WO2023054882A1 - 신규한 아세토하이드록시산 신테아제 변이체 및 이를 이용한 l-이소류신 생산방법 - Google Patents
신규한 아세토하이드록시산 신테아제 변이체 및 이를 이용한 l-이소류신 생산방법 Download PDFInfo
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1022—Transferases (2.) transferring aldehyde or ketonic groups (2.2)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/52—Genes encoding for enzymes or proenzymes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
- C12N15/77—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for Corynebacterium; for Brevibacterium
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/06—Alanine; Leucine; Isoleucine; Serine; Homoserine
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y202/00—Transferases transferring aldehyde or ketonic groups (2.2)
- C12Y202/01—Transketolases and transaldolases (2.2.1)
- C12Y202/01006—Acetolactate synthase (2.2.1.6)
Definitions
- the present application relates to a novel acetohydroxy acid synthase (AHAS) variant that improves L-isoleucine production ability, a microorganism containing the same, and a method for producing L-isoleucine using the microorganism .
- AHAS acetohydroxy acid synthase
- L-isoleucine is one of the branched-chain amino acids among a total of 20 amino acids, and is classified as an essential amino acid and is used in animal feed, food additives, and medicine. Since L-isoleucine performs functions such as post-metabolism energy production, hemoglobin production, blood sugar control, muscle production and repair, L-isoleucine is increasingly used in the field of animal feed as well as infusion solutions, nutritional supplements, and sports supplements.
- the present inventors identified a variant of acetohydroxy acid synthase (AHAS), one of the proteins in the L-isoleucine production pathway, and confirmed that the variant improved the L-isoleucine-producing ability of the strain. By doing so, this application was completed.
- AHAS acetohydroxy acid synthase
- One object of the present application is an acetohydroxy acid synthase (Acetohydroxy acid synthase) in which the amino acid corresponding to the 42nd position in the amino acid sequence of SEQ ID NO: 1 is substituted with another amino acid and the amino acid corresponding to the 47th position is substituted with another amino acid.
- synthase, AHAS acetohydroxy acid synthase
- Another object of the present application is to provide a polynucleotide encoding the variant of the present application.
- Another object of the present application is the variant of the present application; Or a polynucleotide encoding the variant; to provide a strain of the genus Corynebacterium comprising a.
- Another object of the present application is the variant of the present application; Or a polynucleotide encoding the variant; to provide a method for producing L-isoleucine, comprising the step of culturing a strain of the genus Corynebacterium comprising the above in a medium.
- L-isoleucine Since the microorganisms expressing acetohydroxy acid synthase mutations in the present application can significantly improve L-isoleucine production compared to strains that do not express them, L-isoleucine can be effectively produced using them. Accordingly, a wide range of industrial applications such as food, feed, and medicine using L-isoleucine can be expected.
- One aspect of the present application is acetohydroxy acid synthase in which the amino acid corresponding to position 42 in the amino acid sequence of SEQ ID NO: 1 is substituted with another amino acid and the amino acid corresponding to position 47 is substituted with another amino acid.
- synthase, AHAS acetohydroxy acid synthase
- the amino acid corresponding to the 42nd position may be substituted with valine.
- amino acid corresponding to the 47th position may be substituted with leucine.
- the variant of the present application may be one in which the amino acid corresponding to position 42 is substituted with valine and the amino acid corresponding to position 47 is substituted with leucine based on the amino acid sequence set forth in SEQ ID NO: 1, which is the parent sequence. At least 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, 99% or more, 99.5% or more from the amino acid sequence described in 1 , or an amino acid sequence having greater than 99.7% and less than 100% homology or identity.
- sequence additions or deletions naturally occurring mutations, silent mutations or conservations to the amino acid sequence N-terminus, C-terminus and/or within that do not alter the function of the variants of the present application. This is the case with redundant substitution.
- the "conservative substitution” refers to the substitution of one amino acid with another amino acid having similar structural and/or chemical properties. Such amino acid substitutions can generally occur based on similarities in polarity, charge, solubility, hydrophobicity, hydrophilicity and/or amphipathic nature of the residues. Typically, conservative substitutions may have little or no effect on the activity of the protein or polypeptide.
- variant means that one or more amino acids have been subjected to conservative substitution and/or modification, which is different from the amino acid sequence before the mutation, but the functions or properties refers to a polypeptide that is maintained.
- variants can generally be identified by modifying one or more amino acids in the amino acid sequence of the polypeptide and evaluating the properties of the modified polypeptide. That is, the ability of the variant may be increased, unchanged, or reduced compared to the polypeptide before the mutation.
- some variants may include variants in which one or more portions such as an N-terminal leader sequence or a transmembrane domain are removed.
- variants may include variants in which a portion is removed from the N- and/or C-terminus of the mature protein.
- variant may be used interchangeably with terms such as variant, variant, variant polypeptide, mutated protein, mutation and variant (in English, modification, modified polypeptide, modified protein, mutant, mutein, divergent, etc.) And, if the term is used in a mutated sense, it is not limited thereto.
- Variants may also include deletions or additions of amino acids that have minimal impact on the secondary structure and properties of the polypeptide.
- a signal (or leader) sequence involved in protein translocation may be conjugated to the N-terminus of the variant, either co-translationally or post-translationally.
- the variant may be conjugated with other sequences or linkers to enable identification, purification, or synthesis.
- parent sequence means a reference sequence that becomes a variant polypeptide by introducing a modification (modification). That is, the parental sequence may be a target for introducing mutations such as substitution, insertion, and/or deletion as a starting sequence.
- the parental sequence may be a naturally occurring or wild type, or a variant in which one or more substitutions, insertions or deletions have occurred in the natural or wild type, or may be an artificially synthesized sequence. there is.
- the term 'homology' or 'identity' refers to the degree of similarity between two given amino acid sequences or base sequences and can be expressed as a percentage.
- the terms homology and identity are often used interchangeably.
- Sequence homology or identity of conserved polynucleotides or polypeptides can be determined by standard alignment algorithms, together with default gap penalties established by the program used.
- Substantially homologous or identical sequences generally comprise at least about 50%, 60%, 70% or more of the entire or full-length sequence under moderate or high stringent conditions. , can hybridize to 80% or more or 90% or more. It is obvious that hybridization also includes hybridization with polynucleotides containing common codons or codons in consideration of codon degeneracy in polynucleotides.
- GAP program can define the total number of symbols in the shorter of the two sequences divided by the number of similarly arranged symbols (i.e., nucleotides or amino acids).
- the default parameters for the GAP program are (1) a binary comparison matrix (containing values of 1 for identity and 0 for non-identity) and Schwartz and Dayhoff, eds., Atlas Of Protein Sequence And Structure, National Biomedical Research Foundation , pp. 353-358 (1979), Gribskov et al (1986) Nucl. Acids Res. 14: weighted comparison matrix of 6745 (or EDNAFULL (EMBOSS version of NCBI NUC4.4) substitution matrix); (2) a penalty of 3.0 for each gap and an additional penalty of 0.10 for each symbol in each gap (or 10 gap opening penalty, 0.5 gap extension penalty); and (3) no penalty for end gaps.
- the variant of the present application may have acetohydroxy acid synthase (AHAS) activity.
- the variant of the present application may have an activity to increase the L- isoleucine production ability compared to the wild-type polypeptide having acetohydroxy acid synthase activity.
- acetohydroxy acid synthase is the first enzyme in L-valine biosynthesis, and is also referred to as acetolactate acidase.
- Acetohydroxy acid synthase catalyzes the decarboxylation of pyruvate and its condensation reaction with other pyruvic acid molecules to produce acetolactate, a precursor of valine, or decarboxylation of pyruvate and 2-ketobutyrate ( 2-ketobutyrate) to produce acetohydroxybutyrate, a precursor of isoleucine.
- the acetohydroxy acid synthase is encoded by two genes, ilvB and ilvN .
- the ilvB gene represents the large subunit of acetohydroxy acid synthase
- the ilvN gene represents the small subunit of acetohydroxy acid synthase. Each small subunit is coded. Among them, the small subunit encoded by the ilvN gene is considered to be critically involved in feedback inhibition.
- the "feedback inhibition" means that an end product of an enzyme system inhibits a reaction at an early stage of the enzyme system.
- an acetohydroxy acid synthase may be an acetohydroxy acid synthase encoded by the ilvN gene.
- sequence of the acetohydroxy acid synthase encoded by the ilvN gene can be obtained from NCBI's GenBank, a known database, and may specifically have the amino acid sequence of SEQ ID NO: 1, but is not limited thereto.
- corresponding to refers to an amino acid residue at a recited position in a polypeptide, or an amino acid residue that is similar, identical, or homologous to a recited residue in a polypeptide. Identification of the amino acid at the corresponding position may be determining the specific amino acid in the sequence that references the specific sequence.
- corresponding region generally refers to a similar or corresponding position in a related or reference protein.
- any amino acid sequence can be aligned with SEQ ID NO: 1, and based on this, each amino acid residue of the amino acid sequence can be numbered with reference to the numerical position of the amino acid residue corresponding to the amino acid residue of SEQ ID NO: 1.
- sequence alignment algorithms such as those described herein, can identify the location of amino acids, or locations where modifications such as substitutions, insertions, or deletions occur, compared to a query sequence (also referred to as a “reference sequence”).
- Such alignments include, for example, the Needleman-Wunsch algorithm (Needleman and Wunsch, 1970, J. Mol. Biol. 48: 443-453), the Needleman program in the EMBOSS package (EMBOSS: The European Molecular Biology Open Software Suite, Rice et al. , 2000), Trends Genet. 16: 276-277) may be used, but it is not limited thereto, and a sequence alignment program known in the art, a pairwise sequence comparison algorithm, and the like may be appropriately used.
- the variant of the present application may have, include, consist of, or consist essentially of the amino acid sequence set forth in SEQ ID NO: 5.
- Another aspect of the present application is to provide a polynucleotide encoding a variant of the present application.
- polynucleotide is a polymer of nucleotides in which nucleotide monomers are covalently linked in a long chain shape, and is a DNA or RNA strand of a certain length or more, more specifically, encoding the variant means a polynucleotide fragment.
- the polynucleotide encoding the variant of the present application may include a nucleotide sequence encoding the amino acid sequence described in SEQ ID NO: 3, SEQ ID NO: 4, or SEQ ID NO: 5.
- the polynucleotide of the present application may have or include the sequence of SEQ ID NO: 24.
- the polynucleotide of the present application may consist of or essentially consist of the sequence of SEQ ID NO: 24.
- the polynucleotides of the present application are various in the coding region within the range that does not change the amino acid sequence of the variants of the present application in consideration of codon degeneracy or preferred codons in organisms intended to express the variants of the present application. Transformations can be made. Specifically, the polynucleotide of the present application has 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more of the sequence of SEQ ID NO: 2.
- the codon encoding the amino acid corresponding to the 42nd position of SEQ ID NO: 1 may be one of the codons encoding valine, and the codon encoding the amino acid corresponding to the 47th position. can be one of the codons encoding the acid.
- polynucleotide of the present application is included without limitation as long as it is a probe that can be prepared from a known gene sequence, for example, a sequence that can hybridize under stringent conditions with a sequence complementary to all or part of the polynucleotide sequence of the present application.
- stringent condition means a condition that allows specific hybridization between polynucleotides. These conditions are described in J. Sambrook et al., Molecular Cloning, A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory press, Cold Spring Harbor, New York, 1989; F.M. Ausubel et al., Current Protocols in Molecular Biology, John Wiley & Sons, Inc., New York, 9.50-9.51, 11.7-11.8).
- polynucleotides with high homology or identity 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, Or a condition in which polynucleotides having 99% or more homology or identity hybridize and polynucleotides having lower homology or identity do not hybridize, or 60 ° C., which is a washing condition for normal southern hybridization, 1XSSC, 0.1% SDS, specifically 60 ° C, 0.1XSSC, 0.1% SDS, more specifically 68 ° C, 0.1XSSC, 0.1% SDS, at a salt concentration and temperature equivalent to 1 time, specifically 2 to 3 times washing conditions can be enumerated.
- Hybridization requires that two nucleic acids have complementary sequences, although mismatches between bases are possible depending on the stringency of hybridization.
- complementary is used to describe the relationship between nucleotide bases that are capable of hybridizing to each other. For example, with respect to DNA, adenine is complementary to thymine and cytosine is complementary to guanine.
- the polynucleotides of the present application may also include substantially similar nucleic acid sequences as well as isolated nucleic acid fragments complementary to the entire sequence.
- a polynucleotide having homology or identity to the polynucleotide of the present application can be detected using hybridization conditions including a hybridization step at a Tm value of 55°C and using the above-described conditions.
- the Tm value may be 60 ° C, 63 ° C or 65 ° C, but is not limited thereto and may be appropriately adjusted by those skilled in the art according to the purpose.
- Appropriate stringency for hybridizing the polynucleotides depends on the length of the polynucleotides and the degree of complementarity, parameters well known in the art (e.g., J. Sambrook et al., supra).
- Another aspect of the present application is to provide a vector comprising the polynucleotide of the present application.
- the vector may be an expression vector for expressing the polynucleotide in a host cell, but is not limited thereto.
- the vector of the present application may include a DNA product containing the nucleotide sequence of a polynucleotide encoding the target polypeptide operably linked to a suitable expression control region (or expression control sequence) so as to express the target polypeptide in a suitable host.
- the expression control region may include a promoter capable of initiating transcription, an arbitrary operator sequence for regulating such transcription, a sequence encoding a suitable mRNA ribosome binding site, and a sequence regulating termination of transcription and translation.
- the vector After transformation into a suitable host cell, the vector can replicate or function independently of the host genome and can integrate into the genome itself.
- Vectors used in the present application are not particularly limited, and any vectors known in the art may be used.
- Examples of commonly used vectors include natural or recombinant plasmids, cosmids, viruses and bacteriophages.
- pWE15, M13, MBL3, MBL4, IXII, ASHII, APII, t10, t11, Charon4A, and Charon21A can be used as phage vectors or cosmid vectors, and pDZ-based, pBR-based, and pUC-based plasmid vectors , pBluescriptII-based, pGEM-based, pTZ-based, pCL-based, pET-based, etc. can be used.
- pDZ, pDC, pDCM2, pACYC177, pACYC184, pCL, pECCG117, pUC19, pBR322, pMW118, pCC1BAC vectors and the like can be used.
- a polynucleotide encoding a target polypeptide may be inserted into a chromosome through a vector for chromosomal insertion into a cell. Insertion of the polynucleotide into the chromosome may be performed by any method known in the art, for example, homologous recombination, but is not limited thereto.
- a selection marker for determining whether the chromosome is inserted may be further included.
- the selectable marker is used to select cells transformed with a vector, that is, to determine whether a target nucleic acid molecule has been inserted, and can exhibit selectable phenotypes such as drug resistance, auxotrophy, resistance to cytotoxic agents, or surface polypeptide expression. markers may be used. In an environment treated with a selective agent, only cells expressing the selectable marker survive or exhibit other expression traits, so transformed cells can be selected.
- the term "transformation” means introducing a vector containing a polynucleotide encoding a target polypeptide into a host cell or microorganism so that the polypeptide encoded by the polynucleotide can be expressed in the host cell.
- the transformed polynucleotide can be expressed in the host cell, it may be inserted into and located in the chromosome of the host cell or located outside the chromosome.
- the polynucleotide includes DNA and/or RNA encoding a polypeptide of interest.
- the polynucleotide may be introduced in any form as long as it can be introduced and expressed into a host cell.
- the polynucleotide may be introduced into a host cell in the form of an expression cassette, which is a genetic construct containing all elements required for self-expression.
- the expression cassette may include a promoter operably linked to the polynucleotide, a transcription termination signal, a ribosome binding site, and a translation termination signal.
- the expression cassette may be in the form of an expression vector capable of self-replication.
- the polynucleotide may be introduced into a host cell in its own form and operably linked to a sequence necessary for expression in the host cell, but is not limited thereto.
- operably linked means that the polynucleotide sequence is functionally linked to a promoter sequence that initiates and mediates the transcription of the polynucleotide encoding the target variant of the present application.
- Another aspect of the present application is to provide a strain of the genus Corynebacterium , including the variant of the present application or the polynucleotide of the present application.
- the strain of the present application may include the variant polypeptide of the present application, a polynucleotide encoding the polypeptide, or a vector containing the polynucleotide of the present application.
- strain or microorganism
- strain includes both wild-type microorganisms and naturally or artificially genetically modified microorganisms, and causes such as insertion of foreign genes or enhancement or inactivation of endogenous gene activity.
- a microorganism whose specific mechanism is attenuated or enhanced due to, it may be a microorganism containing genetic modification for the production of a desired polypeptide, protein or product.
- the strains of the present application include strains containing any one or more of the variants of the present application, the polynucleotides of the present application, and vectors containing the polynucleotides of the present application; strains modified to express variants of the present application or polynucleotides of the present application; variants of the present application, or strains expressing the polynucleotides of the present application (eg, recombinant strains); Or it may be a strain (eg, a recombinant strain) having the mutant activity of the present application, but is not limited thereto.
- the strain of the present application may be a strain having an L-isoleucine producing ability.
- the strain of the present application is a microorganism naturally having the ability to produce acetohydroxy acid synthase or L-isoleucine, or a mutant of the present application or poly-encoding the same in a parent strain that does not have the ability to produce acetohydroxy acid synthase or L-isoleucine. It may be a microorganism into which a nucleotide (or a vector containing the polynucleotide) is introduced and/or endowed with L-isoleucine-producing ability, but is not limited thereto.
- the strain of the present application is a cell or microorganism that is transformed with a vector containing a polynucleotide of the present application or a polynucleotide encoding a variant of the present application and expresses the variant of the present application, and for the purpose of the present application
- the strains of the application may include all microorganisms capable of producing L-isoleucine, including the variants of the present application.
- a polynucleotide encoding the variant of the present application is introduced into a natural wild-type microorganism or a microorganism that produces L-isoleucine, so that the acetohydroxy acid synthase variant is expressed, and the L-isoleucine-producing ability is increased. It may be an increased recombinant strain.
- the recombinant strain with increased L-isoleucine-producing ability is a natural wild-type microorganism or an acetohydroxy acid synthase unmodified microorganism (ie, a microorganism expressing wild-type acetohydroxy acid synthase (SEQ ID NO: 1) or a mutant form (SEQ ID NO: 1)).
- microorganisms that do not express the protein may be microorganisms with increased L-isoleucine-producing ability, but are not limited thereto.
- the acetohydroxy acid synthase unmodified microorganism which is a target strain for comparing the increase in the L-isoleucine-producing ability, is Corynebacterium glutami, which introduces hom (R407H) and ilvA (T381A, F383A) mutations Coomb ATCC13032 strain (CA10-3101, KCCM12739P) or NTG (N-Methyl-N'-nitro-N-nitrosoguanidine) treated L-isoleucine producing strain KCJI-38 strain (KCCM11248P, Korean Patent No. 10-1335789) It may be, but is not limited thereto.
- the recombinant strain having increased production capacity has an L-isoleucine production capacity of about 1% or more, specifically about 2% or more, about 5% or more, about 10% or more, about 15% or more, about 20% or more, about 25% or more, about 29% or more, about 30% or more, about 35% or more, about 39% or more, about 40% or more, about 41% or more, about 43% or more, about 45% or more, about 46% or more, about 50% or more, about 52% or more, about 55% or more, about 57% or more, about 58% or more, about 60% or more, or about 63% or more , e.g., about 200% or less, about 150% or less, about 100% or less, about 50% or less, about 40% or less, about 30% or less, about 20% or less, or about 15% or less).
- the recombinant strain having increased production capacity has an L-isoleucine production capacity of about 1.01 times or more, about 1.02 times or more, about 1.05 times or more, about 1.10 times or more, about 1.15 times or more, compared to the parental strain or non-modified microorganism before mutation.
- the term "unmodified microorganism” does not exclude strains containing mutations that may occur naturally in microorganisms, and are wild-type strains or wild-type strains themselves, or are genetically modified by natural or artificial factors. It may mean a strain before change.
- the non-modified microorganism may mean a strain before or without introduction of the acetohydroxy acid synthase variant described herein.
- the "unmodified microorganism” may be used interchangeably with "strain before transformation", “microorganism before transformation”, “non-mutated strain”, “unmodified strain”, “non-mutated microorganism” or "reference microorganism".
- the microorganisms of the present application are Corynebacterium genus ( Corynebacterium stationis ), Corynebacterium glutamicum ( Corynebacterium glutamicum ), Corynebacterium crudilactis ( Corynebacterium crudilactis ), Corynebacterium Leeum deserti ( Corynebacterium deserti ), Corynebacterium efficiens ( Corynebacterium efficiens ), Corynebacterium callunae ( Corynebacterium callunae ), Corynebacterium singulare ( Corynebacterium singulare ), Corynebacterium halotoleans ( Corynebacterium halotolerans ), Corynebacterium striatum ( Corynebacterium striatum ), Corynebacterium ammonia Genes ( Corynebacterium ammoniagenes ), Corynebacterium pollutis
- the term "enhancement" of polypeptide activity means that the activity of the polypeptide is increased relative to the intrinsic activity.
- the enhancement may be used interchangeably with terms such as activation, up-regulation, overexpression, and increase.
- activation, enhancement, upregulation, overexpression, and increase may include those that exhibit an activity that was not originally possessed, or those that exhibit enhanced activity compared to intrinsic activity or activity before modification.
- the "intrinsic activity” refers to the activity of a specific polypeptide originally possessed by a parent strain or unmodified microorganism before transformation when a character is changed due to genetic mutation caused by natural or artificial factors. This may be used interchangeably with “activation before transformation”.
- “Enhancement”, “upregulation”, “overexpression” or “increase” of the activity of a polypeptide compared to the intrinsic activity means that the activity and/or concentration (expression amount) is improved.
- the enhancement can be achieved by introducing a foreign polypeptide or by enhancing the activity and/or concentration (expression level) of an endogenous polypeptide. Whether or not the activity of the polypeptide is enhanced can be confirmed from an increase in the activity level, expression level, or amount of a product released from the corresponding polypeptide.
- Enhancement of the activity of the polypeptide can be applied by various methods well known in the art, and is not limited as long as the activity of the target polypeptide can be enhanced compared to the microorganism before transformation. Specifically, it may be using genetic engineering and / or protein engineering, which is well known to those skilled in the art, which is a routine method of molecular biology, but is not limited thereto (e.g., Sitnicka et al. Functional Analysis of Genes. Advances in Cell Biology. 2010, Vol. 2. 1-16, Sambrook et al. Molecular Cloning 2012, etc.).
- modification of the polynucleotide sequence encoding the polypeptide to enhance the activity of the polypeptide eg, modification of the polynucleotide sequence of the polypeptide gene to encode the modified polypeptide to enhance the activity of the polypeptide
- It may be a combination of two or more selected from 1) to 8), but is not particularly limited thereto.
- the increase in the intracellular copy number of the polynucleotide encoding the polypeptide is achieved by introducing into the host cell a vector capable of replicating and functioning independently of the host, to which the polynucleotide encoding the corresponding polypeptide is operably linked. it may be Alternatively, it may be achieved by introducing one copy or two or more copies of a polynucleotide encoding the corresponding polypeptide into the chromosome of the host cell.
- the introduction into the chromosome may be performed by introducing a vector capable of inserting the polynucleotide into the chromosome of the host cell into the host cell, but is not limited thereto.
- the vector is as described above.
- the expression control region may include a promoter, an operator sequence, a sequence encoding a ribosome binding site, and a sequence regulating termination of transcription and translation.
- the original promoter may be replaced with a strong promoter, but is not limited thereto.
- Examples of known strong promoters include cj1 to cj7 promoter (US Patent US 7662943 B2), lac promoter, trp promoter, trc promoter, tac promoter, lambda phage PR promoter, PL promoter, tet promoter, gapA promoter, SPL7 promoter, SPL13 (sm3) promoter (US Patent US 10584338 B2), O2 promoter (US Patent US 10273491 B2), tkt promoter, yccA promoter, etc., but are not limited thereto.
- Modification of the nucleotide sequence encoding the initiation codon or 5'-UTR region of the gene transcript encoding the polypeptide is, for example, a nucleotide sequence encoding another initiation codon with a higher polypeptide expression rate than the endogenous initiation codon. It may be substituted, but is not limited thereto.
- Modification of the amino acid sequence or polynucleotide sequence of 4) and 5) above may include deletion, insertion, non-conservative or conservative substitution of the amino acid sequence of the polypeptide or the polynucleotide sequence encoding the polypeptide to enhance the activity of the polypeptide.
- the combination thereof may be a sequence mutation, or replacement with an amino acid sequence or polynucleotide sequence improved to have stronger activity, or an amino acid sequence or polynucleotide sequence improved to increase activity, but is not limited thereto.
- the replacement may be specifically performed by inserting the polynucleotide into a chromosome by homologous recombination, but is not limited thereto.
- the vector used at this time may further include a selection marker for checking whether the chromosome is inserted.
- the selectable marker is as described above.
- Introduction of a foreign polynucleotide exhibiting the activity of the polypeptide may be introduction of a foreign polynucleotide encoding a polypeptide exhibiting the same/similar activity as the polypeptide into a host cell.
- the foreign polynucleotide is not limited in origin or sequence as long as it exhibits the same/similar activity as the polypeptide.
- the method used for the introduction can be performed by appropriately selecting a known transformation method by a person skilled in the art, and expression of the introduced polynucleotide in a host cell can generate a polypeptide and increase its activity.
- the codon optimization of the polynucleotide encoding the polypeptide is codon optimization of the endogenous polynucleotide to increase transcription or translation in the host cell, or optimization of the transcription or translation of the foreign polynucleotide in the host cell. It may be that the codons of this have been optimized.
- Analyzing the tertiary structure of the polypeptide to select and modify or chemically modify the exposed site for example, by comparing the sequence information of the polypeptide to be analyzed with a database in which sequence information of known proteins is stored, depending on the degree of sequence similarity. It may be to determine a template protein candidate according to the method, confirm the structure based on this, and modify or modify an exposed portion to be chemically modified to be modified or modified.
- Such enhancement of polypeptide activity is an increase in the activity or concentration of the corresponding polypeptide based on the activity or concentration of the polypeptide expressed in the wild-type or unmodified microbial strain, or an increase in the amount of the product produced from the corresponding polypeptide. It may be, but is not limited thereto.
- Modification of some or all of the polynucleotides in the microorganism of the present application is (a) genome editing using homologous recombination or genetic scissors (engineered nuclease, e.g., CRISPR-Cas9) using a vector for chromosomal insertion into the microorganism and / or (b) It may be induced by light and/or chemical treatment, such as ultraviolet light and radiation, but is not limited thereto.
- a method of modifying part or all of the gene may include a method using DNA recombination technology.
- a part or all of a gene may be deleted by injecting a nucleotide sequence or vector containing a nucleotide sequence homologous to a target gene into the microorganism to cause homologous recombination.
- the injected nucleotide sequence or vector may include a dominant selection marker, but is not limited thereto.
- Another aspect of the present application provides a method for producing L-isoleucine, comprising the step of culturing a strain of the genus Corynebacterium containing the variant of the present application or the polynucleotide of the present application in a medium.
- the L-isoleucine production method of the present application may include culturing a strain of the genus Corynebacterium including the variant of the present application, the polynucleotide of the present application, or the vector of the present application in a medium.
- the term "cultivation” means growing the Corynebacterium genus strain of the present application under appropriately controlled environmental conditions.
- the culture process of the present application may be performed according to suitable media and culture conditions known in the art. This culturing process can be easily adjusted and used by those skilled in the art according to the selected strain. Specifically, the culture may be batch, continuous and/or fed-batch, but is not limited thereto.
- the term "medium” refers to a material in which nutrients necessary for culturing the strain of the genus Corynebacterium of the present application are mixed as main components, including water indispensable for survival and growth, as well as nutrients and growth supplies, etc.
- any medium and other culture conditions used for culturing the strain of the genus Corynebacterium of the present application can be used without particular limitation as long as it is a medium used for culturing common microorganisms.
- the strain can be cultured while controlling temperature, pH, etc. under aerobic conditions in a conventional medium containing appropriate carbon sources, nitrogen sources, phosphorus, inorganic compounds, amino acids, and/or vitamins.
- Examples of the carbon source in the present application include carbohydrates such as glucose, saccharose, lactose, fructose, sucrose, and maltose; sugar alcohols such as mannitol and sorbitol; organic acids such as pyruvic acid, lactic acid, citric acid and the like; Amino acids such as glutamic acid, methionine, lysine, and the like may be included.
- natural organic nutrients such as starch hydrolysate, molasses, blackstrap molasses, rice winter, cassava, sorghum pomace and corn steep liquor can be used, specifically glucose and sterilized pretreated molasses (i.e. converted to reducing sugar).
- Carbohydrates such as molasses
- other carbon sources in an appropriate amount may be used in various ways without limitation. These carbon sources may be used alone or in combination of two or more, but are not limited thereto.
- nitrogen source examples include inorganic nitrogen sources such as ammonia, ammonium sulfate, ammonium chloride, ammonium acetate, ammonium phosphate, ammonium carbonate, and ammonium nitrate; Amino acids such as glutamic acid, methionine, glutamine, etc., organic nitrogen sources such as peptone, NZ-amine, meat extract, yeast extract, malt extract, corn steep liquor, casein hydrolysate, fish or degradation products thereof, defatted soybean cake or degradation products thereof, etc. can be used These nitrogen sources may be used alone or in combination of two or more, but are not limited thereto.
- inorganic nitrogen sources such as ammonia, ammonium sulfate, ammonium chloride, ammonium acetate, ammonium phosphate, ammonium carbonate, and ammonium nitrate
- Amino acids such as glutamic acid, methionine, glutamine, etc.
- organic nitrogen sources such as peptone, NZ-amine,
- the number of persons may include monopotassium phosphate, dipotassium phosphate, or a sodium-containing salt corresponding thereto.
- the inorganic compound sodium chloride, calcium chloride, iron chloride, magnesium sulfate, iron sulfate, manganese sulfate, calcium carbonate, etc. may be used, and amino acids, vitamins, and/or appropriate precursors may be included. These components or precursors may be added to the medium either batchwise or continuously. However, it is not limited thereto.
- the pH of the medium can be adjusted by adding compounds such as ammonium hydroxide, potassium hydroxide, ammonia, phosphoric acid, sulfuric acid, etc. to the medium in an appropriate manner during the cultivation of the strain of the genus Corynebacterium of the present application.
- an antifoaming agent such as a fatty acid polyglycol ester.
- oxygen or oxygen-containing gas may be injected into the medium, or nitrogen, hydrogen or carbon dioxide gas may be injected without gas injection or nitrogen, hydrogen or carbon dioxide gas may be injected to maintain the anaerobic and non-aerobic state. It is not.
- the culture temperature may be maintained at 20 to 45 ° C, specifically 25 to 40 ° C, and may be cultured for about 10 to 160 hours, but is not limited thereto.
- L-isoleucine produced by the culture of the present application may be secreted into the medium or remain in the cells.
- the L-isoleucine production method of the present application includes preparing a strain of the genus Corynebacterium of the present application, preparing a medium for culturing the strain, or a combination thereof (regardless of order), for example , Prior to the culturing step, it may be further included.
- the L-isoleucine production method of the present application may further include a step of recovering L-isoleucine from the cultured medium (cultured medium) or Corynebacterium genus strain.
- the recovering step may be further included after the culturing step.
- the recovery may be to collect the desired L-isoleucine using a suitable method known in the art according to the culture method of the microorganism of the present application, for example, batch, continuous or fed-batch culture method. .
- a suitable method known in the art according to the culture method of the microorganism of the present application, for example, batch, continuous or fed-batch culture method.
- the L-isoleucine production method of the present application may additionally include a purification step.
- the purification may be performed using suitable methods known in the art.
- the recovery step and the purification step are performed continuously or discontinuously regardless of order, or simultaneously or integrated into one step. It can be performed, but is not limited thereto.
- variants, polynucleotides, vectors and strains, etc. are as described in the other aspects above.
- Another aspect of the present application is a variant of the present application, a polynucleotide encoding the variant, a vector comprising the polynucleotide, or a strain of the genus Corynebacterium comprising the polynucleotide of the present application; medium in which it was cultured; Or to provide a composition for producing L- isoleucine comprising a combination of two or more of them.
- composition of the present application may further include any suitable excipient commonly used in amino acid production compositions, and such an excipient may be, for example, a preservative, a wetting agent, a dispersing agent, a suspending agent, a buffer, a stabilizer, or an isotonic agent. However, it is not limited thereto.
- composition of the present application variants, polynucleotides, vectors, strains, media, and L-isoleucine are as described in the other embodiments above.
- Another aspect of the present application is a variant of the present application; a polynucleotide encoding the variant; Alternatively, to provide a use of a strain of the genus Corynebacterium containing the variant or a polynucleotide encoding the variant for producing L-isoleucine.
- Wild-type Corynebacterium glutamicum has the ability to produce L-isoleucine, but does not overproduce it. Thus, in order to confirm the genetic trait that increases the L-isoleucine-producing ability, a strain with increased L-isoleucine-producing ability compared to the wild type was prepared.
- primer pairs of SEQ ID NOs: 6 and 7 or SEQ ID NOs: 8 and PCR was performed using the primer pair of SEQ ID NO: 9, respectively.
- the primer sequences are as shown in Table 1 below.
- sequence number designation order 6 primer 1 TCGAGCTCGGTACCCCGCTTTTGCACTCATCGAGC 7 primer 2 CACGATCAGAGTGTGCATCATCAT 8 primer 3 ATGATGATGCACATCTGATCGTG 9 primer 4 CTCTAGAGGATCCCCGAGCATCTTCCAAAACCTTG
- PfuUltra TM high-reliability DNA polymerase (Stratagene) was used as the polymerase for the PCR reaction, and the PCR conditions were denaturation at 95 ° C for 30 seconds; Annealing at 55° C. for 30 seconds; and polymerization reaction at 72 ° C. for 1 minute, and denaturation, annealing, and polymerization under these conditions were repeated 28 times to obtain a 1000 bp DNA fragment at the 5' upper part and 1000 bp at the 3' lower part centered on the mutation of the hom gene. DNA fragments of each were obtained.
- PCR was performed using the primer pair of SEQ ID NO: 6 and SEQ ID NO: 9 using the two amplified DNA fragments as templates. After denaturation at 95°C for 5 minutes under PCR conditions, denaturation at 95°C for 30 seconds; Annealing at 55° C. for 30 seconds; And after repeating 28 times of polymerization at 72° C. for 2 minutes, polymerization was performed at 72° C. for 5 minutes.
- a 2 kb DNA fragment (SEQ ID NO: 16) containing a mutation of the hom gene encoding a homoserine dehydrogenase variant in which the 407th arginine is substituted with histidine was amplified.
- the amplification product was purified using a PCR Purification kit (QUIAGEN) and used as an insert DNA fragment for vector construction.
- the molar concentration (M) ratio of the pDCM2 vector (Korean Patent Publication No. 10-2020-0136813) and the inserted DNA fragment, which is the amplification product, heat-treated at 65 ° C. for 20 minutes
- the vector pDCM2-R407H for introducing the hom(R407H) mutation onto the chromosome was constructed by making it 1:2 and cloning using an Infusion Cloning Kit (TaKaRa) according to the provided manual.
- the prepared vector was transformed into Corynebacterium glutamicum ATCC13032 by electroporation, and a strain containing the hom (R407H) mutation on the chromosome was obtained through a secondary crossing process, which was transformed into Corynebacterium glutamicum It was named ATCC13032 hom (R407H).
- ilvA a gene encoding L-threonine dehydratase, was mutated, -Threonine, the 381st amino acid of threonine dehydratase, was substituted with alanine, and phenylalanine, the 383rd amino acid, was substituted with alanine.
- the primer pair or sequence of SEQ ID NO: 10 and SEQ ID NO: 11 using the chromosome of wild-type Corynebacterium glutamicum ATCC13032 as a template PCR was performed using the primer pair of SEQ ID NO: 12 and SEQ ID NO: 13, respectively.
- the primer sequences are as shown in Table 2 below.
- sequence number designation order 10 primer 5 TCGAGCTCGGTACCCATGAGTGAAACATACGTGTC 11 primer 6 GCGCTTGAGGTACTCtgcCAGCGcGATGTCATCATCCGG 12 primer 7 CCGGATGATGACATCgCGCTGgcaGAGTACCTCAAGCGC 13 primer 8 CTCTAGAGGATCCCCCGTCACCGACACCTCCACA
- PfuUltra TM high-reliability DNA polymerase (Stratagene) was used as the polymerase for the PCR reaction, and the PCR conditions were denaturation at 95 ° C for 30 seconds; Denaturation at 55° C. for 30 seconds; and 72 ° C. for 1 minute polymerization, and denaturation, annealing, and polymerization under these conditions were repeated 28 times to obtain a 1126 bp DNA fragment at the 5' upper part and a 286 bp DNA fragment at the 3' lower part centered on the mutation of the ilvA gene. Fragments were obtained respectively.
- PCR was performed using the primer pair of SEQ ID NO: 10 and SEQ ID NO: 13 using the two amplified DNA fragments as templates. After denaturation at 95°C for 5 minutes under PCR conditions, denaturation at 95°C for 30 seconds; Annealing at 55° C. for 30 seconds; And after repeating 28 times of polymerization at 72° C. for 2 minutes, polymerization was performed at 72° C. for 5 minutes.
- a 1.4 kb DNA fragment (SEQ ID NO: 17) containing a mutation in the ilvA gene encoding an L-threonine dehydratase variant in which the 381st threonine is substituted with alanine and the 383rd phenylalanine is substituted with alanine. ) was amplified.
- the amplification product was purified using a PCR purification kit and used as an insert DNA fragment for vector construction. After treating the purified amplification product with restriction enzyme smaI, the molar concentration (M) ratio of the pDCM2 vector heat-treated at 65 ° C.
- TaKaRa A vector pDCM2-ilvA (T381A, F383A) for introducing the ilvA (T381A, F383A) mutation onto the chromosome was constructed by cloning using an infusion cloning kit according to the provided manual.
- the prepared vector was transformed into Corynebacterium glutamicum ATCC13032 hom (R407H) by electroporation, and a strain containing the ilvA (T381A, F383A) mutation on the chromosome was obtained through a secondary crossing process, which was It was named Nebacterium glutamicum CA10-3101.
- the strain CA10-3101 was internationally deposited with the Korea Center for Microorganisms Conservation (KCCM), an international depository under the Budapest Treaty, on May 27, 2020, and was given an accession number as KCCM12739P.
- KCCM Microorganisms Conservation
- the ilvA (T381A, F383A) strain KCJI-38 (KCCM11248P, Republic of Korea Patent No. 10-1335789)
- an L-isoleucine-producing strain treated with NTG N-Methyl-N'-nitro-N-nitrosoguanidine
- KCCM11248P/pECCG117-ilvA (T381A, F383A) strains were prepared by introducing mutations using the electric pulse method. Then, the fermentation titer was evaluated in the following manner.
- L-isoleucine was produced by shaking culture at 32° C. for 60 hours at 200 rpm.
- the composition of the production medium is as follows.
- Glucose 10% yeast extract 0.2%, ammonium sulfate 1.6%, potassium phosphate monobasic 0.1%, magnesium sulfate heptahydrate 0.1%, iron sulfate heptahydrate 10mg/l, manganese sulfate monohydrate 10mg/l, biotin 200 ⁇ g/l l, pH 7.2
- a mutant library of the ilvN gene encoding the small subunit of acetohydroxy acid synthase (AHAS) was constructed.
- the library was prepared using an error-prone PCR kit (clontech Diversify® PCR Random Mutagenesis Kit), using the chromosome of wild-type Corynebacterium glutamicum ATCC13032 as a template and using a pair of primers of SEQ ID NO: 14 and SEQ ID NO: 15.
- a PCR reaction was performed.
- the primer sequences are as shown in Table 4 below.
- sequence number designation order 14 primer 9 CGAGCTCGGTACCCATGGCTAATTCTGACG 15 primer 10 TAGAGGATCCCCTTAGATCTTGGCCGGAGC
- the process of pre-heating at 94 ° C for 30 seconds, 94 ° C for 30 seconds, and 68 ° C for 1 minute 30 seconds was repeated 25 times under the condition that three mutations occur at 0 per 1000 bl.
- the obtained product was subjected to 25 repetitions of 95 ° C for 50 sec, 60 ° C for 50 sec, and 68 ° C for 12 min using megaprimer (500-125 ng), and then treated with DpnI to transform E. coli DH5 ⁇ .
- About 20,000 transformed E. coli colonies were taken and plasmids were extracted, which was named pTOPO-ilvN-library.
- the pTOPO-ilvN-library prepared in Example 2 was transformed into CA10-3101 (KCCM12739P), an L-isoleucine producing strain prepared in Example 1, by electroporation, followed by nutrition containing 25 mg/L of kanamycin.
- the medium was plated to obtain 5,000 colonies of the strain into which the mutant gene was inserted, and each colony was named from CA10-3101/pTOPO-ilvNm5001 to CA10-3101/pTOPO-ilvNm10000.
- the fermentation titer was evaluated for each colony in the following manner. Specifically, after inoculating the parent strain and the mutant strain in a 250 ml corner-bar pool flask containing 25 ml of isoleucine production medium, L-isoleucine was produced by shaking culture at 32° C. for 60 hours at 200 rpm.
- the composition of the production medium is as follows.
- Example 3 The ilvN (A42V) and ilvN (H47L) mutations identified in Example 3 were introduced into the Corynebacterium glutamicum CA10-3101 strain prepared in Example 1.
- CA10-3101/pTOPO-ilvNm6289 ilvN A42V
- CA10-3101/pTOPO-ilvNm9011 ilvN H47L
- PCR was performed using the chromosome as a template and using the primer pair of SEQ ID NO: 14 and SEQ ID NO: 15, respectively.
- PfuUltra TM high-reliability DNA polymerase (Stratagene) was used as the polymerase for the PCR reaction, and the PCR conditions were denaturation at 95 ° C for 30 seconds; Annealing 55° C.
- the amplified product was purified using a QUIAGEN PCR purification kit and used as an insert DNA fragment for vector construction. After treating the purified amplification product with restriction enzyme SmaI, the molar concentration (M) ratio of the pDCM2 vector heat-treated at 65 ° C.
- TaKaRa TaKaRa
- vectors pDCM2-ilvN A42V
- pDCM2-ilvN H47L
- CA10-3101::ilvN A42V
- CA10-3129 CA10-3101::ilvN (H47L)
- CA10-3130 CA10-3130.
- each strain was prepared by the following method. Fermentation titer was evaluated.
- L-isoleucine was produced by shaking culture at 32° C. for 60 hours at 200 rpm.
- the composition of the production medium is shown below.
- Glucose 10% yeast extract 0.2%, ammonium sulfate 1.6%, potassium phosphate monobasic 0.1%, magnesium sulfate heptahydrate 0.1%, iron sulfate heptahydrate 10mg/l, manganese sulfate monohydrate 10mg/l, biotin 200 ⁇ g/l l, pH 7.2
- PCR was performed using a primer pair of SEQ ID NO: 14 and SEQ ID NO: 20, and a primer pair of SEQ ID NO: 21 and SEQ ID NO: 15 using pDCM2-ilvN (A42V) as a template, and pDCM2-ilvN (H47L) as a template PCR was performed using the primer pair of SEQ ID NO: 14 and SEQ ID NO: 18 or the primer pair of SEQ ID NO: 19 and SEQ ID NO: 15.
- the primer sequences are as shown in Table 7 below.
- sequence number designation order 18 primer 11 TTCGGTCTTAACAGACACGAGGGACACGAG 19 primer 12 GTGTCCCTCGTGTCTGTTAAGACCGAAACA 20 primer 13 CGGTTGATGCCgagTGTTTCGGTCTTTGCA 21 primer 14 AAGACCGAAACactcGGCATCAACCGCATC
- PfuUltra TM high-reliability DNA polymerase (Stratagene) was used as the polymerase for the PCR reaction, and the PCR conditions were denaturation at 95 ° C for 30 seconds; Annealing at 55° C. for 30 seconds; and 72° C. for 1 minute polymerization, these denaturation, annealing, and polymerization were repeated 28 times to obtain DNA fragments of 166 bp and 405 bp, respectively.
- the amplified product was purified using a PCR purification kit from QUIAGEN, and used as an insert DNA fragment for vector construction. After treating the purified amplification product with restriction enzyme smaI, the molar concentration (M) ratio of the pDCM2 vector heat-treated at 65 ° C.
- a vector pDCM2-ilvN (A42V, H47L) for introducing the mutant ilvN into the chromosome was constructed by cloning using an infusion cloning kit according to the provided manual.
- Example 6 Construction of L-isoleucine-producing strain into which the combined variant ilvN was introduced
- CA10-3101::ilvN (A42V, H47L) was named CA10-3132.
- fermentation titer was evaluated in the following manner.
- L-isoleucine was produced by shaking culture at 32° C. for 60 hours at 200 rpm.
- the composition of the production medium is as follows.
- Glucose 10% yeast extract 0.2%, ammonium sulfate 1.6%, potassium phosphate monobasic 0.1%, magnesium sulfate heptahydrate 0.1%, iron sulfate heptahydrate 10mg/l, manganese sulfate monohydrate 10mg/l, biotin 200 ⁇ g/l l, pH 7.2
- ilvN alone mutations ilvN (A42V), ilvN (H47L)
- ilvN combination mutations ilvN (A42V, It was confirmed that the L-isoleucine concentration increased in the mutant strain into which H47L)) was introduced, and it was confirmed that the ilvN combination mutant could increase the L-isoleucine-producing ability of the strain rather than the ilvN single mutant.
- Example 7 Construction of a mutant ilvN-substituted strain in the L-isoleucine-producing strain Corynebacterium glutamicum KCCM11248P strain
- KCJI-38 an L-isoleucine-producing strain, treated with NTG (N-Methyl-N'-nitro-N-nitrosoguanidine) two ilvN mutations and a combination mutation confirmed to be effective in increasing L-isoleucine production ability in Example 6 above.
- NTG N-Methyl-N'-nitro-N-nitrosoguanidine
- KCCM11248P Republic of Korea Patent No. 10-1335789
- L-isoleucine was produced by shaking culture at 32° C. for 60 hours at 200 rpm.
- the composition of the production medium is as follows.
- Glucose 10% yeast extract 0.2%, ammonium sulfate 1.6%, potassium phosphate monobasic 0.1%, magnesium sulfate heptahydrate 0.1%, iron sulfate heptahydrate 10mg/l, manganese sulfate monohydrate 10mg/l, biotin 200 ⁇ g/l l, pH 7.2
- the L-isoleucine-producing ability increased in the mutant strain introduced with two ilvN mutations and a combination mutation, ilvN (A42V).
- the increase rate of L-isoleucine concentration of each strain into which ilvN(H47L) and ilvN(A42V, H47L) was introduced was about 40%, 29%, and 63% compared to the parent strain. It was confirmed that the L-isoleucine production ability could be increased.
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Abstract
Description
서열번호 | 명칭 | 서열 |
6 | primer 1 | TCGAGCTCGGTACCCCGCTTTTGCACTCATCGAGC |
7 | primer 2 | CACGATCAGATGTGCATCATCAT |
8 | primer 3 | ATGATGATGCACATCTGATCGTG |
9 | primer 4 | CTCTAGAGGATCCCCGAGCATCTTCCAAAACCTTG |
서열번호 | 명칭 | 서열 |
10 | primer 5 | TCGAGCTCGGTACCCATGAGTGAAACATACGTGTC |
11 | primer 6 | GCGCTTGAGGTACTCtgcCAGCGcGATGTCATCATCCGG |
12 | primer 7 | CCGGATGATGACATCgCGCTGgcaGAGTACCTCAAGCGC |
13 | primer 8 | CTCTAGAGGATCCCCCGTCACCGACACCTCCACA |
균주명 | L-이소류신(g/L) | L-쓰레오닌(g/L) |
KCCM11248P(모균주) | 1.5 | 0.5 |
KCCM11248P/pECCG117-ilvA(T381A, F383A) | 4.0 | 0.0 |
서열번호 | 명칭 | 서열 |
14 | primer 9 | CGAGCTCGGTACCCATGGCTAATTCTGACG |
15 | primer 10 | TAGAGGATCCCCTTAGATCTTGGCCGGAGC |
균주명 | L-이소류신 농도(g/L) | L-이소류신 농도 증가율(%) |
CA10-3101(모균주) | 2.01 | - |
CA10-3101/pTOPO-ilvNm6289 | 2.91 | 45 |
CA10-3101/pTOPO-ilvNm9011 | 3.16 | 57 |
균주명 | L-이소류신 농도(g/L) | L-이소류신 농도 증가율(%) |
CA10-3101 | 2.12 | - |
CA10-3129(A42V 도입 균주) | 3.10 | 46 |
CA10-3130(H47L 도입 균주) | 2.98 | 41 |
서열번호 | 명칭 | 서열 |
18 | primer 11 | TTCGGTCTTAACAGACACGAGGGACACGAG |
19 | primer 12 | GTGTCCCTCGTGTCTGTTAAGACCGAAACA |
20 | primer 13 | CGGTTGATGCCgagTGTTTCGGTCTTTGCA |
21 | primer 14 | AAGACCGAAACActcGGCATCAACCGCATC |
균주명 | L-이소류신 농도(g/L) | L-이소류신 농도 증가율(%) |
CA10-3101(모균주) | 2.03 | - |
CA10-3129(A42V) | 3.08 | 52 |
CA10-3130(H47L) | 2.90 | 43 |
CA10-3132(A42V, H47L) | 3.21 | 58 |
균주명 | L-이소류신 농도(g/L) | L-이소류신 농도 증가율(%) |
KCCM11248P (모균주) | 1.02 | - |
KCCM11248P△ilvN::ilvN(A42V) | 1.43 | 40 |
KCCM11248P△ilvN::ilvN(H47L) | 1.32 | 29 |
KCCM11248P△ilvN::ilvN(A42V, H47L) | 1.66 | 63 |
Claims (12)
- 서열번호 1의 아미노산 서열에서 42번째 위치에 상응하는 아미노산이 다른 아미노산으로 치환되고 47번째 위치에 상응하는 아미노산이 다른 아미노산으로 치환된, 아세토하이드록시산 신타아제(Acetohydroxy acid synthase) 변이체.
- 제1항에 있어서, 상기 42번째 위치에 상응하는 아미노산은 발린으로 치환되는 것인, 변이체.
- 제1항에 있어서, 상기 47번째 위치에 상응하는 아미노산은 류신으로 치환되는 것인, 변이체.
- 제1항에 있어서, 상기 42번째 위치에 상응하는 아미노산은 알라닌인 것인, 변이체.
- 제1항에 있어서, 상기 47번째 위치에 상응하는 아미노산은 히스티딘인 것인, 변이체.
- 제1항 내지 제5항 중 어느 한 항의 변이체를 코딩하는 폴리뉴클레오티드.
- 제1항 내지 제5항 중 어느 한 항의 변이체; 또는 상기 변이체를 코딩하는 폴리뉴클레오티드;를 포함하는, 코리네박테리움 속 균주.
- 제7항에 있어서, 상기 균주는 서열번호 1의 아미노산 서열을 가지는 야생형 아세토하이드록시산 신타아제 또는 이를 코딩하는 폴리뉴클레오티드를 포함하는 코리네박테리움 속 균주와 비교하여 L-이소류신 생산능이 증가된, 균주.
- 제7항에 있어서, 상기 균주는 코리네박테리움 글루타미쿰인 것인, 균주.
- 제1항 내지 제5항 중 어느 한 항의 변이체; 또는 상기 변이체를 코딩하는 폴리뉴클레오티드;를 포함하는 코리네박테리움 속 균주를 배지에서 배양하는 단계를 포함하는, L-이소류신 생산 방법.
- 제1항 내지 제5항 중 어느 한 항의 변이체, 상기 변이체를 코딩하는 폴리뉴클레오타이드, 상기 폴리뉴클레오타이드를 포함하는 벡터 또는 본 출원의 폴리뉴클레오티드를 포함하는 코리네박테리움 속 균주; 이를 배양한 배지; 또는 이들 중 2 이상의 조합을 포함하는, L-이소류신 생산용 조성물.
- 제1항 내지 제5항 중 어느 한 항의 변이체; 상기 변이체를 코딩하는 폴리뉴클레오티드; 또는 상기 변이체 또는 상기 변이체를 코딩하는 폴리뉴클레오티드를 포함하는 코리네박테리움 속 균주의 L-이소류신 생산 용도.
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AU2022355342A AU2022355342A1 (en) | 2021-09-29 | 2022-08-05 | Novel acetohydroxy acid synthase mutant and l-isoleucine production method using same |
CA3233425A CA3233425A1 (en) | 2021-09-29 | 2022-08-05 | Novel acetohydroxy acid synthase mutant and l-isoleucine production method using same |
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