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微生物拜耳-维利格氧化反应:通过定向进化制备的环己酮单加氧酶突变体的立体选择性和底物接受性

Microbial Baeyer-Villiger oxidation: stereopreference and substrate acceptance of cyclohexanone monooxygenase mutants prepared by directed evolution.

作者信息

Mihovilovic Marko D, Rudroff Florian, Winninger Alexander, Schneider Toni, Schulz Frank, Reetz Manfred T

机构信息

Vienna University of Technology, Institute of Applied Synthetic Chemistry, Getreidemarkt 9/163-OC, A-1060 Vienna, Austria.

出版信息

Org Lett. 2006 Mar 16;8(6):1221-4. doi: 10.1021/ol0601040.

Abstract

[reaction: see text] An array of random mutants of cyclohexanone monooxygenase (CHMO) from Acinetobacter sp. NCIMB 9871 was screened against a library of structurally diverse ketones for modifications in the substrate acceptance profile and stereopreference of the enzymatic Baeyer-Villiger biooxidation. While the set of mutant biocatalysts was initially evolved for the enantiocomplementary oxidation of 4-hydroxycyclohexanone, improved and/or divergent stereoselectivities were observed for several substrates. In addition, expanded substrate acceptance to facilitate biotransformation of sterically demanding ketones was found.

摘要

[反应:见正文] 针对一系列结构多样的酮类文库,筛选了不动杆菌属NCIMB 9871中环己酮单加氧酶(CHMO)的随机突变体阵列,以研究酶促拜耳-维利格生物氧化反应中底物接受谱和立体选择性的变化。虽然最初开发这组突变生物催化剂是用于4-羟基环己酮的对映互补氧化反应,但对几种底物观察到了提高的和/或不同的立体选择性。此外,还发现扩大了底物接受范围,以促进空间位阻较大的酮的生物转化。

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