化学
类固醇
羟基化
单加氧酶
过氧化氢
突变
辅因子
蛋白质工程
生物化学
组合化学
合理设计
催化作用
立体化学
部分
细胞色素P450
醇脱氢酶
生物催化
机制(生物学)
动力学
电子转移
酶
对接(动物)
定向进化
劈理(地质)
活动站点
酶催化
氧化还原酶
细胞色素
催化循环
作者
Xiao-Dong Zhang,Yongchao Wang,Xiaoqing Jiang,Di Deng,Qian Li,Binju Wang,Aitao Li
标识
DOI:10.1021/acs.jafc.5c11530
摘要
Cytochrome P450 CYP109B4 is a characterized 16β-steroid hydroxylase with significant potential in steroid drug biosynthesis, but its application is limited by reliance on costly coenzymes and complex electron transfer processes. To address this, we constructed a hydrogen peroxide (H2O2)-driven catalytic system through structure-guided engineering. Screening a combinatorial variant library identified the L240V/S387F double mutant, which exhibited emergent peroxygenase activity (baseline TTN = 11). Using focused rational iterative site-specific mutagenesis (FRISM), we obtained optimized variant B4-Pm9 exhibiting a 4-fold higher total turnover number (TTN = 44). Coupling with an alcohol dehydrogenase (Aldo)-based H2O2 regeneration system further enhanced catalytic efficiency, achieving a TTN of 348 (31-fold improvement over L240V/S387F mutant). Computational studies revealed the H2O2 activation mechanism in Pm7 and Pm9. Notably, variant B4-Pm7 demonstrated a novel mechanism of H2O2 cleavage mediated by the "alcohol-hydroxyl" moiety, showcasing a significant breakthrough in the realm of P450 peroxygenase.
科研通智能强力驱动
Strongly Powered by AbleSci AI