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    • 专利摘要:
    Host cell myceliophthora thermophila with improved cellulolytic activity and enzymatic compositions obtained therefrom. The present invention relates to a host cell, preferably a cell of myceliophthora thermophila, which shows a lower expression and/or secretion of non-contributive cellulolytic enzymes, preferably where the non-contributive cellulolytic enzyme is the endoglucanase 6 comprising seq id no: 2, thus favoring the presence of contributive cellulolytic enzymes in the enzymatic cocktail synthesized by said host cell. The present invention also relates to the use of said host cells and enzymatic cocktails synthesized by said host cells for obtaining fermentable sugars from the biomass and a process for producing bioproducts, preferably bioethanol, comprising the use of said host cell or of the composition of the invention. (Machine-translation by Google Translate, not legally binding)
    公开号:ES2647322A1
    申请号:ES201630658
    申请日:2016-05-20
    公开日:2017-12-20
    发明作者:Bruno DÍEZ GARCÍA；Noelia VALBUENA CRESPO；Francisco Manuel REYES SOSA；Antonio Javier MORENO PÉREZ；Dolores PÉREZ GÓMEZ；Ana Isabel PLATERO GÓMEZ；Lucía MARTÍN PÉREZ；Sandra GAVALDÁ MARTÍN；Laura VIÑAS DE LA CRUZ；Laura SÁNCHEZ ZAMORANO；Consolación ÁLVAREZ NÚÑEZ；María De Los Ángeles BERMÚDEZ ALCÁNTARA；Javier ROCHA MARTÍN；Laura LEDESMA GARCÍA；Ricardo Arjona Antolín；Juan Luis RAMOS MARTÍN
    申请人:Abengoa Bioenergia Nuevas Technologias SA；
    IPC主号:
    专利说明:

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    Enzymatic composition expressed and / or secreted by the modified host cells of the invention has a higher cellulolytic efficiency and a higher concentration of contributory cellulolytic enzymes that are selected from those that have a higher cellulolytic efficiency within the group of enzymes that are part of the diversity Enzymatic cocktail. This higher concentration of contributory cellulolytic enzymes in the enzyme composition of the invention is a consequence of the lower expression and / or secretion of non-contributory cellulolytic enzymes, since the contributory cellulolytic enzymes occupy the space left, in terms of the amount present in the composition enzymatic, by the non-contributory enzymes eliminated (Figure 1).
    Thus, the present invention describes a modified host cell that produces a less diverse enzyme cocktail, by presenting a reduced expression and / or secretion of at least one non-contributory cellulolytic enzyme with respect to the expression of the same non-contributory cellulolytic enzyme in a host cell parental or wild (wild-type) or unmodified. Additionally, the modified host cell of the invention has a higher cellulolytic efficiency, of transforming the cellulosic material into fermentable sugars, than a parental or wild host cell, not genetically modified.
    Said modified host cell, as defined in the present invention, may additionally have an increase in the expression of at least one contributory cellulolytic enzyme with respect to the expression of said contributory cellulolytic enzyme (s) in a wild host cell, not genetically modified. The contributory cellulolytic enzyme (s) whose expression may be increased in the host cell of the invention may be selected, preferably from homologous contributive cellulolytic enzyme (s) (s) and / or heterologous contributory cellulolytic enzyme (s).
    The inventors have shown that a lower expression and / or secretion of non-contributory cellulolytic enzymes in host cells, results in the expression and / or secretion of an enzymatic composition that presents an increase in the concentration (or a greater representation) of cellulolytic enzymes Contributory factors that have greater efficiency than non-contributory cellulolytic enzymes, which translates into the use of a lower diversity of cellulolytic enzymes in industrial biomass degradation processes and, therefore, also in an increase in process efficiency of saccharification and, finally, in the overall performance of bioproduct production processes,
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    preferably biofuel, since, as previously mentioned, less enzymatic diversity is needed to obtain a higher production of fermentable sugars at the end of the hydrolysis or saccharification process.
    Therefore, a first aspect of the present invention is related to a modified host cell that has a reduced expression and / or secretion of at least 10% in at least one of the non-contributory cellulolytic enzymes with respect to the percentage of expression and / or secretion of said non-contributory cellulolytic enzyme in a wild-type parental or wild host cell. From this moment and throughout this document, this first aspect of the invention will be referred to as the "host cell of the invention".
    In some preferred embodiments, the host cell of the invention has been genetically modified to reduce the expression and / or secretion of at least one non-contributory cellulolytic enzyme by approximately at least 1%, approximately at least 2%, approximately at least one 3%, about at least 4%, about at least 5%, about at least 10%, about at least 15%, about at least 20%, about at least 25%, about at least 30 %, about at least 35%, about at least 40%, about at least 45%, about at least 50%, about at least 55%, about at least 60%, about at least 65% , about at least 70%, about at least 75%, about at least 80%, about at least 85%, about at least 90%, about at least 95%, about at least 100% resp The expression of said non-contributory cellulolytic enzymes in a parental or wild host cell. In a more preferred embodiment, the host cell of the invention exhibits a 100% reduction in the expression and / or secretion of at least one non-contributory cellulolytic enzyme relative to a parental or wild host cell.
    For the purposes of the present invention, the terms "parental or wild host cell" or "wild-type host cell" may be used interchangeably and refer to that host cell that has not been modified to exhibit reduced expression and / or secretion. of one or more of a non-contributory cellulolytic enzyme as described in the present invention. Preferably, the parental or wild cell of the present invention is Myceliophtora thermophila, more preferably M. thermophila C1.
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    In another preferred embodiment, the secretion of one or more non-contributory cellulases may be inhibited, decreased or canceled. Alterations in the secretion of cellulolytic enzymes in the host cell of the invention may affect both the secretion of the non-contributory cellulase (s) and the general enzyme secretion system that specifically inhibits, decreases or nullifies the secretion of the non-contributory cellulase (s). Using recombinant technology, nucleic acid molecules that code for the signal peptide or sequences that allow the secretion of the non-contributory cellulolytic enzyme (s) can be introduced, deleted, disrupted, silenced, modified, inhibited, so that a decreased secretion occurs or null of the non-contributory cellulolytic enzymes or enzymes. In a genetic engineering approach, homologous recombination can be used to induce modifications in the secretion system of the non-contributory cellulolytic enzymes. Thus, in a preferred embodiment, the host cells of the invention are modified to decrease or cancel the secretion of at least one non-contributory cellulase.
    For the purposes of the present invention, the term "expression" or "gene expression" refers to the transcription of a specific gene or specific genes or specific genetic construct in mRNA with the subsequent translation of the latter into a protein. Additionally it includes the secretion of the protein to the outside of the cell.
    For the purposes of the present invention, the term "secretion" refers to the transport of a protein from inside the cell to the outside. For the purposes of the present invention, the term "secretion" refers, preferably to the secretion of enzymes with cellulolytic activity, which by effect of this transport appear in the enzymatic cocktail produced by said cell.
    For the purposes of the present invention, the terms "increased expression" or "overexpression" may be used interchangeably throughout this document and refer to any form of expression that is additional or greater than the original level of expression in a parental cell or wild Methods for increasing the expression of genes or gene products are well documented in the art and include, for example, overexpression driven by appropriate promoters, the use of transcription enhancers or translation enhancers. The isolated nucleic acids can also serve as promoters or enhancers and can be introduced in an appropriate position in a non-heterologous form of a polynucleotide in order to regulate by increasing the expression of a nucleic acid encoding the polypeptide of interest. For example, the
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    preferably selected from the list consisting of: biomass rich in fermentable sugars, such as sugarcane, starch biomass, for example, cereal grains, corn straw, wheat straw, barley straw, sorghum straw, Sugarcane straw, weeds, logs, branch and leaves.
    The predominant polysaccharide in the primary cell wall of biomass is cellulose, the second most abundant is hemicellulose, and the third is pectin. The secondary cell wall, produced after the cell has stopped its growth, also contains polysaccharides and is reinforced by polymeric lignin covalently crosslinked with hemicellulose. Cellulose is a homopolymer of anhydrocellulose and is thus a linear ȕ- (1,4) -D-glucan, while hemicellulose includes a variety of compounds, such as xylans, xyloglucans, arabinoxylans, and mannans in complex branched structures With a range of substituents. Although generally polymorphic, cellulose is found in plant tissue primarily as an insoluble crystalline matrix of parallel glucan chains. Hemicelluloses normally bind by hydrogen bonds to cellulose, as well as to other hemicelluloses, which helps stabilize the cell wall matrix.
    For the purposes of the present invention the term "cellulose" refers to a linear polysaccharide comprising hundreds to thousands of D-glucose units linked by ȕ- (1,4) bonds. This polysaccharide is also known as ȕ- (1,4) glucan.
    The term "cellulolytic enzyme or cellulase" refers to a category of enzymes that can degrade complex polymers, such as cellulose and / or hemicellulose (ȕ-1,4-glucan or ȕ-D-glucosidic bonds) to shorter oligosaccharides, such as cellobiose and / or glucose and xylobiose and / or xylose, respectively. Within this category of enzymes, the following groups are preferably found: 1,4-ȕ-D-glucan glucanhydrolase ("endoglucanase"
    or "EG"); 1,4-ȕ-D-glucan cellobiohydrolase ("exoglucanase", "cellobiohydrolase", or "CBH"); ȕD-glycosidoglucohydrolase ("ȕ-glucosidase", "cellobiase" or "BGL"), endoxylanases or xylanases ("Xyl"), beta-xylosidases ("beta-Xyl") and mono-oxygenase polysaccharides ("PMO"). Endoglucanases break internal bonds and alter the crystalline structure of cellulose, exposing individual cellulose polysaccharide chains ("glucans"). Cellobiohydrolases gradually shorten the glucan molecules, mainly releasing cellobiose units (a water-soluble d-1,4 linked glucose dimer), as well as glucose, celotriose and celotetraose. The glu-glucosidases fraction cellobiose in glucose monomers. Xylanases catalyze the random hydrolysis of polymeric xylan, pectin
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    polymeric or hemicellulose containing xylose residues that results in the formation of sugar oligomers containing xylose and / or monomeric xylose residues. Betaxylosidases are enzymes with 4-ȕ-D-xylan xylohydrolase activity catalyzing the reaction from xylose oligomers, including xylobiose, finally releasing D-xylose. PMOs are metalloproteins with endocellulolytic activity that act with a different mechanism than endoglucanases, since they break cellulose chains by oxidation of their glucose monomers in carbons 1, 4 and / or 6.
    The term "efficiency" of an enzyme, group of enzymes or enzymatic composition, refers to the catalytic activity of the enzyme, group of enzymes or enzymatic composition, under appropriate conditions under which the enzyme converts specific polymeric or artificial substrates into oligomeric products. or specific monomers. Preferably, a "greater efficiency" or "better efficiency" of the enzymes of the invention or of the enzyme cocktail of the invention, refers to obtaining an equal, or preferably greater amount of fermentable sugars obtained at the end of the hydrolytic process (it is ie, an equal or greater yield), with a lower diversity of cellulolytic enzymes present in the cocktail, with respect to an enzymatic cocktail obtained from a wild or parental host cell.
    The term "contributory cellulolytic enzymes" refers to those cellulases within the diversity of cellulases present in enzymatic cocktails, such as preferably, endoglucanases, cellobiohydrolases, ȕ-glucosidases, ȕ-xylosidases, xylanases, mono-oxygen polysaccharides, among others, which have a cellulolytic activity such that when removed from an enzymatic cocktail, the yield is reduced in terms of releasing fermentable sugars per unit mass. In a preferred embodiment, a contributory cellulolytic enzyme of any of the families or cellulolytic activities described in the present invention can be selected from a homologous or heterologous cellulase.
    The term "non-contributory cellulolytic enzyme" refers to those cellulases within the diversity of cellulases present in enzyme cocktails, such as preferably, endoglucanases, cellobiohydrolases, ȕ-glucosidases, ȕ-xylosidases, xylanases, mono-oxygen polysaccharides, among others, which have a cellulolytic activity such that being eliminated or reduced from an enzymatic cocktail improves its efficiency. In a preferred embodiment, a non-contributory cellulolytic enzyme of any of the families or cellulolytic activities described in the present invention may preferably be selected from a homologous or heterologous cellulase. In a preferred embodiment, the non-contributory cellulase of the invention is a homologous cellulase.
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    additionally they are genetically modified to increase the expression or insert more than one copy of the coding sequences of contributory cellulolytic enzymes that can be both homologous and heterologous. In a preferred embodiment, the over-expression of one or more contributory cellulases is carried out to increase the production or proportion of the contributory cellulases. In still more particular embodiments, the host cells of the invention are characterized in that in addition to presenting an increase in the expression of at least one of the contributory cellulolytic enzymes, said enzymes also have a greater cellulolytic activity. The genetic modification to obtain said characteristics in the strains of the invention can be achieved by genetic engineering techniques or by using classical microbiological techniques such as chemical or UV mutagenesis and subsequent selection. A combination of recombinant modification and classical selection techniques can be used to produce the organism of interest. Using recombinant technology, nucleic acid molecules can be introduced, over-expressed or modified, in a way that produces high yield of the secretion of contributory cellulolytic enzymes within the organism or in the culture. In a genetic engineering approach, homologous recombination can be used to induce modifications of genes chosen as the target, specifically targeting an in vivo gene to increase the expression of the encoded protein.
    In some preferred embodiments, the host cell described in the present invention has been genetically modified to over-express at least one of the contributory cellulolytic enzymes in about at least 1%, about at least 5%, about at least 10% , about at least 20%, about at least 25%, about at least 30%, about at least 35%, about at least 40%, about at least 45%, about at least 50%, approximately at least 55%, approximately at least 60%, approximately at least 65%, approximately at least 70%, approximately at least 75%, approximately at least 80%, approximately at least 85%, approximately at least 90%, approximately at least 95%, approximately at least 96%, approximately at least 97%, approximately at least 98%, approximately at least 99%, approximately at least 100% r specific to the expression of said contributory cellulolytic enzymes in a wild host cell.
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    In another preferred embodiment, the host cells of the invention are characterized by the overexpression of at least one of the contributory cellulolytic enzymes selected by the method described in the present invention.
    In another more preferred embodiment, the host cells of the invention are characterized in that the contributory cellulases can be derived from the host cell of the invention (homologous) or from other microorganisms producing cellulolytic enzymes other than the host cell of the invention (heterologous) . They can also be produced naturally or recombinantly.
    In another more preferred embodiment, the host cells of the invention are characterized in that the contributive cellulolytic enzyme that can increase its expression is preferably a cellobiohydrolase. In a more preferred embodiment, said cellobiohydrolase is preferably any cellobiohydrolase that has the highest efficiency within its family.
    In another more preferred embodiment, the host cells of the invention are characterized in that the contributive cellulolytic enzyme that can increase its expression is preferably an endoglucanase. In an even more preferred embodiment, the endoglucanase is preferably any endoglucanase that has the highest efficiency within its own family. In another more preferred embodiment, the preferred endoglucanase is endoglucanase 2. In another more preferred embodiment, endoglucanase 2 preferably comprises a sequence that has at least 60% identity with SEQ ID NO: 6, and optionally encoded by a nucleotide sequence. comprising a sequence that has at least 60% identity with SEQ ID NO: 5. More preferably, endoglucanase 2 is endoglucanase 2 comprising SEQ ID NO: 6, optionally encoded by the nucleotide sequence comprising SEQ ID NO: 5.
    In another more preferred embodiment, the host cells of the invention are characterized in that the contributive cellulolytic enzyme that can increase its expression is preferably a beta-glucosidase. In a still more preferred embodiment, beta-glucosidase is preferably any beta-glucosidase that has the highest efficiency within its own family.
    In another more preferred embodiment, the host cells of the invention are characterized in that the contributive cellulolytic enzyme that can increase its expression is
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    In another preferred embodiment, the host cell of the invention is characterized in that it has a reduced expression of a homologous non-contributory endoglucanase that has at least 60% identity with endoglucanase 6 comprising SEQ ID NO: 2, optionally encoded by a nucleotide sequence that has at least 60% identity with endoglucanase 6 comprising SEQ ID NO: 1 and a reduced expression of a homologous non-contributory mono-oxygenase polysaccharide that has at least 60% identity with the mono polysaccharide -oxygenase 09768 comprising SEQ ID NO: 4, optionally encoded by a nucleotide sequence that has at least 60% identity with the 09768 mono-oxygenase polysaccharide comprising SEQ ID NO: 3.
    In yet another more preferred embodiment, the host cell of the invention is characterized in that it has a reduced expression of endoglucanase 6 of SEQ ID NO: 2 and of the mono-oxygenase polysaccharide 09768 of SEQ ID NO: 4. Preferably, the reduced expression of endoglucanase 2 and 09768 mono-oxygenase polysaccharide refers to the deletion of the genes encoding said enzymes.
    As described herein, the "host cell" includes any type of cell that is susceptible to transformation, transfection, transduction, and the like with one or more nucleic acid constructs or expression vector comprising a polynucleotide that it codes for the cellulases described here, both contributory and non-contributory cellulases. The host cell can be a eukaryotic cell or a prokaryotic cell.
    In a particular embodiment the host cell is a prokaryotic cell that is preferably selected from the group of bacteria of the genera Bacillus, Clostridium, Esherichia, Klebsiella, Pseudomonas, Streptomyces, Thermoanaerobacterium or Zymomonas.
    In another particular embodiment, the host cell is a eukaryotic cell that is preferably selected from the group of fungi of the genera Candida, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces, Yarrowia, Acremonium, Agaricus, Alternaria, Aspergillus, Aureobasidium, Botryospaisium, Ceriporiopaisium, Ceriporioidium , Chrysosporium, Claviceps, Cochliobolus, Coprinopsis, Coptotermes, Corynascus, Cryphonectria, Cryptococcus, Diplodia, Exidia, Filibasidium, Fusarium, Gibberella, Holomastigotoides, Humícola, Irpex, Lentinula, Leptospaiprous, Magnaporiocamorathio, Nenapusimorus, Magnapus, Neopus, Neopus, Neopus , Paecilomyces, Penicillium, Phanerochaete, Piromyces, Poitrasia, Pseudoplectania, Pseudotrichonympha, Rhizomucor, Schizophyllum,
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    Scytalidium, Talaromyces, Thermoascus, Thielavia, Tolypocladium, Trichoderma, Trichophaea, Verticillium, Volvariella or Xylaria.
    In an even more preferred embodiment, the host cell of the invention is any strain of the Myceliophthora thermophila species. In an even more preferred embodiment, the host cell of the invention is strain C1 of Myceliophthora thermophila.
    It will be understood that for the aforementioned genera and species, the invention encompasses the perfect and imperfect states, and other taxonomic equivalents, for example, the anamorphs, with respect to the name of the species by which they are known. Those skilled in the art will readily recognize the identity of suitable equivalents. For example, Myceliophthora thermophila is equivalent to Chrysosporium lucknowense.
    Another aspect of the present invention relates to an enzyme cocktail obtained by the host cells of the invention. Said enzymatic cocktail comprises, at least, the contributory cellulolytic enzymes as defined above and which are secreted by the host cells of the invention, so that it will lack at least one of the non-contributory cellulolytic enzymes as defined above. From here and throughout this document, this cocktail will be called "cocktail of the invention". Preferably, in a particular embodiment, the enzyme cocktail referred to in the present invention comprises the contributory cellulolytic enzymes as defined above and lacks the enzymatic activity of at least one cellulase with endoglucanase activity, preferably, endoglucanase 6 ( Eg6), and / or at least one cellulase with monooxygenase polysaccharide activity, preferably PMO-09768.
    The cocktail of the invention can also be supplemented by adding other accessory or additional enzymes, which can be both homologous and heterologous, and which are also characterized in that their specific enzymatic activity cannot be replaced by any of the enzymatic activities exhibited by contributory cellulolytic enzymes. Said accessory or additional enzymes are selected from any of the following: aminopeptidases, amylases, carbohydrases, carboxypeptidases, catalases; chitinases, cutinases, cyclodextrin glucosyltransferases, deoxyribonucleases, esterases, alpha-galactosidase, beta-galactosidase, glucoamylase, alpha-glucosidases, haloperoxidases, invertases, lacases, lipases, mannosidases, oxidases, oxidoreductases, proteimasases, phylostasases, proteimasases, proteases polyphenoloxidases,
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    proteolytic enzymes, ribonucleases, transglutamines, or any combination thereof, provided that it does not present non-contributory cellulolytic enzymes.
    This accessory (s) or additional (s) enzyme (s) may come from both the host cell itself and other microorganisms capable of secreting cellulolytic enzymes that exhibit the activities indicated above, for example, by means of a microorganism belonging to the genus Aspergillus, such as Aspergillus aculeatus, Aspergillus awamori, Aspergillus fumigatus, Aspergillus foetidus, Aspergillus japonicus, Aspergillus nidulans, Aspergillus niger, or Aspergillus oryzae; Fusarium, such as Fusarium bactridioides, Fusarium cerealis, Fusarium crookwellense, Fusarium culmorum, Fusarium graminearum, Fusarium graminum, Fusarium heterosporum, Fusarium negundi, Fusarium oxysporum, Fusarium pseudograminearum, Fusarium reticulatum, Fusarium sausarium, Fusarium roseusus, Fusarium sausarium, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus, Fusarium roseusus toruloseum, Fusarium trichothecioides, or Fusarium venenatum; Gibberella, such as Gibberella zeae; Humicola, such as Humicola insolens or Humicola lanuginosa; Trichoderma, such as Trichoderma harzianum, Trichoderma koningii, Trichoderma longibrachiatum, Trichoderma reesei, or Trichoderma viride; or Myceliophthora, such as Myceliophthora thermophila.
    Therefore, in a more preferred embodiment, the cocktail of the invention further comprises other accessory or additional cellulolytic enzymes as described in the preceding paragraphs, which can be produced naturally or recombinantly.
    In a more preferred embodiment, the cocktail of the invention is an enzymatic mixture obtained from the host cell of the invention. In an even more preferred embodiment, the cocktail of the invention is an enzymatic mixture obtained by the host cell of the invention, preferably M. thermophila, which has a lower expression and / or secretion of homologous non-contributory cellulolytic enzymes in relation to a cell host, preferably M. thermophila parental or wild, which has a normal expression and / or secretion of all cellulolytic enzymes.
    The cocktail of the invention can be prepared according to the procedures known in the art and can be in liquid form or be a dry composition. The enzymes to be included in the cocktail can be stabilized according to the procedures known in the art.
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    权利要求:
    Claims (1)
    [1]
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    类似技术:
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    同族专利:
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    ES2647322B1|2018-10-05|
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE69922978T2|1998-10-06|2005-12-08|Emalfarb, Mark Aaron, Jupiter|TRANSFORMATION SYSTEM IN FILAMENTOUS FUNGICIDES CHRYSOSPORIUM HOST CELLS|
    US7923236B2|2007-08-02|2011-04-12|Dyadic International , Inc.|Fungal enzymes|
    ES2845200T3|2009-03-16|2021-07-26|Danisco Us Inc|Chrysosporium lucknowense protein production system|
    DK2635690T3|2010-11-02|2016-02-15|Codexis Inc|FORMATIONS AND PROCESSES FOR PREPARING fermentable SUGAR|
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    PCT/ES2017/070339| WO2017198890A1|2016-05-20|2017-05-22|Myceliophthora thermophila host cell having improved cellulolytic activity and enzymatic compounds produced with same|
    US16/303,088| US11254956B2|2016-05-20|2017-05-22|Myceliophthora thermophila host cell having improved cellulolytic activity and enzymatic compounds produced with same|
    EP17798810.2A| EP3460045A4|2016-05-20|2017-05-22|Myceliophthora thermophila|
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