硝化酶
化学
腈
生物催化
组合化学
高通量筛选
酶
羧酸
基因组
计算生物学
有机化学
生物化学
催化作用
基因
反应机理
生物
作者
Carine Vergne‐Vaxelaire,Franck Bordier,Aurélie Fossey,Marielle Besnard‐Gonnet,Adrien Debard,Aline Mariage,Virginie Pellouin,Alain Perret,Jean‐Louis Petit,Mark Stam,Marcel Salanoubat,Jean Weissenbach,Véronique de Berardinis,Anne Zaparucha
标识
DOI:10.1002/adsc.201201098
摘要
Abstract A high‐throughput screening of candidate nitrilases against 25 structurally diverse substrates allowed us to create a wide collection of 125 experimentally validated nitrilases. The enzymes were selected by genomic approach from 700 diverse prokaryotic species and one metagenome as representative of the nitrilase family diversity. The enzymatic screening of this collection expands the biocatalytic toolbox for chemical synthesis by providing a large number of tested nitrilases with their assigned substrates. Three examples illustrate the synthetic potential of our enzyme collection. The syntheses of carboxylic acid building blocks, a β‐substituted phenylpropanoic acid, a cyclic γ‐keto carboxylic acid and a mononitrile monocarboxylic acid, were achieved from the corresponding nitrile substrates, using three new nitrilases (two from Sphingomonas wittichii and one from Syntrophobacter fumaroxidans). Improvements of nitrilase activities through the optimization of reaction parameters and the preparative biocatalytic synthesis are presented for these three examples.
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