诱饵
化学
基质(水族馆)
分子
突变
细胞色素
组合化学
酶
生物化学
有机化学
突变
受体
基因
海洋学
地质学
作者
Joshua Kyle Stanfield,Osami Shoji
出处
期刊:Chemistry Letters
[Oxford University Press]
日期:2021-10-13
卷期号:50 (12): 2025-2031
被引量:10
摘要
Cytochrome P450BM3 is a haemoenzyme that catalyses the monooxygenation of unactivated C–H bonds. In the absence of an appropriate substrate, however, P450BM3 remains in an inactive state and catalysis does not proceed. Traditionally, mutagenesis has been the mainstay technique employed to overcome this limitation, opening P450BM3 up for non-native substrate hydroxylations. This highlight review will discuss a different approach, wherein native substrate mimics (decoy molecules) are employed to trick P450BM3 into mistakenly hydroxylating non-native substrates. This decoy molecule system has the advantage that the wild-type enzyme can be utilised, and laborious mutagenesis can be avoided. Major developments from the first discovery of decoy molecules to the present day will be briefly covered herein. Cytochrome P450BM3 is a haemoenzyme that catalyses the monooxygenation of unactivated C-H bonds with high substrate specificity. This highlight review will introduce a different approach to alter the substrate specificty of wild-type P450BM3, wherein native substrate mimics (decoy molecules) trick P450BM3 into mistakenly hydroxylating non-native substrates. Major developments from the first discovery of decoy molecules through to the present day will be briefly covered herein.
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