Wang_2024_Enzyme.Microb.Technol_176_110411

Reference

Title : Biomanufacture of L-homoserine lactone building block: A strategy for preparing gamma-substituted L-amino acids by modular reaction - Wang_2024_Enzyme.Microb.Technol_176_110411
Author(s) : Wang Y , Wu M , Zheng H , Wu D , Yao P , Li W , Jin K , Yu X
Ref : Enzyme Microb Technol , 176 :110411 , 2024
Abstract :

A strain high-performance of esterase producing bacteria was screened from soil, which could selectively hydrolyze D-homoserine lactone from its racemate to achieve the resolution of L- homoserine lactone with more than 99% e.e. in 48% yield. L-homoserine lactone building block was then converted to L-alpha-amino-gamma-bromobutyronic acid chiral blocks, which reacted with various nucleophilic reagent modules could to be applied to prepare L-gamma- substituted alpha-amino acids such as L-selenomethionine, L-methionine, L-glufosinate and L-selenocystine. Its advantages included high selectivity of biocatalytic resolution reactions, high optical purity of products, racemic recycle of D-substrates and modular reaction, which simplified the production process of these products and highlighted the power of biological manufacturing.

PubMedSearch : Wang_2024_Enzyme.Microb.Technol_176_110411
PubMedID: 38377656

Related information

Citations formats

Wang Y, Wu M, Zheng H, Wu D, Yao P, Li W, Jin K, Yu X (2024)
Biomanufacture of L-homoserine lactone building block: A strategy for preparing gamma-substituted L-amino acids by modular reaction
Enzyme Microb Technol 176 :110411

Wang Y, Wu M, Zheng H, Wu D, Yao P, Li W, Jin K, Yu X (2024)
Enzyme Microb Technol 176 :110411