IP Library Granted Patent US 10,954,539
Granted Patent B2
US 10,954,539 · App. 15/765,148 · Granted Mar 23, 2021

Method for producing hydroxy-L-pipecolic acid

Inventors: Ryoma Miyake (Tokyo, JP); Hiroshi Kawabata (Tokyo, JP)
Assignee: API CORPORATION
C12P17/12C12N9/0016C12N9/0022C12N9/0071C12N9/1096C12Y114/11028C12N15/09
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Quick Facts
Patent No.
US 10,954,539
App. No.
15/765,148
Granted
Mar 23, 2021
Kind
B2
Abstract

A novel method of producing high-purity hydroxy-L-pipecolic acids in an efficient and inexpensive manner while suppressing the production of hydroxy-L-proline is provided. The method includes allowing an L-pipecolic acid hydroxylase, a microorganism or cell having the ability to produce the enzyme, a processed product of the microorganism or cell, and/or a culture liquid comprising the enzyme and obtained by culturing the microorganism or cell, to act on L-pipecolic acid as a substrate in the presence of 2-oxoglutaric acid and ferrous ion, wherein the L-pipecolic acid hydroxylase has the properties: (1) the enzyme can act on L-pipecolic acid in the presence of 2-oxoglutaric acid and ferrous ion to add a hydroxy group to the carbon atom at positions 3, 4, and/or 5 of L-pipecolic acid; and (2) the enzyme has a catalytic efficiency (kcat/Km) with L-proline that is equal to or less than 7 times the catalytic efficiency (kcat/Km) with L-pipecolic acid.

Claims (25)

1. A method of producing a hydroxy-L-pipecolic acid, the method comprising:

allowing an L-pipecolic acid hydroxylase, a microorganism or cell having the ability to produce the enzyme, a processed product of the microorganism or cell comprising the enzyme, and/or a culture liquid comprising the enzyme and obtained by culturing the microorganism or cell, to act on L-pipecolic acid as a substrate in the presence of 2-oxoglutaric acid and ferrous ion, wherein the L-pipecolic acid hydroxylase has the properties (1) and (2) below:

(1) the enzyme can act on L-pipecolic acid in the presence of 2-oxoglutaric acid and ferrous ion to add a hydroxy group to the carbon atom at positions 3, 4, and/or 5 of L-pipecolic acid; and

(2) the enzyme has a catalytic efficiency (kcat/Km) with L-proline that is equal to or less than 7 times the catalytic efficiency (kcat/Km) with L-pipecolic acid,

wherein the content of L-proline in the L-pipecolic acid as the substrate is not more than 10% (w/w), and

wherein the L-pipecolic acid hydroxylase comprises the protein (A), (B), or (C) below:

(A) a protein having an amino acid sequence of SEQ ID NO: 18 or 20;

(B) a protein having an amino acid sequence with an identity of not less than 95% to the amino acid sequence of SEQ ID NO: 18, which protein has the aforementioned properties (1) and (2);

(C) a protein having an amino acid sequence with an identity of not less than 95% to the amino acid sequence of SEQ ID NO: 20 and which comprises at least one of a tyrosine residue at position 5, an alanine residue at position 23 and/or a glutamic acid residue at position 282, which protein has the aforementioned properties (1) and (2).

2. The method of producing a hydroxy-L-pipecolic acid according to claim 1 , further comprising:

allowing L-lysine and/or DL-lysine to react with

(i-1) one or more enzymes selected from the group consisting of an L-amino acid oxidase, an L-amino acid dehydrogenase and an L-amino acid aminotransferase, or

(i-2) an amino acid racemase and one or more enzymes selected from the group consisting of a D-amino acid oxidase, a D-amino acid dehydrogenase and a D-amino acid aminotransferase,

for the production of 3,4,5,6-tetrahydropyridine-2-carboxylic acid; and subsequently

allowing an N-methyl-L-amino acid dehydrogenase to act on the 3,4,5,6-tetrahydropyridine-2-carboxylic acid for the production of the L-pipecolic acid as the substrate.

3. The method of producing a hydroxy-L-pipecolic acid according to claim 1 , further comprising:

allowing L-lysine to react with one or more enzymes selected from the group consisting of an L-lysine 6-oxidase, an L-lysine 6-dehydrogenase and an L-lysine 6-aminotransferase, for the production of 2,3,4,5-tetrahydropyridine-2-carboxylic acid; and subsequently

allowing a pyrroline-5-carboxylate reductase to act on the 2,3,4,5-tetrahydropyridine-2-carboxylic acid for the production of the L-pipecolic acid as the substrate.

4. The method of producing a hydroxy-L-pipecolic acid according to claim 1 , further comprising allowing a lysine cyclodeaminase to act on L-lysine for the production of the L-pipecolic acid as the substrate.

5. The method of producing a hydroxy-L-pipecolic acid according to claim 1 , wherein the L-pipecolic acid is contacted with a microorganism or cell having the ability to produce the L-pipecolic acid hydroxylase, and wherein the microorganism or cell having the ability to produce the L-pipecolic acid hydroxylase, or the processed product of the microorganism or cell has a hydroxy-L-proline-producing activity that is not more than 55%, where a ratio of 100% corresponds to the hydroxy-L-pipecolic acid-producing activity of the same microorganism or cell, or of the same processed product.

6. The method of producing a hydroxy-L-pipecolic acid according to claim 1 , wherein the L-pipecolic acid is contacted with a microorganism or cell having the ability to produce the L-pipecolic acid hydroxylase, wherein the microorganism or cell having the ability to produce the L-pipecolic acid hydroxylase is a microorganism or cell transformed with DNA encoding the L-pipecolic acid hydroxylase, and

wherein the DNA encoding the L-pipecolic acid hydroxylase comprises the DNA (D), (E), or (F) below:

(D) DNA having a nucleotide sequence of SEQ ID NO: 17 or 19;

(E) DNA comprising a nucleotide sequence which hybridizes with a complementary strand of the nucleotide sequence of SEQ ID NO: 17 under stringent conditions, wherein the conditions comprise a hybridization at 65° C. in the presence of 0.7 mol/L to 1.0 mol/L sodium chloride aqueous solution and a washing under a temperature condition of 65° C. by using one solution with an SSC concentration of 0.1×SSC (the composition of 1×SSC: 150 mmol/L sodium chloride aqueous solution, 15 mmol/L sodium citrate aqueous solution), which DNA encodes a protein having the aforementioned properties (1) and (2);

(F) DNA comprising a nucleotide sequence which hybridizes with a complementary strand of the nucleotide sequence of SEQ ID NO: 19 under stringent conditions, wherein the conditions comprise a hybridization at 65° C. in the presence of 0.7 mol/L to 1.0 mol/L sodium chloride aqueous solution and a washing under a temperature condition of 65° C. by using one solution with an SSC concentration of 0.1×SSC (the composition of 1×SSC: 150 mmol/L sodium chloride aqueous solution, 15 mmol/L sodium citrate aqueous solution), which DNA encodes a protein having the aforementioned properties (1) and (2) and comprising at least one of a tyrosine residue at position 5, an alanine residue at position 23 and/or a glutamic acid residue at position 282.

Assignments (3)
CHANGE OF ADDRESS Recorded Aug 21, 2025
From: API CORPORATION
To: API CORPORATION
Reel/Frame 072498/0511 →
MERGER Recorded Aug 21, 2025
From: API CORPORATION
To: UBE CORPORATION
Reel/Frame 072554/0211 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2018
From: MIYAKE, RYOMA; KAWABATA, HIROSHI
To: API CORPORATION
Reel/Frame 045906/0418 →
Priority Claims (1)
JP 2015-197231 · Oct 2, 2015 · national
Continuity (1)
Related Publication 20180273993A1 · Sep 27, 2018