诱饵
化学
细胞色素
分子
细胞色素P450
基质(水族馆)
催化作用
生物化学
突变
酶
组合化学
立体化学
生物物理学
有机化学
突变
基因
海洋学
地质学
受体
生物
作者
Osami Shoji,Yoshihito Watanabe
标识
DOI:10.1002/ijch.201400096
摘要
Abstract To bring out the potential of wild‐type cytochrome P450s, we have developed a series of “decoy molecules” to change their high substrate specificity without any mutagenesis. Decoy molecules are inert dummy substrates with structures that are very similar to those of natural substrates. The decoy molecules force long‐alkyl‐chain fatty acid hydroxylases (P450 BSβ , P450 SPα , and P450BM3) to generate the active species and to catalyze oxidation of various substrates other than fatty acids. Interestingly, the catalytic activity was highly dependent on the structure of decoy molecules. Furthermore, the enantioselectivity of reactions catalyzed by P450 BSβ and P450 SPα was also dependent on the structure of decoy molecules. The decoy molecule system allows us to control reactions catalyzed by wild‐type enzymes by designing decoy molecules.
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