摘要
Aromatic aldehydes are important industrial raw materials mainly synthesized by anti-Markovnikov (AM) oxidation of corresponding aromatic olefins. The AM product selectivity remains a big challenge. P450 aMOx is the first reported enzyme that could catalyze AM oxidation of aromatic olefins. Here, we reported a rational design strategy based on the “butterfly” model of the active site of P450 aMOx. Constrained molecular dynamic simulations and a binding energy analysis of key residuals combined with an experimental alanine scan were applied. As a result, the mutant A275G showed high AM selectivity of >99%. The results also proved that the “butterfly” model is an effective design strategy for enzymes.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 888721 |
| 期刊 | Frontiers in Molecular Biosciences |
| 卷 | 9 |
| DOI | |
| 出版状态 | 已出版 - 23 5月 2022 |
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