Mutant L-pipecolic acid hydroxylase and method for producing cis-5-hydroxy-L-pipecolic acid using the same

Abstract

The present invention addresses the problem of providing: a mutant L-pipecolic acid hydroxylase for producing cis-5-hydroxy-L-pipecolic acid in a highly productive and highly selective manner by hydrating L-pipecolic acid; and a novel method for industrially producing cis-5-hydroxy-L-pipecolic acid from L-pipecolic acid in a highly productive and low-cost manner. The present invention provides a mutant L-pipecolic acid hydroxylase that has an amino acid sequence in which a specific amino acid mutation is introduced in the amino acid sequence represented by SEQ ID NO: 2.

Description

[Technical Field]

[0001] The present invention relates to a mutant L-pipecolic acid hydroxylase and a method for producing cis-5-hydroxy-L-pipecolic acid using the same. More specifically, the present invention relates to a mutant L-pipecolic acid hydroxylase that has a high ability to produce cis-5-hydroxy-L-pipecolic acid by hydroxylating L-pipecolic acid, and a method for producing cis-5-hydroxy-L-pipecolic acid from L-pipecolic acid with high productivity by using the enzyme. [Background technology]

[0002] Cis-5-hydroxy-L-pipecolic acid (hereinafter sometimes referred to as "5HPA") is a compound useful as a pharmaceutical intermediate, etc. It is known that cis-5-hydroxy-L-pipecolic acid can be produced from L-pipecolic acid by biological methods.

[0003] For example, the alfalfa root nodule bacteria Sinorhizobium meliloti (Sinorhizobiu mm el il oti) It is known that a protein (hereinafter referred to as "SruPH") encoded by a polynucleotide (cis gene) expressed from 48 bases (corresponding to 16 amino acids) upstream of the annotation of the CAC47686 protein (hereinafter referred to as "SmPH") derived from Saccharomyces cerevisiae 1021 and the EFV12517 protein (hereinafter referred to as "SruPH") derived from Segniliparus rugosus ATCC BAA-974 possesses the cis-5-hydroxylase activity of L-pipecolic acid and can convert L-pipecolic acid to 5HPA. However, these proteins only produced a few percent of cis-3-hydroxypipecolic acid (hereinafter sometimes referred to as "3HPA") in addition to 5HPA.

[0004] Therefore, there is a need for a protein that has a high ability to add a hydroxyl group to the carbon atom at position 5 of L-pipecolic acid (high regioselectivity at position 5), and a protein derived from Xenorhabdus doucetiae FRM16 strain (hereinafter sometimes referred to as "XdPH") has been reported as an L-pipecolic acid hydroxylase that has higher regioselectivity at position 5 than SmPH and SruPH (Patent Document 1). However, when XdPH is expressed in Escherichia coli as a host, the majority of the protein is expressed as an insoluble, inactive protein.

[0005] Furthermore, from an industrial perspective, it is desirable from a cost perspective to be able to express enzyme proteins as active enzymes or soluble proteins using heterologous hosts such as Escherichia coli. However, when expressed in a heterologous expression system, an enzyme that is naturally active may not be expressed as an active enzyme, or a protein that is naturally soluble may be expressed as an insoluble protein.

[0006] Therefore, when industrially producing 5HPA from L-pipecolic acid, it is desirable to have an L-pipecolic acid hydroxylase that has L-pipecolic acid hydroxylation activity (the ability to add a hydroxyl group to the carbon atom at position 5 of L-pipecolic acid) when expressed in Escherichia coli as a host and that is expressed as a soluble protein. Here, a method has been reported for expressing, as an active mutant enzyme or soluble protein, an enzyme that is not expressed as an active enzyme or soluble protein in a heterologous expression system, or that is expressed in only trace amounts even if an active enzyme is expressed (Patent Document 2). Patent Document 2 describes a method of expressing, in a heterologous expression system, a gene having a base sequence encoding an amino acid sequence in which at least one hydrophobic amino acid present in a hydrophilic region of an α-helix structure has been substituted (provided that the substituted amino acid is substituted with an amino acid that is more hydrophilic or less hydrophobic than the original amino acid) and / or at least one hydrophilic amino acid present in a hydrophobic region of an α-helix structure has been substituted (provided that the substituted amino acid is substituted with an amino acid that is more hydrophobic or less hydrophobic), thereby expressing the active mutant enzyme or soluble protein. [Prior art documents] [Patent documents]

[0007] [Patent Document 1] WO2016 / 076159 [Patent Document 2] WO2016 / 199898 Summary of the Invention [Problem to be solved by the invention]

[0008] An object of the present invention is to provide a mutant L-pipecolic acid hydroxylase for producing cis-5-hydroxy-L-pipecolic acid with high productivity and high selectivity by hydroxylating L-pipecolic acid. Another object of the present invention is to provide a novel method for industrially producing cis-5-hydroxy-L-pipecolic acid from L-pipecolic acid with high productivity and low cost. [Means for solving the problem]

[0009] In order to solve the above-mentioned problems, the present inventors conducted extensive research on XdPH mutants with reference to the method described in Patent Document 2. As a result, they found that mutants in which glutamic acid at position 15, isoleucine at position 28, valine at position 31, cysteine ​​at position 76, isoleucine at position 108, leucine at position 142, glutamine at position 202, alanine at position 239, phenylalanine at position 246, or isoleucine at position 271 in the amino acid sequence of XdPH were substituted with other amino acids, respectively, had a high ability to selectively hydroxylate the carbon atom at position 5 of L-pipecolic acid to produce cis-5-hydroxy-L-pipecolic acid (L-pipecolic acid hydroxylation activity), and when expressed in Escherichia coli as a host, the mutants were expressed as soluble proteins with high L-pipecolic acid hydroxylation activity, thereby completing the present invention.

[0010] That is, the gist of the present invention is as follows. [1] A mutant L-pipecolic acid hydroxylase having an amino acid sequence represented by SEQ ID NO: 2, in which at least one amino acid mutation selected from the group consisting of the following (a) to (o) has been introduced: (a) Amino acid mutation in which glutamic acid at position 15 is replaced by alanine (b) Amino acid mutation in which isoleucine at position 28 is replaced by proline (c) Amino acid mutation in which isoleucine at position 28 is replaced with arginine (d) Amino acid mutation in which valine at position 31 is replaced by glutamic acid (e) Amino acid mutation in which cysteine ​​at position 76 is replaced with tyrosine (f) Amino acid mutation in which isoleucine at position 108 is replaced by arginine (g) Amino acid mutation in which leucine at position 142 is replaced by arginine (h) Amino acid mutation in which leucine at position 142 is replaced by lysine (i) Amino acid mutation in which leucine at position 142 is replaced by asparagine (j) Amino acid mutation in which leucine at position 142 is replaced by glutamine (k) Amino acid mutation in which leucine at position 142 is replaced by histidine (l) Amino acid mutation in which glutamine at position 202 is replaced by proline (m) Amino acid mutation in which alanine at position 239 is replaced by aspartic acid (n) Amino acid mutation in which phenylalanine at position 246 is replaced by tyrosine (o) Amino acid mutation in which isoleucine at position 271 is replaced by glycine [2] The mutant L-pipecolic acid hydroxylase according to [1], characterized in that it has an amino acid sequence represented by SEQ ID NO: 2, into which at least two amino acid mutations selected from the group consisting of (a) to (o) have been introduced. [3] The mutant L-pipecolic acid hydroxylase according to [1] or [2], characterized in that it has an amino acid sequence in which at least three amino acid mutations selected from the group consisting of (a) to (o) have been introduced into the amino acid sequence represented by SEQ ID NO: 2. [4] A method for producing cis-5-hydroxy-L-pipecolic acid, comprising contacting L-pipecolic acid with the mutant L-pipecolic acid hydroxylase according to any one of [1] to [3], a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell, to produce cis-5-hydroxy-L-pipecolic acid. [5] A method for producing cis-5-hydroxy-L-pipecolic acid according to [4], characterized in that the mutant L-pipecolic acid hydroxylase, a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell is contacted with L-pipecolic acid in the presence of 2-oxoglutaric acid and divalent iron ions. [Effects of the Invention]

[0011] The mutant L-pipecolic acid hydroxylase of the present invention has a high ability to selectively hydroxylate the carbon atom at position 5 of L-pipecolic acid to produce cis-5-hydroxy-L-pipecolic acid (L-pipecolic acid hydroxylating activity). Furthermore, when expressed in Escherichia coli as a host, it has high L-pipecolic acid hydroxylating activity and is expressed as a soluble protein. Therefore, the mutant L-pipecolic acid hydroxylase of the present invention is useful for industrially producing cis-5-hydroxy-L-pipecolic acid from L-pipecolic acid. Furthermore, the method for producing cis-5-hydroxy-L-pipecolic acid of the present invention using the mutant L-pipecolic acid hydroxylase enables industrial production of cis-5-hydroxy-L-pipecolic acid from L-pipecolic acid with high productivity and low cost. [Brief explanation of the drawings]

[0012] [Figure 1] 1 shows the results (electrophoresis photographs) of solubility evaluation of XdPH mutants (single mutation introduced) after low-temperature culture in Example 6. In Fig. 1, the area enclosed by a square (dotted line) indicates the XdPH mutant expressed in the soluble fraction. [Figure 2] 2 shows the results (electrophoresis photographs) of solubility evaluation of XdPH mutants (in which single or multiple mutations have been introduced) after low-temperature culture and normal culture in Example 6. In Fig. 2, the area enclosed by a square (dotted line) indicates the XdPH mutant expressed in the soluble fraction. [Figure 3] 3 shows the results of evaluating the solubility of XdPH mutants after low-temperature (15°C) culture (electrophoresis photograph) in Example 7. In Fig. 3, the area enclosed by a square (dotted line) indicates the XdPH mutant expressed in the soluble fraction. [Figure 4] 4 shows the results of evaluating the solubility of XdPH mutants after low-temperature (20°C) culture in Example 7 (electrophoresis photographs). In FIG. 4, the area enclosed by a square (dotted line) indicates the XdPH mutant expressed in the soluble fraction. [Figure 5] FIG. 1 shows the results of HPLC analysis in Example 4. DETAILED DESCRIPTION OF THE INVENTION

[0013] The present invention will be described in detail below.

[0014] As used herein, "L-pipecolic acid hydroxylation activity" means the ability to add a hydroxyl group to the carbon atom at position 5 of L-pipecolic acid (the ability to convert L-pipecolic acid to cis-5-hydroxy-L-pipecolic acid).

[0015] As used herein, "L-pipecolic acid hydroxylation activity" can be evaluated by, for example, contacting a target enzyme with L-pipecolic acid and measuring the amount of cis-5-hydroxy-L-pipecolic acid converted from L-pipecolic acid. Specifically, a reaction solution containing L-pipecolic acid, 2-oxoglutaric acid, L-ascorbic acid, and ferrous iron as reaction aids, and the target enzyme (or a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, a culture solution containing the enzyme obtained by culturing the microorganism or cell, or a protein purified from the microorganism or cell) is reacted at an appropriate temperature (e.g., about 10°C to 45°C) and pressure (e.g., about atmospheric pressure), and the amount of cis-5-hydroxy-L-pipecolic acid produced is measured, allowing the activity to be evaluated as the amount of cis-5-hydroxy-L-pipecolic acid produced (e.g., U / g) per cell mass (unit: g or turbidity) or total protein mass (unit: g) added to the reaction solution. Here, unit (U) represents the ability to produce 1 μmole of cis-5-hydroxy-L-pipecolic acid per minute.

[0016] As used herein, the term "enzyme" includes purified enzymes (including partially purified enzymes) and enzymes immobilized on a carrier using known immobilization techniques, such as those immobilized on a carrier such as polyacrylamide or carrageenan gel.

[0017] Furthermore, in the present specification, whether a protein after heterologous expression has been expressed as a soluble protein can be determined by the amount of soluble protein in an extract after heterologous expression. The amount of soluble protein can be measured, for example, by chemically, physically, or mechanically disrupting the bacterial cells used for heterologous expression in the presence of a buffer (e.g., by surfactant treatment, ultrasonic disruption, crushing, French press, etc.) to obtain an extract, and then measuring the amount of protein contained in the supernatant obtained by removing insoluble components such as insoluble proteins contained in the extract by centrifugation, filtration, etc. This measurement can be performed using known protein quantification methods, such as electrophoresis, ELISA, and Western blotting.

[0018] 1. Mutant L-pipecolic acid hydroxylase of the present invention The mutant L-pipecolic acid hydroxylase of the present invention has an amino acid sequence represented by SEQ ID NO: 2, into which at least one amino acid mutation selected from the group consisting of the following (a) to (o) has been introduced: (a) Amino acid mutation in which glutamic acid at position 15 is replaced by alanine (b) Amino acid mutation in which isoleucine at position 28 is replaced by proline (c) Amino acid mutation in which isoleucine at position 28 is replaced with arginine (d) Amino acid mutation in which valine at position 31 is replaced by glutamic acid (e) Amino acid mutation in which cysteine ​​at position 76 is replaced with tyrosine (f) Amino acid mutation in which isoleucine at position 108 is replaced by arginine (g) Amino acid mutation in which leucine at position 142 is replaced by arginine (h) Amino acid mutation in which leucine at position 142 is replaced by lysine (i) Amino acid mutation in which leucine at position 142 is replaced by asparagine (j) Amino acid mutation in which leucine at position 142 is replaced by glutamine (k) Amino acid mutation in which leucine at position 142 is replaced by histidine (l) Amino acid mutation in which glutamine at position 202 is replaced by proline (m) Amino acid mutation in which alanine at position 239 is replaced by aspartic acid (n) Amino acid mutation in which phenylalanine at position 246 is replaced by tyrosine (o) Amino acid mutation in which isoleucine at position 271 is replaced by glycine

[0019] In the present invention, the amino acid sequence shown in SEQ ID NO: 2 is the amino acid sequence of a wild-type L-pipecolic acid hydroxylase protein (XdPH) derived from Xenorhabdus doucetiae FRM16 strain.

[0020] The mutant L-pipecolic acid hydroxylase of the present invention has an L-pipecolic acid hydroxylating activity equal to or greater than that of XdPH. Furthermore, when expressed in Escherichia coli as a host, the mutant L-pipecolic acid hydroxylase has an L-pipecolic acid hydroxylating activity equal to or greater than that of XdPH, and is expressed as a soluble protein. An amino acid sequence having at least one amino acid mutation selected from the group consisting of (a) to (n) introduced into the amino acid sequence represented by SEQ ID NO: 2 is preferred because it tends to have higher L-pipecolic acid hydroxylating activity and higher solubility. In particular, an amino acid sequence having at least one amino acid mutation selected from the group consisting of (g) to (k) introduced into it, i.e., an amino acid sequence having leucine at position 142 substituted with another amino acid in the amino acid sequence represented by SEQ ID NO: 2, is more preferred because it is believed to exhibit high L-pipecolic acid hydroxylating activity even when cultured at temperatures around 28°C to 30°C, at which E. coli grows well. Examples of such other amino acids include amino acids that are less hydrophobic than leucine and do not have a negative charge. The amino acid mutation represented by (g) is more preferred.

[0021] In the amino acid sequence represented by SEQ ID NO: 2, an amino acid sequence into which at least two amino acid mutations selected from the group consisting of (a) to (o) have been introduced is preferred because it tends to have higher L-pipecolic acid hydroxylating activity and higher solubility. The combination of mutations is arbitrary, and examples thereof include combinations of (g) and any one other than (g), such as (g) and (a), (g) and (b), (g) and (c), (g) and (d), (g) and (e), and (g) and (n). Further examples include combinations of (b) and any one other than (b), such as (b) and (e). Further examples include combinations of (e) and any one other than (e), such as (e) and (b). Furthermore, an amino acid sequence represented by SEQ ID NO: 2 into which at least three amino acid mutations selected from the group consisting of (a) to (o) have been introduced is even more preferred because it has a higher L-pipecolic acid hydroxylating activity. The combination of mutations is arbitrary, and examples thereof include a combination of (g) and any two other than (g), a combination of (g) and two selected from (a), (b), (c), (d), (e), and (n), a combination of (g), (b), and (e), (g), (b), and (d), and a combination of (g), (b), and (n).

[0022] The mutant L-pipecolic acid hydroxylase of the present invention can be produced from the amino acid sequence represented by SEQ ID NO: 2 by methods known to those skilled in the art, such as site-directed mutagenesis and PCR.

[0023] The mutant L-pipecolic acid hydroxylase of the present invention can also be produced by culturing a transformant containing a nucleic acid encoding it and isolating and purifying the mutant L-pipecolic acid hydroxylase from the resulting culture. The nucleic acid encoding the mutant L-pipecolic acid hydroxylase of the present invention may be DNA or RNA, or may be a DNA / RNA chimera. DNA is preferred. The nucleic acid may be double-stranded or single-stranded. If double-stranded, it may be double-stranded DNA, double-stranded RNA, or a DNA:RNA hybrid. If single-stranded, it may be the sense strand (i.e., coding strand) or the antisense strand (i.e., non-coding strand).

[0024] Examples of DNA from which the mutant L-pipecolic acid hydroxylase of the present invention can be derived include DNA cloned from the Xenorhabdus doucetiae FRM16 strain. For example, the DNA can be obtained by known PCR or hybridization from a DNA fraction prepared from cells or tissues derived from the Xenorhabdus doucetiae FRM16 strain. Other examples include full-length L-pipecolic acid hydroxylase cDNA directly amplified by reverse transcriptase-PCR using total RNA or mRNA fractions prepared from cells or tissues derived from the Xenorhabdus doucetiae FRM16 strain as a template. Such DNA can be converted (mutated) using a known kit, such as Mutan-super Express Km (TAKARA BIO INC.) or Mutan-K (TAKARA BIO INC.), according to a known method, such as ODA-LA PCR, gapped duplex, or Kunkel, or a method modified therefrom, to obtain a DNA encoding the mutant L-pipecolic acid hydroxylase of the present invention. Alternatively, the cDNA can be obtained by converting the cDNA cloned by colony or plaque hybridization or PCR from a cDNA library prepared by inserting the total RNA or mRNA fragment into an appropriate vector, according to the above-mentioned method. The vector used for the library may be any of bacteriophage, plasmid, cosmid, phagemid, etc.

[0025] An example of a nucleic acid encoding a protein having the amino acid sequence represented by SEQ ID NO: 2 is a nucleic acid comprising the nucleotide sequence represented by SEQ ID NO: 1. The nucleotide sequence represented by SEQ ID NO: 1 is a synthetic nucleotide sequence obtained by optimizing the codons of a gene from Xenorhabdus doucetiae strain FRM16 encoding the amino acid sequence represented by SEQ ID NO: 2 for expression in E. coli. Not only genes from Xenorhabdus doucetiae, but also nucleic acids whose codons have been optimized in accordance with the host to be transformed are naturally encompassed in the nucleic acids encoding proteins having L-pipecolic acid hydroxylating activity of the present invention.

[0026] Those skilled in the art can obtain a nucleic acid encoding the amino acid sequence of a mutant L-pipecolic acid hydroxylase containing the mutations (a) to (o) by appropriately substituting, deleting, inserting, and / or adding bases to the nucleic acid represented by SEQ ID NO: 1 using site-directed mutagenesis (Nucleic Acids Res. 10, pp. 6487 (1982), Methods in Enzymol. 100, pp. 448 (1983), Molecular Cloning, PCR A Practical Approach IRL Press, pp. 200 (1991)) or the like to introduce base substitutions that result in desired mutations.

[0027] In the production method of the present invention described below, the mutant L-pipecolic acid hydroxylase may be directly used in the reaction of L-pipecolic acid as a substrate. However, it is preferable to use a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell.

[0028] The microorganisms or cells capable of producing the mutant L-pipecolic acid hydroxylase of the present invention may be microorganisms or cells that originally have the ability to produce the mutant L-pipecolic acid hydroxylase, or microorganisms or cells to which the production ability has been imparted by breeding. The microorganisms or cells may be live or dead, and for example, resting cells may be suitably used. Examples of types of microorganisms or cells capable of producing the mutant L-pipecolic acid hydroxylase of the present invention include those described below as "host microorganisms" or "host cells."

[0029] As a means for imparting the above-mentioned productivity by breeding, known methods such as genetic recombination (transformation) and mutation can be used. Transformation methods include a method of introducing a target DNA and a method of enhancing the expression of a target DNA by modifying an expression regulatory sequence such as a promoter on a chromosome.

[0030] Among these, it is preferable to use a microorganism or cell transformed with DNA encoding the protein of the present invention (mutant L-pipecolic acid hydroxylase).

[0031] As described above, the nucleic acid (DNA) encoding the mutant L-pipecolic acid hydroxylase of the present invention can be obtained by cloning and converting the DNA by PCR using, for example, chromosomal DNA derived from the Xenorhabdus doucetiae FRM16 strain as a template and appropriate primers.

[0032] Furthermore, the nucleic acid (DNA) encoding the mutant L-pipecolic acid hydroxylase of the present invention can be obtained, as described above, by directly amplifying the full-length mutant L-pipecolic acid hydroxylase cDNA by RT-PCR using, for example, total RNA or mRNA derived from Xenorhabdus doucetiae FRM16 strain as a template, followed by cloning and conversion by PCR using appropriate primers.

[0033] For example, the protein gene expression vector of the present invention is provided by inserting the DNA encoding the mutant L-pipecolic acid hydroxylase of the present invention obtained as described above into a known expression vector in an expressible configuration. Then, by transforming a host cell with the expression vector, a transformant into which the DNA encoding the protein of the present invention has been introduced can be obtained. The transformant can also be obtained by expressibly incorporating the DNA encoding the protein of the present invention into the chromosomal DNA of the host by a technique such as homologous recombination.

[0034] As used herein, the term "expression vector" refers to a genetic element used to replicate and express a protein having a desired function in a host organism by incorporating a polynucleotide encoding the protein and introducing the vector into the host organism. Examples of such vectors include, but are not limited to, plasmids, viruses, phages, and cosmids. Preferably, the expression vector is a plasmid.

[0035] As used herein, the term "transformant" refers to a microorganism or cell into which a gene of interest has been introduced using an expression vector or the like, and which is now capable of expressing a desired trait associated with a protein having a desired function.

[0036] Specific examples of methods for producing transformants include a method in which DNA encoding the protein of the present invention (mutant L-pipecolic acid hydroxylase) is introduced into a plasmid vector, phage vector, or viral vector that stably exists in host cells, and the resulting expression vector is then introduced into the host cells, or a method in which the DNA is directly introduced into the host genome and the genetic information is transcribed and translated. In this case, it is preferable to link a suitable promoter upstream of the 5' end of the DNA in the host, and more preferably to link a terminator downstream of the 3' end. Such promoters and terminators are not particularly limited as long as they are known to function in cells used as hosts. For example, vectors, promoters, and terminators described in detail in "Basic Lectures on Microbiology 8: Genetic Engineering, Kyoritsu Shuppan" can be used.

[0037] The host microorganism to be transformed to express the mutant L-pipecolic acid hydroxylase of the present invention is not particularly limited, as long as the host itself does not adversely affect the substrate L-pipecolic acid or the target product cis-5-hydroxy-L-pipecolic acid. Examples of the host microorganism include the following microorganisms:

[0038] Bacteria for which host-vector systems have been established, such as those belonging to the genera Escherichia, Bacillus, Pseudomonas, Serratia, Brevibacterium, Corynebacterium, Streptococcus, and Lactobacillus. Actinomycetes belonging to the genera Rhodococcus and Streptomyces, for which host-vector systems have been established. Yeasts for which host-vector systems have been established, such as those belonging to the genera Saccharomyces, Kluyveromyces, Schizosaccharomyces, Zygosaccharomyces, Yarrowia, Trichosporon, Rhodosporidium, Hansenula, Pichia, and Candida. Fungi with established host-vector systems, such as those belonging to the genera Neurospora, Aspergillus, Cephalosporium, and Trichoderma.

[0039] The procedures for preparing transformants, the construction of recombinant vectors suitable for the host, and the method for culturing the host can be carried out in accordance with techniques commonly used in the fields of molecular biology, biotechnology, and genetic engineering (e.g., the methods described in Green et al., Molecular Cloning: A Laboratory Manual (4th ed.), Cold Spring Harbor Press, Cold Spring Harbor, NY (2012)).

[0040] Specific examples of preferred host microorganisms, preferred transformation techniques for each microorganism, vectors, promoters, terminators, etc. are given below, but the present invention is not limited to these examples. In the genus Escherichia, particularly Escherichia coli, examples of plasmid vectors include pBR and pUC-based plasmids, and examples of promoters include those derived from lac (β-galactosidase), trp (tryptophan operon), tac, trc (lac and trp fusion), λ phage PL, PR, T7 phage, etc. Examples of terminators include those derived from trpA, phage, and rrnB ribosomal RNA. In the genus Bacillus, examples of vectors include pUB110-based plasmids and pC194-based plasmids, and they can also be integrated into chromosomes. As promoters and terminators, promoters and terminators of enzyme genes such as alkaline protease, neutral protease, and α-amylase can be used. In the genus Pseudomonas, examples of vectors include general host-vector systems established for Pseudomonas putida, Pseudomonas cepacia, etc., plasmids involved in the degradation of toluene compounds, and the broad-host-range vector pKT240 (Gene, 26, 273-82 (1983)) based on the TOL plasmid (containing genes necessary for autonomous replication derived from RSF1010, etc.). For Brevibacterium species, particularly Brevibacterium lactofermentum, examples of vectors include plasmid vectors such as pAJ43 (Gene 39, 281 (1985)).Various promoters and terminators used in Escherichia coli can be used. For the genus Corynebacterium, particularly Corynebacterium glutamicum, examples of vectors include plasmid vectors such as pCS11 (Japanese Patent Laid-Open Publication No. 57-183799) and pCB101 (Mol. Gen. Genet. 196, 175 (1984)). For the genus Saccharomyces, particularly Saccharomyces cerevisiae, vectors include YRp, YEp, YCp, and YIp plasmids. Promoters and terminators for various enzyme genes, such as alcohol dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, acid phosphatase, β-galactosidase, phosphoglycerate kinase, and enolase, are also available. In the genus Schizosaccharomyces, examples of vectors include the plasmid vector derived from Schizosaccharomyces pombe described in Mol. Cell. Biol. 6, 80 (1986). In particular, pAUR224 is commercially available from Takara Bio Inc. and can be easily used. Within the Aspergillus genus, Aspergillus niger and Aspergillus oryzae are the most extensively studied fungi, and plasmid and chromosomal integration are available, and promoters derived from extracellular proteases and amylases can be used (Trends in Biotechnology 7, 283-287 (1989)). In addition to the above, host-vector systems have been established for various microorganisms, and these can be used as appropriate.

[0041] In addition to microorganisms, various host-vector systems have been established in plants and animals. In particular, systems for expressing large amounts of heterologous proteins in animals such as insects (e.g., silkworms) (Nature 315, 592-594 (1985)) and plants such as rapeseed, corn, and potato, as well as systems using cell-free protein synthesis systems such as Escherichia coli cell-free extracts and wheat germ, have been established and can be used advantageously.

[0042] Examples of processed products of microorganisms or cells capable of producing the mutant L-pipecolic acid hydroxylase of the present invention include cell preparations such as those obtained by treating the microorganisms or cells with organic solvents such as acetone, dimethyl sulfoxide (DMSO), or toluene, or surfactants, freeze-drying, or physically or enzymatically disrupting the microorganisms or cells, as well as crude or purified enzyme fractions extracted from the microorganisms or cells, and those immobilized on carriers such as polyacrylamide gel and carrageenan gel.

[0043] Examples of a culture medium containing the mutant L-pipecolic acid hydroxylase of the present invention obtained by culturing a microorganism or cell capable of producing the enzyme include a suspension of the microorganism or cell with a liquid medium, and, when the microorganism or cell is a secretory expression cell, a supernatant obtained by removing the microorganism or cell by centrifugation or a concentrate thereof. The culture may be carried out under any conditions suitable for culturing the microorganism or cell, and may be appropriately adjusted to optimize the activity, physical properties, productivity, etc. of the mutant L-pipecolic acid hydroxylase of the present invention. For example, when Escherichia coli is used as a host, the culture conditions are typically a culture temperature of 15°C to 37°C and a time period of approximately 12 to 48 hours. Low-temperature culture may be preferable from the viewpoint of enzyme activity and solubility. In such cases, the culture is preferably carried out at a culture temperature of 15°C to 25°C or 15°C to 20°C.

[0044] 2. Method for producing cis-5-hydroxy-L-pipecolic acid of the present invention The method for producing cis-5-hydroxy-L-pipecolic acid of the present invention comprises contacting L-pipecolic acid with the mutant L-pipecolic acid hydroxylase of the present invention, a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell (hereinafter, these may be collectively referred to as "the mutant L-pipecolic acid hydroxylase of the present invention, etc.").

[0045] The production method of the present invention can use a purified or roughly purified mutant L-pipecolic acid hydroxylase of the present invention, a microorganism or cell capable of producing the mutant L-pipecolic acid hydroxylase of the present invention (e.g., a transformant having a DNA encoding the mutant L-pipecolic acid hydroxylase of the present invention), a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell. Among these, it is preferable to use a microorganism or cell capable of producing the mutant L-pipecolic acid hydroxylase of the present invention (e.g., a transformant having a DNA encoding the mutant L-pipecolic acid hydroxylase of the present invention), a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell, and it is more preferable to use a transformant having a DNA encoding the mutant L-pipecolic acid hydroxylase of the present invention.

[0046] In the production method of the present invention, multiple types of mutant L-pipecolic acid hydroxylases may be used in combination.

[0047] The amount of the mutant L-pipecolic acid hydroxylase or the like of the present invention to be contacted with L-pipecolic acid is not particularly limited, as long as it is an amount that can produce cis-5-hydroxy-L-pipecolic acid. For example, when the microorganism or cells are added to a reaction solution containing L-pipecolic acid, the microorganism or cell concentration in the reaction solution is typically about 0.1 w / v% to 50 w / v%, preferably 1 w / v% to 20 w / v%, based on wet cell weight. Furthermore, when the processed product or culture solution is added to a reaction solution containing L-pipecolic acid, the specific activity of the mutant L-pipecolic acid hydroxylase to be used is determined, and an amount is added so that the microorganism or cell concentration in the reaction solution reaches the aforementioned concentration. Here, w / v% represents weight / volume %.

[0048] The contact method is not particularly limited, and for example, L-pipecolic acid as a substrate can be added to a liquid containing the mutant L-pipecolic acid hydroxylase of the present invention, etc. Alternatively, the mutant L-pipecolic acid hydroxylase of the present invention, etc. may be added to a liquid containing L-pipecolic acid as a substrate (reaction substrate). When L-pipecolic acid comes into contact with the mutant L-pipecolic acid hydroxylase of the present invention, etc., L-pipecolic acid is hydroxylated to produce cis-5-hydroxy-L-pipecolic acid.

[0049] The amount of L-pipecolic acid used as a substrate can be appropriately selected depending on the amount of cis-5-hydroxy-L-pipecolic acid to be produced. L-pipecolic acid can be used at a substrate concentration of typically 0.01 w / v% to 90 w / v%, preferably 0.1 w / v% to 30 w / v%, in a liquid containing L-pipecolic acid and the mutant L-pipecolic acid hydroxylase of the present invention (hereinafter sometimes referred to as a "reaction liquid").

[0050] L-pipecolic acid, the mutant L-pipecolic acid hydroxylase of the present invention, and the like may be added all at once at the start of the reaction, or may be added continuously or intermittently from the viewpoint of reducing the influence of substrate inhibition of the enzyme or increasing the accumulated concentration of the product.

[0051] The contact is preferably carried out in the presence of 2-oxoglutaric acid and divalent iron ions. 2-oxoglutaric acid is usually added in an equimolar or greater amount relative to the substrate L-pipecolic acid, preferably in an equimolar to 2-fold molar amount. 2-oxoglutaric acid may be added all at once at the start of the reaction, or may be added continuously or intermittently to reduce the influence of any inhibitory effects on the enzyme or to increase the accumulated concentration of the product. Alternatively, an inexpensive compound that can be metabolized by the host, such as glucose, may be added instead of 2-oxoglutaric acid and allowed to metabolize by the host, with the 2-oxoglutaric acid produced during the process being used in the reaction.

[0052] Divalent iron ions can be used in a reaction solution at a concentration of typically 0.001 mmol / L to 100 mmol / L, preferably 0.01 mmol / L to 50 mmol / L, and particularly preferably 0.1 mmol / L to 10 mmol / L. Divalent iron ions can be added all at once at the start of the reaction, as iron sulfate or the like. Furthermore, if the divalent iron ions added during the reaction are oxidized to trivalent iron or precipitated and reduced, it is also effective to add additional iron. Note that if the mutant L-pipecolic acid hydroxylase or the like of the present invention already contains a sufficient amount of divalent iron ions, adding additional iron is not necessarily required. The contact is preferably carried out in the presence of L-ascorbic acid. The concentration of L-ascorbic acid in the reaction solution is usually 0.001 mmol / L to 50 mmol / L, preferably 0.01 mmol / L to 30 mmol / L, and particularly preferably 0.1 mmol / L to 25 mmol / L. The addition of L-ascorbic acid can reduce the oxidation of divalent iron ions.

[0053] The contact can usually be carried out in an aqueous medium or a mixture of an aqueous medium and an organic solvent, but is preferably carried out in an aqueous medium from the viewpoint of post-reaction treatment and industrial applications.

[0054] Examples of aqueous media include water and known buffers such as Good's buffer, phosphate buffer, Tris buffer, and borate buffer. Organic solvents that have high solubility for the substrate L-pipecolic acid, such as methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, tert-butanol, acetone, and dimethyl sulfoxide, can be used. Furthermore, organic solvents that can effectively remove reaction by-products, such as ethyl acetate, butyl acetate, toluene, chloroform, and n-hexane, can also be used.

[0055] The contact can be carried out, for example, under atmospheric pressure, usually at a temperature ranging from 4°C to 60°C, preferably from 10°C to 45°C, and particularly preferably from 15°C to 40°C. The contact can also be carried out usually at a pH of 3 to 11, preferably from 5 to 8. The contact time is not particularly limited, as long as it is long enough for L-pipecolic acid to be hydroxylated to produce cis-5-hydroxy-L-pipecolic acid, but is usually 10 minutes or longer, preferably 30 minutes or longer, and usually within 90 hours, preferably within 72 hours.

[0056] The produced cis-5-hydroxy-L-pipecolic acid can be separated from the bacterial cells and proteins in the reaction solution by a separation or purification method known to those skilled in the art, such as centrifugation or membrane treatment, and then purified by an appropriate combination of methods known to those skilled in the art, such as extraction with an organic solvent such as 1-butanol or tert-butanol, distillation, column chromatography using an ion exchange resin or silica gel, crystallization at the isoelectric point, or crystallization with the monohydrochloride, dihydrochloride, calcium salt, or the like.

[0057] According to the production method of the present invention, cis-5-hydroxy-L-pipecolic acid, which is useful as an intermediate for pharmaceuticals, can be produced industrially with high productivity and low cost. [Example]

[0058] The present invention will be explained in more detail below with reference to examples, but the present invention is not limited to these examples. In the examples, amino acids may be abbreviated as follows:

[0059] [Table 1]

[0060] <Example 1: Obtaining the XdPH gene and introducing a mutation into the XdPH gene 1> The gene sequence (xdph_Ecodon, SEQ ID NO: 1) encoding L-proline cis-4-hydroxylase XdPH (GenBank Accession No. CDG16639, SEQ ID NO: 2) derived from Xenorhabdus doucetiae FRM16 strain was codon-optimized for expression in Escherichia coli. DNA2.0 (now ATUM) artificially synthesized this gene and inserted it into pJExpress411 (DNA2.0) to produce the plasmid pJ411XdPH. Furthermore, the resulting plasmid pJ411XdPH was used as a template for the following PCR amplifications according to standard methods: 2 Expression plasmids for the mutants shown in Table 1 (Nos. m1 to m25 and m37 to m59) were constructed.

[0061] <Example 2: Introduction of mutations into the XdPH gene 2> Using the plasmid pJ411XdPH_m15 obtained in Example 1, which carries the mutant gene in which leucine at position 142 has been replaced with arginine, as a template, further mutations were introduced in the same manner as in Example 1 to obtain plasmid pJ411XdPH_m26, which expresses a double mutant. This plasmid carries a gene encoding the mutant enzyme XdPHm26 in which leucine at position 142 has been replaced with arginine and glutamic acid at amino acid position 15 has been replaced with alanine. In a similar manner, the mutant expression plasmids (pJ411XdPH_m27 to pJ411XdPH_m36) shown in Table 2 were prepared.

[0062] [Table 2-1]

[0063] [Table 2-2]

[0064] <Example 3: Obtaining mutant XdPH gene-expressing bacteria 1> The wild-type plasmid pJ411XdPH and each of the mutant expression plasmids obtained in Examples 1 and 2 were used to transform Escherichia coli BL21(DE3) (Invitrogen) according to standard methods to obtain each recombinant Escherichia coli.

[0065] <Example 4: Activity evaluation of mutant L-pipecolic acid hydroxylase (XdPH mutant) 1> (1) Preparation of enzyme solution To obtain cells expressing the introduced genes, each of the recombinant E. coli strains obtained in Example 3 (recombinant E. coli strains transformed with the wild-type plasmid pJ411XdPH, and the mutant expression plasmids pJ411XdPH_m1 to pJ411XdPH_m31 and pJ411XdPH_m33 to pJ411XdPH_m36) was pre-cultured in 1 mL of liquid LB medium containing kanamycin and a lac promoter inducer at 30°C for approximately 5 hours. Subsequently, cells were harvested after normal or low-temperature culture. In the case of normal culture, the cells were harvested after approximately 20 hours of culture at 28°C or 30°C following pre-culture. In the case of low-temperature culture, the cells were harvested after approximately 24 hours of culture at 15°C following pre-culture.

[0066] Next, 0.6 mL of each recombinant E. coli was collected by centrifugation and suspended in 50 mmol / L MES (2-morpholinoethanesulfonic acid) buffer at pH 6.5. A container containing 0.5 mL of the resulting suspension was immersed in ice water and sonicated, followed by centrifugation at 12,000 rpm. The resulting supernatant was used as the enzyme solution for evaluating L-pipecolic acid hydroxylation activity.

[0067] (2) Activity evaluation 0.2 mL of a reaction solution in which the components were mixed to the concentrations shown in Table 3 was placed in a plastic tube and shaken at 30°C for 30 minutes.

[0068] [Table 3]

[0069] After adding 0.1 mL of hydrochloric acid with a concentration of 1 mmol / L to the oscillated reaction solution to stop the reaction, 0.1 mL of an aqueous sodium hydroxide solution with a concentration of 1 mmol / L was added to neutralize the reaction solution. The neutralized reaction solution was centrifuged, and the solution obtained by removing the precipitate was analyzed by HPLC (High Performan ce Liquid Chromatography) under the following conditions to measure the concentration of the generated cis-5-hydroxy-L-pipecolic acid.

[0070] <HPLC analysis conditions> Equipment used: Chromaster (registered trademark) (manufactured by Hitachi High-Tech Sciences Corporation) Column: Astec (registered trademark) CLC-D Chiral HPLC Column, 5 μm, 150 × 4.6 mm Detection wavelength: 254 nm Injection volume: 10 μL Developing solution: 2 mmol / L copper sulfate Flow rate: 1 mL / min Column temperature: 45 °C

[0071] The evaluation results of the L-pipecolic acid hydroxylation activity of the wild-type enzyme XdPH and each XdPH mutant are shown in Table 4 [low-temperature culture] and Table 5 [normal culture]. In Table 4 and Table 5, the L-pipecolic acid hydroxylation activity was evaluated as the amount of cis-5-hydroxy-L-pipecolic acid produced (U / g-total protein) per total protein amount (unit: g). Here, the unit (U) represents the ability to produce 1 μmol of cis-5-hydroxy-L-pipecolic acid per minute. The display of the L-pipecolic acid hydroxylation activity in Table 4 and Table 5 means the following.

[0072] Display Amount of cis-5-hydroxy-L-pipecolic acid produced (U / g-total protein) - 0 + 1 - 5 ++ 5 - 10 +++ 10 - 50 ++++ 50 - 100 +++++ 100~150

[0073] [Table 4]

[0074] [Table 5]

[0075] As is clear from Tables 4 and 5, the wild-type enzyme XdPH exhibits slight L-pipecolic acid hydroxylation activity when the recombinant E. coli is cultured at low temperatures (around 15°C to 20°C), but does not exhibit any L-pipecolic acid hydroxylation activity when cultured at temperatures around 28°C to 30°C, at which E. coli grows well. As shown in Table 4, the L-pipecolic acid hydroxylation activity of XdPH mutants containing a single mutation was evaluated after low-temperature incubation (15°C). The following mutants exhibited improved L-pipecolic acid hydroxylation activity compared to the wild-type XdPH enzyme: m9 (glutamic acid at position 15 is substituted with alanine), m10 (isoleucine at position 28 is substituted with proline), m11 (isoleucine at position 28 is substituted with arginine), m12 (valine at position 31 is substituted with glutamic acid), m13 (cysteine ​​at position 76 is substituted with tyrosine), m14 (isoleucine at position 108 is substituted with arginine), m15 (leucine at position 142 is substituted with arginine), and m23 (phenylalanine at position 246 is substituted with tyrosine). Among these, m15 exhibited particularly improved L-pipecolic acid hydroxylation activity.

[0076] Furthermore, by combining multiple mutations that improved L-pipecolic acid hydroxylation activity by single mutations, L-pipecolic acid hydroxylation activity was further improved (m26 to m36). Among these, those with a mutation in which leucine at position 142 was replaced with arginine (m26 to m31 and m34 to m36), those with a mutation in which isoleucine at position 28 was replaced with proline (m27 and m33 to m36), and those with a mutation in which cysteine ​​at position 76 was replaced with tyrosine (m29 and m33 to m34) in the amino acid sequence represented by SEQ ID NO: 2 showed significantly improved L-pipecolic acid hydroxylation activity. In particular, those with a mutation in which leucine at position 142 was replaced with arginine, isoleucine at position 28 was replaced with proline, and cysteine ​​at position 76 was replaced with tyrosine (m34) showed significantly improved L-pipecolic acid hydroxylation activity.

[0077] As is clear from Table 5, the L-pipecolic acid hydroxylation activity of XdPH mutants with a single mutation introduced was evaluated after conventional culture (28°C or 30°C). The wild-type enzyme XdPH did not exhibit L-pipecolic acid hydroxylation activity during conventional culture, but m15 and m26 to m36 exhibited good L-pipecolic acid hydroxylation activity. In particular, mutants m26 to m36 with multiple mutations introduced exhibited extremely high L-pipecolic acid hydroxylation activity.

[0078] Furthermore, by combining multiple mutations that improved L-pipecolic acid hydroxylation activity by single mutations, L-pipecolic acid hydroxylation activity was further improved (m26 to m36). Among these, those with a mutation in which leucine at position 142 was replaced with arginine (m26 to m31 and m34 to m36), those with a mutation in which isoleucine at position 28 was replaced with proline (m27 and m33 to m36), and those with a mutation in which cysteine ​​at position 76 was replaced with tyrosine (m29 and m33 to m34) in the amino acid sequence represented by SEQ ID NO: 2 showed significantly improved L-pipecolic acid hydroxylation activity. In particular, those with a mutation in which leucine at position 142 was replaced with arginine, isoleucine at position 28 was replaced with proline, and cysteine ​​at position 76 was replaced with tyrosine (m34) showed significantly improved L-pipecolic acid hydroxylation activity.

[0079] Furthermore, m29 to m30 and m33 to m36 had higher L-pipecolic acid hydroxylation activity when cultured at temperatures around 28°C to 30°C, at which E. coli grows well, than when cultured at low temperatures.

[0080] The mutants XdPHm1 to XdPHm8, XdPHm16 to XdPHm22, XdPHm24, and XdPHm25 showed little or no L-pipecolic acid hydroxylation activity in both low-temperature and normal culture. Furthermore, the HPLC analysis results (chart) of the L-pipecolic acid hydroxylation activity of the wild-type enzyme XdPH and mutant XdPHm27 cultured under normal conditions are shown in Figure 5. Figure 5 also shows that cis-5-hydroxy-L-pipecolic acid is produced by mutant XdPHm27.

[0081] Example 5: Activity evaluation of XdPH mutants 2 (1) Preparation of enzyme solution To obtain cells expressing the introduced genes, each recombinant E. coli strain obtained in Example 3 (recombinant E. coli strains transformed with the wild-type plasmid pJ411XdPH, and the mutant expression plasmids pJ411XdPH_m34 and pJ411XdPH_m37 to pJ411XdPH_m59) was pre-cultured in 1 mL of liquid LB medium containing kanamycin and a lac promoter inducer at 30°C for approximately 5 hours. Subsequently, the strains were cultured at low temperature (at 15°C or 20°C for approximately 24 hours) and then harvested.

[0082] After cultivation, the culture medium was centrifuged to collect the cells and suspended in 0.5 mL of 50 mmol / L MES (2-morpholinoethanesulfonic acid) buffer at pH 7. The resulting suspension (0.5 mL) was placed in a container and sonicated in ice water, then centrifuged at 12,000 rpm to separate the supernatant and residue. The resulting supernatant was used as the enzyme solution for evaluating L-pipecolic acid hydroxylation activity.

[0083] (2) Activity evaluation 0.1 mL of a reaction solution in which the components were mixed to the concentrations shown in Table 6 was placed in a plastic tube and shaken at 30°C for 30 minutes.

[0084] [Table 6]

[0085] The reaction was stopped by transferring 20 μL of the reaction mixture to a separate plastic tube containing 10 μL of 1 mmol / L hydrochloric acid. The reaction mixture was then neutralized by adding 10 μL of 1 mmol / L aqueous sodium hydroxide. 40 μL of 2 mmol / L aqueous copper sulfate was added, and the precipitate was removed by centrifugation. 20 μL of the resulting supernatant was mixed with 20 μL of 1 mol / L borate buffer (pH 9.0) and 50 μL of 20 mmol / L 1-fluoro-2,4-dinitrophenyl-5-L-alanine amide (FDAA) in acetonitrile, and the mixture was incubated at 40°C for 60 minutes.

[0086] 10 μL of hydrochloric acid with a concentration of 1 mol / L was added to stop the reaction. After adding 100 μL of methanol, the precipitate was removed by centrifugation, and 150 μL of the obtained supernatant was analyzed by UPLC (registered trademark) (Ultra Performance LC) under the following conditions to measure the concentration of the generated cis-5-hydroxy-L-pipecolic acid.

[0087] <UPLC (registered trademark) analysis conditions> Equipment used: ACQUITY UPLC (registered trademark) system (manufactured by Waters) Column: ACQUITY UPLC BEH C18 (1.7 μm) 2.1×100 mm (manufactured by Waters) Detection wavelength: 340 nm Injection volume: 5 μL Eluent A: 0.1% formic acid Eluent B: Acetonitrile (0.1% formic acid) Flow rate: 0.2 mL / min Gradient conditions: Time (min) Eluent B (%) 0 20 12 55 12.5 100 14.5 100 14.6 20​​​​​​​​​​​​​​​​​​​​

[0090] [Table 7]

[0091] The L-pipecolic acid hydroxylation activity of XdPH mutants with a single mutation introduced was evaluated after low-temperature culture (15°C or 20°C). As is clear from Table 7, m50, in which alanine at position 239 was replaced with aspartic acid, and m56, in which glutamine at position 202 was replaced with proline in the amino acid sequence represented by SEQ ID NO: 2, had improved L-pipecolic acid hydroxylation activity compared to the wild-type enzyme XdPH. Furthermore, m34, which had multiple (3) mutations introduced, had significantly improved L-pipecolic acid hydroxylation activity compared to the wild-type enzyme XdPH. Among the XdPH mutants into which a single mutation was introduced, m37 to m49, m51 to m55, and m57 to m59 did not show improved L-pipecolic acid hydroxylation activity compared to the wild-type enzyme XdPH.

[0092] <Example 6: Solubility evaluation 1 of XdPH mutants> (1) Preparation of solutions for solubility evaluation To obtain bacterial cells expressing the introduced genes, each of the recombinant E. coli strains obtained in Example 3 (recombinant E. coli strains transformed with the wild-type plasmid pJ411XdPH, and the mutant expression plasmids pJ411XdPH_m1 to pJ411XdPH_m23, pJ411XdPH_m26 to pJ411XdPH_m30, and pJ411XdPH_m34) was pre-cultured in 1 mL of liquid LB medium containing kanamycin and a lac promoter inducer at 30°C for approximately 5 hours, followed by normal culture (culture at 28°C for approximately 20 hours) or low-temperature culture (culture at 15°C for approximately 24 hours), and then harvested by centrifugation at 12,000 rpm.

[0093] The entire amount of each recombinant E. coli obtained was suspended in 50 mmol / L MES buffer at pH 7 to a turbidity (OD630) of approximately 10. A container containing 0.5 mL of the resulting suspension was immersed in ice water and subjected to ultrasonic disruption, followed by centrifugation at 12,000 rpm to separate the supernatant and residue. The resulting supernatant was designated the soluble fraction, and the residue the insoluble fraction.

[0094] (2) Solubility evaluation The protein concentration of each soluble fraction obtained was quantified according to standard methods, and then each fraction was divided into plastic tubes so that the total protein amount was 10 μg. The tubes were suspended in a solubilization buffer containing SDS (sodium dodecyl sulfate), and heated at 90°C for approximately 10 minutes to prepare solutions for solubility evaluation. Each of the obtained insoluble fractions was suspended in 0.5 mL of SDS-containing solubilization buffer, and then heated at 90°C for 10 minutes to solubilize the suspension. This solution was used as a solution for solubility evaluation.

[0095] Each of the obtained solutions was subjected to SDS-polyacrylamide electrophoresis according to a standard method to confirm the amount of expressed XdPH protein. The results of solubility evaluation after low-temperature culture for XdPH mutants into which a single mutation had been introduced are shown in Table 8 and FIG. Furthermore, the results of evaluating the solubility of XdPH mutants with single or multiple mutations after low-temperature culture and normal culture are shown in Table 9 and Figure 2. The solubility was evaluated by visually inspecting the electrophoresis results and using the solubility level as an index based on the soluble expression amount of the wild-type enzyme XdPH. The solubility levels in Tables 8 and 9 have the following meanings.

[0096] Display solubility level - Less than wild type * Slightly more soluble than wild type ** Slightly more soluble than wild type *** Significantly more soluble than wild type

[0097] [Table 8]

[0098] [Table 9]

[0099] The wild-type enzyme XdPH is expressed in a slightly soluble form in the active form in E. coli when recombinant E. coli is cultured at low temperatures, but it is difficult to express it in a soluble form in E. coli when cultured at temperatures around 28°C to 30°C, where E. coli grows well.

[0100] The XdPH mutants shown in Table 8, which had undergone single mutation introduction, were evaluated for solubility after low-temperature incubation (15°C). As a result, m6, in which arginine at position 262 was replaced with valine, m8, in which isoleucine at position 271 was replaced with tyrosine, m9, in which glutamic acid at position 15 was replaced with alanine, and m14, in which isoleucine at position 108 was replaced with arginine in the amino acid sequence represented by sequence number 2, had slightly improved solubility compared to the wild-type enzyme XdPH.

[0101] In the amino acid sequence represented by sequence number 2, m7 in which the 271st isoleucine is replaced with glycine, m10 in which the 28th isoleucine is replaced with proline, m11 in which the 28th isoleucine is replaced with arginine, m12 in which the 31st valine is replaced with glutamic acid, m13 in which the 76th cysteine ​​is replaced with tyrosine, m15 in which the 142nd leucine is replaced with arginine, and m23 in which the 246th phenylalanine is replaced with tyrosine had slightly improved solubility compared to the wild-type enzyme XdPH.

[0102] Furthermore, the XdPH mutants shown in Table 9, which had undergone single or multiple mutations, were evaluated for solubility after low-temperature culture (15°C) and normal culture (28°C).

[0103] Among the XdPH mutants with a single mutation, m14, in which the 108th isoleucine in the amino acid sequence represented by sequence number 2 was replaced with arginine, showed slightly improved solubility compared to the wild-type enzyme XdPH, both after low-temperature incubation (15°C) and normal incubation (28°C).

[0104] Among the XdPH mutants with a single mutation, m10, in which the 28th isoleucine in the amino acid sequence shown in SEQ ID NO: 2 is replaced with proline; m11, in which the 28th isoleucine is replaced with arginine; m12, in which the 31st valine is replaced with glutamic acid; m13, in which the 76th cysteine ​​is replaced with tyrosine; and m23, in which the 246th phenylalanine is replaced with tyrosine, all had slightly improved solubility compared to the wild-type enzyme XdPH, both after low-temperature cultivation (15°C) and after normal cultivation (28°C).

[0105] Among the XdPH mutants with a single mutation, m15, in which the 142nd leucine in the amino acid sequence shown in sequence number 2 was replaced with arginine, showed slightly improved solubility compared to the wild-type XdPH enzyme after low-temperature incubation (15°C), and significantly improved solubility compared to the wild-type XdPH enzyme after normal incubation (28°C).

[0106] The multiple mutation-introduced strains m26-m30 and m34 showed significantly improved solubility compared to the wild-type XdPH enzyme after low-temperature incubation (15°C). Furthermore, the multiple mutation-introduced strains m26-m29 showed significantly improved solubility compared to the wild-type XdPH enzyme even after normal incubation (28°C). These results confirmed that the introduction of multiple mutations increases the efficiency of soluble expression.

[0107] Among the XdPH mutants shown in Tables 8 and 9, the solubility of m1 to m5 and m16 to m22 was lower than that of the wild-type enzyme XdPH.

[0108] <Example 7: Evaluation of solubility of XdPH mutants 2> (1) Preparation of enzyme solution To obtain bacterial cells expressing the introduced genes, each of the recombinant E. coli strains obtained in Example 3 (recombinant E. coli strains transformed with the wild-type plasmid pJ411XdPH, the mutant expression plasmids pJ411XdPH_m34, and pJ411XdPH_m37 to pJ411XdPH_m59) was pre-cultured in 1 mL of liquid LB medium containing kanamycin and a lac promoter inducer at 30°C for approximately 5 hours, followed by low-temperature culture (at 15°C or 20°C for approximately 24 hours) and harvested by centrifugation at 12,000 rpm.

[0109] The entire amount of recombinant E. coli obtained was suspended in 0.5 mL of 50 mmol / L MES buffer at pH 7. The resulting container was immersed in ice water and subjected to ultrasonic disruption, followed by centrifugation at 12,000 rpm to separate the supernatant and residue. The resulting supernatant was designated as the soluble fraction, and the residue as the insoluble fraction.

[0110] (2) Solubility evaluation 20 μL of each of the obtained soluble fractions was transferred to a plastic tube, suspended in an SDS-containing solubilization buffer, and heated at 100° C. for about 10 minutes to be used as a solution for solubility evaluation. Each of the obtained insoluble fractions was suspended in 0.5 mL of SDS-containing solubilization buffer, and then heated at 100°C for 10 minutes to solubilize the suspension. This solution was used as a solution for solubility evaluation. Each of the resulting solutions was subjected to SDS-polyacrylamide gel electrophoresis according to a standard method to confirm the amount of expressed XdPH protein. The solubility evaluation results are shown in Table 10, Figures 3 and 4. The solubility was evaluated by visually inspecting the electrophoresis results and using the solubility level as an index based on the soluble expression amount of the wild-type enzyme XdPH. The solubility levels in Table 10 have the following meanings.

[0111] Display solubility level - Less than wild type ** Slightly more soluble than wild type *** Significantly more soluble than wild type

[0112] [Table 10]

[0113] Among the XdPH mutants with a single mutation, m50, in which alanine at position 239 in the amino acid sequence shown in SEQ ID NO: 2 was replaced with aspartic acid, and m56, in which glutamine at position 202 was replaced with proline, had slightly improved solubility compared to the wild-type enzyme XdPH. Furthermore, m34, which had undergone multiple mutations, had significantly improved solubility compared to the wild-type enzyme XdPH, confirming that the efficiency of soluble expression was improved by introducing multiple mutations. Among the XdPH mutants shown in Table 10, m37 to m49, m51 to m55, and m57 to m59 had solubility lower than that of the wild-type enzyme XdPH.

[0114] <Example 8: Introduction of mutations into the XdPH gene 3> Using the plasmid pJ411XdPH obtained in Example 1 as a template, a plasmid pET28aXdPH was prepared by inserting it into the plasmid pET-28a(+) (Merck Millipore) according to a standard method. Furthermore, using the obtained pET28aXdPH as a template, expression plasmids for mutants (No. m15 and m60 to m77) in which the 142nd amino acid shown in Table 11 had been site-specifically modified were prepared according to a standard method.

[0115] [Table 11]

[0116] <Example 9: Obtaining mutant XdPH gene-expressing bacteria 2> The wild-type plasmid pET28aXdPH and each of the mutant expression plasmids obtained in Example 8 were used to transform Escherichia coli BL21(DE3) (Invitrogen) according to a standard method to obtain each recombinant Escherichia coli.

[0117] Example 10: Activity evaluation of XdPH mutants 3 (1) Preparation of enzyme solution To obtain cells expressing the introduced genes, the recombinant E. coli obtained in Example 9 (recombinant E. coli transformed with the wild-type plasmid pET28aXdPH, and the mutant expression plasmids pET28aXdPH_m15 and pET28aXdPH_m60 to pET28aXdPH_m77) were cultured at 30°C at OD 200 using LB autoinduction medium (Novagen). 600 After culturing until the pH reached 0.6 to 0.8, the bacteria were cultured at 15°C for approximately 24 hours and then harvested.

[0118] Next, 2 mL of each recombinant E. coli was collected by centrifugation and suspended in 100 mmol / L MES buffer at pH 6.5. A container containing 0.5 mL of the resulting suspension was immersed in ice water and sonicated, followed by centrifugation at 20,000 rpm. The resulting supernatant was used as the enzyme solution for evaluating L-pipecolic acid hydroxylation activity.

[0119] (2) Activity evaluation 0.05 mL of a reaction solution prepared by mixing components to the concentrations shown in Table 12 was placed in a plastic tube and allowed to stand at 20°C for 10 minutes to allow the reaction to occur.

[0120] [Table 12]

[0121] The reaction was terminated by transferring 12.5 μL of the resulting reaction mixture to a separate plastic tube containing 25 μL of 31.8 mmol / L FDLA (1-fluoro-2,4-dinitrophenyl-L-leucinamide) acetone solution. 5 μL of 1 mol / L sodium carbonate was then added, and the mixture was incubated at 37°C for 60 minutes. The reaction was terminated by adding 5 μL of 2 mol / L hydrochloric acid, followed by dilution with 427.5 μL of eluent (3.83 mol / L aqueous acetonitrile solution containing 26.5 mmol / L formic acid). The resulting diluted solution was passed through a filter to remove precipitate. The effluent was analyzed by UPLC® under the same conditions as in Example 5 to measure the concentration of the cis-5-hydroxy-L-hydroxypipecolic acid produced.

[0122] Table 13 shows the evaluation results of the L-pipecolic acid hydroxylation activity of wild-type XdPH and XdPH mutants (m15 and m60 to m77). In Table 13, the L-pipecolic acid hydroxylation activity was evaluated as the relative production amount (relative activity) to the amount of cis-5-hydroxy-L-pipecolic acid produced per total protein (unit: g) obtained in the reaction using the wild-type enzyme XdPH (U / g-total protein). Here, unit (U) represents the ability to produce 1 μmole of cis-5-hydroxy-L-pipecolic acid per minute. The L-pipecolic acid hydroxylation activity in Table 13 has the following meanings.

[0123] Display Relative activity ★ 0~2 ★★ 2~5 ★★★ 5~10 ★★★★ >10

[0124] [Table 13]

[0125] Among the XdPH mutants with a single mutation, m15, m60, m61, m63, m65, m72, and m74, in which leucine at position 142 was substituted with arginine, lysine, asparagine, glutamine, histidine, alanine, or cysteine, had improved L-pipecolic acid hydroxylation activity compared to the wild-type XdPH enzyme. Among these, m15, m60, m61, m63, and m65, in which leucine at position 142 was substituted with arginine, lysine, asparagine, glutamine, or histidine, had particularly improved L-pipecolic acid hydroxylation activity. The L-pipecolic acid hydroxylation activity tends to be improved by substituting leucine, a highly hydrophobic amino acid, with arginine, lysine, asparagine, glutamine, histidine, alanine, or cysteine, which are amino acids that are less hydrophobic (more hydrophilic) than leucine, preferably arginine, lysine, asparagine, glutamine, or histidine. Furthermore, even if the amino acid had low hydrophobicity, substitution with a negatively charged amino acid (m64: glutamic acid, m62: aspartic acid) did not improve the L-pipecolic acid hydroxylation activity.

[0126] Modeling the crystal structure of the wild-type enzyme XdPH using SWISS-MODEL (https: / / swissmodel.expasy.org / ) revealed that leucine 142 is located on the surface of the enzyme. Substitution of a highly hydrophobic amino acid with a less hydrophobic amino acid improved the solubility in water, increasing the expression level as a soluble protein and improving the L-pipecolic acid hydroxylation activity.

[0127] <Description of Sequence Listing> SEQ ID NO: 1: XdPH gene sequence codon-optimized for E. coli SEQ ID NO: 2: XdPH amino acid sequence

Claims

1. A mutant L-pipecolic acid hydroxylase having an amino acid sequence represented by SEQ ID NO: 2, wherein any one of the following amino acid mutations (a) to (o) has been introduced, and having L-pipecolic acid hydroxylating activity: (a) Amino acid mutation in which glutamic acid at position 15 is replaced with alanine (b) Amino acid mutation in which isoleucine at position 28 is replaced with proline (c) Amino acid mutation in which isoleucine at position 28 is replaced with arginine (d) Amino acid mutation in which valine at position 31 is replaced by glutamic acid (e) an amino acid mutation in which cysteine ​​at position 76 is replaced with tyrosine (f) an amino acid mutation in which isoleucine at position 108 is replaced with arginine; (g) Amino acid mutation in which leucine at position 142 is replaced with arginine (h) Amino acid mutation in which leucine at position 142 is replaced by lysine (i) an amino acid mutation in which leucine at position 142 is replaced by asparagine (j) an amino acid mutation in which leucine at position 142 is replaced by glutamine (k) Amino acid mutation in which leucine at position 142 is replaced with histidine (l) Amino acid mutation in which glutamine at position 202 is replaced by proline (m) Amino acid mutation in which alanine at position 239 is replaced by aspartic acid (n) an amino acid mutation in which phenylalanine at position 246 is replaced by tyrosine (o) Amino acid mutation in which isoleucine at position 271 is replaced with glycine

2. A mutant L-pipecolic acid hydroxylase having an amino acid sequence represented by SEQ ID NO: 2 into which two types of amino acid mutations selected from the group consisting of a combination of (g) and (a); a combination of (g) and (b); a combination of (g) and (c); a combination of (g) and (d); a combination of (g) and (e); and a combination of (g) and (n) have been introduced, among the following amino acid mutations (a) to (o), and having L-pipecolic acid hydroxylating activity. (a) Amino acid mutation in which glutamic acid at position 15 is replaced with alanine (b) Amino acid mutation in which isoleucine at position 28 is replaced with proline (c) Amino acid mutation in which isoleucine at position 28 is replaced with arginine (d) Amino acid mutation in which valine at position 31 is replaced by glutamic acid (e) an amino acid mutation in which cysteine ​​at position 76 is replaced with tyrosine (f) an amino acid mutation in which isoleucine at position 108 is replaced with arginine; (g) Amino acid mutation in which leucine at position 142 is replaced with arginine (h) Amino acid mutation in which leucine at position 142 is replaced by lysine (i) an amino acid mutation in which leucine at position 142 is replaced by asparagine (j) an amino acid mutation in which leucine at position 142 is replaced by glutamine (k) Amino acid mutation in which leucine at position 142 is replaced with histidine (l) Amino acid mutation in which glutamine at position 202 is replaced by proline (m) Amino acid mutation in which alanine at position 239 is replaced by aspartic acid (n) an amino acid mutation in which phenylalanine at position 246 is replaced by tyrosine (o) Amino acid mutation in which isoleucine at position 271 is replaced with glycine

3. A mutant L-pipecolic acid hydroxylase having an amino acid sequence represented by SEQ ID NO: 2 into which three types of amino acid mutations selected from the group consisting of a combination of (g), (b), and (e); a combination of (g), (b), and (d); and a combination of (g), (b), and (n) among the following amino acid mutations (a) to (o) have been introduced, and having L-pipecolic acid hydroxylating activity. (a) Amino acid mutation in which glutamic acid at position 15 is replaced with alanine (b) Amino acid mutation in which isoleucine at position 28 is replaced with proline (c) Amino acid mutation in which isoleucine at position 28 is replaced with arginine (d) Amino acid mutation in which valine at position 31 is replaced by glutamic acid (e) an amino acid mutation in which cysteine ​​at position 76 is replaced with tyrosine (f) an amino acid mutation in which isoleucine at position 108 is replaced with arginine; (g) Amino acid mutation in which leucine at position 142 is replaced with arginine (h) Amino acid mutation in which leucine at position 142 is replaced by lysine (i) an amino acid mutation in which leucine at position 142 is replaced by asparagine (j) an amino acid mutation in which leucine at position 142 is replaced by glutamine (k) Amino acid mutation in which leucine at position 142 is replaced with histidine (l) Amino acid mutation in which glutamine at position 202 is replaced by proline (m) Amino acid mutation in which alanine at position 239 is replaced by aspartic acid (n) an amino acid mutation in which phenylalanine at position 246 is replaced by tyrosine (o) Amino acid mutation in which isoleucine at position 271 is replaced with glycine

4. A method for producing cis-5-hydroxy-L-pipecolic acid, comprising contacting L-pipecolic acid with the mutant L-pipecolic acid hydroxylase according to any one of claims 1 to 3, a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell, to produce cis-5-hydroxy-L-pipecolic acid. Method for producing si-L-pipecolic acid.

5. The cis-5-hydroxy-L-pipecolic acid according to claim 4, characterized in that the mutant L-pipecolic acid hydroxylase, a microorganism or cell capable of producing the enzyme, a processed product of the microorganism or cell, and / or a culture solution containing the enzyme obtained by culturing the microorganism or cell is contacted with L-pipecolic acid in the presence of 2-oxoglutaric acid and divalent iron ions. Method for producing phosphoric acid.

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