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    • 专利摘要:
    SUMMARY A process for producing stratified heart-leafed somatic coniferous embryos is described, the method comprising (a) incubating a culture including immature somatic coniferous embryos in a culture vessel including a developing medium having an osmolality of 300 kg / m to 450 mM / kg at a temperature of from 22 ° C to 25 ° C during the first incubation period long enough for at least some of the embryos to reach anatomical maturity; and (b) the step of subjecting the embryos in the culture vessel of step (a) to a temperature of from 0 ° C to 10 ° C during a second incubation period of at least one week for the production of stratified cardiac somatic embryos.
    公开号:SE1050412A1
    申请号:SE1050412
    申请日:2008-09-22
    公开日:2010-04-26
    发明作者:Amy M Jamruszka
    申请人:Weyerhaeuser Nr Co；
    IPC主号:
    专利说明:

    2 conifer embryos formed in vivo in conifer seeds. The present invention provides methods that meet this need with respect to conifers of the genus Pinus.
    Summary In one aspect, a process is provided for the production of stratified heart-leafed somatic conifer embryos. The method comprises (a) incubating a culture comprising immature somatic conifer embryos in a culture vessel comprising a development medium having an osmolality in the range of 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C for a first time. incubation period long enough for at least a portion of the embryos to reach anatomical maturity; and (b) the step of subjecting the embryos in the culture vessel of step (a) to a temperature of from 0 ° C to 10 ° C for a second incubation period of at least 1 week to produce stratified somatic heart-leaf embryos.
    In another aspect, a process is provided for the production of cardiac somatic embryos. The method comprises (a) incubating a culture comprising pre-cardiac somatic conifer embryos in or on a first development medium during a first incubation period; (b) singularizing a plurality of embryos treated according to step (a); (c) culturing the diversity of singularized leaf-like somatic conifer embryos in a culture vessel comprising a development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C during a second incubation period which is long enough for at least some of the embryos to reach anatomical maturity; and (d) the step of subjecting the embryos in the culture vessel of step (c) to a temperature of from 0 ° C to 10 ° C during a third incubation period of at least 1 week pre-preparing stratified somatic heart-leafed embryos.
    The methods of the present invention are useful for preparing mature stratified heart-leafed somatic embryos with increased germination rate and a vigor that can be further characterized, such as genetically or biochemically, and / or which can be subjected to germination to produce conifers, if necessary. desirable. The methods according to the invention can thus be used, for example, for more efficient production of clones of individual conifers with one or more desirable properties, such as high growth rate or improved wood quality.
    DESCRIPTION OF THE DRAWINGS The above aspects and many of the attendant advantages of the present invention will be more readily understood by reference to the following detailed description taken in conjunction with the accompanying drawings.
    FIGURE 1 shows a schematic representation of the development of somatic conifer embryos at an early and late stage.
    FIGURE 2 shows a set of photographs of germs produced under the conditions (FIGURE 2A-2C) for treatment group 1 (control) or produced under the conditions (FIGURE 2D-2F) for treatment group 14, which show the improved germination vigor obtained. using the conditions of treatment 14, as described in EXAMPLE 2.
    FIGURE 2A shows a photograph of germs from treatment group 1, S-frame 1.
    FIGURE 2B shows a photograph of germs from treatment group 1, S-frame 2.
    FIGURE 2C shows a photograph of germs from treatment group 1, S-frame 3.
    FIGURE 2D shows a photograph of germs from treatment group 14, S-frame 1.
    FIGURE 2E shows a photograph of germs from treatment group 14, S-frame 2.
    FIGURE 2F shows a photograph of germs from treatment group 14, S-frame 3.
    Detailed Description Unless otherwise specifically defined herein, all terms used herein have the same meaning as they would be to one skilled in the art to the present invention.
    The term "developmental stage" as used herein refers to the period during somatic cloning during which histogenesis and growth of tissues and organs takes place in an immature embryo to achieve a full-size mature embryo capable of germinating a plant. 10 15 20 25 30 4 The term "immature embryo" as used herein refers to an embryo which is not yet capable of germinating in a plant and includes embryos in an early stage of development (ie pre-cardiac embryos) and development in an intermediate stage (ie embryos with heart leaves or hypocotyls that are not yet fully developed).
    The term “anatomical maturity” used here refers to an embryo that has developed heart leaves and hypocotyls.
    The term “heart-leafed embryo” as used herein refers to an embryo having a well-defined elongated bipolar structure with latent meristematic centers with one or fl clearly visible heart-leafed primordia at one end and a latent root substance at the opposite end.
    The term "pre-cardiac embryo" as used herein refers to an embryo that does not yet have a cardiac leaf.
    The term "normal seedling" as used herein denotes the presence of all expected parts of a plant at the time of evaluation. The expected parts of a plant may include a rootstock, a hypocotyl, one or more heart leaves and an epicotyl. In the case of gymnosperms, a normal germ substance is characterized by the fact that the root substance has a length of more than 3 mm and that it lacks visible discernible malformations compared with the appearance of embryos as a germ based on a natural seed.
    The term “root substance” as used herein refers to the portion of a plant embryo that develops into the primary root of the resulting plant.
    The term "hypocotyl" used here refers to that part of a plant embryo or a seedling which is located below the heart leaves, but above the rootstock.
    The term “epicotyl” used herein refers to the portion of a seedling stalk that is located above the heart leaves.
    As used herein, the term "embryonic suspender mass" or "ESM" refers to a cell mass that is spread on the surface of a nutrient medium enclosed in either a semi-solid gel or as a liquid in a porous matrix capable of providing physical support and provided to germinate for a period of up to three months. During this three-month incubation period, somatic embryos starting from microscopic precursor cell groups grow into visible embryos at an early stage and finally into anatomically mature embryos. The structure of the ESM after several weeks of incubation usually consists of a proliferated mat with a few embryos in direct contact with the medium, but most of the embryos are formed on top or on the side of the still proliferating cell mass.
    The term “stratification” as used herein refers to the step of subjecting embryos to cold treatment (eg 0 ° C to 10 ° C) before germination. Stratification (cooling with moisture) is a treatment used to circumvent germination resistance in seeds of many temperate species (Taylor & Waring, Plant, Cell, And Environment 2: 165-171, 1979).
    Unless otherwise indicated, all concentration values expressed as percent are weight percent per unit volume.
    In accordance with the methods of the present invention, it has been unexpectedly discovered that culturing immature somatic conifer embryos in or on a development medium including an osmolality in the range of from 300 mM / kg to 450 mM / kg during an initial incubation period, followed by culturing the embryos on the same development medium at a temperature of from 0 ° C to 10 ° C during a second incubation period, gives embryos with increased germination frequency and vigor compared to embryos which are incubated in a development medium and then transferred to a stratification medium having an osmolality of less than 150 mM / kg and which are subjected to cold treatment (stratification), as described in EXAMPLES 2-4. In addition to the improved germination rate and germination vigor, the exclusion of the medium transfer step between development and stratification provides a number of other benefits, including simplified production of leaf-bearing embryos, and possible cold storage of embryos on development medium prior to germination, thereby enabling flexibility and time use. of embryos. The methods of the present invention allow, for example, the accumulation and synchronization of embryo populations prior to field testing.
    According to the above, in one aspect a process is provided for the production of stratified heart-leaf-like somatic conifer embryos. The method comprises (a) incubating a culture comprising immature somatic conifer embryos in a culture vessel comprising a development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C during an initial incubation period long enough for at least some of the embryos to reach anatomical maturity; and (b) the step of subjecting the embryos in the culture vessel of step (a) to a temperature of from 0 ° C to 10 ° C during a second incubation period of at least 1 week for the production of stratified cardiac somatic embryos.
    The methods of the invention can be used to produce heart-leafed somatic embryos starting from any conifer, such as members of the genus Pinus, such as southern yellow pine (Loblolly pine) (Pinus taeda) and Radiata pine. Embryos for Douglas fir can also be produced, for example, by means of the methods according to the invention.
    A population of mature somatic coniferous embryos produced by the methods of the invention has a higher efficiency for germination to coniferous plants than a population of somatic coniferous embryos produced by any other identical control method which includes the subsequent development step of transferring embryos from a developing medium with a osmolality in the range from 300 Mm / kg to 450 mM / kg to a stratification medium with an osmolality of less than 150 mM / kg.
    Prior to stratification, in accordance with the methods of the present invention, a culture including immature somatic conifer embryos, such as embryonic suspender cell masses (ESM), is incubated in a development medium that promotes the development of cardiac leaf embryos during an initial incubation period.
    Immature somatic coniferous embryos, such as pre-cardiac somatic coniferous embryos, can be prepared from somatic coniferous cells, such as cells obtained from coniferous embryos. Cells from conifer embryos can be induced, for example, by hormones to form embryonic suspender cell masses (ESM), which can be treated by the present invention to obtain mature somatic conifer embryos. ESM can, for example, be prepared on the basis of pre-cardiac embryos that have been removed from seeds. The seed is surface sterilized, for example, before the removal of the pre-cardiac embryos, which are then grown on or in an induction medium which enables the formation of ESM, which during the propagation process induces embryos at an early stage by budding and cleavage. . ESM is usually grown in a maintenance medium to form pre-cardiac somatic embryos. Non-limiting examples of ESM culture conditions and suitable induction and maintenance media are further described below.
    Thus, in some embodiments, somatic coniferous cells are grown in or on an induction medium to obtain embryogenic cells. Embryogenic cells are cells capable of producing one or more heart-shaped somatic conifer embryos and include, for example, embryonic coniferous suspension masses. The induction medium usually includes inorganic salts and organic nutrients. The osmolality of the induction medium is usually about 160 mg / kg or even lower, but can be as high as 170 mM / kg. The induction medium usually includes growth hormones. Examples of hormones that may be included in the induction medium are auxins (eg 2,4-dichlorophenoxyacetic acid (2,4-D)) and cytokinins (eg 6-benzylaminopurine (BAP)). Auxins can, for example, be used in a concentration of from 1 mg / l to 200 mg / l. Cytokinins can be used, for example, in a concentration of from 0.1 mg / l to 10 mg / l. The induction medium may contain an absorbent composition, especially when high levels of growth hormones are used. The absorbent composition can be any composition which is not toxic to the embryogenic cells at the concentrations used in the practice of the present methods and which is capable of absorbing growth-promoting hormones as well as toxic compounds present in the medium produced by the plant cells during embryonic development. Non-limiting examples of useful absorbent compositions include activated carbon, soluble poly (vinylpyrrolidone), insoluble poly (vinylpyrrolidone), activated alumina and silica gel. The absorbent composition may be present in an amount of, for example, from about 0.1 g / l to about 5 g / l. An example of an induction medium useful in the practice of the present invention is BM1 medium, which is described in EXAMPLE 1 below. The induction medium is usually solid and can be solidified by the inclusion of a gelling agent.
    Somatic coniferous cells are usually grown in or on an induction medium for a period of from 3 weeks to 10 weeks, such as from 6 weeks to 8 weeks, at a temperature of from 10 ° C to 30 ° C, such as from 15 ° C to 25 ° C, or as from 20 ° C to 23 ° C.
    Maintenance The maintenance medium may be a solid medium, or it may be a surface medium which can be agitated to promote growth and proliferation of the embryogenic tissue. The osmolality of the maintenance medium is usually higher than the osmolality of the induction medium and is usually in the range 180-400 mM / kg. The maintenance medium may contain nutrients that maintain the embryogenic tissue and may include hormones, such as one or more auxins and / or cytokinins, which promote cell division and growth of the embryogenic tissue. In general, the concentrations of hormones in the maintenance medium are lower than the corresponding concentration in the induction medium.
    It is generally desirable, but not necessary, to include maltose as the sole or major metabolizable sugar source in the maintenance medium. Examples of useful maltose concentrations range from about 1% to about 2.5%. An example of a suitable maintenance medium is BMZ medium, which is described in EXAMPLE 1 below. Embryogenic conifer cells are usually transferred to fresh maintenance medium once a week.
    Development In accordance with the methods of this aspect of the present invention, a culture including immature somatic conifer embryos is incubated in a development medium that promotes the development of cardiac embryos during an initial incubation period.
    The development medium for use in this aspect of the invention usually contains nutrients that maintain the somatic embryos. Suitable developmental media usually do not include any growth-promoting hormones, such as auxins and cytokinins. The osmolality of the development medium ranges from 300 mM / kg to 450 mM / kg. In some embodiments, the development medium has an osmolality of 350 mM or higher.
    The development medium can be liquid, solid or semi-solid. An example of a suitable BM3 development medium is described in EXAMPLE 1 below. Other examples of a suitable development medium are described in EXAMPLES 2-4 below.
    In certain embodiments of the method, the development medium has an initial osmolality of at least 300 mM / kg, which is maintained at a level of at least 200 mM / kg during stratification.
    In some embodiments, the development medium PEG comprises a concentration of from 1% to 15%. In some embodiments, the development medium PEG comprises a concentration of 7-15% (eg, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%). In some embodiments, the development medium comprises PEG at a concentration of from 10 to 12% and an osmolality of at least 350 mM / kg to 450 mM / kg.
    Maltose may be included in the development medium as the main or sole source of sugar for the somatic embryos. Useful maltose concentrations range from about 1% to about 2.5%.
    The development medium may contain gellan gum. Gellan gum is a gelling agent that is marketed under the names GELRITE and PHYTAGEL, for example. If gellan gum is included in the development medium, it is usually present in a concentration of less than about 0.5%, usually in a concentration of from about 0% to about 0.4%. The development medium is usually a solid medium, although it may be a liquid medium.
    The developing medium may contain an absorbent composition, such as activated carbon, as described herein, for the induction medium.
    In some embodiments, the development medium further includes sucrose and / or abscisic acid. The concentration of abscisic acid in the development medium can be between 0.5 mg / l and 500 mg / l. In certain embodiments of the methods of the invention, the concentration of abscisic acid in the developing medium is between 1 mg / l and 100 mg / l. In some embodiments, the concentration of abscisic acid in the development medium is between 5 mg / L and 20 mg / L.
    In certain embodiments of the invention, the development medium contains sucrose as the main or sole source of metabolizable sugar. Usable sucrose concentrations are in the range of about 1% to about 6%.
    According to the methods of this aspect of the invention, the culture including immature somatic conifer embryos is incubated in a culture vessel including the development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C for a first time. incubation period that is long enough for at least some of the embryos to reach anatomical maturity (ie have developed heart leaves and hypocotyl, respectively).
    In some embodiments, the first incubation period is long enough for at least a portion (eg, at least one embryo, at least 10% of the embryos, at least 25%, at least 50%, more than 50% or at least 75%) of the diversity of embryos in the embryo. - the ryoculture must achieve anatomical maturity.
    As shown in FIGURE 1, the developmental stage of somatic embryos can be divided into the early stage, which involves histogenesis (ie formation of various tissues starting from undifferentiated cells), the intermediate stage, which involves organ growth and initiation of hypocotyl and cardiac development, and the late stage. , which involves the completion of organ growth, the completion of hypocotyl and cardiac leaf development (ie anatomical maturation) and the deposition of storage products. The early stage of development of an immature embryo includes, in particular, initial root development, the onset of root cap development, differentiation of the stele promeristem, and shoot tip formation. The development in the intermediate stage includes the initiation of hypocotyl development and heart leaf development, and the development in the late stage includes the completion of hypocotyl development and heart leaf development, which results in an anatomically mature embryo.
    The formation of one or fl your structures or one or fl your embryos (eg heart-leafed primordia or heart leaves) can be determined by visual inspection or imaging analysis of the cultured embryos. Visual inspection or image generation analysis can possibly be performed at a magnification of 5-10 times.
    The first incubation period may be different depending on the genotype. In some embodiments, the initial incubation period is from at least 6 weeks to at least 12 weeks in length, such as from 8 to 12 weeks. The first incubation on the developing medium can be performed at a temperature of from 10 ° C to 30 ° C, such as from 15 ° C to 25 ° C, or as from 20 ° C to 23 ° C.
    Stratification Stratification (cooling with moisture) is a treatment used to circumvent germination resistance in seeds in many temperate species (Taylor & Waring, Plant, Cell, And Environment 2: 165-171, 1979). As described herein, it has unexpectedly been found that stratification can be performed on development media including an osmolality of at least 300 mM / kg up to 450 mM / kg, which results in an increased yield of embryos with a increased germination rate (as described in EXAMPLES 2-4) compared to embryos produced using the stratification medium with an osmolality of less than 150 mM / kg (such as BM4).
    After incubation of the somatic embryos on the development medium for the first incubation period, which is long enough for at least some of the embryos to reach anatomical maturity, the embryos are then subjected to the temperature of from 0 ° C according to the procedures of this aspect of the present invention. to 10 ° C for a second incubation period of at least 1 week for the preparation of stratified cardiac somatic embryos.
    In one embodiment, heart-leafed somatic pine embryos in or on the development medium, including an osmosis of at least 300 mM / kg up to 450 mM / kg, are subjected to a temperature of from 0 ° C to 10 ° C for a second incubation period of at least 1 week up to 8 weeks (eg from 1 week to 8 weeks, such as from 4 weeks to 6 weeks) for the production of stratified cardiac somatic embryos. In another embodiment, heart-shaped somatic pine embryos are subjected in or on the development medium comprising an osmosis of at least 300 mM / kg up to 450 mM / kg for a temperature of from 0 ° C to 10 ° C for a period of other incubation periods of at least 2 months up to 6 months (eg at least 2 months, at least 3 months, at least 4 months, at least 5 months and up to 6 months) for the production of stratified cardiac somatic embryos stored before germination. The second incubation period usually takes place in the dark at a temperature of from 1 ° C to 6 ° C, such as from 1 ° C to 4 ° C.
    In one embodiment of the method of the invention, the initial osmolality of the development medium at the start of the first incubation period according to step (a) is at least 300 mM / kg and is maintained at a level of at least 200 mM / kg during the second incubation period according to step (b). ). The level of osmolality can be maintained by adding various osmotically active agents ("osmoticants") to the development medium (eg PEG, adding various sugars, myoinositol or other osmotically active agents to increase the osmolality), or by adjusting the volume. of the development medium the embryos are incubated in or on during development and stratification, as described in EXAMPLE 4.
    Usually, embryos are formed on the surface of a mass of embryogenic cells, such as an embryonic suspension mass. The heart-leafed embryos can be separated into individual (singularized) heart-leafed embryos before culturing them in or on the stratification medium, or they can be grown as a mass of non-singularized embryos. The cardiac embryos can be separated into individual (singularized) cardiac embryos before being subjected to a temperature of from 0 ° C to 10 ° C for a second incubation period of at least 1 week to produce stratified cardiac somatic embryos, or they can be cultured. as a mass of non-singularized embryos.
    Post-stratification Following stratification, the heart-leafed embryos prepared using the methods of the present invention may be subjected to germination to form pine plants which can be allowed to grow into trees, if desired. Typically, the heart-leafed embryos are subjected to a pre-germination drying treatment, as described in EXAMPLE 1. The heart-leafed embryos can also be placed in manufactured seed for subsequent germination. The heart-leafed embryos can be subjected to germination on, for example, a solid germination medium, such as BM5 medium, as described in EXAMPLE 1 below. The cardiac somatic embryos are usually illuminated to stimulate germination. Generally, all steps in the processes of the present invention, except germination, are performed in the dark. The germinated plants can be transferred to soil for further growth. The germinated plants can, for example, be planted in soil in a greenhouse and allowed to grow before transfer to a place outdoors.
    In certain embodiments, the methods in this aspect of the invention provide a higher yield of somatic cardiac embryos than an identical method in which the embryogenic cells are grown on a developing medium with an osmolality of at least 300 mM / kg up to 450 mM / kg ( containing, for example, PEG), followed by stratification in or on a stratification medium having an osmolality of less than 150 mM / kg (for example, not containing PEG), as shown in EXAMPLES 2-4. In another aspect, there is provided a process for producing cardiac leaf somatic embryos. The method comprises (a) incubating a culture comprising pre-cardiac somatic conifer embryos in or on a first development medium during a first incubation period; (b) singularizing a number of embryos treated according to step (a); (c) culturing the diversity of singularized leaf-like somatic conifer embryos in a culture vessel comprising a development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C during a second incubation period which is long enough for at least some of the embryos to reach anatomical maturity; and (d) the step of subjecting the embryos in the culture vessel of step (c) to a temperature of from 0 ° C to 10 ° C during a third incubation period of at least 1 week to produce stratified cardiac somatic embryos.
    According to this aspect of the invention, immature somatic conifer embryos, such as pre-cardiac somatic conifer embryos, can be prepared from somatic conifer cells, such as cells obtained from conifer embryos, by culturing the cells in or on an induction medium for preparation. of embryogenic cells, as described above.
    The embryogenic cells can then be cultured in or on a maintenance medium to propagate the embryogenic cells, as described above. The proliferated embryogenic cells can then be cultured in or on a first development medium during a first incubation period, singularized and incubated in a second development medium during a second incubation period, followed by stratification on the second development medium.
    The first and second developmental media usually contain nutrients that maintain the somatic embryos. Suitable developmental media usually do not include any growth-promoting hormones, such as auxins and cytokinins. In some embodiments, the first and second development media have the same formulation. In some embodiments, the first and second development media have different formulations.
    The osmolality of the first and / or second development medium can be adjusted to a value that falls within a desired range, such as from about 300 mM / kg to about 450 mM / kg. In general, an osmolality of 350 mM or higher is more advantageous in the methods of the invention. An example of a suitable BM3 development medium is described in EXAMPLE 1 below. Other examples of suitable development media are described in EXAMPLES 2-4 below. In certain embodiments of the method, the second development medium has a higher osmolality (eg from 350 mM / kg to 450 mM / kg) than the first development medium (eg from 300 mM / kg to 400 mM / kg). In some embodiments, the osmolality of the second development medium is selected to match the osmolality of the first development medium at the end of the first incubation period.
    In some embodiments, the first and / or second development medium comprises PEG in a concentration of from 1% to 15%. In some embodiments, the first development medium comprises PEG at a concentration of 7% to 10% (eg, 7%, 8%, 9%, 10%). In some embodiments, the second development medium comprises PEG at a concentration of 8% -15% (eg, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%). In some embodiments, the second development medium includes PEG at a higher concentration than the first development medium.
    Maltose may be included in the first and / or second development medium as the main or only carbon source for the somatic embryos. Useful maltose concentrations range from about 1% to about 2.5%.
    The first and / or the second development medium may contain gelling rubber. Gellan gum is a gelling agent that is marketed under the names GELRITE and PHYTAGEL, for example. If gellan gum is included in the development medium, it is usually present in a concentration of less than 0.5%, usually in a concentration of from about 0% to about 0.4%. The first and second developing media are usually a solid medium, although one or both of them may be a liquid medium.
    The first and / or the second developing medium may contain an absorbent composition, such as activated carbon, as described herein, for the induction medium.
    In some embodiments, the first and / or second developmental medium also includes sucrose and / or abscisic acid. The concentration of abscisic acid in the development medium can be between 0.5 mg / l and 500 mg / l. In certain embodiments of the methods of the invention, the concentration of abscisic acid in the development medium is between 1 mg / l and 100 mg / l. In some embodiments, the concentration of abscisic acid in the development medium is between 5 mg / lg and 20 mg / l.
    In certain embodiments of the invention, the first and / or second development medium contains sucrose as the main or only carbon source for metabolizable sugar. Useful sucrose concentrations range from about 1% to about 6%.
    The first and second development media may be liquid, solid or semi-solid. The concentrations of the osmotic agents, such as polyethylene glycol (PEG), or other osmotic agents may be elevated in the liquid medium to achieve the same osmolality as in the corresponding solid medium.
    Typically, a solid development medium equivalent to a liquid development medium has an osmolality that is within about 50 mM / kg of the osmolality of the liquid development medium.
    In some embodiments of this aspect of the process, the first incubation period is long enough to form at least one of the following structures on a portion (eg, at least one embryo, at least 10% of the embryos, at least 25%, at least 50%, more than 50% or at least 75%) of the diversity of embryos in the first embryo culture: one or more embryos with heart-leafed primordia; one or more embryos with heart leaves; one or more embryos with at least 4 heart leaves; one or more embryos with distinct heart leaves with present hypocotyl and root regions.
    The first incubation period may be different depending on the genotype. In some embodiments, the initial incubation period is from at least 6 weeks to at least 8 weeks, such as from 7 to 8 weeks. The first incubation on the first developing medium can be performed at a temperature of from 10 ° C to 30 ° C, such as from 15 ° C to 25 ° C, or as from 20 ° C to 23 ° C.
    At the end of the first incubation period, for example when the presence of one or more heart-leafed primordia is observed on a portion of the embryos, or after a period of about 6 weeks, the procedure involves singularizing a plurality of individual embryos from the first culture of embryos. Any means for physically separating individual embryos from the first culture of embryos can be used to singularize the embryos in accordance with the methods of the present invention. As for the culture with embryonic suspension mass (ESM), physical separation methods can be used, for example, such as washing away the ESM (eg spraying singularization via pressure-controlled spraying of aqueous liquid), vacuum elimination of ESM, vibration or picking up of embryos from mentioned ESM. Other non-limiting examples of useful singularization methods include filtering or sorting embryos based on a physical property, such as size, shape, eg via a screen, or based on other physical properties, such as surface roughness, hydrophobicity, density or pulp.
    In some embodiments, the singularization step also involves picking up individual embryos based on one or more selection criteria. Visually evaluated selection criteria can be used, for example, by a person skilled in the art or a computerized imaging system for the selection of embryos based on one or more morphological characteristics, which include, but are not limited to, the size, shape (eg axial symmetry), surface texture, color of the embryo. (eg no visible green staining), absence of split hypocotyls and lack of transparent heart leaves. Embryos can also be selected on the basis of criteria related to chemistry or adsorption based on external structure, reflectance, transmittance or emission spectra using near infrared spectroscopy (NIR), as described in U.S. Patent Application No. 2004/0072143 entitled "Methods for Classification of Somatic Embryos", which is hereby incorporated by reference. Desirable embryos can be picked up individually (via a manual or automated procedure) from the first embryo culture (eg as an embryonic suspension mass) using any instrument The embryo can be picked up manually or via an automated procedure, as described in U.S. Patent Application No. 2004/0267457 entitled "Automated System and Method for Harvesting and Multi-Stage Screening of Plant Embryos". , which is hereby incorporated by reference.
    In certain embodiments of the method, the picked embryos are laid directly on the surface of a second development medium or on a porous substrate in contact with a second development medium, which may be in solid or surface form.
    A porous substrate useful in the practice of various embodiments of the methods of the invention typically has a pore diameter in the range of from about 5 microns to about 1200 microns, such as from about 50 to 500 microns, such as from about 70 to about 25 microns. 150 μm, such as about 100 μm. The porous material is usually flat and can have any desired shape or dimension chosen to simplify handling and to provide contact with the other development medium. Examples of porous materials include materials that are sterilizable and strong enough to resist breakage when the material is lifted for the purpose of transferring singularized embryos to the subsequent stage of the somatic embryo production process, such as stratification.
    Examples of useful porous materials include, but are not limited to, membranes, nylon fibers, nonwovens (eg, nylon, stainless steel, or plastic) and polymeric fibers.
    In some embodiments, the singularized embryos are transferred to a second developmental medium or porous substrate that is in contact with a second developmental medium so that the singularized embryos are not in physical contact with each other.
    In accordance with the methods of the present invention, after the singularization, the singularized immature embryos are contacted with a second development medium during a second incubation period. In some embodiments, the second incubation period is long enough to at least some (eg, at least one embryo, at least 10% of the embryos, at least 25%, at least 50%, more than 50% or at least 75%) of the diversity of singularized embryos should achieve anatomical maturity (ie have developed heart leaves and hypocotyl, respectively), as described above with reference to FIGURE 1.
    The second incubation period may be different depending on the genotype. In some embodiments, the second incubation period is at least 3 weeks long, such as 3 weeks to 5 weeks. In some embodiments, the embryos are incubated for a total period of time (including the first incubation period and the second incubation period) of at least 12 weeks on the development medium. The second incubation on the second development medium can be performed at a temperature of from 10 ° C to 30 ° C, such as from 15 ° C to 25 ° C, or as from 20 ° C to 23 ° C.
    In accordance with this aspect of the methods of the invention, the singularized embryos are then stratified after incubation in or on the second development medium by the step of subjecting them to a temperature of from 0 ° C to | 10 ° C for a third incubation period of at least 1 week.
    In one embodiment, cardiac somatic pine embryos in or on the development medium, including an osmolality of at least 300 mM / kg up to 450 mM / kg, are subjected to a temperature of from 0 ° C to 10 ° C for a third incubation period of at least 1 week up to 8 weeks ( for example, from 1 week to 8 weeks, such as from 4 weeks to 6 weeks), for the production of stratified cardiac somatic embryos. In another embodiment, heart-leafed somatic pine embryos in or on the developing medium, including an osmolality of at least 300 mM / kg up to 450 mM / kg, are subjected to a temperature of from 0 ° C to 10 ° C for a third incubation period of at least 2 months. up to 6 months (eg at least 2 months, at least 3 months, at least 4 months, at least 5 months and up to 6 months) for the production of stratified cardiac somatic embryos stored before germination. The third incubation period usually proceeds in the dark at a temperature of from 1 ° C to 6 ° C, such as from 1 ° C to 4 ° C.
    In one embodiment of the method of the invention, the initial osmolality of the development medium at the start of the second incubation period according to step (a) is at least 300 mM / kg and is maintained at a level of at least 200 mM / kg during the third incubation period according to step (c). ).
    The methods of the various aspects of the invention each include the step of incubating a culture including immature somatic conifer embryos in a development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg during an initial incubation period, followed by the step of subject the embryos in the culture vessel to a temperature of from 0 ° C to 10 ° C for at least 1 week to produce stratified embryos. The methods of the invention can be used, for example, to produce clones of individual pine trees with one or more desirable properties, such as high growth rate. In one aspect, the present invention provides methods for producing a population of genetically identical somatic pine embryos. The term "genetically identical somatic pine embryos" as used herein refers to embryos derived from the same original plant. The term includes somatic pine embryos containing a small number of mutations that can occur during the development of somatic embryos. Any of the methods described herein can be used to produce populations of genetically identical somatic heart-leafed pine embryos.
    The following examples illustrate only the presently best mode of practice of the invention, but should not be construed as limiting the invention.
    EXAMPLE 1 This example describes a process for the preparation of somatic pine embryos starting from southern yellow pine using a development medium (BM3) and a stratification medium (BIVI4).
    Methods: Hongamethophytes containing zygotic embryos are removed from seeds 4 weeks to 5 weeks after fertilization. The seed coatings are removed, but the embryos are not dissected further out of the surrounding gametophyte other than the nuclear end is cut off. The cones are stored at 4 ° C until use. Immediately before removal of the immature embryos, the seeds are sterilized using an initial wash and detergent treatment, followed by sterilization for ten minutes in 15% H 2 O 2. The explants are thoroughly washed with sterile distilled water after each treatment.
    Tables 1 and 2 describe the compositions of media that are useful for the production of somatic pine embryos. TABLE 1 Basal medium (BM) for Pinus taeda Ingredient Concentration (mg / I) NH4NO3 150.0 KNO3 909.9 KH2PO4 136.1 Ca (NO3) 2-4H2O 236.2 CaCl2-4H2O 50.0 MgSO4-7H2O 246 .5 Mg (NO3) 2-6H2O 256.5 MgCl2-6H2O 50.0 Kl 4.15 H3BO3 15.5 MnSO4-H2O 10.5 ZnSO4-7H2O 14.4 NaMoO4-2H2O 0.125 CuSO4-5H2O 0.125 CoCl2-6H2O 0.125 FeSO4-7H2O 27.86 NazEDTA 37.36 Maltose 30,000 Myoinositol 200 Casamino acids 500 L-glutamine 1000 Thiamine-HCl 1.00 Pyridoxine-HCl 0.50 Nicotinic acid 0.50 Glycine 2.00 Gelrite 1600 pH-adjusted to 5.7 + Used if a solid medium is desired TABLE 2 Composition of media for different treatment steps BM1 induction medium BM + 2,4-D (15 μM) + kinetin (2 μM) + BAP (2 μM).
    BMz maintenance medium BM + 2,4-D (5 μM) + kinetin (0.5 μM) + BAP (0.5 μM), Gelrite (1600 mg / L) is added when a solid medium is desired.
    BM3 development medium BM + 25 mg / l abscisic acid + 10% PEG-8000 + 0.01% myo-inositol, + 0.1% activated carbon + 1% glucose, + 2.5% maltose.
    The following amino acid mixture is added: L-proline (100 mg / l), L-asparagine (100 mg / l), L-arginine (50 mg / l), L-alanine (20 mg / l) and L-serine (20 mg /IN). Gelrite (2500 mg / L) is added when a solid medium is desired. 10 15 20 25 21 Osmolality = 365 mM / kg BM4 stratification medium BM3 modified by exclusion of abscisic acid and exclusion of PEG-8000. Gelrite (2500 mg / L) is added when a solid medium is desired.
    Osmolality = 120 mM / kg BlV | 5-germination medium BM modified by replacing maltose with 2% sucrose. Myoinositol is reduced to 100 mg / l, glutamine and casamino acids are reduced to 0.0 mg / l, FeSO4-7H2O is reduced to 13.9 mg / l and NaZEDTA is reduced to 18.6 mg / l. Gelrite is replaced with 8 g / l agar, and 0.25% activated carbon is added.
    Induction: Sterile gametophytes with intact embryos are placed on solid ßMj culture medium and stored in an environment of 22-25 ° C with a dark photoperiod of 24 hours for a period of 3-5 weeks. The length of the time period depends on the particular genotype being grown. At the end of this time period, a white mucous mass is formed in association with the original explants. A microscopic examination usually reveals several embryos at an early stage associated with the mass. These are generally characterized as having a thin-walled suspender associated with a small head with a dense cytoplasm and large nuclei.
    The osmolality of the induction medium can in some cases be as high as 150 mM / kg and is usually about 120 mM / kg or even lower (such as 110 mM / kg).
    Maintenance and propagation: Early-stage embryos removed from the masses formed in the induction step are first placed on a gelled BM; maintenance and propagation medium. This differs from the induction medium in that the growth hormones (both auxins and cytokinins) have been reduced by at least an entire order of magnitude. The osmolality of this medium is 120 mM / kg or higher (usually in the range of about 120-150 mM / kg for Pinus taeda). The temperature and photoperiod were also here 22-25 ° C with 24 hours in the dark. The embryos are grown for 12-14 days on the solid BM2 medium before transfer to a surface medium for further subculture. This surface medium has the same composition as BM2, but lacks the gelling medium.
    At the end of the maintenance stage on solid medium, the embryos are usually similar in appearance to those from the induction stage. After 5-6 subcultures per week on the liquid maintenance medium, advanced embryos have formed at an early stage.
    These are characterized by smooth embryonic heads and were estimated to usually have more than 100 individual cells with multiple suspensions.
    Embryo development: Immature embryos are transferred from the maintenance medium to a fixed development medium at an early stage. The development medium either lacks hormones altogether or has such present in only very low levels. Abscisic acid is usually included to facilitate further development. The further inclusion of adsorbent composition in this medium is advantageous. The absorbent composition can be selected from a number of chemical materials with a large surface area and / or controlled pore size, such as activated carbon, soluble and insoluble forms of poly (vinylpyrrolidone), activated alumina and silica gel. The adsorbent composition is usually present in a concentration of about 0.1-5 g / l, more specifically about 0.25-2.5 g / l. Gellan gum may be included in a concentration of about 0.25%.
    The osmotic potential of the development medium can be significantly increased beyond that of the maintenance medium. It has been found to be advantageous to have an osmolality as high as 360 mM / kg or higher (eg up to 450 mM / kg). Development preferably takes place in complete darkness at a temperature of 22-25 ° C until embryonic embryos have developed (ie reached anatomical maturity).
    Maturation and stratification: After 7-12 weeks on BM3 development medium, heart-leafed embryos are singularized and transferred to a filter paper support on a BIV14 stratification medium. The BM4 stratification medium is similar to the BM3 development medium, but lacks abscisic acid, PEG-8000 and gellan gum. The osmolality of the stratification medium without PEG is usually below 150 mM / kg, such as about 120 mM / kg. Embryos are grown on the stratification medium at between 1 ° C and 10 ° C in the dark for between 1 week and 8 weeks, such as between 2 weeks and 6 weeks.
    Drying: The mature embryos, which are still on the filter paper carrier, are lifted from the pad and placed in a closed container over water at a relative humidity of 97-99% for a period of about 3 weeks. 10 15 20 25 30 23 Germination: The dried mature embryos are rehydrated by placing them, while still on the filter paper carrier, for about 24 hours on a pad saturated with liquid germination medium.
    The embryos are then placed individually on solid BM5 medium for germination. This is a basal medium that lacks growth hormones and has been modified by reducing sucrose, myoinositol and organic nitrogen. The embryos are incubated on BM5 medium for about 10 weeks at ambient conditions of 23-25 ° C and a photoperiod of 16 hours in light and 8 hours in the dark until the resulting seedlings have a well-developed root substance and a ditto hypocotyl and a green heart-shaped structure and epicotyl.
    Due to the reduced carbohydrate concentration, the osmotic potential of the germination medium is further reduced to below that of the development medium. It is usually lower than about 150 mM / kg (such as about 100 mM / kg).
    EXAMPLE 2 This example shows that incubation of immature embryo seeds from southern yellow pine (Pinus taeda) on a development medium (+ 10% PEG) with an osmolality of 365 mM / kg, followed by stratification while still on the same development medium, improves embryo yield and germination-successful germination compared with incubation of embryos on development medium with an osmolality of 365 mM / kg, followed by stratification on a stratification medium (0.0% PEG) with an osmolality of less than 150 mM / kg.
    Methods: Hongamethophytes containing zygotic embryos were removed from seeds of seven different genotypes according to the methods described in EXAMPLE 1. The induction and maintenance steps were performed as described in EXAMPLE 1, and stocks of embryonic suspension mass (ESM) cultures were frozen.
    Recovery of ESM cultures from in vitro storage: A bottle of each genotype was thawed on filter paper over BMZ maintenance medium. Once the ESM of the cultures had grown sufficiently to form an elevation of about 1 cm in width and 0.4 cm in height, the ESM was collected from the filter paper and freed from the callus. This transfer procedure continued over a 14-day cycle until 1-4 elevations of ESM with a width of approximately 1 cm and a height of 0.4 cm were collected for each genotype. 10 15 20 25 24 Maintenance and Propagation Approximately 7 weeks after the recovery of ESM from frozen stock cultures, the ESM cultures were filled into a 500 ml flask containing 100 ml of maintenance medium in a ratio of 1: 5.
    Development: The ESM culture was spread on a nylon membrane over 600 ml semi-solid BM3 development medium (+ 10% PEG, osmolality = 365 mM / kg) in Cambro boxes with halved size (shallow) (a depth of 5.08 cm (2 inches)), resulting in a medium depth of about 1.27 cm (1/2 inch). A total of 24 ml cells were plated for each genotype on two half-sized Cambro boxes. Each frame in a Cambro box contained 6 ml of cells, giving a total of 12 ml of cells per box in a twelve-drop configuration. The cells were dispensed as 12 drops of 0.5 ml each per frame. After smearing, the Cambro boxes were placed in the dark at room temperature for a development period of 12 weeks. After the development period, the following stratification treatments were tested, as described in TABLE 3.
    Stratification: After incubation for 12 weeks on BM3 development medium, embryos from treatment groups 1 and 8 were transferred to a pad over 320 ml BM4 stratification medium (0.0% PEG, osmolality = 120 mM / kg) in half-sized Cambroboxes. . Embryos in treatment group 14 were maintained on BM3 development medium during stratification. The stratification of all treatment groups was performed for 4 weeks at 4 ° C to 7 ° C. 10 15 20 25 TABLE 3: DESCRIPTION OF TREATMENT CONDITIONS BY DEVELOPMENT _ number of Treatment _ _ _ Description of treatment tested reference number clones 1 (control) Incubation for 12 weeks in BM3 development medium at room temperature 61, stratification in BM4 -stratification medium for 1 month, COW for 1 week, germination for 5 weeks. 8 incubation for 12 weeks in BM3 development medium at room temperature, storage for 3 months in the dark at 4-8 ° C, stratification in BM4 stratification medium for 1 month, COW for 1 week, germination for 5 weeks. 14 incubation for 12 weeks in BM3 development medium at room temperature, after development Cambro boxes were stored in the dark at 4 ° C to 8 ° C for 3 months in BM3 development medium (no medium change), COW for 1 week, germination under 5 weeks.
    Conditioning over water (COW) and sincularization: After stratification, the embryos were singularized by separation by spraying and then placed in an environment with 98% relative humidity and conditioned over water at room temperature for 1 week in COW boxes.
    Germination: After conditioning over water, 75 embryos from each treatment group (per genotype) were transferred by hand to BM5 germination medium (150 ml medium dispensed per Cambro box). These embryos were placed on top of the germination medium, but were not planted. 25 embryos were placed in each box, resulting in 3 germination boxes per treatment group per genotype. Any remaining embryos were counted to determine the total embryo yield.
    Embryos were visually selected for germination using the following criteria: three or more visible heart leaves; even embryo (no callus formation); the embryo is ivory, yellow or green and is opaque; fused embryos were not selected; embryos with wide flattened hypocotyls were not selected; elongated embryos were accepted.
    After manual embryo transfer to germination boxes containing germination medium, the boxes were placed at 1 ° C to 2 ° C for 3 months. The germination boxes were then moved to room temperature in the dark for 7 days and then placed in a bright room for further germination. After 8 weeks of incubation on the germination medium, the seedlings were monitored to determine whether they were ready for transfer to the greenhouse. Seedling plants from treatment group 1 (control) were harvested when the majority met the selection criteria. All subsequent experimental groups were harvested using the control germination period for each individual genotype clone.
    Results: Comparison between Treatment 1 (control) and Treatment 14 In the experiments, continued incubation of embryos on development medium during stratification (exclusion of use of stratification medium) (treatment 14) is compared with control treatment 1, in which embryos were incubated on development medium and transferred to stratification medium before stratification. As shown below in TABLE 4, treatment yielded 14 embryos with a higher germination rate as well as seedlings with improved vigor compared to embryos produced in treatment 1.
    TABLE 4: ESTIMATED AVERAGE GROWTH FREQUENCY AND CONFIDENCE INTERVIEW FOR TREATMENT 1 AND 14 (N = 15 GENOTYPES) U estimated by Lower limit for Upper limit for Treatment _ p _ g 90% confidence- 90% confidence- sn | tt | g germination frequency _ _ interval (Cl) interval (Cl) 1 (control) 0.335 0.280 0.395 14 (stratification on ut- 0.373 0.316 0.434 development medium in cold storage) As shown above in TABLE 4, embryos from treatment group 14 had a slightly higher germination rate (37%) than control treatment 1 (34%), although the observed difference was not statistically significant (p = 0.42). 10 15 20 25 27 TABLE 5: ESTIMATED AVERAGE SURVIVAL AND CONFIDENCE INTERVALS FOR TREATMENTS 1 AND 14 (N = 15 GENOTYPES) Estimated by_ Lower limit for Upper limit for Treatment snim survival (90% confidence interval 90% confidence interval 90% confidence interval Cl) 1 0.756 0.690 0.812 14 0.748 0.668 0.802 As shown in TABLE 5, seedlings formed using treatment 14 had a slightly lower survival than treatment 1 (control) (75% compared to 76%), but the difference was not statistical. significant (p = 0.87).
    An improvement in seedling vigor was observed for treatment 14. 13 of the 15 genotypes included in treatment group 14 were observed to have more potent epicotyl, longer roots, or both, than embryos from treatment group 1. Although organ lengths were not measured in this experiment, photographs of the seedlings in each treatment group before transfer. FIGURE 2 shows a set of photographs of seedlings prepared under the conditions of treatment group 1 (control) (FIGURES 2A-2C) or prepared under the conditions of treatment group 14 (FIGURES 2D-2F). As shown in FIGURE 2, an improvement in the vigor of the seedlings was obtained by using the conditions of treatment group 14 (FIGURES 2D-F) compared to treatment group 1 (control) (FIGURES 2A-C).
    Comparison between treatments 1, 8 and 14 In this analysis, the results of genotypes common to treatments 1, 8 and 14 were compared in order to determine whether transfer of embryos to stratification medium after incubation and possible storage in development medium was detrimental to embryos. germination. Germination frequency results are shown in TABLE 6. 10 15 20 25 28 TABLE 6: AVERAGE GROWTH FREQUENCY AND CONFIDENCE INTERVALS FOR TREATMENTS 1, 8 AND 14 (N = 7 GENOTYPS) Lower limit for Upper limit for Treatment Estimated average 90% % confidence average germination frequency interval interval 1 (control) 0.396 0.315 0.484 8 0.180 0.125 0.254 14 0.403 0.321 0.491 The difference in germination sequences among the controls and treatments shown in TABLE 6 is statistically significant (p = 0.0005). In a direct comparison between treatments 8 and 14, significantly lower values are obtained for treatment 8 compared with treatment 14 (p = 0.0008) and the control (p = 0.0011).
    In addition, the embryos from treatment 8 were observed to be deformed after separation by spraying (data not shown).
    Summary and conclusion: These results show that continued incubation of embryos on development medium (10% PEG, osmolality = 365 mM / kg) during stratification (exclusion of use of stratification medium) (treatment group 14) gives embryos with a higher germination sequence and seedlings with improved viability compared to the embryos prepared from treatment group 1 and treatment group 8, where embryos were incubated on development medium (10% PEG, osmolality = 365 mM / kg), and transferred to stratification medium (0.0% PEG , osmolality = 120 mM / kg) before stratification. In addition, as shown in FIGURE 2, an improvement in seedling growth in favor of treatment 14 was observed, with thirteen of the fifteen genotypes included in treatment group 14 being observed to have more potent epicotyledons, longer roots, or both, than treatment group embryos. 1.
    EXAMPLE 3 This example shows that exclusion of the media exchange step between development and stratification results in embryos with increased germination sequence. Methods: Hongamethophytes containing zygotic embryos were removed from seeds from four different genotypes according to the methods described in EXAMPLE 1. The induction, maintenance and development steps were performed as described in EXAMPLE 1.
    TABLE 7 describes the experimental treatment conditions after development.
    TABLE 7: TREATMENT CONDITIONS AFTER DEVELOPMENT Treatment reference number Description 1 (control) 12 weeks incubation on modified BM3 development medium (10% PEG, osmolality = 336 mM / kg), stratification on BM4 stratification medium (0% PEG, mMolality) for 4 weeks 2 12 weeks incubation on modified Blvly development medium (10% PEG, osmolality = 336 mM / kg), stratification on BM4 stratification medium (0% PEG, osmolality = 120 mM / kg) for 8 weeks 3 12 weeks incubation on modified BM3 development medium (10% PEG, osmolality = 336 mM / kg), and after development Cambro boxes were stored in the dark at 4 ° C for 4 weeks on the same development medium (no medium exchange) 4 same as for treatment 3 with 8 weeks storage on development medium at 4 ° C After the stratification treatments shown in TABLE 7 above, the embryos on the d-frames were sprayed separately on 3 s-frames (complete Cambroboxes) per genotype / treatment. Two germination boxes of 25 embryos each were selected from each s-frame. A total of 6 germination boxes were produced per genotype / treatment. The embryos were placed on the germination medium and not planted out in the medium. The seedlings were assessed after incubation for 6 weeks on germination medium. The root length was also measured for all plants according to category 1.
    A seedling plant of category 1 includes the following characteristics: the presence of a 1 mm long root (no undeveloped stumps ("nubbins")), the presence of about 5 epicotyledons with an approximate length of 5 mm, no large-scale hypocotyl ruptures and a hypocotyl which is not bent more than 90 degrees. 10 15 20 25 30 A seedling plant (bipolar) of category 1 + 2 includes the following characteristics: the presence of a 1 mm long root (no undeveloped stumps) and the presence of epicotyledonous leaves (no size or no number) that are visible to the eye.
    Statistical analysis: 4 treatments were performed, a complete faculty (“factorial”) included 2 stratification media (standard and old development medium) times two durations (4 weeks and 8 weeks). The different media were applied to full-plot experimental units, and the duration of the incubation was applied to the divided plots. The results were assessed with respect to germination frequency (category 1 and category 1 + category 2) and root length. The root length was analyzed using a mixed model after achieving a transformation using a natural logarithm for stabilizing the variance.
    Category 1 and Category 1 + Category 2 seedlings were analyzed using a generalized linear mixed model.
    The germination frequency results for category 1 are shown below in TABLE 8.
    TABLE 8: AVERAGE GROWTH FREQUENCY FOR CATEGORY 1 (ALL GENOTYPS INCLUDED) _ _ Lower Limit for Upper Limit for Treatment Average 90% confidence 90% confidence germination frequency range (Cl) control14 (0.046 control) 0.113 3 0.098 0.056 0.167 4 0.104 0.059 0.176 As shown in TABLE 8, the germination frequency of Category 1 seedlings was higher in treatments 3 and 4, where embryos were maintained on development medium during the stratification step (ie incubation at 4 ° C).
    The results for the total bipolar germination frequency (category 1 + category 2) are shown below in TABLE 9. 10 15 31 TABLE 9: AVERAGE FOR TOTAL BIPOLAR GROWTH (CATEGORY 1 + CATEGORY 2) (ALL GENOTYPES INCLUDED LIMITS FOR LIMITED LIMITS _ GENERALS Treatment germination rate 90% Cl 90% Cl 1 (control) 0,300 0,202 0,422 2 0,296 0,199 0,417 3 0,243 0,147 0,374 4 0,205 0,122 0,325 Mean value of the germination rate for category 1 or for the bipolar sample (category 1 + category 2) for each of the four genotypes tested varied only by about 10-20% (data not shown).
    The results of the measurements of the average root length are shown in TABLE 10.
    TABLE 10: AVERAGE ROOT LENGTH (ALL GENOTYPS INCLUDED) _ Mean (mm) Lower limit for Upper limit for Treatment 90% cl 90% cl 1 (control) 13.5 10.3 17.7 2 19.0 14.5 24, 8 3 12.8 9.8 16.8 4 17.4 13.3 22.8 TABLE 11: COMPARISON OF EXPERIMENTAL RESULTS FROM 3 MODELS Category 1 Bipolar seedlings __ _ _ _ Root-length Variable Seedlings (category 1 + category 2) __ __ __ P-value P-value P-value Medium for stratification (stratification- 0 07 (_k I, deviating celebration medium compared with __ __ 0.42 0.40 _ _ ar better) development medium) _ _. <0.01 Duration (4 weeks compared to __ __ __ 0.30 0.09 (4 weeks are better) (8 weeks with 8 weeks) __ better) Medium * Duration 0.10 0.16 0.85 P-values <0.10 indicates a significant result Summary of results: With respect to germination according to category 1, a statistically significant difference (p = 0.07) was observed in the germination frequencies of embryos maintained on development medium (modified BM3, 10 15 20 25 30 32 10% PEG, osmolality = 336 mM / kg) during the stratification step (ie incubation at 4 ° C), as shown in TABLE 8. In terms of duration, embryos stratified on development medium (modified BMg, 10% PEG, osmolality = drug 336 mM / kg) benefit from an additional 4 weeks of incubation, unlike those on stratification medium (BM4, 0.0% PEG, osmolality = 120 mM / kg). The overall low observed values for germination can be increased by using early singularization during development, followed by maintenance of the embryos on development medium after singularization during the stratification period.
    In summary, these results indicate that performing the stratification step on the original development medium (ie excluding the step of transferring embryos to stratification medium) is advantageous for obtaining embryos with more vigorous germination according to category 1. This is a significant result, since the exclusion of the transfer to the stratification medium enables development, storage and stratification on the same development medium, which makes the procedure much more efficient. The exclusion of embryo transfer from the development medium to the stratification medium reduces, for example, the workload, the preparation of stratification medium and the preparation of additional Cambro boxes.
    EXAMPLE 4 In this example, the effect of medium volume and medium depth during development and stratification treatment on germination rates for somatic embryos is measured.
    Methods: Hongamethophytes containing zygotic embryos were removed from the seeds of four different genotypes according to the methods described in EXAMPLE 1. The induction and maintenance steps were performed as described in EXAMPLE 1, except that ESM was spread over the tree network on the developmental frame instead of via drops.
    The development and stratification steps were performed as shown in TABLE 12. All embryos in this experiment were incubated on development medium with an initial osmolality of 336 mM / kg (10% PEG) for 12 weeks, followed by stratification, as shown in TABLE 12, during 4 weeks. 33 TABLE 12: DEVELOPMENT AND STRATIFICATION TREATMENTS Medium_ Depth of Transfer between Treatment Volume Cam bridge development and Stratification at 4 ° C container stratification medium 1 (control) 600 ml primer (5.08 yes stratification medium (BM4, cm (2 inches)) 0.0% PEG, osmolality = 120 mM / kg 2,900 ml primer (5.08 yes stratification medium (BM4, cm (2 inch)) 0.0% PEG, osmolality = 120 mM / kg 3 1200 ml primer (5.08 yes stratification medium (BM4, cm (2 inches)) 0.0% PEG, osmolality = 120 mM / kg 4 (control) 600 ml depth (10.16 yes stratification medium (BM4, cm (4 inches)) 0.0% PEG, osmolality = 120 mM / kg 5 900 ml depth (10.16 yes stratification medium (BM4, cm (4 inches)) 0 .0% PEG, osmolality = 120 mM / kg 6 1200 ml depth (10.16 yes stratification medium (BM4, cm (4 inches)) 0.0% PEG, osmolality = 120 mM / kg 7 600 ml base (5.08 no development medium (modim (2 inches)) celebrated BM3 10% PEG, osmolality = 336 mM / kg 8,900 ml base (5.08 no development medium (modim (2 inches)) celebrated BM3 10% PEG, osmolality = 336 mM / kg 9 1200 ml base (5.08 no development medium (modim (2 inches)) celebrated BM3 10% PEG, osmolality = 336 mM / kg 10 600 ml depth (10.16 no development medium (mod (cm)) 4 inches)) celebrated BM3 1 0% PEG, osmolality = 336 mM / kg 11 900 ml depth (10.16 no development medium (modim (4 inches)) celebrated BM3 10% PEG, osmolality = 336 mM / kg 12 1200 ml depth (10.16 no development medium (modim (4 inches)) celebrated BM3 10% PEG, osmolality = 336 mM / kg After development, all treatment groups germinated, as described below. Stratification: As shown in TABLE 12 for the treatments, 1-6 embryos plated on a D-frame were transferred to stratification medium (BM4, 0.0% PEG, osmolality = 120 mM / kg). For treatments 7-12, embryos smeared on a D-frame on a development medium (modified BlVl3, 10% PEG, osmolality = 336 mM / kg) remained on the same development medium during stratification.
    The total yield of embryos per treatment was determined after 12 weeks of incubation on development medium. Conditioning over water (COW) was performed in a large Cambro box with the dimension 1x1 for 1 week.
    Germination: 100 embryos per treatment were transferred manually to germination boxes. Embryo selection criteria for germination: Symmetrical embryos with all three parts (heart leaves, hypocotyls and root canal regions) were selected without obvious defects and with four or more heart leaves without any fused heart leaves or heart leaves protruding from the center. The size of the embryos varied. The embryos were opaque with colors in all shades of white, yellow or green. No transparent or vitrified green embryos were selected.
    The germination frequency was determined after 6 weeks.
    Results: TABLE 13 shows the effect of medium volume, container depth and medium depth during development and stratification on the average embryo yield by analysis using a linear mixed model.
    TABLE 13: STATISTICAL SIGNIFICANCE FOR MEDIUM VOLUME, CONTAINER DEPTH AND IVIEDIUM DEPTH DURING DEVELOPMENT AND STRATIFICATION Treatment variable DF (degrees of freedom) P-value Medium volume 2 0.073 Container depth 1 as the box is shown above ) on the embryo yield is statistically significant with a p-value of 0.009. The effect of the medium volume is weakly significant with a p-value of 0.073, while no statistical significance was observed for an interaction effect between these variables.
    TABLE 14 shows the estimated average yield ("LS mean") for each level of medium volume and container depth together with 95% confidence intervals.As shown in the Group column in TABLE 14, the variables within the same letter group are not statistically significant on a cone confidence level of 90%, while factors within different letter groups are significantly different.
    TABLE 14: EFFECT OF MEDIUM VOLUME AND CONTAINER DEPTH DURING DEVELOPMENT AND STRATIFICATION OF EMBRYOUS EXCHANGE variable Estimated Lower limit Upper limit for Group embryo exchange for 90% Cl 90% Cl Medium volume: 600 ml 641 421 861 A Medium volume 780 570 990 B Container depth: shallow (5.08 650 432 869 A cm (2 inches)) Container depth: depth (10.16 820 616 1024 B cm (4 inches)) As shown in TABLE 14, the Cambro boxes with medium volumes of 900 ml and 1200 ml in a statistically significantly higher embryo yield than the boxes with a medium volume of 600 ml. The treatments with volumes of 900 ml and 1200 ml were not significantly different from each other, and each had an estimated yield that was approximately 140 embryos per box greater than the yield of the Cambro box with a volume of 600 ml. 10 15 36 TABLE 15: COMPARISON OF EIVIBRYO YIELD AFTER STRATIFICATION (IE INCUBATION AT 4 ° C) ON STRATIFYING MEDIUM OR DEVELOPMENT MEDIUM _ Medium- _, _ _ _ Embryo- Treatment Cambro-volume container 600 ), (medium depth = stratification medium 668 1.27 cm (1/2 inch)) 2,900 ml base (2 inches), (medium depth = stratification medium 746 1.91 om (% inch)) 3 1200 ml base (2 inches), (medium depth = stratification medium 755 2.54 cm (1 inch)) 4 (control) 600 ml depth (10.16 cm (4 inches)) stratification medium 863 5 900 ml depth (10.16 cm (4 inches)) stratification medium 794 6 1200 ml depth (10.16 cm (4 inches)) stratification medium 843 7 600 ml base (5.08 cm (2 inches)) development medium 612 8 900 ml base (5.08 cm (2 inches)) development medium 821 9 1200 ml base (5.08 cm (2 inches)) development medium 803 10 600 ml depth (10.16 cm (4 inches)) development medium 757 11 900 ml depth (10.16 cm (4 inches)) development medium 843 12 1200 ml depth ( 10.16 cm (4 inches)) development medium 821 S as shown in TABLE 15, the development and stratification of embryos on Cambro boxes with larger amounts of medium (900 ml and 1200 ml) showed statistically significantly higher embryo yields than the control amount of medium (600 ml). The estimated difference between these medium volume treatments was approximately 140 embryos per box. In addition, the deep Cambro boxes (10.16 cm (4 inches)) showed statistically significantly higher embryo yields than the shallow Cambro boxes (5.08 (2 inches)). The estimated difference between these two treatments at different box depths was about 170 per box.
    Osmolality measurements: The osmolality of the medium was measured after 12 weeks of incubation on development medium. The development medium had an initial osmolality of 336 mM / kg (10% PEG). The results are shown below in TABLE 16. (control) 160 base Cambro-box: 900 ml 200 base Cambro-box: 1200 ml 220 deep control Cambro-box (10.16 cm (4 inches)) (600 ml) 170 deep Cambro-box: 900 ml 190 deep Cambro -box: 1200 ml 210 Conclusion: As shown in TABLE 16, larger volumes of development medium maintained higher osmolalities after incubation for 12 weeks. With development medium with an initial osmolality of 336 mM / kg, even m with additional medium volume, none of the boxes maintained an osmolality of more than 250 mM after 12 weeks.
    Germination data The effect of medium volume, box depth and stratification treatment on the embryo germination frequency was analyzed using a generalized linear mixed model. The random effects in this model were present in sets and Cambro boxes within sets.
    Seedlings according to category 1: Germination for category 1 was assessed as described in Example 3.
    TABLE 17 SHOWS THE ESTIMATED AVERAGE GROWTH FREQUENCY FOR CATEGORY 1 FOR EACH STRATIFICATION TREATMENT TOGETHER WITH 90% CONFIDENCE INTERVALS Lower Upper Treatment Condition Cl. 4.1% 0.020 0.084 A development medium to stratification medium afterwards) (w / o PEG) Maintained on development medium 6.7% 0.034 0.130 B (+ PEG) 10 15 20 25 38 The treatment conditions shown in TABLE 17 on the same letter group level is not statistically significant at the 90% confidence level, while the treatment conditions for different group letters are significantly different.
    As shown above in TABLE 17, there was a significant difference in the frequency of seedlings in category 1 (p = 0.007, confidence level 90%) derived from embryos maintained on development medium (+ PEG) during stratification compared to the frequency of seedling category 1 from embryos transferred from development medium to stratification medium (no PEG) before stratification.
    Seedlings of category 1 + 2 were assessed as follows: a seedling (bipolar) of category 1 + 2 includes the following characteristics: the presence of a 1 mm long root (no undeveloped stumps) and the presence of epicotyledonous leaves (no size or no number) which are visible to the eye.
    TABLE 18 SHOWS THE ESTIMATED MEAN CATEGORY germination frequency of 1 every STRATIFICATION treatment along with 90% confidence intervals Lower Upper treatment condition Gâgïï /: srïrïtëïïtïëïrllinfï gçšrrïs gçärrß Group 90% CI 90% Cl stratification media (change of departure 7.0% 0.037 0.128 A development medium to stratification medium afterwards) (w / o PEG) Maintained on development medium 11.5% 0.064 0.198 B (+ PEG) The treatment conditions shown in TABLE 18 at the same letter group level are not statistically significant at a 90% confidence level, while treatment conditions with different letter groups are significantly different.
    As shown in TABLE 18, there was a significant difference in the frequency of seedlings according to category 1 + 2 (p = 0.002, confidence level 90%) derived from embryos maintained on development medium (+ 10% PEG, osmolality = 336 mM / kg) during stratification compared to the frequency of seedlings of category 1 + 2 derived from embryos transferred from development medium to stratification medium (0.0% PEG, osmolality = 120 mM / kg) before stratification.
    The germination frequency was also assessed for seedlings in category 1 and category 1 + 2 derived from embryos formed using treatments 1-6, as described in TABLE 12. The results of the statistical analysis of the differences observed in germination frequency are shown below in TABLE 19.
    TABLE 19: STATISTICAL SIGNIFICANCE OF DIFFERENCES IN GROWING OBSERVED BY USING DIFFERENT TREATMENT METHODS Difference observed Difference observed in Treatment condition DF in germination frequency in germination frequency in category 1 (p-value 2) with p-value 2 0.453 0.454 compared to 900 ml or 1200 ml) Box depth (shallow, 5.08 cm (2 inches) 1 0.943 0.791 compared to depth, 10.16 cm (4 inches)) Stratification medium (change from 1 0.007 0.002 development medium to ex-post stratification medium (w / o PEG) compared to maintained on development medium during stratification) Medium * Depth 2 0.820 0.879 Medium * Stratification 2 0.424 0.654 Depth * Stratification 1 0.348 0.340 Medium * Depth * Stratification 2 0.914 0.918 analysis of the significance of the differences observed in germination frequency after embryo treatment with different medium volumes, different box depths and different stratification medium conditions, was, as shown above in TABLE 19, only ski The conditions observed under different stratification medium conditions are statistically significant. A statistically significant difference in stratification medium conditions was observed both for seedlings in category 1 (0.007) and for seedlings in category 1 + category 2 (0.002).
    This is an important result, indicating that the procedure for incubating embryos on development medium with an initial osmolality of at least 300 mM / kg to 450 mM / kg for a period of from 7 to 12 weeks at room temperature, was followed. of stratification of the embryos on the same development medium, ie conversion of the conditions of the embryos on the development medium from 0 ° C to 10 ° C for at least 1 week, results in increased embryo yield (as described in EXAMPLES 2-3), increased embryo frequency and improved germination vigor plants (as shown in EXAMPLE 2 and in FIGURE 2) (showing that 13 of 15 genotypes at treatment 14 were observed to have more potent epicotyledonous, longer roots, or both) .These results are compared with those of a control method involving transfer of embryos from development medium (an osmolality of at least 300 mM / kg) to stratification medium (an osmolality of 120 mM / kg), followed by stratification of 1 ° C to 10 ° C for at least 1 week.
    The procedure for maintaining embryos on development medium during stratification therefore provides the unexpected advantage of increased embryo yield and increased germination frequency. The methods according to the invention also bring advantages with simplified handling of a large number of embryos due to the reduced number of steps and the possibility to stratify and possibly store embryos in a subsequent development step at 1 ° C to 10 ° C for up to 3 months to 6 months before germination. Although preferred embodiments of the invention have been elucidated and described, it will be appreciated that various changes may be made without departing from the spirit and scope of the invention.
    权利要求:
    Claims (17)
    [1]
    A process for producing stratified cardiac somatic conifer embryos comprising: (a) incubating a culture comprising immature somatic conifer embryos in a culture vessel comprising a development medium having an osmolality in the range of from 300 mM / kg to 450 mM / kg to 450 mM / kg; a temperature of from 22 ° C to 25 ° C during a first incubation period long enough for at least a portion of the embryos to reach anatomical maturity; and (b) the step of subjecting the embryos in the culture vessel of step (a) to a temperature of from 0 ° C to 10 ° C for a second incubation period of at least one week to produce stratified cardiac somatic embryos.
    [2]
    The method of claim 1, wherein the developing medium comprises PEG in a concentration of from about 1% to about 15%.
    [3]
    The method of claim 1, wherein the developing medium comprises PEG in a concentration of from about 7% to about 15%.
    [4]
    The method of claim 1, wherein the first incubation period is from 7 weeks to 12 weeks.
    [5]
    The method of claim 1, wherein the second incubation period is from 1 week to 8 weeks.
    [6]
    The method of claim 1, wherein the second incubation period is from 1 week to 6 months. 10 15 20 25 30 42
    [7]
    The method of claim 1, further comprising culturing the embryos treated according to step (b) in or on a germination medium for the production of seedlings.
    [8]
    The method of claim 1, wherein the osmolality of the development medium is maintained at a level of at least 200 mM / kg during the second incubation period.
    [9]
    The method of claim 1, wherein the embryos in the first culture are singularized before the first incubation period.
    [10]
    A method of producing cardiac somatic embryos, comprising: (a) incubating a culture comprising pre-cardiac somatic conifer embryos in or on a first development medium during a first incubation period; (b) singularizing a number of embryos treated according to step (8): (c) culturing the diversity of singularized leaf-like somatic conifer embryos in a culture vessel including a second developmental medium having an osmolality in the range of 300 mM / kg to 450 mM / kg at a temperature of from 22 ° C to 25 ° C during a second incubation period long enough for at least some of the embryos to reach anatomical maturity; and (d) the step of subjecting the embryos in the culture vessel of step (c) to a temperature of from 0 ° C to 10 ° C during a third incubation period for at least one week to produce stratified cardiac somatic embryos.
    [11]
    The method of claim 10, wherein the second development medium comprises PEG in a concentration of from about 1% to about 15%. 10 15 20 43
    [12]
    The method of claim 10, wherein the first incubation period is from 6 weeks to 8 weeks.
    [13]
    The method of claim 10, wherein the combination of the first incubation period and the second incubation period totals a time period of at least 12 weeks.
    [14]
    The method of claim 10, wherein the third incubation period is from 1 week to 6 months.
    [15]
    The method of claim 10, wherein the third incubation period is from 1 week to 8 weeks.
    [16]
    The method of claim 10, wherein the singularized embryos in the culture vessel are not in physical contact with each other.
    [17]
    The method of claim 10, further comprising culturing the embryos treated according to step (d) in or on a germination medium for the production of seedlings.
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    同族专利:
    公开号 | 公开日
    UY31358A1|2009-04-30|
    WO2009042553A1|2009-04-02|
    FI20105297A|2010-03-24|
    CN101808506A|2010-08-18|
    AR068567A1|2009-11-18|
    US8216840B2|2012-07-10|
    US20090087908A1|2009-04-02|
    AU2008304630B2|2012-01-19|
    SE534887C2|2012-02-07|
    CA2698134A1|2009-04-02|
    FI126715B|2017-04-13|
    NZ584616A|2011-11-25|
    CA2698134C|2013-01-15|
    AU2008304630A1|2009-04-02|
    CN101808506B|2013-03-20|
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    法律状态:
    2018-05-02| NUG| Patent has lapsed|
    优先权:
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    US97571707P| true| 2007-09-27|2007-09-27|
    PCT/US2008/077264|WO2009042553A1|2007-09-27|2008-09-22|Methods for stratification and storage of somatic embryos|
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