Department of Chemistry, Center of Chemistry for Frontier Technologies, Zhejiang University, Hangzhou, 310027, China.
College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing, 314001, China.
Angew Chem Int Ed Engl. 2021 Apr 19;60(17):9326-9329. doi: 10.1002/anie.202100534. Epub 2021 Mar 12.
The reliable design and prediction of enzyme promiscuity to access transformations not observed in nature remains a long-standing challenge. Herein, we present the first example of an intramolecular stereoselective Stetter reaction catalyzed by benzaldehyde lyase, guided by the rational structure screening of various ThDP-dependent enzymes using molecular dynamics (MD) simulations. After optimization, high productivity (up to 99 %) and stereoselectivity (up to 99:1 e.r.) for this novel enzyme function was achieved.
可靠地设计和预测酶的杂化活性,以实现自然界中未观察到的转化,仍然是一个长期存在的挑战。在此,我们通过使用分子动力学(MD)模拟对各种依赖于 ThDP 的酶进行合理的结构筛选,首次展示了苯甲醛裂解酶催化的分子内立体选择性 Stetter 反应的实例。经过优化,这种新酶功能的生产效率(高达 99%)和立体选择性(高达 99:1 e.r.)都很高。