Use of stereoselective transaminase in asymmetric synthesis of chiral amine
Use of a stereoselective transaminase in the asymmetric synthesis of a chiral amine. In particular, provided is use of a polypeptide in the production of a chiral amine or a downstream product using a chiral amine as a precursor. Further provided is a method for producing a chiral amine, comprising culturing a strain expressing the polypeptide so as to obtain a chiral amine. Further provided are a chiral amine production strain and a method for constructing the chiral amine production strain. The stereoselective transaminase has a broad substrate spectrum and thus has a broad application potential in the preparation of a chiral amine.
1. A method for producing a chiral amine, comprising:
(a) carrying out a reaction shown in equation Ito form a chiral amine in a liquid reaction system, using a prochiral carbonyl compound as a substrate, reacting the substrate with an amino donor in the presence of a prosthetic group and under the catalysis of a stereoselective transaminase; and
(b) isolating the chiral amine from the reaction system after carrying out the reaction in (a), wherein the stereoselective transaminase has an amino acid sequence having at least 90% sequence identity to the amino acid sequence shown in SEQ ID NO: 1; and
wherein the prochiral carbonyl compound comprises any one of compounds 6- 8, or a pharmaceutically acceptable salt thereof:
2. The method of claim 1 , wherein the chiral amine is used as a precursor for producing sitagliptin and the precursor is selected from group consisting of compound 6a, compound 7a, and compound 8a.
3. The method of claim 1 , wherein the chiral amine produced comprises any one of compounds 6a-8a or a pharmaceutically acceptable salt thereof:
4. The method according to claim 1 , wherein the amino donor comprises α-phenethylamine, β-aminobutyric acid, glycine, or isopropylamine.
5. The method according to claim 1 , wherein the prochiral carbonyl compound is selected from the group consisting of compounds 6-8,
and wherein the chiral amine produced is used as a precursor for producing sitagliptin.
6. A method for producing a chiral amine, comprising the steps of:
1) culturing a chiral amine producing Escherichia bacterial strain comprising a modification to express an R-selective-ω-transaminase having an amino acid sequence having at least 90% sequence identity to the amino acid sequence shown in SEQ ID NO: 1 under production conditions sufficient to induce the expression of the (R)-selective-ω-transaminase;
2) homogenizing and disrupting the cultured chiral amine producing Escherichia bacterial strain;
3) adding the disrupted cultured chiral amine producing Escherichia bacterial strain to a liquid reaction system comprising a prochiral carbonyl compound and an amino donor;
4) carrying out the reaction in the liquid reaction system to obtain the chiral amine; and
5) isolating the chiral amine from the liquid reaction system of 4); and
wherein the prochiral carbonyl compound comprises any one of compounds 6-8, or a pharmaceutically acceptable salt thereof:
7. The method for producing a chiral amine according to claim 6 , wherein the amino donor comprises α-phenethylamine, β-aminobutyric acid, glycine, or isopropylamine.
8. The method of claim 6 , wherein the modification to express an R-selective-ω-transaminase is expression of a full-length transaminase gene selected from the group consisting of a nucleotide sequence having at least 90% sequence identity to the sequence shown in SEQ ID NO: 2 and a complementary sequence thereof.