硝化酶
腈水合酶
酰胺
化学
酶
腈
生物化学
组合化学
酰胺酶
功能(生物学)
底物特异性
计算生物学
产量(工程)
基质(水族馆)
突变
蛋白质工程
生物催化
突变体
立体化学
催化作用
催化效率
酶分析
酶催化
药物发现
肽
活动站点
功能分析
二肽
作者
Shuiqin Jiang,Zhelin ZHENG,Hua Dong,Siwei Zhang,Qi Tong,Dong Yi
标识
DOI:10.1021/acs.jafc.5c14148
摘要
Catalytic promiscuity provides fundamental insights into enzyme evolution. To address the multiobjective challenges in discovering and evolving promiscuous activities, we developed EnzySFC, an AI-assisted platform that combines de novo enzyme discovery with functional evolution, enabling coordinated optimization of activity and specificity. Using EnzySFC, we experimentally validated 10 uncharacterized nitrilases from 1113 candidates: 90% showed catalytic activity toward the target substrate, and 80% demonstrated amide formation. Notably, a wild-type nitrilase from a Phototrophicales bacterium exhibited exclusive nitrile hydratase activity. Through AI-driven evolution, 16 mutants of a nitrilase from an Actinomycetia bacterium were experimentally verified within a single prediction cycle. Seven variants displayed increased amide production, five of which exceeded 80% amide proportion. The top four variants achieved a 100% amide yield with complete substrate conversion. This platform establishes a transferable framework for multiobjective enzyme engineering and accelerates the development of efficient enzyme catalysts.
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