Bringing out the Potential of Wild-type Cytochrome P450s using Decoy Molecules: Oxygenation of Nonnative Substrates by Bacterial Cytochrome P450s

被引:17
|
作者
Shoji, Osami [1 ]
Watanabe, Yoshihito [2 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Dept Chem, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, Res Ctr Mat Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
关键词
bacterial cytochrome P450; biocatalysis; decoy molecule; hydroxylation; substrate misrecognition; ACID ALPHA-HYDROXYLASE; HYDROGEN-PEROXIDE; PERFLUOROCARBOXYLIC ACIDS; SPHINGOMONAS-PAUCIMOBILIS; BACILLUS-SUBTILIS; CRYSTAL-STRUCTURE; ELECTRON-TRANSFER; FATTY-ACIDS; PHENOL; BENZENE;
D O I
10.1002/ijch.201400096
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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(BS beta), P450(SP alpha), and P450BM3) to generate the active species and to catalyze oxidation of various sub-strates 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(BS beta) and P450(SP alpha) 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.
引用
收藏
页码:32 / 39
页数:8
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