详细信息

Asymmetric bioreduction of γ- and δ-keto acids by native carbonyl reductases from Saccharomyces cerevisiae    

文献类型:期刊文献

中文题名:Asymmetric bioreduction of γ- and δ-keto acids by native carbonyl reductases from Saccharomyces cerevisiae

作者:Chunlei Ren[1];Tao Wang[1];Xiaoyan Zhang[1];Jiang Pan[1];Jianhe Xu[1,2];Yunpeng Bai[1,2]

机构:[1]State Key Laboratory of Bioreactor Engineering,East China University of Science and Technology,Shanghai 200237,China;[2]Shanghai Collaborative Innovation Centre for Biomanufacturing,East China University of Science and Technology,Shanghai 200237,China

年份:2021

卷号:34

期号:1

起止页码:305

中文期刊名:Chinese Journal of Chemical Engineering

外文期刊名:中国化学工程学报(英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2021_2022】;

基金:financially sponsored by the National Key Research and Development Program of China (2016YFA0204300, 2019YFA09005000);the National Natural Science Foundation of China (21536004, 21776085, 21871085);the Natural Science Foundation of Shanghai (18ZR1409900);Key Project of the Shanghai Science and Technology Committee (18DZ1112703);the Fundamental Research Funds for the Central Universities (WF1714026)。

语种:英文

中文关键词:Keto acids/esters;(R)-γ-/δ-Decalactones;Carbonyl reductase;Asymmetric reduction;Saccharomyces cerevisiae

摘要:Optically pure(R)-γ-and(R)-δ-lactones can be prepared by intramolecular cyclization of chiral hydroxy acids/esters reduced asymmetrically from γ-and δ-keto acids/esters using Saccharomyces cerevisiae(S.cerevisiae) as a whole-cell biocatalyst.However,some of the enzymes catalyzing these reactions in S.cerevisiae are still unknown up to date.In this report,two carbonyl reductases,OdCRl and OdCR2,were successfully discovered,and cloned from S.cerevisiae using a genome-mining approach,and overexpressed in Escherichia coli(E.coli).Compared with OdCR1,OdCR2 can reduce 4-oxodecanoic acid and 5-oxodecanoic acid asymmetrically with higher stereoselectivity,generating(R)-γ-decalactone(99% ee) and(R)-δ-decalactone(98% ee) in 85% and 92%yields,respectively.This is the first report of native enzymes from S.cerevisiae for the enzymatic synthesis of chiral γ-and δ-lactones which is of wide uses in food and cosmetic industries.

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