Method for enzymatic preparation of R-3 aminobutyric acid
An R-3-aminobutyric acid preparation method with high efficiency and high stereoselectivity. The method comprises using aspartase with stereoisomerization catalytic activity derived from Escherichia coli to efficiently convert butenoic acid into R-3-aminobutyric acid. After only 24 h of reaction, the conversion rate is as high as ≥98%, and the ee value is ≥99.9%. The conversion efficiency is greatly improved, the reaction time is shortened, and the production costs are reduced. The method features a high yield, a high conversion rate, low costs, a short production cycle, a simple process, ease of enlargement, suitability for mass production and the like.
1. A method for producing an R-3-aminobutyric acid comprising the steps of:
(1) using butenoic acid as a substrate and carrying out a stereoisomeric catalytic reaction shown in equation I to form the R-3-aminobutyric acid under the catalysis of an aspartase in a reaction system;
(b) optionally, isolating the R-3-aminobutyric acid from the reaction system after the reaction of the step (1);
wherein, the aspartase is obtained from E. coli , and
the aspartase is a mutant having 90% sequence identity to the amino acid sequence of SEQ ID NO: 5 which has two to four amino acid mutations in the amino acid sequence corresponding to the wild type aspartase shown in SEQ ID NO: 5, wherein the amino acid mutation is selected from the group consisting of threonine (T) at position 204, methionine (M) at position 338, Lysine (K) at position 341, asparagine (N) at position 343, or a combination thereof.
2. The method of claim 1 , wherein the ee value of the R-3-aminobutyric acid is ≥99.5%, and/or the conversion rate of the reaction is ≥90%.
3. The method of claim 1 , wherein the mutation in the mutant is selected from the group consisting of T204C, M338I, K341M, N343C, or a combination thereof.
4. A method for producing an R-3-aminobutyric acid comprising the steps of:
1) culturing a production strain under production conditions to obtain an R-3-aminobutyric acid;
2) optionally, isolating the R-3-aminobutyric acid from the culture system of 1),
wherein the production strain is an R-3-aminobutyric acid production strain expressing a polypeptide, and the polypeptide is an exogenous aspartase obtained from E. coli and is used to catalyze the stereoisomeric catalytic reaction as below:
wherein the exogenous aspartase is a mutant having 90% sequence identity to the amino acid sequence of SEQ ID NO: 5 which has two to four amino acid mutations in the amino acid sequence corresponding to the wild type aspartase shown in SEQ ID NO: 5, wherein the amino acid mutation is selected from the group consisting of threonine (T) at position 204, methionine (M) at position 338, Lysine (K) at position 341, asparagine (N) at position 343, or a combination thereof.
5. The method of claim 1 , wherein the aspartase has the amino acid sequence as shown in SEQ ID NO: 3.
6. The method of claim 4 , wherein the aspartase has the amino acid sequence as shown in SEQ ID NO: 3.