. A method to control soy cyst nematode (Heterodera glycines) that infests a soybean nematode resistant plant characterized by understanding the application of N- {2- [3-chloro-5- (trifluoromethyl) -2-pyridinyl] ethyl} -2- (trifluoromethyl) benzamide (fluopyram) of formula (I)
[0002]
Method according to claim 1, characterized in that the fluopyram is applied at a rate of 100 g to 5 kg per ha.
[0003]
Method according to claim 1, characterized in that the fluopyram is applied to a plant seed resistant to soybean nematode.
[0004]
Method according to claim 3, characterized in that fluopyram is applied at a rate of 10 to 10,000 mg per kilogram of seed.
[0005]
Method according to claim 3, characterized in that fluopyram is applied at a rate of 10 to 300 mg per kilogram of seed.
[0006]
Method according to claim 1, characterized in that the soybean resistant plant comprises a transgenic soybean plant comprising Axmi031 or Axn2.

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---

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---

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---

WO2012038480A2|2012-03-29|

---

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---

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---

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---

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---

UY33625A|2012-04-30|

---

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---

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---

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引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

---

US2036008A|1934-11-07|1936-03-31|White Martin Henry|Plug fuse|

---

US3247908A|1962-08-27|1966-04-26|Robook Nicolay Nikolaevich|Adjustable blades hydraulic turbine runner|

---

US4272417A|1979-05-22|1981-06-09|Cargill, Incorporated|Stable protective seed coating|

---

US4245432A|1979-07-25|1981-01-20|Eastman Kodak Company|Seed coatings|

---

MA19709A1|1982-02-17|1983-10-01|Ciba Geigy Ag|APPLICATION OF QUINOLEIN DERIVATIVES TO THE PROTECTION OF CULTIVATED PLANTS.|

---

DE3382743D1|1982-05-07|1994-05-11|Ciba Geigy|Use of quinoline derivatives to protect crops.|

---

JPS6087254A|1983-10-19|1985-05-16|Japan Carlit Co Ltd:The|Novel urea compound and herbicide containing the same|

---

US5304732A|1984-03-06|1994-04-19|Mgi Pharma, Inc.|Herbicide resistance in plants|

---

US5331107A|1984-03-06|1994-07-19|Mgi Pharma, Inc.|Herbicide resistance in plants|

---

US4761373A|1984-03-06|1988-08-02|Molecular Genetics, Inc.|Herbicide resistance in plants|

---

DE3525205A1|1984-09-11|1986-03-20|Hoechst Ag, 6230 Frankfurt|PLANT PROTECTIVE AGENTS BASED ON 1,2,4-TRIAZOLE DERIVATIVES AND NEW DERIVATIVES OF 1,2,4-TRIAZOLE|

---

EP0191736B1|1985-02-14|1991-07-17|Ciba-Geigy Ag|Use of quinoline derivatives for the protection of crop plants|

---

ES2018274T5|1986-03-11|1996-12-16|Plant Genetic Systems Nv|VEGETABLE CELLS RESISTANT TO GLUTAMINE SYNTHETASE INHIBITORS, PREPARED BY GENETIC ENGINEERING.|

---

US5637489A|1986-08-23|1997-06-10|Hoechst Aktiengesellschaft|Phosphinothricin-resistance gene, and its use|

---

US5273894A|1986-08-23|1993-12-28|Hoechst Aktiengesellschaft|Phosphinothricin-resistance gene, and its use|

---

US5276268A|1986-08-23|1994-01-04|Hoechst Aktiengesellschaft|Phosphinothricin-resistance gene, and its use|

---

US5605011A|1986-08-26|1997-02-25|E. I. Du Pont De Nemours And Company|Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase|

---

US5378824A|1986-08-26|1995-01-03|E. I. Du Pont De Nemours And Company|Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase|

---

US5013659A|1987-07-27|1991-05-07|E. I. Du Pont De Nemours And Company|Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase|

---

DE3633840A1|1986-10-04|1988-04-14|Hoechst Ag|PHENYLPYRAZOLIC CARBONIC ACID DERIVATIVES, THEIR PRODUCTION AND USE AS PLANT GROWTH REGULATORS AND SAFENERS|

---

DE3775527D1|1986-10-22|1992-02-06|Ciba Geigy Ag|1,5-DIPHENYLPYRAZOLE-3-CARBONIC ACID DERIVATIVES FOR THE PROTECTION OF CROPS.|

---

US4808430A|1987-02-27|1989-02-28|Yazaki Corporation|Method of applying gel coating to plant seeds|

---

US5638637A|1987-12-31|1997-06-17|Pioneer Hi-Bred International, Inc.|Production of improved rapeseed exhibiting an enhanced oleic acid content|

---

DE3808896A1|1988-03-17|1989-09-28|Hoechst Ag|PLANT PROTECTION AGENTS BASED ON PYRAZOL CARBON SEA DERIVATIVES|

---

GB8810120D0|1988-04-28|1988-06-02|Plant Genetic Systems Nv|Transgenic nuclear male sterile plants|

---

DE3817192A1|1988-05-20|1989-11-30|Hoechst Ag|PLANT-PROTECTIVE AGENTS CONTAINING 1,2,4-TRIAZOLE DERIVATIVES AND NEW DERIVATIVES OF 1,2,4-TRIAZOLE|

---

US5084082A|1988-09-22|1992-01-28|E. I. Du Pont De Nemours And Company|Soybean plants with dominant selectable trait for herbicide resistance|

---

EP0365484B1|1988-10-20|1993-01-07|Ciba-Geigy Ag|Sulfamoyl phenyl ureas|

---

US6013861A|1989-05-26|2000-01-11|Zeneca Limited|Plants and processes for obtaining them|

---

DK0412911T3|1989-08-10|2001-10-29|Aventis Cropscience Nv|Plants with modified flowers|

---

DE3939010A1|1989-11-25|1991-05-29|Hoechst Ag|ISOXAZOLINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PLANT PROTECTIVE AGENT|

---

DE3939503A1|1989-11-30|1991-06-06|Hoechst Ag|NEW PYRAZOLINE FOR THE PROTECTION OF CULTURAL PLANTS AGAINST HERBICIDES|

---

US5908810A|1990-02-02|1999-06-01|Hoechst Schering Agrevo Gmbh|Method of improving the growth of crop plants which are resistant to glutamine synthetase inhibitors|

---

US5739082A|1990-02-02|1998-04-14|Hoechst Schering Agrevo Gmbh|Method of improving the yield of herbicide-resistant crop plants|

---

AT152572T|1990-04-04|1997-05-15|Pioneer Hi Bred Int|MANUFACTURE OF RAPESEED WITH A REDUCED LEVEL OF SATURATED FATTY ACIDS|

---

US5198599A|1990-06-05|1993-03-30|Idaho Resarch Foundation, Inc.|Sulfonylurea herbicide resistance in plants|

---

AU655197B2|1990-06-25|1994-12-08|Monsanto Technology Llc|Glyphosate tolerant plants|

---

WO1992000964A1|1990-07-05|1992-01-23|Nippon Soda Co., Ltd.|Amine derivative|

---

FR2667078B1|1990-09-21|1994-09-16|Agronomique Inst Nat Rech|DNA SEQUENCE GIVING MALE CYTOPLASMIC STERILITY, MITOCHONDRIAL, MITOCHONDRIA AND PLANT CONTAINING THE SAME, AND PROCESS FOR THE PREPARATION OF HYBRIDS.|

---

DE59108636D1|1990-12-21|1997-04-30|Hoechst Schering Agrevo Gmbh|New 5-chloroquinoline-8-oxyalkanecarboxylic acid derivatives, process for their preparation and their use as antidots of herbicides|

---

DE4104782B4|1991-02-13|2006-05-11|Bayer Cropscience Gmbh|Novel plasmids containing DNA sequences that cause changes in carbohydrate concentration and carbohydrate composition in plants, as well as plants and plant cells containing these plasmids|

---

US5731180A|1991-07-31|1998-03-24|American Cyanamid Company|Imidazolinone resistant AHAS mutants|

---

US6270828B1|1993-11-12|2001-08-07|Cargrill Incorporated|Canola variety producing a seed with reduced glucosinolates and linolenic acid yielding an oil with low sulfur, improved sensory characteristics and increased oxidative stability|

---

GB2264726A|1992-02-27|1993-09-08|Chu Rey Chin|Demountable multi-storey car park|

---

GB9204388D0|1992-02-29|1992-04-15|Tioxide Specialties Ltd|Water-in-oil emulsions|

---

TW259690B|1992-08-01|1995-10-11|Hoechst Ag|

---

DE4227061A1|1992-08-12|1994-02-17|Inst Genbiologische Forschung|A polyfructane sucrase DNA sequence from Erwinia Amylovora|

---

GB9218185D0|1992-08-26|1992-10-14|Ici Plc|Novel plants and processes for obtaining them|

---

US5743477A|1992-08-27|1998-04-28|Dowelanco|Insecticidal proteins and method for plant protection|

---

EP0664835B1|1992-10-14|2004-05-19|Syngenta Limited|Novel plants and processes for obtaining them|

---

GB9223454D0|1992-11-09|1992-12-23|Ici Plc|Novel plants and processes for obtaining them|

---

AU684068B2|1993-03-25|1997-12-04|Syngenta Participations Ag|Novel pesticidal proteins and strains|

---

EP1329154A3|1993-04-27|2004-03-03|Cargill, Inc.|Non-hydrogenated canola oil for food applications|

---

WO1995004826A1|1993-08-09|1995-02-16|Institut Für Genbiologische Forschung Berlin Gmbh|Debranching enzymes and dna sequences coding them, suitable for changing the degree of branching of amylopectin starch in plants|

---

DE4330960C2|1993-09-09|2002-06-20|Aventis Cropscience Gmbh|Combination of DNA sequences that enable the formation of highly amylose-containing starch in plant cells and plants, processes for producing these plants and the modified starch that can be obtained therefrom|

---

DE4331448A1|1993-09-16|1995-03-23|Hoechst Schering Agrevo Gmbh|Substituted isoxazolines, processes for their preparation, compositions containing them and their use as safeners|

---

CN1066487C|1993-10-01|2001-05-30|三菱商事株式会社|Gene that identifies sterile plant cytoplasm and process for preparing hybrid plant by using the same|

---

AU692791B2|1993-10-12|1998-06-18|Agrigenetics, Inc.|Brassica napus variety AG019|

---

US5908975A|1993-11-09|1999-06-01|E. I. Du Pont De Nemours And Company|Accumulation of fructans in plants by targeted expression of bacterial levansucrase|

---

US5837458A|1994-02-17|1998-11-17|Maxygen, Inc.|Methods and compositions for cellular and metabolic engineering|

---

US5605793A|1994-02-17|1997-02-25|Affymax Technologies N.V.|Methods for in vitro recombination|

---

AU688006B2|1994-03-25|1998-03-05|Brunob Ii B.V.|Method for producing altered starch from potato plants|

---

DK0759993T3|1994-05-18|2007-11-12|Bayer Bioscience Gmbh|DNA sequences encoding enzymes capable of facilitating the synthesis of linear alpha 1,4-glucans in plants, fungi and microorganisms|

---

US5824790A|1994-06-21|1998-10-20|Zeneca Limited|Modification of starch synthesis in plants|

---

CN1156951A|1994-06-21|1997-08-13|曾尼卡有限公司|Novel plants and processes for obtaining them|

---

NL1000064C1|1994-07-08|1996-01-08|Stichting Scheikundig Onderzoe|Production of oligosaccharides in transgenic plants.|

---

DE4441408A1|1994-11-10|1996-05-15|Inst Genbiologische Forschung|DNA sequences from Solanum tuberosum encoding enzymes involved in starch synthesis, plasmids, bacteria, plant cells and transgenic plants containing these sequences|

---

DE4447387A1|1994-12-22|1996-06-27|Inst Genbiologische Forschung|Debranching enzymes from plants and DNA sequences encoding these enzymes|

---

DK0795018T3|1995-01-06|2008-01-21|Plant Res Int Bv|DNA sequences encoding carbohydrate polymer synthesizing enzymes and method for producing transgenic plants|

---

DE19509695A1|1995-03-08|1996-09-12|Inst Genbiologische Forschung|Process for the preparation of a modified starch in plants, and the modified starch isolatable from the plants|

---

US6406690B1|1995-04-17|2002-06-18|Minrav Industries Ltd.|Bacillus firmus CNCM I-1582 or Bacillus cereus CNCM I-1562 for controlling nematodes|

---

US5853973A|1995-04-20|1998-12-29|American Cyanamid Company|Structure based designed herbicide resistant products|

---

BR9604993B1|1995-04-20|2009-05-05|a mutant encoding a mutant ahas protein of acetohydroxy acid synthesis and mutant ahas proteins.|

---

WO1996034968A2|1995-05-05|1996-11-07|National Starch And Chemical Investment Holding Corporation|Improvements in or relating to plant starch composition|

---

FR2734842B1|1995-06-02|1998-02-27|Rhone Poulenc Agrochimie|DNA SEQUENCE OF A HYDROXY-PHENYL PYRUVATE DIOXYGENASE GENE AND OBTAINING PLANTS CONTAINING A HYDROXY-PHENYL PYRUVATE DIOXYGENASE GENE, TOLERANT TO CERTAIN HERBICIDES|

---

US6284479B1|1995-06-07|2001-09-04|Pioneer Hi-Bred International, Inc.|Substitutes for modified starch and latexes in paper manufacture|

---

US5712107A|1995-06-07|1998-01-27|Pioneer Hi-Bred International, Inc.|Substitutes for modified starch and latexes in paper manufacture|

---

GB9513881D0|1995-07-07|1995-09-06|Zeneca Ltd|Improved plants|

---

FR2736926B1|1995-07-19|1997-08-22|Rhone Poulenc Agrochimie|5-ENOL PYRUVYLSHIKIMATE-3-PHOSPHATE SYNTHASE MUTEE, CODING GENE FOR THIS PROTEIN AND PROCESSED PLANTS CONTAINING THIS GENE|

---

DK1435205T3|1995-09-19|2010-03-29|Bayer Bioscience Gmbh|Process for preparing a modified starch|

---

GB9524938D0|1995-12-06|1996-02-07|Zeneca Ltd|Modification of starch synthesis in plants|

---

DE19601365A1|1996-01-16|1997-07-17|Planttec Biotechnologie Gmbh|Nucleic acid molecules from plants encoding enzymes involved in starch synthesis|

---

DE19608918A1|1996-03-07|1997-09-11|Planttec Biotechnologie Gmbh|Nucleic Acid Molecules Encoding New Debranching Enzymes from Maize|

---

US5773704A|1996-04-29|1998-06-30|Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College|Herbicide resistant rice|

---

DE19618125A1|1996-05-06|1997-11-13|Planttec Biotechnologie Gmbh|Nucleic acid molecules that encode new potato debranching enzymes|

---

DE19619918A1|1996-05-17|1997-11-20|Planttec Biotechnologie Gmbh|Nucleic acid molecules encoding soluble starch synthases from maize|

---

DE19621522A1|1996-05-29|1997-12-04|Hoechst Schering Agrevo Gmbh|New N-acylsulfonamides, new mixtures of herbicides and antidots and their use|

---

DE69737448T2|1996-05-29|2007-11-15|Bayer Cropscience Ag|NUCLEIC ACID MOLECULES CODING FOR ENZYMES FROM WHEAT INVOLVED IN STARCH SYNTHESIS|

---

AU731253B2|1996-06-12|2001-03-29|Pioneer Hi-Bred International, Inc.|Substitutes for modified starch in paper manufacture|

---

JP2001503607A|1996-06-12|2001-03-21|パイオニアハイ―ブレッドインターナショナル，インコーポレイテッド|A substitute for modified starch in papermaking.|

---

WO1997047807A1|1996-06-12|1997-12-18|Pioneer Hi-Bred International, Inc.|Substitutes for modified starch in paper manufacture|

---

US5876739A|1996-06-13|1999-03-02|Novartis Ag|Insecticidal seed coating|

---

AUPO069996A0|1996-06-27|1996-07-18|Australian National University, The|Manipulation of plant cellulose|

---

US5850026A|1996-07-03|1998-12-15|Cargill, Incorporated|Canola oil having increased oleic acid and decreased linolenic acid content|

---

US5773702A|1996-07-17|1998-06-30|Board Of Trustees Operating Michigan State University|Imidazolinone herbicide resistant sugar beet plants|

---

EP0929543B1|1996-09-26|2001-10-31|Syngenta Participations AG|Herbicidal composition|

---

GB9623095D0|1996-11-05|1997-01-08|Nat Starch Chem Invest|Improvements in or relating to starch content of plants|

---

US6232529B1|1996-11-20|2001-05-15|Pioneer Hi-Bred International, Inc.|Methods of producing high-oil seed by modification of starch levels|

---

DE19653176A1|1996-12-19|1998-06-25|Planttec Biotechnologie Gmbh|New maize nucleic acid molecules and their use to produce a modified starch|

---

DE19652961A1|1996-12-19|1998-06-25|Hoechst Schering Agrevo Gmbh|New 2-fluoroacrylic acid derivatives, new mixtures of herbicides and antidots and their use|

---

CA2193938A1|1996-12-24|1998-06-24|David G. Charne|Oilseed brassica containing an improved fertility restorer gene for ogura cytoplasmic male sterility|

---

US5981840A|1997-01-24|1999-11-09|Pioneer Hi-Bred International, Inc.|Methods for agrobacterium-mediated transformation|

---

US6071856A|1997-03-04|2000-06-06|Zeneca Limited|Herbicidal compositions for acetochlor in rice|

---

DE19708774A1|1997-03-04|1998-09-17|Max Planck Gesellschaft|Enzymes encoding nucleic acid molecules which have fructosyl polymerase activity|

---

DE19709775A1|1997-03-10|1998-09-17|Planttec Biotechnologie Gmbh|Nucleic acid molecules encoding corn starch phosphorylase|

---

DE19727410A1|1997-06-27|1999-01-07|Hoechst Schering Agrevo Gmbh|3- -2-quinolones and crop protection agents containing them|

---

GB9718863D0|1997-09-06|1997-11-12|Nat Starch Chem Invest|Improvements in or relating to stability of plant starches|

---

DE19742951A1|1997-09-29|1999-04-15|Hoechst Schering Agrevo Gmbh|Acylsulfamoylbenzoic acid amides, crop protection agents containing them and process for their preparation|

---

DE19749122A1|1997-11-06|1999-06-10|Max Planck Gesellschaft|Enzymes encoding nucleic acid molecules that have fructosyl transferase activity|

---

FR2770854B1|1997-11-07|2001-11-30|Rhone Poulenc Agrochimie|DNA SEQUENCE OF A GENE OF HYDROXY-PHENYL PYRUVATE DIOXYGENASE AND PRODUCTION OF PLANTS CONTAINING SUCH A GENE, HERBICIDE TOLERANT|

---

FR2772789B1|1997-12-24|2000-11-24|Rhone Poulenc Agrochimie|PROCESS FOR THE ENZYMATIC PREPARATION OF HOMOGENTISATE|

---

AU3478499A|1998-04-09|1999-11-01|E.I. Du Pont De Nemours And Company|Starch r1 phosphorylation protein homologs|

---

WO1999053933A1|1998-04-17|1999-10-28|Her Majesty The Queen In Right Of Canada As Represented By The Minister Of Agrigulture And Agri-Food Canada|Process for recovery and purification of saponins and sapogenins from quinoa |

---

DE69934224T2|1998-04-27|2007-10-04|Kumiai Chemical Industry Co., Ltd.|3-ARYLPHENYLSULFIDE DERIVATIVES AND INSECTICIDES AND MITICIDES|

---

DE19820608A1|1998-05-08|1999-11-11|Hoechst Schering Agrevo Gmbh|New nucleic acid encoding isoamylase from wheat and related transgenic plants producing starch with altered properties|

---

DE19820607A1|1998-05-08|1999-11-11|Hoechst Schering Agrevo Gmbh|New enzyme with starch synthase activity, useful for producing starch for foods and packaging materials|

---

DE59913709D1|1998-05-13|2006-09-07|Bayer Bioscience Gmbh|TRANSGENIC PLANTS WITH CHANGED ACTIVITY OF A PLASTIC ADP / ATP TRANSLOCATOR|

---

DE19821614A1|1998-05-14|1999-11-18|Hoechst Schering Agrevo Gmbh|Sugar beet mutants which are tolerant to sulfonylurea herbicides|

---

DK1092033T3|1998-06-15|2009-05-18|Brunob Ii Bv|Improvements to or relating to plants and plant products|

---

US6693185B2|1998-07-17|2004-02-17|Bayer Bioscience N.V.|Methods and means to modulate programmed cell death in eukaryotic cells|

---

DE19836099A1|1998-07-31|2000-02-03|Hoechst Schering Agrevo Gmbh|Nucleic acid molecules coding for a β-amylase, plants which synthesize a modified starch, process for the preparation of the plants, their use and the modified starch|

---

DE19836097A1|1998-07-31|2000-02-03|Hoechst Schering Agrevo Gmbh|Nucleic acid molecules coding for an alpha-glucosidase, plants that synthesize a modified starch, process for producing the plants, their use and the modified starch|

---

DE19836098A1|1998-07-31|2000-02-03|Hoechst Schering Agrevo Gmbh|Plants that synthesize a modified starch, process for producing the plants, their use and the modified starch|

---

AU6018399A|1998-08-25|2000-03-14|Pioneer Hi-Bred International, Inc.|Plant glutamine: fructose-6-phosphate amidotransferase nucleic acids|

---

EP1109916A1|1998-09-02|2001-06-27|Planttec Biotechnologie GmbH|Nucleic acid molecules encoding an amylosucrase|

---

DK1117802T3|1998-10-09|2010-05-25|Bayer Bioscience Gmbh|Nucleic acid molecules encoding a branching enzyme from bacteria of the genus Neisseria as well as a process for producing alpha-1,6-branched alpha-1,4-glucans|

---

EP1131452B1|1998-11-09|2014-01-22|Bayer CropScience Aktiengesellschaft|Nucleic acid molecules from rice and their use for the production of modified starch|

---

US6503904B2|1998-11-16|2003-01-07|Syngenta Crop Protection, Inc.|Pesticidal composition for seed treatment|

---

US6531648B1|1998-12-17|2003-03-11|Syngenta Participations Ag|Grain processing method and transgenic plants useful therein|

---

DE19905069A1|1999-02-08|2000-08-10|Planttec Biotechnologie Gmbh|Alternansucrase encoding nucleic acid molecules|

---

US6323392B1|1999-03-01|2001-11-27|Pioneer Hi-Bred International, Inc.|Formation of brassica napus F1 hybrid seeds which exhibit a highly elevated oleic acid content and a reduced linolenic acid content in the endogenously formed oil of the seeds|

---

IL146063D0|1999-04-29|2002-07-25|Marlow Foods Ltd|Herbicide resistant plants|

---

AU4133100A|1999-04-29|2000-11-17|Syngenta Limited|Herbicide resistant plants|

---

DE19924342A1|1999-05-27|2000-11-30|Planttec Biotechnologie Gmbh|Genetically modified plant cells and plants with increased activity of an amylosucrase protein and a branching enzyme|

---

DE19926771A1|1999-06-11|2000-12-14|Aventis Cropscience Gmbh|Nucleic acid molecules from wheat, transgenic plant cells and plants and their use for the production of modified starch|

---

DE19937348A1|1999-08-11|2001-02-22|Aventis Cropscience Gmbh|Nucleic acid molecules from plants encoding enzymes involved in starch synthesis|

---

DE19937643A1|1999-08-12|2001-02-22|Aventis Cropscience Gmbh|Transgenic cells and plants with altered activity of the GBSSI and BE proteins|

---

WO2001014569A2|1999-08-20|2001-03-01|Basf Plant Science Gmbh|Increasing the polysaccharide content in plants|

---

US6423886B1|1999-09-02|2002-07-23|Pioneer Hi-Bred International, Inc.|Starch synthase polynucleotides and their use in the production of new starches|

---

US6472588B1|1999-09-10|2002-10-29|Texas Tech University|Transgenic cotton plants with altered fiber characteristics transformed with a sucrose phosphate synthase nucleic acid|

---

GB9921830D0|1999-09-15|1999-11-17|Nat Starch Chem Invest|Plants having reduced activity in two or more starch-modifying enzymes|

---

AR025996A1|1999-10-07|2002-12-26|Valigen Us Inc|NON-TRANSGENIC PLANTS RESISTANT TO HERBICIDES.|

---

ES2414438T3|2000-03-09|2013-07-19|E.I. Du Pont De Nemours And Company|Sunflower plants tolerant to sulfonylureas|

---

DE60111613T2|2000-03-09|2006-05-18|Monsanto Technology Llc.|METHOD FOR PRODUCING GLYPHOSATE TOLERANT PLANTS|

---

US6768044B1|2000-05-10|2004-07-27|Bayer Cropscience Sa|Chimeric hydroxyl-phenyl pyruvate dioxygenase, DNA sequence and method for obtaining plants containing such a gene, with herbicide tolerance|

---

US6303818B1|2000-08-08|2001-10-16|Dow Agrosciences Llc|Unsaturated oxime ethers and their use as fungicides|

---

BR0114322A|2000-09-29|2004-06-15|Syngenta Ltd|Glyphosate-resistant epsps enzyme, isolated polynucleotide, vector, plant material, fertile, morphologically normal whole plants, soybean, canola, brassica, cotton, sugar beet, sunflower, peas, potatoes and weeds, methods for selectively controlling weeds in a field, and to produce plants that are substantially tolerant or substantially resistant to glyphosate herbicide, use of polynucleotide, methods for selecting transformed biological material to express a gene of interest, and for regenerating a transformed fertile plant to contain a foreign one. and diagnostic kit|

---

US6660690B2|2000-10-06|2003-12-09|Monsanto Technology, L.L.C.|Seed treatment with combinations of insecticides|

---

US6734340B2|2000-10-23|2004-05-11|Bayer Cropscience Gmbh|Monocotyledon plant cells and plants which synthesise modified starch|

---

AR031027A1|2000-10-23|2003-09-03|Syngenta Participations Ag|AGROCHEMICAL COMPOSITIONS|

---

FR2815969B1|2000-10-30|2004-12-10|Aventis Cropscience Sa|TOLERANT PLANTS WITH HERBICIDES BY METABOLIC BYPASS|

---

EP1399566A2|2000-10-30|2004-03-24|Maxygen, Inc.|Novel glyphosate n-acetyltransferase genes|

---

EP2322629A3|2003-04-29|2011-11-02|Pioneer Hi-Bred International Inc.|Novel glyphosate-n-acetyltransferase genes|

---

AU1415802A|2000-12-07|2002-06-18|Syngenta Ltd|Herbicide resistant plants|

---

BR0115782A|2000-12-08|2004-01-20|Commonwealh Scient And Ind Res|Modification of sucrose synthase gene expression in plant tissue and uses|

---

US20020134012A1|2001-03-21|2002-09-26|Monsanto Technology, L.L.C.|Method of controlling the release of agricultural active ingredients from treated plant seeds|

---

WO2002079410A2|2001-03-30|2002-10-10|Basf Plant Science Gmbh|Glucan chain length domains|

---

CA2465884A1|2001-06-12|2002-12-19|Bayer Cropscience Gmbh|Transgenic plants synthesising high amylose starch|

---

US6582770B2|2001-07-31|2003-06-24|E.I. Du Pont De Nemours And Company|Process for coating|

---

AU2002322435A1|2001-08-09|2003-02-24|Cibus Genetics|Non-transgenic herbicide resistant plants|

---

JP2005508166A|2001-10-17|2005-03-31|ビーエーエスエフプラントサイエンス，ゲーエムベーハー|Starch|

---

AR037328A1|2001-10-23|2004-11-03|Dow Agrosciences Llc|COMPOSITE OF [7-BENCIL-2,6-DIOXO-1,5-DIOXONAN-3-IL] -4-METOXIPIRIDIN-2-CARBOXAMIDE, COMPOSITION THAT UNDERSTANDS AND METHOD THAT USES IT|

---

DE10208132A1|2002-02-26|2003-09-11|Planttec Biotechnologie Gmbh|Process for the production of maize plants with an increased leaf starch content and their use for the production of maize silage|

---

WO2003092360A2|2002-04-30|2003-11-13|Verdia, Inc.|Novel glyphosate-n-acetyltransferase genes|

---

CN1319946C|2002-08-12|2007-06-06|拜尔农科股份有限公司|Novel 2-pyridylethylbenzamide derivative|

---

EP1389614A1|2002-08-12|2004-02-18|Bayer CropScience S.A.|Novel N-[2-ethyl]benzamide derivatives as fungicides|

---

FR2844142B1|2002-09-11|2007-08-17|Bayer Cropscience Sa|TRANSFORMED PLANTS WITH ENHANCED PRENYLQUINON BIOSYNTHESIS|

---

PL377055A1|2002-10-29|2006-01-23|Basf Plant Science Gmbh|Compositions and methods for identifying plants having increased tolerance to imidazolinone herbicides|

---

AU2003275716A1|2002-10-31|2004-05-25|Ishihara Sangyo Kaisha, Ltd.|3-benzoyl-2,4,5-substituted pyridine derivatives or salts thereof and bactericides containing the same|

---

US20040110443A1|2002-12-05|2004-06-10|Pelham Matthew C.|Abrasive webs and methods of making the same|

---

DK1578973T3|2002-12-19|2008-11-24|Bayer Cropscience Ag|Plant cells and plants that synthesize a starch with increased final viscosity|

---

GB0230155D0|2002-12-24|2003-02-05|Syngenta Participations Ag|Chemical compounds|

---

JP2006521099A|2003-03-07|2006-09-21|ビーエーエスエフプラントサイエンスゲーエムベーハー|Promotion of amylose production in plants|

---

WO2004084631A1|2003-03-26|2004-10-07|Bayer Cropscience Gmbh|Use of aromatic hydroxy compounds as safeners|

---

US6743752B2|2003-03-28|2004-06-01|Northern Quinoa Corporation|Method of protecting plants from bacterial diseases|

---

ZA200508019B|2003-04-09|2006-12-27|Bayer Bioscience Nv|Methods and means for increasing the tolerance of plants to stress conditions|

---

WO2005002359A2|2003-05-22|2005-01-13|Syngenta Participations Ag|Modified starch, uses, methods for production thereof|

---

EP1633875B1|2003-05-28|2012-05-02|Basf Se|Wheat plants having increased tolerance to imidazolinone herbicides|

---

EP1493328A1|2003-07-04|2005-01-05|Institut National De La Recherche Agronomique|Method of producing double low restorer lines of brassica napus having a good agronomic value|

---

ES2354696T3|2003-07-31|2011-03-17|Toyo Boseki Kabushiki Kaisha|PLANT THAT PRODUCES HIALURONIC ACID.|

---

GB0318109D0|2003-08-01|2003-09-03|Syngenta Ltd|Improvements in or relating to organic compounds|

---

DE10335726A1|2003-08-05|2005-03-03|Bayer Cropscience Gmbh|Use of hydroxyaromatics as safener|

---

DE10335725A1|2003-08-05|2005-03-03|Bayer Cropscience Gmbh|Safener based on aromatic-aliphatic carboxylic acid derivatives|

---

WO2005017157A1|2003-08-15|2005-02-24|Commonwealth Scientific And Industrial Research Organisation |Methods and means for altering fiber characteristics in fiber-producing plants|

---

AR047107A1|2003-08-29|2006-01-11|Inst Nac De Tecnologia Agropec|RICE PLANTS THAT HAVE A GREATER TOLERANCE TO IMIDAZOLINONA HERBICIDES|

---

AT491784T|2003-09-30|2011-01-15|Bayer Cropscience Ag|PLANTS WITH REDUCED ACTIVITY OF A CLASS 3 BRANCHING SYSTEM|

---

WO2005030941A1|2003-09-30|2005-04-07|Bayer Cropscience Gmbh|Plants with increased activity of a class 3 branching enzyme|

---

BRPI0415972A|2003-10-31|2007-01-23|Mitsui Chemicals Inc|diamine derivatives, process for producing these derivatives, and plant disease control agents which contain these derivatives as active ingredients|

---

JP4939057B2|2004-01-23|2012-05-23|三井化学アグロ株式会社|3- isoquinolin-1-yl) quinoline compounds|

---

US7622301B2|2004-02-24|2009-11-24|Basf Plant Science Gmbh|Compositions and methods using RNA interference for control of nematodes|

---

EP1725666B1|2004-03-05|2012-01-11|Bayer CropScience AG|Plants with reduced activity of the starch phosphorylating enzyme phosphoglucan, water dikinase|

---

AR048026A1|2004-03-05|2006-03-22|Bayer Cropscience Gmbh|PROCEDURES FOR THE IDENTIFICATION OF PROTEINS WITH ENZYMATIC ACTIVITY FOSFORILADORA DE ALMIDON|

---

AR048025A1|2004-03-05|2006-03-22|Bayer Cropscience Gmbh|PLANTS WITH INCREASED ACTIVITY OF AN ALMIDON FOSFORILING ENZYME|

---

AR048024A1|2004-03-05|2006-03-22|Bayer Cropscience Gmbh|PLANTS WITH INCREASED ACTIVITY OF DIFFERENT ENZYMES FOSFORILANTES DEL ALMIDON|

---

US7432082B2|2004-03-22|2008-10-07|Basf Ag|Methods and compositions for analyzing AHASL genes|

---

DE102004023332A1|2004-05-12|2006-01-19|Bayer Cropscience Gmbh|Quinoxaline-2-one derivatives, crop protection agents containing them, and processes for their preparation and their use|

---

EP1766030A2|2004-06-16|2007-03-28|BASF Plant Science GmbH|Polynucleotides encoding mature ahasl proteins for creating imidazolinone-tolerant plants|

---

DE102004029763A1|2004-06-21|2006-01-05|Bayer Cropscience Gmbh|Plants that produce amylopectin starch with new properties|

---

TR200700491T2|2004-07-30|2007-04-24|Basf Agrochemical Products B.V.|Herbicide resistant sunflower plants, polynucleotides encoding herbicide resistant acetohydroxyacid synthase wide subunit proteins|

---

AR050095A1|2004-08-04|2006-09-27|Basf Plant Science Gmbh|SEQUENCES OF SMALL SUBINITIES OF SINTASA ACETOHIDROXIACIDE OF MONOCOTILEDONEAS AND METHODS OF USE.|

---

BRPI0514342A2|2004-08-13|2009-10-06|Basf Plant Science Gmbh|double stranded rna molecule, grouping of double stranded rna molecules, transgenic plant, and methods for controlling a parasitic nematode's infection of a plant and for manufacturing a transgenic plant|

---

ES2340183T3|2004-08-18|2010-05-31|Bayer Cropscience Ag|PLANTS WITH GREATER PLASTIC ACTIVITY OF ENZIMA R3 FOSFORILANTE DE ALMIDON.|

---

WO2006021972A1|2004-08-26|2006-03-02|Dhara Vegetable Oil And Foods Company Limited|A novel cytoplasmic male sterility system for brassica species and its use for hybrid seed production in indian oilseed mustard brassica juncea|

---

PL1805312T3|2004-09-23|2009-12-31|Bayer Ip Gmbh|Methods and means for producing hyaluronan|

---

EP1807519B1|2004-10-29|2012-02-01|Bayer BioScience N.V.|Stress tolerant cotton plants|

---

AR051690A1|2004-12-01|2007-01-31|Basf Agrochemical Products Bv|MUTATION INVOLVED IN THE INCREASE OF TOLERANCE TO IMIDAZOLINONE HERBICIDES IN PLANTS|

---

EP1672075A1|2004-12-17|2006-06-21|Bayer CropScience GmbH|Transformed plant expressing a dextransucrase and synthesizing a modified starch|

---

EP1679374A1|2005-01-10|2006-07-12|Bayer CropScience GmbH|Transformed plant expressing a mutansucrase and synthesizing a modified starch|

---

DE102005008021A1|2005-02-22|2006-08-24|Bayer Cropscience Ag|New spiroketal-substituted cyclic ketoenol compounds used for combating animal parasites, undesired plant growth and/or undesired microorganisms|

---

CN101128111B|2005-02-24|2013-01-30|辛根塔参与股份公司|Method of improving nematode tolerant or resistant plant growth|

---

JP2006304779A|2005-03-30|2006-11-09|Toyobo Co Ltd|Plant producing hexosamine in high productivity|

---

EP1707632A1|2005-04-01|2006-10-04|Bayer CropScience GmbH|Phosphorylated waxy potato starch|

---

EP1710315A1|2005-04-08|2006-10-11|Bayer CropScience GmbH|High phosphate starch|

---

WO2006129204A2|2005-05-31|2006-12-07|Devgen Nv|Rnai for control of insects and arachnids|

---

WO2006133827A2|2005-06-15|2006-12-21|Bayer Bioscience N.V.|Methods for increasing the resistance of plants to hypoxic conditions|

---

MX2008000097A|2005-06-24|2008-03-19|Bayer Bioscience Nv|Methods for altering the reactivity of plant cell walls.|

---

AR054174A1|2005-07-22|2007-06-06|Bayer Cropscience Gmbh|OVERPRINTING OF ALMIDON SYNTHEASE IN VEGETABLES|

---

TW200738701A|2005-07-26|2007-10-16|Du Pont|Fungicidal carboxamides|

---

JPWO2007023719A1|2005-08-22|2009-02-26|クミアイ化学工業株式会社|Pesticide mitigation agent and herbicide composition with reduced phytotoxicity|

---

RS20080076A|2005-08-24|2009-07-15|Pioneer Hi-Brend International Inc.,|Compositions providing tolerance to multiple herbicides and methods of use thereof|

---

JPWO2007023764A1|2005-08-26|2009-02-26|クミアイ化学工業株式会社|Pesticide mitigation agent and herbicide composition with reduced phytotoxicity|

---

EA015908B1|2005-08-31|2011-12-30|Монсанто Текнолоджи, Ллс|Insecticidal protein b.thuringiensis cry1a.105, encoding polynucleotide thereof and use thereof|

---

SG166097A1|2005-09-16|2010-11-29|Monsanto Technology Llc|Methods for genetic control of insect infestations in plants and compositions thereof|

---

PT2295584E|2005-09-16|2015-09-22|Devgen Nv|Transgenic plant-based methods for plant pests using rnai|

---

CA2624973C|2005-10-05|2016-01-19|Bayer Cropscience Ag|Production of hyaluronan from plants transgenic for hyaluronan synthase, gfat and udp-glucose dehydrogenase|

---

WO2007039314A2|2005-10-05|2007-04-12|Bayer Cropscience Ag|Plants with increased hyaluronan production|

---

CN101297041A|2005-10-05|2008-10-29|拜尔作物科学股份公司|Plants with an increased production of hyaluronan II|

---

JP5474356B2|2006-01-12|2014-04-16|デブジェンエヌブイ|Method for controlling pests using RNAi|

---

WO2007080126A2|2006-01-12|2007-07-19|Devgen N.V.|Dsrna as insect control agent|

---

CA2637665A1|2006-02-10|2007-08-23|Monsanto Technology Llc|Identification and use of target genes for control of the plant parasitic nematodes heterodera glycines|

---

TW201309635A|2006-02-10|2013-03-01|Dow Agrosciences Llc|Insecticidal N-substituted alkyl sulfoximines|

---

US20070214515A1|2006-03-09|2007-09-13|E.I.Du Pont De Nemours And Company|Polynucleotide encoding a maize herbicide resistance gene and methods for use|

---

WO2007104570A2|2006-03-16|2007-09-20|Devgen N.V.|Nematode control|

---

KR20090007718A|2006-03-21|2009-01-20|바이엘 바이오사이언스 엔.브이.|Stress resistant plants|

---

CN101405296B|2006-03-21|2014-04-30|拜尔作物科学公司|Novel genes encoding insecticidal proteins|

---

DE102006015468A1|2006-03-31|2007-10-04|Bayer Cropscience Ag|New cyclic enamine ketone derivatives useful for controlling pests, especially insects|

---

DE102006015467A1|2006-03-31|2007-10-04|Bayer Cropscience Ag|New cyclic enamine ketone derivatives useful for controlling pests, especially insects|

---

DE102006015470A1|2006-03-31|2007-10-04|Bayer Cropscience Ag|New cyclic enamine ketone derivatives useful for controlling pests, especially insects|

---

US7923602B2|2006-06-14|2011-04-12|Athenix Corp.|AXMI-031, AXMI-039, AXMI-040 and AXMI-049, a family of novel delta endotoxin genes and methods for their use|

---

TWI381811B|2006-06-23|2013-01-11|Dow Agrosciences Llc|A method to control insects resistant to common insecticides|

---

WO2008013622A2|2006-07-27|2008-01-31|E. I. Du Pont De Nemours And Company|Fungicidal azocyclic amides|

---

AT509113T|2006-11-29|2011-05-15|Athenix Corp|IMPROVED GRG23 EPSP SYNTHASES: COMPOSITIONS AND METHODS FOR THEIR USE|

---

DE102006057036A1|2006-12-04|2008-06-05|Bayer Cropscience Ag|New biphenyl substituted spirocyclic ketoenol derivatives useful for the manufacture of herbicides and for combating parasites|

---

CA2672083A1|2006-12-12|2008-06-19|Basf Plant Science Gmbh|Pathogen inducible plant trehalose-6-phophate phophatase gene promoters and regulatory elements|

---

BRPI0720574A2|2006-12-22|2014-02-04|Basf Plant Science Gmbh|PROMOTER, EXPRESSION CASSETTE, TRANSGENIC PLANT, AND METHOD OF CHECKING OR IMPROVING NEMATO RESISTANCE ON A PLANT|

---

BRPI0808371A2|2007-02-06|2014-07-08|Basf Plant Science Gmbh|TRANSGENIC PLANT, SEED, EXPRESSION VECTOR, AND METHOD OF PRODUCING A TRANSGENIC PLANT HAVING ENHANCED NEMATOID RESISTANCE|

---

CA2674494A1|2007-02-06|2008-08-14|Basf Plant Science Gmbh|Compositions and methods using rna interference for control of nematodes|

---

BRPI0806995A2|2007-02-08|2014-04-08|Basf Plant Science Gmbh|TRANSGENIC PLANT, SEED, EXPRESSION VECTOR, METHOD FOR INCREASING NEMATOID RESISTANCE ON A PLANT|

---

MX2009007729A|2007-02-08|2009-07-27|Basf Plant Science Gmbh|Polynucleotides encoding truncated sucrose isomerase polypeptides for control of parasitic nematodes.|

---

US20100115660A1|2007-02-08|2010-05-06|Basf Plant Science Gmbh|Compositions and Methods Using RNA Interference of OPR3-Like Gene For Control of Nematodes|

---

BRPI0807018A2|2007-02-08|2014-04-22|Basf Plant Science Gmbh|DSRNA Molecule, DSRNA Molecule Collection, Transgenic Plant, and Method of Preparing a Transgenic Plant|

---

EP2126094A1|2007-02-09|2009-12-02|BASF Plant Science GmbH|Compositions and methods using rna interference targeting mthfr - like genes for control of nematodes|

---

MX2009008356A|2007-02-09|2009-08-20|Basf Plant Science Gmbh|Compositions and methods of using rna interference of sca1-like genes for control of nematodes.|

---

WO2008095970A1|2007-02-09|2008-08-14|Basf Plant Science Gmbh|Compositions and methods using rna interference of cdpk-like for control of nematodes|

---

BRPI0808389A2|2007-03-15|2014-07-08|Basf Plant Science Gmbh|TRANSGENIC PLANT, SEED, EXPRESSION VECTOR, AND METHOD FOR INCREASING NEMATODE RESISTANCE ON A PLANT.|

---

CA2682156C|2007-04-12|2012-03-20|Nihon Nohyaku Co., Ltd.|Nematicidal agent composition and method of using the same|

---

CN101998988A|2007-05-30|2011-03-30|先正达参股股份有限公司|Cytochrome P450 genes conferring herbicide resistance|

---

CL2008001647A1|2007-06-08|2008-10-10|Syngenta Participations Ag|COMPOUNDS DERIVED FROM FENILETIL-AMIDA ACIDO-1H-PIRAZOL-4-CARBOXILICO; COMPOUNDS DERIVED FROM AMINA; METHOD TO CONTROL OR PREVENT INFRASTATION OF PLANTS BY PHYTOOPATHOGEN MICROORGANISMS; AND COMPOSITION FOR CONTROL|

---

BRPI0813165A2|2007-06-15|2014-11-11|Basf Plant Science Gmbh|DOUBLE TAPE RNA Molecule, TRANSGENIC PLANT, METHODS FOR PREPARING A TRANSGENIC PLANT, AND FOR GIVING A NEMATOID RESISTANCE PLANT, AND EXPRESSION CASSETTE AND EXPRESSION VECTOR.|

---

EP2198028A2|2007-08-31|2010-06-23|BASF Plant Science GmbH|Method for producing a transgenic plant cell, a plant or a part thereof with increased resistance to plant disease|

---

US20110258736A1|2007-08-31|2011-10-20|Basf Plant Science Gmbh|Pathogen Control Genes and Methods of Use in Plants|

---

WO2009048847A1|2007-10-12|2009-04-16|Monsanto Technology Llc|Methods and compositions for high yielding soybeans with nematode resistance|

---

WO2009068313A2|2007-11-28|2009-06-04|Bayer Bioscience N.V.|Brassica plant comprising a mutant indehiscent allele|

---

EP2064952A1|2007-11-29|2009-06-03|Bayer CropScience AG|Method for reducing mycotoxin contamination in maize|

---

EP2562175A1|2008-01-22|2013-02-27|Dow AgroSciences LLC|5-fluoro pyrimidine derivatives as fungicides|

---

TWI501728B|2008-04-07|2015-10-01|Bayer Cropscience Ag|Combinations of biological control agents and insecticides or fungicides|

---

US20110039706A1|2008-04-14|2011-02-17|Marco Busch|New mutated hydroxyphenylpyruvate dioxygenase, dna sequence and isolation of plants which are tolerant to hppd inhibitor herbicides|

---

NZ589991A|2008-06-25|2012-09-28|Athenix Corp|Toxin genes from bacillus thuringiensis and methods for their use|

---

EP2949659A1|2008-07-02|2015-12-02|Athenix Corporation|AXMI-115, AXMI-113, AXMI-005, AXMI-163 and AXMI-184: insecticidal proteins and methods for their use|

---

AU2009270539B2|2008-07-17|2015-04-23|BASF Agricultural Solutions Seed US LLC|Brassica plant comprising a mutant indehiscent allelle|

---

US8268843B2|2008-08-29|2012-09-18|Dow Agrosciences, Llc.|5,8-difluoro-4--phenyl)ethylamino)quinazolines and their use as agrochemicals|

---

JP2012502100A|2008-09-10|2012-01-26|バイエル・クロツプサイエンス・エル・ピー|Genetically modified seeds combining spore-forming bacteria and any insect control agent|

---

EP2039772A2|2009-01-06|2009-03-25|Bayer CropScience AG|Method for improved utilization of the production potential of transgenic plants introduction|

---

ES2585816T3|2009-03-25|2016-10-10|Bayer Cropscience Ag|Combinations of nematicidal active ingredients comprising fluopiram and Bacillus firmus|

---

WO2012004293A2|2010-07-08|2012-01-12|Bayer Cropscience Ag|Insecticide and fungicide active ingredient combinations|

---

AR083922A1|2010-11-22|2013-04-10|Bayer Cropscience Lp|PROCEDURES TO PREVENT AND / OR TREAT FUNGICAL DISEASES OR NEMATODES, SUCH AS THE SUBITA DEATH DEATH SYNDROME |

---

EA036053B1|2011-04-05|2020-09-21|Басф Агрикалчерал Солюшнс Сид Юс Ллк|Axmi115 VARIANT INSECTICIDAL GENE AND METHODS FOR ITS USE|CA2682156C|2007-04-12|2012-03-20|Nihon Nohyaku Co., Ltd.|Nematicidal agent composition and method of using the same|

---

AR083922A1|2010-11-22|2013-04-10|Bayer Cropscience Lp|PROCEDURES TO PREVENT AND / OR TREAT FUNGICAL DISEASES OR NEMATODES, SUCH AS THE SUBITA DEATH DEATH SYNDROME |

---

WO2012140207A2|2011-04-15|2012-10-18|Syngenta Participations Ag|Method for controlling nematode pests|

---

MX351526B|2011-07-28|2017-10-18|Athenix Corp|Axmi205 variant proteins and methods for their use.|

---

EP2737068A1|2011-07-29|2014-06-04|Athenix Corp.|Axmi279 pesticidal gene and methods for its use|

---

WO2013110594A1|2012-01-25|2013-08-01|Bayer Intellectual Property Gmbh|Active compound combinations containing fluopyram and biological control agent|

---

JP6182158B2|2012-01-25|2017-08-16|バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ|Active compound combination comprising fluopyram, Bacillus and a biological control agent|

---

NZ742943A|2012-05-30|2019-04-26|Bayer Cropscience Ag|Compositions comprising a biological control agent and a fungicide from the group consisting of inhibitors of the respiratory chain at complex i or ii|

---

KR102023962B1|2012-05-30|2019-09-23|바이엘 크롭사이언스 악티엔게젤샤프트|Compositions comprising a biological control agent and an insecticide|

---

CN103451117B|2012-06-04|2015-03-04|华中农业大学|Bacillus preparation for preventing and controlling pathogenic bacteria in soil environments as well as preparation method and application thereof|

---

AR092435A1|2012-09-12|2015-04-22|Bayer Cropscience Lp|COMPOSITIONS AND METHODS FOR CONTROLLING PARASITES OF PLANT NEMATODES|

---

US20150289516A1|2012-10-26|2015-10-15|Bayer Cropscience Lp|Biocontrol of nematodes|

---

EP2730570A1|2012-11-13|2014-05-14|Bayer CropScience AG|Pyridyloxyal alkyl carboxamides and their use as endoparasiticides and nematicide|

---

MX360582B|2012-12-13|2018-11-07|Inst De Ecologia A C Star|Biocontrol of phyto-parasitic nematodes using paecilomyces.|

---

CL2013000307A1|2013-01-30|2014-04-04|Bio Insumos Nativa Ltda|Bionematicide composition comprising at least two strains of bacillus or the fermentation products thereof, and an agronomically acceptable vehicle; formulation comprising the composition; bacillus nematicide strain|

---

EP2971143A4|2013-03-15|2016-08-24|Dow Agrosciences Llc|Markers linked to reniform nematode resistance|

---

MX360160B|2013-03-15|2018-10-24|Pioneer Hi Bred Int|PHI-4 POLYPEPTIDES and METHODS FOR THEIR USE.|

---

US9661857B2|2013-11-01|2017-05-30|Thomas T. Yamashita|Compositions for controlling plant parasitic nematodes|

---

JP2017501178A|2013-12-19|2017-01-12|バイエル・クロップサイエンス・アクチェンゲゼルシャフト|Compounds with nematicidal activity|

---

CN103789233A|2014-01-15|2014-05-14|河南农业大学|Biocontrol strain 09B18 for preventing and controlling cereal cyst nematode of wheat, method for preparing biocontrol agent and application of biocontrol agent|

---

CN103975925A|2014-05-24|2014-08-13|深圳诺普信农化股份有限公司|Fungicidal composition taking Fluopicolide as main ingredient|

---

ES2561908B2|2014-07-31|2016-12-01|Universidad De Granada|Use of Bacillus methylotrophicus as a plant growth stimulant and biological control medium, and strains isolated from that species|

---

CN104371959B|2014-11-18|2017-12-05|吴山功|Biological deodorizing fly eradication composite bacteria agent and its application|

---

EP3227274B1|2014-12-02|2019-07-03|Bayer CropScience Aktiengesellschaft|Bicyclic compounds as pest controllers|

---

CN113736809A|2014-12-12|2021-12-03|先正达参股股份有限公司|Compositions and methods for controlling plant pests|

---

EP3240403B1|2014-12-29|2019-11-13|FMC Corporation|Microbial compositions and methods of use for benefiting plant growth and treating plant disease|

---

UY36335A|2014-12-29|2017-04-28|Fmc Corp|MICROBIAL COMPOSITIONS INTENDED TO BE USED IN COMBINATION WITH INSECTICIDES FOR SOILS, TO BENEFIT THE GROWTH OF PLANTS|

---

CR20170327A|2015-01-16|2017-11-02|Valent Biosciences Llc|COMBINED FORMULATIONS OF BACILLUS THURINGIENSIS SUBESPECIE KURSTAKI AND BACILLUS THURINGIENSIS SUBESPECIE AIZAWAI|

---

CN104839227A|2015-04-08|2015-08-19|江苏省农业科学院|Application of Bacillus amyloliquefaciens B-1619 in control of root-knot nematode disease|

---

CN104770391A|2015-04-16|2015-07-15|广东中迅农科股份有限公司|Pesticide composition for preventing and controlling capsicum meloidogyne|

---

CN107846882A|2015-07-07|2018-03-27|拜耳作物科学有限合伙公司|For reducing grain nematode nematosis and improving the method and composition of herbaceous stem amount|

---

CN105660706B|2016-01-27|2018-05-25|山东省科学院生物研究所|Applications of the bacillus cereus BCJB01 in terms of root-knot nematode is prevented|

---

CN105613505B|2016-02-02|2017-12-19|山东省联合农药工业有限公司|A kind of nematicide of fluorine-containing ether bacterium acid amides|

---

US20190159455A1|2016-04-11|2019-05-30|Basf Se|Pesticidally Active Mixtures of Tioxazafen|

---

CN109068655A|2016-04-11|2018-12-21|巴斯夫欧洲公司|The pesticide activity mixture of tioxazafen|

---

BR112018075323A2|2016-06-06|2019-03-19|Bayer Cropscience Lp|methods of increasing plant yield and improving pest resistance|

---

CN106282067B|2016-08-24|2019-10-11|李丽丽|Multifunctional agricultural complex micro organism fungicide and probiotics and application|

---

CN106399159B|2016-08-30|2019-08-23|江西顺泉生物科技有限公司|A kind of bacillus firmus microbial inoculum and the preparation method and application thereof|

---

CN107318880A|2017-07-20|2017-11-07|佛山市普尔玛农化有限公司|A kind of composition pesticide of containing fluopyram, pyraclostrobin and imidacloprid|

---

CN107771859A|2017-11-30|2018-03-09|广西南宁益土生物科技有限责任公司|A kind of containing fluopyram and the nematicide of bacillus subtilis|

---

CN108130289B|2017-12-13|2021-03-30|中国科学院兰州化学物理研究所|Special compound microbial agent for hot peppers and preparation method thereof|

---

CN108353913A|2018-03-16|2018-08-03|佛山市普尔玛农化有限公司|A kind of nematicidal composition containing fluopyram|

---

CN111316995A|2018-12-17|2020-06-23|中化国际股份有限公司|Pesticide composition, pesticide preparation and application of pesticide composition and pesticide preparation|

---

CN110184198A|2019-05-16|2019-08-30|杭州市园林工程有限公司|A kind of preparation method of the microbial bacterial agent of controlling plant diseases|

法律状态:
2018-04-17| B06F| Objections, documents and/or translations needed after an examination request according art. 34 industrial property law|

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2018-10-09| B07A| Technical examination (opinion): publication of technical examination (opinion)|

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2018-10-23| B15K| Others concerning applications: alteration of classification|Free format text: A CLASSIFICACAO ANTERIOR ERA: A01N 43/40 Ipc: A01N 43/40 (1980.01), A01P 5/00 (2006.01) |

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2019-02-26| B06G| Technical and formal requirements: other requirements|

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2019-04-30| B06G| Technical and formal requirements: other requirements|

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2020-02-18| B07A| Technical examination (opinion): publication of technical examination (opinion)|

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2020-09-01| B06A| Notification to applicant to reply to the report for non-patentability or inadequacy of the application according art. 36 industrial patent law|

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2020-12-08| B09A| Decision: intention to grant|

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2021-01-19| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 21/09/2011, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

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申请号 | 申请日 | 专利标题

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US38524710P| true| 2010-09-22|2010-09-22|

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US61/385,247|2010-09-22|

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US41852010P| true| 2010-12-01|2010-12-01|

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EP10193328.1|2010-12-01|

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EP10193328A|EP2460406A1|2010-12-01|2010-12-01|Use of fluopyram for controlling nematodes in nematode resistant crops|

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EP10193341.4|2010-12-01|

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US61/418,520|2010-12-01|

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EP10193341|2010-12-01|

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US41943310P| true| 2010-12-03|2010-12-03|

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US61/419,433|2010-12-03|

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PCT/EP2011/066448|WO2012038476A1|2010-09-22|2011-09-21|Use of active ingredients for controlling nematodes in nematode-resistant crops|

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