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人工金属酶的定向进化:催化活性的遗传优化

Directed Evolution of Artificial Metalloenzymes: Genetic Optimization of the Catalytic Activity.

作者信息

Hestericová Martina

机构信息

Department of Chemistry, University of Basel, Mattenstrasse 24a, BPR 1096, CH-4002 Basel, Switzerland.

出版信息

Chimia (Aarau). 2018 Apr 25;72(4):189-192. doi: 10.2533/chimia.2018.189.

Abstract

Artificial metalloenzymes (ArMs) based on the incorporation of a biotinylated metal cofactor within a streptavidin (Sav) combine attractive features of both enzymatic and homogeneous catalysis. To speed up their optimization, we present a directed evolution of an artificial transfer hydrogenase (ATHase) based on a stream-lined and optimized protocol for the design, overexpression and screening of Sav isoforms. Ten positions have been subjected to mutagenesis to yield two variants with improved catalytic activity and selectivity for the reduction of cyclic imines, along with greater stability in a biphasic medium.

摘要

基于在链霉亲和素(Sav)中掺入生物素化金属辅因子的人工金属酶(ArM)结合了酶催化和均相催化的诱人特性。为了加速其优化,我们提出了一种基于简化和优化方案的人工转移氢化酶(ATHase)的定向进化方法,用于Sav异构体的设计、过表达和筛选。对十个位点进行了诱变,以产生两个变体,它们对环状亚胺的还原具有更高的催化活性和选择性,并且在双相介质中具有更高的稳定性。

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