Patent Grant
10633679
This application is a U.S. national phase application of International PCT Patent Application No. PCT/KR2015/003065, which was filed on Mar. 27, 2015, which claims priority to Korean Patent Application Nos. 10-2014-0049870, filed Apr. 25, 2014. These applications are incorporated herein by reference in their entireties.
The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is HANO_050_00US_ST25.txt. The text file is 62 KB, was created on Oct. 25, 2016, and is being submitted electronically via EFS-Web.
The present disclosure relates to a microorganism for producing diamine and a method of producing diamine using the same.
Biogenic amines (BAs) are nitrogenous compounds which are mainly produced by decarboxylation of amino acids or by amination and transamination of aldehydes and ketones. These biogenic amines are low molecular weight compounds and synthesized in the metabolism of microorganisms, plants and animals, and thus biogenic amines are known as components frequently found in these cells. In particular, biogenic amines are polyamines such as spermidine, spermine, putrescine or 1,4-butanediamine, and cadaverine.
In general, putrescine is an important raw material for production of polyamine nylon-4,6 which is produced by reacting putrescine with adipic acid. Putrescine is usually produced by chemical synthesis involving conversion of propylene to acrylonitrile and to succinonitrile.
As a production method of putrescine using a microorganism, a method of producing putrescine at a high concentration by transformation of E. coli and Corynebacterium has been reported (International Patent Publication No. WO06/005603; International Patent Publication No. WO09/125924; Qian Z D et al., Biotechnol. Bioeng. 104: 4, 651-662, 2009; Schneider et al., Appl. Microbiol, Biotechnol. 88; 4, 859-868, 2010; Schneider et al., Appl. Microbiol. Biotechnol. 95, 169-178, 2012). Furthermore, studies have been actively conducted on putrescine transporters in E. coli, yeast, plant and animal cells (K Igarashi, Plant Physiol. Biochem. 48: 506-512, 2010).
Meanwhile, cadaverine is a foul-smelling diamine compound produced by protein hydrolysis during putrefaction of animal tissues. Cadaverine has the chemical formula of NH2(CH2)5NH2, which is similar to that of putrescine.
Cadaverine serves as a component of polymers such as polyamide or polyurethane, chelating agents, or other additives. In particular, polyamide having an annual global market of 3.5 million tons is known to be prepared by polycondensation of cadaverine or succinic acid, and thus cadaverine has received much attention as an industrially useful compound.
Cadaverine is a diamine found in a few microorganisms (Tabor and Tabor, Microbiol Rev., 49:81-99, 1985). In the gram negative bacterium E. coli, cadaverine is biosynthesized from L-lysine by L-lysine decarboxylase. The level of cadaverine in E. coli is regulated by biosynthesis, degradation, uptake and export of cadaverine (Soksawatmaekhin et al., Mol Microbiol., 51:1401-1412, 2004).
The present inventors have made intensive efforts to investigate a protein having an ability to export diamine such as putrescine or cadaverine so as to improve diamine productivity in a microorganism having the diamine productivity. As a result, they found that a Corynebacterium efficiens-derived protein or a protein having high amino acid sequence homology therewith has a diamine export activity, and this protein is introduced into a microorganism for producing diamine to enhance its activity, resulting in a remarkable increase in the ability to export diamine such as putrescine and cadaverine, thereby completing the present invention.
An object of the present invention is to provide a microorganism for producing diamine.
Another object of the present invention is to provide a method of producing diamine, including the steps of (i) culturing the microorganism for producing diamine to obtain a cell culture; and (ii) recovering diamine from the cultured microorganism or the cell culture.
In an aspect to achieve the above objects, the present invention provides a microorganism for producing diamine, in which activity of a protein having an amino acid sequence of SEQ ID NO: 6 or an amino acid sequence having 55% or higher sequence homology with SEQ ID NO:6 is introduced or enhanced.
As used herein, the term “diamine” collectively refers to a compound having two amine groups, and specific examples thereof may include putrescine and cadaverine. Putrescine is tetramethylenediamine which may be produced from ornithine as a precursor. Cadaverine is called 1,5-pentanediamine or pentamethylenediamine, which may be produced from lysine as a precursor. Such diamines are industrially applicable compounds that serve as valuable raw materials for synthesis of polymers such as polyamine nylon, polyamide or polyurethane.
As used herein, the term “protein having an amino acid sequence of SEQ ID NO: 6” is a protein found in Corynebacterium efficiens, and also called CE2495. It was investigated that this protein retains high homology with a membrane protein of Corynebacterium, NCgl2522. In an embodiment of the present invention, CE2495 protein is identified as a putative protein which is involved in diamine export in a strain having diamine productivity, thereby remarkably increasing diamine productivity.
Here, CE2495 protein having the amino acid sequence of SEQ ID NO: 6 may be a protein that is encoded by a nucleotide sequence of SEQ ID NO: 5. In the polynucleotide encoding the CE2495 protein, however, various modifications may be made in the coding region provided that they do not change the amino acid sequence of the polypeptide expressed from the coding region, due to codon degeneracy or in consideration of the codons preferred by an organism in which the protein is to be expressed. Thus, the CE2495 protein may be encoded by various nucleotide sequences as well as by the nucleotide sequence of SEQ ID NO: 5.
Further, the CE2495 protein of the present invention may be any protein having the amino acid sequence of SEQ ID NO: 6, or having 55% or higher, preferably 75% or higher, more preferably 90% or higher, much more preferably 95% or higher, even much more preferably 98% or higher, and most preferably 99% or higher homology therewith, as long as the protein exhibits a substantial diamine export activity. It is apparent that an amino acid sequence having such homology, of which a part is deleted, modified, substituted, or added, is also within the scope of the present invention, as long as the resulting amino acid sequence has a biological activity substantially equivalent or corresponding to the protein of SEQ ID NO: 6.
As used herein, the term “protein having an amino acid sequence having 55% or higher sequence homology with the amino acid sequence of SEQ ID NO: 6” means any protein without limitation, as long as the protein has an amino acid sequence having 55% or higher sequence homology with the amino acid sequence of SEQ ID NO: 6 and it also has substantially diamine export activity. For example, the protein may be a protein having an amino acid sequence of SEQ ID NO: 22 or SEQ ID NO: 24, but is not limited thereto.
For example, the protein having the amino acid sequence of SEQ ID NO: 22 is a protein found in Corynebacterium ammoniagenes, and also called HMPREF0281_01446. It was investigated that this protein retains 59% homology with a membrane protein of Corynebacterium, NCgl2522 and 61% homology with CE2495 of Corynebacterium efficiens. In an embodiment of the present invention, it was investigated that the HMPREF0281_01446 protein exhibits diamine export activity in a strain having diamine productivity, thereby remarkably increasing diamine productivity.
The HMPREF0281_01446 protein having the amino acid sequence of SEQ ID NO. 22 may be a protein that is encoded by a nucleotide sequence of SEQ ID NO: 21. In the polynucleotide encoding this protein, however, various modifications may be made in the coding region provided that they do not change the amino acid sequence of the polypeptide expressed from the coding region, due to codon degeneracy or in consideration of the codons preferred by an organism in which the protein is to be expressed. Thus, this protein may be encoded by various nucleotide sequences as well as by the nucleotide sequence of SEQ ID NO: 21.
Further, the protein having the amino acid sequence of SEQ ID NO: 24 is a protein found in Corynebacterium lipophiloflavum, and also called HMPREF0298_0262. It was investigated that this protein retains 52% homology with a membrane protein of Corynebacterium, NCgl2522 and 56% homology with CE2495 of Corynebacterium efficiens. In an embodiment of the present invention, it was investigated that the HMPREF0298_0262 protein exhibits diamine export activity in a strain having diamine productivity, thereby remarkably increasing diamine productivity.
The HMPREF0298_0262 protein having the amino acid a nucleotide sequence of SEQ ID NO: 23. In the polynucleotide encoding this protein, however, various modifications may be made in the coding region provided that they do not change the amino acid sequence of the polypeptide expressed from the coding region, due to codon degeneracy or in consideration of the codons preferred by an organism in which the protein is to be expressed. Thus, this protein may be encoded by various nucleotide sequences as well as by the nucleotide sequence of SEQ ID NO: 23.
The term “homology”, as used herein with regard to a sequence, refers to identity with a given amino acid sequence or nucleotide sequence, and the homology may be expressed as a percentage. In the present invention, a homology sequence having identical or similar activity to the given amino acid sequence or nucleotide sequence is expressed as “% homology”. For example, homology may be identified using a standard software program which calculates parameters of score, identity and similarity, specifically BLAST 2.0, or by comparing sequences in a Southern hybridization experiment under stringent conditions as defined. Defining appropriate hybridization conditions are within the skill of the art (e.g., see Sambrook et al., 1989, infra), and determined by a method known to those skilled in the art.
As used herein, the term “microorganism for producing diamine” refers to a microorganism prepared by providing diamine productivity for a parent strain having no diamine productivity or a microorganism having endogenous diamine productivity. Specifically, the microorganism having diamine productivity may be a microorganism having putrescine or cadaverine productivity.
The “microorganism having putrescine productivity” may be, but is not limited to, a microorganism in which the activity of acetylglutamate synthase that converts glutamate to N-acetylglutamate, ornithine acetyltransferase (ArgJ) that converts acetyl ornithine to ornithine, acetylglutamate kinase (ArgB) that converts acetyl glutamate to N-acetylglutamyl phosphate, acetyl-gamma-glutamyl-phosphate reductase (ArgC) that converts acetyl glutamyl phosphate to N-acetyl glutamate semialdehyde, or acetylornithine aminotransferase (ArgD) that converts acetyl glutamate semialdehyde to N-acetylornithine is enhanced compared to its endogenous activity, in order to enhance the biosynthetic pathway from glutamate to ornithine, and the productivity of ornithine which is used as a precursor for putrescine biosynthesis is enhanced, but is not limited thereto.
Further, the microorganism having putrescine productivity may be a microorganism which is modified to have activity of ornithine carbamoyl transferase (ArgF) involved in synthesis of arginine from ornithine, a protein (NCgl1221) involved in glutamate export, and/or a protein (NCgl469) involved in putrescine acetylation weaker than its endogenous activity, and/or is modified to be introduced with activity of ornithine decarboxylase (ODC).
Here, as non-limiting examples, the acetyl gamma glutamyl phosphate reductase (ArgC) may have an amino acid sequence of SEQ ID NO: 14, the acetylglutamate synthase or ornithine acetyltransferase (ArgJ) may have an amino acid sequence of SEQ ID NO: 15, the acetyl glutamate kinase (ArgB) may have an amino acid sequence of SEQ ID NO: 16, and the acetylornithine aminotransferase (ArgD) may have an amino acid sequence of SEQ ID NO: 14. However, the amino acid sequences of respective enzyme proteins are not particularly limited thereto, and the enzymes may be proteins having amino acid sequences having 80% or higher, preferably 90% or higher, or more preferably 95% or higher homology therewith, as long as they have activities of the respective enzymes.
Further, as non-limiting examples, the ornithine carbamoyl transferase (ArgF) may have an amino acid sequence of SEQ ID NO: 18, the protein involved in glutamate export may have an amino acid sequence of SEQ ID NO: 19, and ornithine decarboxylase (ODC) may have an amino acid sequence of SEQ ID NO: 20. However, the amino acid sequences of respective enzyme proteins are not limited thereto, and the enzymes may be proteins having amino acid sequences having 80% or higher, preferably 90% or higher, more preferably 95% or higher, or particularly preferably 97% or higher homology therewith, as long as they have activities of the respective enzymes.
Meanwhile, the “microorganism having cadaverine productivity” may be, but is not limited to, a microorganism prepared by additionally introducing or enhancing activity of lysine decarboxylase (LDC) in a microorganism having lysine productivity. For example, the microorganism may be one having enhanced lysine productivity in order to increase cadaverine production. A method of enhancing lysine productivity may be performed by a known method which is predictable to those skilled in the art.
The lysine decarboxylase is an enzyme catalyzing conversion of lysine to cadaverine, and its activity is introduced or enhanced, thereby effectively producing cadaverine.
The lysine decarboxylase may have an amino acid sequence of SEQ ID NO: 26, but is not particularly limited thereto. The enzyme may have an amino acid sequence having 80% or higher, preferably 90% or higher, or more preferably 95% or higher homology therewith, as long as it has the above activity.
As used herein, the term “production” is a concept including extracellular release of diamine, for example, release of diamine into a culture medium, as well as production of diamine within a microorganism.
Meanwhile, the term “introduction of protein activity”, as used herein, means that a microorganism having no endogenous protein is externally provided with an activity of the protein, and for example, it may be performed by introduction of a foreign gene. Further, the term “enhancement of protein activity” means that active state of the protein retained in or introduced into the microorganism is enhanced, compared to its intrinsic active state.
Non-limiting examples of the introduction or enhancement of the protein activity may include improvement of the activity of the protein itself present in a microorganism due to mutation so as to achieve effects beyond the endogenous functions, and/or improvement in endogenous gene activity of the protein present in the microorganism, amplification of the endogenous gene by internal or external factors, increase in the gene copy number, increase in the activity by additional introduction of a foreign gene or replacement or modification of a promoter, but are not limited thereto.
The increase in the gene copy number may be, but is not particularly limited to, performed by operably linking the gene to a vector or by integrating it into the host cell genome. Specifically, the copy number of the polynucleotide in the host cell genome may be increased by introducing into the host cell the vector which is operably linked to the polynucleotide encoding the protein of the present invention and replicates and functions independently of the host cell, or by introducing into the host cell the vector which is operably linked to the polynucleotide and is able to integrate the polynucleotide into the host cell genome.
As used herein, “modification of the expression regulatory sequence for increasing the polynucleotide expression” may be, but is not particularly limited to, done by inducing a modification on the expression regulatory sequence through deletion, insertion, non-conservative or conservative substitution of nucleotide sequence, or a combination thereof in order to further enhance the activity of expression regulatory sequence, or by replacing the expression regulatory sequence with a nucleotide sequence having stronger activity. The expression regulatory sequence includes, but is not particularly limited to, a promoter, an operator sequence, a sequence coding for a ribosome-binding site, and a sequence regulating the termination of transcription and translation.
As used herein, the replacement or modification of a promoter, although not particularly limited thereto, may be performed by replacement or modification with a stronger promoter than the original promoter. A strong heterologous promoter instead of the original promoter may be linked upstream of the polynucleotide expression unit, and examples of the strong promoter may include a CJ7 promoter, a lysCP1 promoter, an EF-Tu promoter, a groEL promoter, an aceA or aceB promoter, and specifically, a Corynebacterium-derived promoter, lysCP1 promoter or CJ7 promoter is operably linked to the polynucleotide encoding the enzyme so that its expression rate may be increased. Here, the lysCP1 promoter is a promoter improved through nucleotide sequence substitution of the promoter region of the polynucleotide encoding aspartate kinase and aspartate semialdehyde dehydrogenase (WO 2009/096689). Further, CJ7 promoter is a strong promoter derived from Corynebacterium ammoniagenes (Korean Patent No. 0620092 and WO 2006/065095).
Furthermore, modification of a polynucleotide sequence on chromosome, although not particularly limited thereto, may be performed by inducing a mutation on the expression regulatory sequence through deletion, insertion, non-conservative or conservative substitution of polynucleotide sequence, or a combination thereof in order to further enhance the activity of the polynucleotide sequence, or by replacing the sequence with a polynucleotide sequence which is modified to have stronger activity.
As used herein, the term “vector” refers to a DNA construct including a nucleotide sequence encoding the desired protein, which is operably linked to an appropriate expression regulatory sequence to express the desired protein in a suitable host cell. The regulatory sequence may include a promoter that can initiate transcription, an optional operator sequence for regulating the transcription, a sequence encoding a suitable mRNA ribosome binding site, and a sequence regulating the termination of transcription and translation. After the vector is introduced into the suitable host cell, it may replicate or function independently of the host genome, and may be integrated into the genome itself.
The vector used in the present invention is not particularly limited, as long as it is able to replicate in the host cell, and any vector known in the art may be used. Examples of conventional vectors may include a natural or recombinant plasmid, cosmid, virus and bacteriophage. For instance, pWE15, M13, λMBL3, λMBL4, λIXII, λASHII, λAPII, λt10, λt11, Charon4A, and Charon21A may be used as a phage vector or cosmid vector. pBR type, pUC type, pBluescriptII type, pGEM type, pTZ type, pCL type and pET type may be used as a plasmid vector. A vector usable in the present invention is not particularly limited, and any known expression vector may be used. Preferably, pDZ, pACYC177, pACYC184, pCL, pECCG117, pUC19, pBR322, pMW118, or pCC1BAC vector may be used.
Further, the polynucleotide encoding the desired endogenous protein in the chromosome can be replaced by a mutated polynucleotide using a vector for bacterial chromosomal insertion. The insertion of the polynucleotide into the chromosome may be performed by any method known in the art, for example, homologous recombination. Since the vector of the present invention may be inserted into the chromosome by homologous recombination, it may further include a selection marker to confirm chromosomal insertion. The selection marker is to select cells that are transformed with the vector, that is, to confirm insertion of the desired polynucleotide, and the selection marker may include markers providing selectable phenotypes, such as drug resistance, auxotrophy, resistance to cytotoxic agents, or surface protein expression. Only cells expressing the selection marker are able to survive or to show different phenotypes under the environment treated with the selective agent, and thus the transformed cells may be selected.
As used herein, the term “transformation” means the introduction of a vector including a polynucleotide encoding a target protein into a host cell in such a way that the protein encoded by the polynucleotide is expressed in the host cell. As long as the transformed polynucleotide can be expressed in the host cell, it can be either integrated into and placed in the chromosome of the host cell, or exist extrachromosomally. Further, the polynucleotide includes DNA and RNA encoding the target protein. The polynucleotide may be introduced in any form, as long as it can be introduced into the host cell and expressed therein. For example, the polynucleotide may be introduced into the host cell in the form of an expression cassette, which is a gene construct including all elements required for its autonomous expression. Typically, the expression cassette includes a promoter operably linked to the polynucleotide, transcriptional termination signals, ribosome binding sites, or translation termination signals. The expression cassette may be in the form of a self-replicable expression vector. Also, the polynucleotide as it is may be introduced into the host cell and operably linked to sequences required for expression in the host cell.
Further, as used herein, the term “operably linked” means a functional linkage between a polynucleotide sequence encoding the desired protein of the present invention and a promoter sequence which initiates and mediates transcription of the polynucleotide sequence.
Further, the microorganism having diamine productivity may be a microorganism, in which the diamine acetyltransferase activity is weakened compared to the endogenous activity, in order to increase diamine production.
As used herein, the term “diamine acetyltransferase” is an enzyme catalyzing transfer of an acetyl group from acetyl-CoA to diamine, and it may be exemplified by Corynebacterium glutamicum NCgl1469 or E. coli SpeG, but its name may differ depending on the species of a microorganism having diamine productivity. NCgl1469 may have an amino acid sequence of SEQ ID NO: 11 or 12, and SpeG may have an amino acid sequence of SEQ ID NO: 13, but the sequence may differ depending on the species of the microorganism. The protein may have an amino acid sequence having 80% or higher, preferably 90% or higher, or more preferably 95% or higher, or particularly preferably 97% or higher homology therewith, as long as it has the diamine acetyltransferase activity.
Since the diamine acetyltransferase converts diamine to acetyl-diamine (e.g., N—Ac-putrescine or N—Ac-cadaverine), diamine productivity may be increased by weakening its activity, compared to the endogenous activity.
As used herein, the term “endogenous activity” refers to activity of the protein that the original microorganism possesses in its native or undenatured state, and “modified to have weakened activity, compared to the endogenous activity” means that activity of the protein is further weakened compared to the activity of the corresponding protein that the original microorganism possesses in the native or undenatured state.
The weakening of the protein activity means that the protein activity is reduced, compared to a non-modified strain, or the activity is eliminated. It is possible to apply a method well known in the art to the weakening of the protein activity.
Examples of the method may include a method of replacing the gene encoding the protein on the chromosome by a gene that is mutated to reduce the enzyme activity or to eliminate the protein activity, a method of introducing a mutation into the expression regulatory sequence of the gene encoding the protein on the chromosome, a method of replacing the expression regulatory sequence of the gene encoding the protein by a sequence having weaker activity, a method of deleting a part or an entire of the gene encoding the protein on the chromosome, a method of introducing antisense oligonucleotide that complementarily binds to a transcript of the gene on the chromosome to inhibit translation of mRNA to the protein, a method of artificially adding a sequence complementary to SD sequence at upstream of SD sequence of the gene encoding the protein to form a secondary structure, thereby preventing access of the ribosomal subunits, and a reverse transcription engineering (RTE) method of adding a promoter for reverse transcription at 3′-terminus of open reading frame (ORF) of the corresponding sequence, and combinations thereof, but are not particularly limited thereto.
In detail, a partial or full deletion of the gene encoding the protein may be done by introducing a vector for chromosomal insertion into a microorganism, thereby substituting the polynucleotide encoding an endogenous target protein on chromosome with a polynucleotide having a partial deletion or a marker gene. The “partial” may vary depending on the type of polynucleotide, but specifically refers to 1 to 300, preferably 1 to 100, and more preferably 1 to 50 nucleotides.
Meanwhile, the microorganism of the present invention is a microorganism having diamine productivity, and includes a prokaryotic microorganism expressing the protein having the amino acid sequence of SEQ ID NO: 6, and examples thereof may include microorganisms belonging to Escherichia sp., Shigella sp., Citrobacter sp., Salmonella sp., Enterobacter sp., Yersinia sp., Klebsiella sp., Erwinia sp., Corynebacterium sp., Brevibacterium sp., Lactobacillus sp., Selenomanas sp., Vibrio sp., Pseudomonas sp., Streptomyces sp., Arcanobacterium sp., Alcaligens sp. or the like, but are not limited thereto. The microorganism of the present invention is specifically a microorganism belonging to Corynebacterium sp. or Escherichia sp., and more specifically, Corynebacterium glutamicum or Escherichia coli, but is not limited thereto.
A specific example may be a microorganism prepared by deleting NCgl2522, which is a protein having putrescine export activity, from a Corynebacterium glutamicum ATCC13032-based putrescine-producing strain KCCM11240P (Korean Patent Publication No. 2013-0082478) and then introducing CE2495 into the transposon gene. Therefore, this microorganism KCCM11240P ΔNCgl2522 Tn:P (cj7)-CE2495 is designated as CC01-0757, and deposited under the Budapest Treaty to the Korean Culture Center of Microorganisms (KCCM) on Nov. 15, 2013, with Accession No. KCCM11475P.
In another aspect, the present invention provides a method of producing diamine, comprising: (i) culturing the microorganism having putrescine diamine, in which activity of the protein having the amino acid sequence of SEQ ID NO: 6 or 55% or higher sequence homology therewith is introduced or enhanced, so as to obtain a cell culture; and (ii) recovering diamine from the cultured microorganism or the cell culture.
The protein having the amino acid sequence of SEQ ID NO: 6 or the protein having the amino acid sequence having 55% or higher sequence homology therewith, the introduction of the protein activity, the enhancement of the protein activity, the diamine, and the microorganism having diamine productivity are the same as described above.
In the method, the step of culturing the microorganism may be, although not particularly limited to, preferably performed by batch culture, continuous culture, and fed-batch culture known in the art. In this regard, the culture conditions are not particularly limited, but an optimal pH (e.g., pH 5 to 9, preferably pH 6 to 8, and most preferably pH 6.8) may be maintained by using a basic chemical (e.g., sodium hydroxide, potassium hydroxide or ammonia) or acidic chemical (e.g., phosphoric acid or sulfuric acid). Also, an aerobic condition may be maintained by adding oxygen or oxygen-containing gas mixture to a cell culture. The culture temperature may be maintained at 20 to 45° C., and preferably at 25 to 40° C., and the cultivation may be performed for about 10 to 160 hours.
Furthermore, a medium to be used for culture may include sugar and carbohydrate (e.g., glucose, sucrose, lactose, fructose, maltose, molasse, starch and cellulose), oil and fat (e.g., soybean oil, sunflower seed oil, peanut oil and coconut oil), fatty acid (e.g., palmitic acid, stearic acid and linoleic acid), alcohol. (e.g., glycerol and ethanol), and organic acid (e.g., acetic acid) individually or in combination as a carbon source; nitrogen-containing organic compound (e.g., peptone, yeast extract, meat juice, malt extract, corn solution, soybean meal powder and urea), or inorganic compound (e.g., ammonium sulfate, ammonium, chloride, ammonium phosphate, ammonium carbonate, and ammonium nitrate) individually or in combination as a nitrogen source; potassium dihydrogen phosphate, dipotassium phosphate, or sodium-containing salt corresponding thereto individually or in combination as a phosphorus source; other essential growth-stimulating substances including metal salts (e.g., magnesium sulfate or iron sulfate), amino acids, and vitamins. In the present invention, the medium may be used as a synonym for the culture liquid.
As used herein, the term “cell culture” is a material obtained by culturing a microorganism, and includes the medium, the microorganism cultured, and substances released from the microorganism cultured. For example, a nutrient supply source required for cell culture, such as minerals, amino acids, vitamins, nucleic acids and/or other components generally contained in culture medium (or culture liquid) in addition to the carbon source, and the nitrogen source may be included. Further, a desired substance or an enzyme produced/secreted by the cells may be included.
Since diamine produced by culture may be secreted into the medium or remain in the cells, the cell culture may include diamine that is produced by culturing the microorganism.
The method of recovering diamine such as putrescine or cadaverine produced in the culturing step of the present invention may be carried out, for example, using a suitable method known in the art according to a culturing method, for example, batch culture, continuous culture, or fed-batch culture, thereby collecting the desired amino acids from the culture liquid.
In the present invention, it is demonstrated that Corynebacterium efficiens-derived CE2495 protein is a protein having diamine export activity, and putrescine export activity can be enhanced by introducing this protein activity into Corynebacterium sp. microorganism which has a putrescine synthetic pathway, but low putrescine export activity. It is also demonstrated that putrescine and cadaverine can be increased at the same time by introducing this protein activity into E. coli which has synthetic pathways of putrescine and cadaverine. Accordingly, diamine can be effectively produced by applying Corynebacterium efficiens-derived CE2495 protein to a microorganism having diamine productivity.
Hereinafter, the present invention will be described in more detail with reference to Examples. However, these Examples are for illustrative purposes only, and the invention is not intended to be limited by these Examples.
It was confirmed that putrescine production was reduced when NCgl2522, a permease belonging to major facilitator superfamily (MFS), was deleted in a Corynebacterium glutamicum ATCC13032-based putrescine-producing strain KCCM11240P (Korean Patent Publication NO. 2013-0082478) and a Corynebacterium glutamicum ATCC13869-based putrescine-producing strain DAB12-a ΔNCgl1469 (argF deletion, NCgl1221 deletion, E. coli speC introduction, arg operon promoter substitution, NCgl1469 deletion; designated as DAB12-b, Korean Patent Publication No. 2013-0082478) as Corynebacterium sp. microorganisms having putrescine productivity.
It was also confirmed that putrescine was produced in a high yield in Corynebacterium glutamicum strains prepared by additional introduction of NCgl2522 gene into the transposon in KCCM11240P or DAB12-b, or by substitution of NCgl2522 promoter on the chromosome with cj7 promoter to enhance NCgl2522 activity. Further, the intracellular amount of putrescine was measured in the strain in which NCgl2522 expression was enhanced, and as a result, a smaller amount of putrescine was observed, compared to that of a control group. It is indicating that NCgl2522 has an ability to export putrescine.
In detail, based on the nucleotide sequence of the gene encoding NCgl2522 of Corynebacterium glutamicum ATCC13032, a pair of primers of SEQ ID NOS: 1 and 2 for obtaining a homologous recombination fragment of the N-terminal region of NCgl2522 and a pair of primers of SEQ ID NOS: 3 and 4 for obtaining a homologous recombination fragment of the C-terminal region of NCgl2522 were used as in the following Table 1.
PCR was performed using the genomic DNA of Corynebacterium glutamicum ATCC13032 as a template and two pairs of primers so as to amplify PCR fragments of the N-terminal and C-terminal regions, respectively. These PCR fragments were electrophoresed to obtain the desired fragments. At this time, PCR reaction was carried out for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 30 seconds at 72° C. The fragment of the N-terminal region thus obtained was treated with restriction enzymes, BamHI and SalI and the fragment of the C-terminal region thus obtained was treated with restriction enzymes, SalI and XbaI. The fragments thus treated, were cloned into the pDZ vector treated with restriction enzymes, BamHI and XbaI, so as to construct a plasmid pDZ-1′NCgl2522 (K/O).
The plasmid pDZ-1′NCgl2522(K/O) was introduced into Corynebacterium glutamicum KCCM11240P by electroporation, so as to obtain a transformant. Then, the transformant was plated and cultured on BHIS plate (37 g/l of Braine heart infusion, 91 g/l of sorbitol, and 2% agar) containing kanamycin (25 μg/ml) and X-gal (5-bromo-4-chloro-3-indolin-D-galactoside) for colony formation. From the colonies thus formed, blue-colored colonies were selected as the strain introduced with the plasmid pDZ-1′NCgl2522(K/O).
The selected strains were cultured with shaking in CM medium (10 g/l of glucose, 10 g/l of polypeptone, 5 g/l of yeast extract, 5 g/l of beef extract, 2.5 g/l of NaCl, and 2 g/l of urea, pH 6.8) at 30° C. for 8 hours. Subsequently, each cell culture was serially diluted from 10−4 to 10−10. Then, the diluted samples were plated and cultured on an X-gal-containing solid medium for colony formation. From the colonies thus formed, the white colonies which appeared at relatively low frequency were selected, to finally obtain a Corynebacterium glutamicum strain in which the gene encoding NCgl2522 was deleted and putrescine productivity was weakened. The Corynebacterium glutamicum strain in which putrescine export activity was weakened was designated as KCCM11240P ΔNCgl2522.
In the same manner, PCR was performed using the genomic DNA of Corynebacterium glutamicum ATCC13869 as a template and two pairs of primers given in Table 1 so as to construct a plasmid pDZ-2′NCgl2522(K/O) by the above described method. A Corynebacterium glutamicum strain, in which the gene encoding NCgl2522 of DAB12-b strain was deleted using the vector according to the above described method to weaken putrescine productivity, was constructed. This Corynebacterium glutamicum strain having weakened putrescine export activity was designated as DAB12-b ΔNCgl2522.
As confirmed in Reference Example 1, the NCgl2522 membrane protein was found to function to export putrescine. Therefore, based on the amino acid sequence of NCgl2522, the present inventors acquired genes having homology therewith using BlastP program of National Center for Biotechnology Information (NCBI, www.ncbi.nlm.nih.gov).
From Corynebacterium sp. other than Corynebacterium glutamicum, Corynebacterium efficiens YS-314 was found to have CE2495 which shows 71% homology with the amino acid sequence of NCgl2522. Its nucleotide sequence (SEQ ID NO: 5) and amino acid sequence (SEQ ID NO: 6) were obtained.
In the same manner, the nucleotide sequence (SEQ ID NO: 21) and amino acid sequence (SEQ ID NO: 22) of HMPREF0281_01446 derived from Corynebacterium ammoniagenes DSM 20306, which shows 59% homology with the amino acid sequence of NCgl2522, and the nucleotide sequence (SEQ ID NO: 23) and amino acid sequence (SEQ ID NO: 24; of HMPREF0298_0262 derived from Corynebacterium lipophiloflavum DSM 44291, which shows 52% homology with the amino acid sequence of NCgl2522, were obtained. The amino acid sequence of HMPREF0281_01446 and the amino acid sequence of HMPREF0298_0262 show 61% and 56% homology with the amino acid sequence of CE2495 of Corynebacterium efficiens YS-314, respectively, as shown in the following Table 2.
Meanwhile, Corynebacterium sp. microorganisms having genes showing homology with NCgl2522, and homology thereof are given in the following Table 3.
Corynebacterium accolens
Corynebacterium ammoniagenes
Corynebacterium amycolatum
Corynebacterium atypicum
Corynebacterium aurimucosum
Corynebacterium auriscanis
Corynebacterium callunae
Corynebacterium camporealensis
Corynebacterium capitovis
Corynebacterium casei
Corynebacterium casei LMG S-19264
Corynebacterium caspium
Corynebacterium diphtheriae
Corynebacterium efficiens
Corynebacterium falsenii DSM 44353
Corynebacterium genitalium
Corynebacterium glutamicum 13032
Corynebacterium glutamicum R
Corynebacterium glutamicum 13869
Corynebacterium glutamicum ATCC 14067
Corynebacterium glycinophilum AJ 3170
Corynebacterium halotolerans
Corynebacterium jeikeium
Corynebacterium lipophiloflavum
Corynebacterium maris
Corynebacterium massiliense
Corynebacterium mastitidis
Corynebacterium matruchotii
Corynebacterium nuruki
Corynebacterium pilosum
Corynebacterium pseudodiphtheriticum
Corynebacterium pseudogenitalium
Corynebacterium pseudotuberculosis
Corynebacterium resistens
Corynebacterium sp. ATCC 6931
Corynebacterium sp. HFH0082
Corynebacterium sp. KPL1818
Corynebacterium sp. KPL1824
Corynebacterium striatum
Corynebacterium terpenotabidum
Corynebacterium tuberculostearicum
Corynebacterium tuscaniense DNF00037
Corynebacterium ulcerans
Corynebacterium urealyticum
Corynebacterium ureicelerivorans
Corynebacterium variabile
Corynebacterium vitaeruminis DSM 20294
<2-1> Introduction of CE2495 into Transposon Gene in Chromosome of ATCC13032-Based Putrescine-Producing Strain
In order to examine whether chromosomal insertion of CE2495 gene affects putrescine export in KCCM11240P ΔNCgl2522 having reduced putrescine export activity which was prepared in Reference Example 1, CE2495 was introduced into a transposon gene by the following method.
As a vector for transformation, which allows a gene insertion into the chromosome using a transposon gene of Corynebacterium sp. microorganism, pDZTn (WO 2009/125992) was used, and cj7 (WO 2006/65095) was used as a promoter.
A CE2495 gene fragment of about 1.44 kb was amplified using the chromosome of Corynebacterium efficiens YS-314 strain as a template and a pair of primers of SEQ ID NOS: 9 and 10 (See Table 4). At this time, PCR reaction was carried out for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 1 minute and 30 seconds at 72° C. Next, this PCR product was electrophoresed on a 0.8% agarose gel to elute and purify a band of the desired size.
Further, the cj7 promoter region was obtained by carrying out PCR for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 30 seconds at 72° C. using p117-Pcj7-gfp as a template and a pair of primers of SEQ ID NOs. 7 and 8 (See Table 4). A fragment of the cj7 promoter gene was electrophoresed on a 0.8% agarose gel to elute and purify a band of the desired size.
pDZTn vector was treated with XhoI, and fusion cloning of the PCR product obtained above was performed. In-Fusion@HD Cloning Kit (Clontech) was used in the fusion cloning. The resulting plasmid was designated as pDZTn-P(cj7)-CE2495.
Next, the plasmid pDZTn-P(cj7)-CE2495 was introduced into Corynebacterium glutamicum KCCM11240P ΔNCgl2522 described in Reference Example 1 by electroporation to obtain a transformant. The transformant was cultured with shaking in CM medium (10 g/l of glucose, 10 g/l of polypeptone, 5 g/l of yeast extract, 5 g/l of beef extract, 2.5 g/l of NaCl, and 2 g/l of urea, pH 6.8) (30° C. for 8 hours). Subsequently, cell culture was serially diluted from 10−4 to 10−10. Then, the diluted samples were plated and cultured on an X-gal-containing solid medium for colony formation.
From the colonies formed, the white colonies which appeared at relatively low frequency were selected to finally obtain strains in which the gene encoding CE2495 was introduced by secondary crossover. The strains finally selected were subjected to PCR using a pair of primers of SEQ ID NOS: 7 and 10 to confirm introduction of the gene encoding CE2495. This Corynebacterium glutamicum mutant strain was designated as KCCM11240P ΔNCgl2522 Tn:P(cj7)-CE2495.
<2-2> Introduction of CE2495 into Transposon Gene in Chromosome of ATCC13869-Based Putrescine-Producing Strain
In order to examine whether the chromosomal insertion of CE2495 gene affects putrescine export in DAB12-b ΔNCgl2522 having reduced putrescine export activity which was prepared in Reference Example 1, pDZTn-P(cj7)-CE2495 prepared above was introduced into Corynebacterium glutamicum DAB12-ΔNCgl2522 and strain is confirmed introduction of CE2495 into the transposon gene in the same manner as in Example <2-1>.
A Corynebacterium glutamicum mutant strain thus selected was designated as DAB12-b ΔCgl2522 Tn:P(cj7)-CE24 95.
<2-3> Evaluation of Putrescine Productivity of Corynebacterium sp.-Derived Putrescine-Producing Strain Introduced with CE2495
In order to confirm the effect of CE2495 introduction on putrescine productivity in the putrescine-producing strain, putrescine productivities of the Corynebacterium glutamicum mutant strains prepared in Examples <2-1> and <2-2> were compared.
In detail, 6 types of Corynebacterium glutamicum mutants (KCCM11240P; KCCM11240P ΔNCgl2522; KCCM11240P ΔNCgl2522 Tn:P(cj7)-CE2495; DAB12-b; DAB12-b ΔNCgl2522; DAB12-b ΔNCgl2522 Tn:P (cj7)-CE2495) were plated, on 1 mM arginine-containing CM plate media (1% glucose, 1% polypeptone, 0.5% yeast extract, 0.5% beef extract, 0.25% NaCl, 0.2% urea, 100 μl of 50% NaOH, and 2% agar, pH 6.8, based on 1 L), and cultured at 30° C. for 24 hours, respectively. 1 platinum loop of each strain thus cultured was inoculated in 25 ml of titer medium (8% Glucose, 0.25% soybean protein, 0.50% corn steep solids, 4% (NH4)2SO4, 0.1% KH2PO4, 0.05% MgSO4. 7H2O, 0.15% urea, 100 μg of biotin, 3 mg of thiamine hydrochloride, 3 mg of calcium-pantothenic acid, 3 mg of nicotinamide, and 5% CaCO3, pH 7.0, based on 1 L), and then cultured with shaking at 30° C. and 200 rpm for 98 hours. 1 mM arginine was added to all media for culturing the strains. The putrescine concentration in each cell culture was measured, and the results are shown in the following Table 5.
As shown in Table 5, putrescine production was found to be increased in both 2 types of the CE2495-introduced Corynebacterium glutamicum mutant strains.
<3-1> Introduction of CE2495 into Transposon Gene in Chromosome of L-Lysine-Producing Corynebacterium Glutamicum KCCM11016P
In order to confirm cadaverine export activity of CE2495 protein, CE2495 gene was introduced into the chromosome of a lysine-producing strain KCCM11016P (this microorganism was deposited at the Korean Culture Center of Microorganisms on Dec. 18, 1995 with Accession No. KFCC10881, and then deposited at the International Depository Authority under Budapest Treaty with Accession No. KCCM11016P, Korean Patent No. 10-0159812), pDZTn-P (cj7)-CE2495 prepared above was introduced into Corynebacterium glutamicum KCCM11016P and strain is confirmed introduction of CE2495 into transposon in the same manner as in Example <2-1>.
A Corynebacterium glutamicum mutant strain thus selected was designated as KCCM11016P Tn:P (cj7)-CE2495.
<3-2> Introduction of E. Coli-Derived Lysine Decarboxylase Gene into L-Lysine-Producing Strain Introduced CE2495
The L-lysine-producing strain introduced CE2495, KCCM11016P Tn:P (cj7)-CE2495 which was prepared in Example <3-1> was introduced with E. coli-derived lysine decarboxylase gene in a plasmid form for cadaverine production. The nucleotide sequence (SEQ ID NO; 25) and amino acid sequence (SEQ ID NO: 26) of lysine decarboxylase ldcC were obtained from NCBI data base.
An ldcC gene fragment of about 2.1 kb was obtained by carrying out PCR for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 52° C., and extension for 2 minutes at 72° C. using the chromosome of E. coli W3110 strain as a template and a pair of primers of SEQ ID NOS: 29 and 30 (See Table 6). This product was treated with HindIII and XbaI, and then electrophoresed in a 0.8% agarose gel to elute and purify a band of the desired size.
Further, the cj7 promoter region was obtained by carrying out PCR for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 30 seconds at 72° C. using p117-Pcj7-gfp as a template and a pair of primers of SEQ ID NOs. 27 and 28 (See Table 6). A gene fragment of the cj7 promoter gene was treated with KpnI and HindII, and then electrophoresed on a 0.8% agarose gel to elute and purify a band of the desired size.
A gene fragment which was obtained by performing electrophoresis of KpnI and XbaI-treated pECCG117 (Biotechnology letters vol 13, No. 10, p. 721-726 (1991)) vector in a 0.8% agarose gel and then eluting and purifying a band of the desired size, the cj7 promoter gene fragment treated with KpnI and HindIII, and the lysine decarboxylase ldcC gene fragment treated with HindIII and XbaI were cloned using T4 DMA ligase (NEB). The E. coli ldcC-encoding plasmid obtained by the above experiment was designated as pECCG117-Pcj7-ldcC.
The prepared pECCG117-Pcj7-ldcC vector or pECCG117 vector was introduced into KCCM11016P and KCCM11016P Tn:P (cj7)-CE2495 by electroporation, respectively. The transformants were plated on BHIS plate containing 25 μg/ml kanamycin for selection. The selected strains were designated as KCCM11016P pECCG117, KCCM11016P pECCG117-Pcj7-ldcC, KCCM11016P Tn:P(cj7)-CE2495 pECCG117, and KCGM11016P Tn:P(cj7)-CE2495 pECCG117-Pcj7-ldcC, respectively.
<3-3> Evaluation of Cadaverine Productivity of Corynebacterium sp.-Derived Lysine-Producing Strain Having Chromosomal Insertion of CE2495 and Lysine Decarboxylase Gene as Plasmid
In order to examine whether introduction of CE2495 into the cadaverine-producing strain affects cadaverine production, cadaverine productivity was compared between Corynebacterium glutamicum mutant strains prepared in Example <3-2>.
In detail, 4 types of Corynebacterium glutamicum mutant strains (KCCM11016P pECCG117; KCCM11016P pECCG117-Pcj7-ldcC; KCCM11016P Tn:P(cj7)-CE2495 pECCG117; and KCCM11016P Tn:P(cj7)-CE2495 pECCG117-Pcj7-ldcC) were cultured by the following method, and cadaverine productivity was compared therebetween.
The respective mutant strains were plated on CM plate media (1% glucose, 1% polypeptone, 0.5% yeast extract, 0.5% beef extract, 0.25% NaCl, 0.2% urea, 100 μl of 50% NaOH, and 2% agar, pH 6.8, based on 1 L), and cultured at 30° C. for 24 hours. Each of the strains cultured was inoculated to a 250 ml corner-baffled flask containing 25 ml of seed medium (2% glucose, 1% peptone, 0.5% yeast extract, 0.15% urea, 0.4% KH2PO4, 0.8% K2HPO4, 0.05% MgSO4 7H2O, 100 μg of biotin, 1000 μg of thiamine HCl, 2000 μg of calcium-pantothenic acid, and 2000 μg of nicotinamide, pH 7.0, based on 1 L), and cultured with shaking at 30° C. and 200 rpm for 20 hours.
Then, 1 ml of the seed culture was inoculated to a 250 ml corner-baffled flask containing 24 ml of production medium (4% Glucose, 2% (NH4)2SO4, 2.5% soybean protein, 5% corn steep solids, 0.3% urea, 0.1% KH2PO4, 0.05% MgSO4 7H2O, 100 μg of biotin, 1000 μg of thiamine hydrochloride, 2000 μg of calcium-pantothenic acid, 3000 μg of nicotinamide, 0.2 g of leucine, 0.1 g of threonine, 0.1 g of methionine, and 5% CaCO3, pH 7.0, based on 1 L), and then cultured with shaking at 30° C. and 200 rpm for 72 hours.
After culture, cadaverine productivities were measured by HPLC. The concentrations of cadaverine in the cell culture of each strain are given in the following Table 7.
As shown in Table 7, cadaverine production was increased in the CE2495-introduced Corynebacterium glutamicum mutant strains.
<4-1> Preparation of Strain by Introduction of CE2495, HMPREF0281_01446, or HMPREF0298_0262 into W3110
The diamine export activities of Corynebacterium ammoniagenes DSM 20306-derived HMPREF0281_01446 protein and HMPREF0298_0262 protein, which show 59% and 52% homology with NCgl2522, in addition to CE24952, respectively, were examined in E. coli.
Vectors for introduction of HMPREF0281_01446 and HMPREF0281_01446 were constructed in the same manner as in the construction of pDZTn-P(cj7)-CE2495 of Example 2-1.
HMPREF0281_01446 gene was amplified using the chromosome of Corynebacterium ammoniagenes DSM 20306 strain as a template and a pair of primers of SEQ ID NOS: 31 and 32 (see Table 8) so as to obtain a gene fragment of about 1.4 kb.
In the same manner, HMPREF0298_0262 gene was amplified using the chromosome of Corynebacterium lipophiloflavum DSM 44291 strain as a template and a pair of primers of SEQ ID NOS: 33 and 34 (see Table 8) so as to obtain a gene fragment of about 1.36 kb.
In this regard, PCR was carried out for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 1 minute and 30 seconds at 72° C. Then, each of the PCR products was electrophoresed on a 0.8% agarose gel to elute and purify a band of the desired size.
Further, the cj7 promoter region was obtained by carrying out PCR for 30 cycles of denaturation for 30 seconds at 95° C., annealing for 30 seconds at 55° C., and extension for 30 seconds at 72° C. using p117-Pcj7-gfp as a template and a pair of primers of SEQ ID NOS: 7 and 8. A fragment of the cj7 promoter gene was electrophoresed on a 0.8% agarose gel to elute and purify a band of the desired size.
pDZTn vector was treated with XhoI, and fusion cloning of the PCR products obtained above was performed. In-Fusion@HD Cloning Kit (Clontech) was used in the fusion cloning. The resulting plasmids were designated as pDZTn-P (cj7)-HMPREF0281_01446 and pDZTn-P(cj7)-HMPREF029_0262, respectively.
Thereafter, in order to examine whether expression of Corynebacterium efficiens YS-314-derived CE2495, Corynebacterium ammoniagenes-derived HMPREF0281_01446, or Corynebacterium lipophiloflavum-derived HMPREF0298_0262 protein increases putrescine and cadaverine productions in E. coli wild-type strain W3110 having biosynthetic pathway of putrescine and cadaverine, Corynebacterium and E. coli shuttle vector-based pDZTn-P (cj7)-CE2495, pDZTn-P (cj7)-HMPREF0281_01446, or pDZTn-P (cj7)-HMPREF0298_0262 was introduced into W3110, respectively.
A 2×TSS solution (Epicentre) was used for transformation into E. coli, and the transformant was plated and cultured on LB plate (10 g of Tryptone, 5 g of Yeast extract, 10 g of NaCl, and 2% agar, based on 1 L) containing kanamycin (50 μg/ml) for colony formation. The colonies thus formed were designated as W3110 pDZTn-P(cj7)-CE2495, W3110 pDZTn-P(cj7)-HMPREF0281_01446, and W3110 pDZTn-P (cj7)-HMPREF0298_0262, respectively.
<4-2> Comparison of Diamine Productivity of E. coli Introduced with CE2495, HMPREF0281_01446, or HMPREF0298_0262
Putrescine and cadaverine productivities of the strains obtained above were examined.
In detail, E. coli W3110 and W3110 pDZTn-P(cj7)-CE2495, W3110 pDZTn-P (cj7)-HMPREF0281_01446, or W3110 pDZTn-P(cj7)-HMPREF0298_0262 were cultured on LB solid media at 37° C. for 24 hours.
Then, each of them was cultured in 25 ml of titer medium (2 g of (NH4)2PO4, 6.75 g of KH2PO4, 0.85 g of citric acid, 0.7 g of MgSO4.7H2O, 0.5% (v/v) trace element, 10 g of glucose, 3 g of AMS, and 30 g of CaCO3, based on 1 L) at 37° C. for 24 hours. A trace metal solution contained 5 M HCl: 10 g of FeSO4.7H2O, 2.25 g of ZnSO4.7H2O, 1 g of CuSO4.5H2O, 0.5 g of MnSO4.5H2O, 0.23 g of Na2B4O7.10H2O, 2 g of CaCl2.2H2O, and 0.1 g of (NH4)6Mo7O2.4H2O per 1 liter.
The concentrations of putrescine and cadaverine produced from each cell culture were measured, and the results are given in the following Table 9.
As shown in Table 9, CE2495-introduced W3110 pDZTn-P(cj7)-CE2495 strain showed high putrescine and cadaverine concentrations in ceil culture, compared to the parent strain W3110. Further, putrescine and cadaverine productions were remarkably increased in W3110 pDZTn-P (cj7)-HMPREF0281_01446 and W3110 pDZTn-P (cj7)-HMPREF0298_0262 strains which were introduced with HMPREF0281_01446 and HMPREF0298_0262, respectively.
That is, it was confirmed that diamine in cell culture was remarkably increased by enhancing activity of CE2495 or the protein having 55% or higher sequence homology therewith, suggesting that the ability to export diamine such as putrescine and cadaverine can be improved by enhancing activity of CE2495 or the protein having 55% or higher sequence homology therewith.
As such, the present inventors demonstrated that Corynebacterium glutamicum having enhanced CE2495 activity prepared by introducing CE2495 into transposon of Corynebacterium sp. microorganism KCCM11240P ΔNCgl2522 which has a putrescine synthetic pathway, but reduced putrescine export activity has enhanced putrescine export activity, thereby producing putrescine in a high yield.
Accordingly, this strain KCCM11240P ΔNCgl2522 Tn:P(cj7)-CE2495 was designated as CC01-0757, and deposited under the Budapest Treaty to the Korean Culture Center of Microorganisms (KCCM) on Nov. 15, 2013, with Accession No. KCCM11475P.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2014-0049870 | Apr 2014 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2015/003065 | 3/27/2015 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2015/163591 | 10/29/2015 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 20170044581 | Lee et al. | Feb 2017 | A1 |
| Number | Date | Country |
|---|---|---|
| 103492553 | Jan 2014 | CN |
| 2009-531042 | Sep 2009 | JP |
| 2014-507152 | Mar 2014 | JP |
| 2016-514466 | May 2016 | JP |
| 10-0159812 | Aug 1998 | KR |
| 10-0620092 | Aug 2006 | KR |
| 1020120064046 | Jun 2012 | KR |
| 1020130082478 | Jul 2013 | KR |
| 101732788 | May 2017 | KR |
| 2006005603 | Jan 2006 | WO |
| 2006065095 | Jun 2006 | WO |
| 2009096689 | Aug 2009 | WO |
| 2009125924 | Oct 2009 | WO |
| 2009125992 | Oct 2009 | WO |
| 2012114256 | Aug 2012 | WO |
| 2013093737 | Jun 2013 | WO |
| 2013105827 | Jul 2013 | WO |
| 2014148743 | Sep 2014 | WO |
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| Number | Date | Country | |
|---|---|---|---|
| 20170044581 A1 | Feb 2017 | US |
