孕烯醇酮
肾上腺毒素
胆固醇侧链裂解酶
细胞色素
雅罗维亚
细胞色素P450
生物化学
类固醇
代谢工程
喜树酯
泛醇
生物
化学
甾醇
酶
胆固醇
细胞色素c
辅酶Q-细胞色素c还原酶
基因
线粒体
激素
作者
Ruosi Zhang,Yu Zhang,Ying Wang,Mingdong Yao,Jinlai Zhang,Hong Liu,Xiao Zhou,Wenhai Xiao,Ying‐Jin Yuan
标识
DOI:10.1021/acssynbio.9b00018
摘要
Microbial production of steroid drugs exhibits great potentials in much greener and more sustainable manners, in which engineering multiple cytochrome P450s is the prerequisite requirement. The pairing of multicomponents of P450 systems is a tremendous challenge. Herein, biosynthesis of pregnenolone (a common precursor of steroid drugs) in Yarrowia lipolytica was taken as a typical instance to explore the engineering strategy of the cytochrome P450 side-chain cleavage enzyme (P450scc) system. The mature forms of the components belonging to P450scc system, CYP11A1, adrenodoxin (Adx), and adrenodoxin reductase (AdR), were coexpressed in a former constructed campesterol producing strain. To maximize pregnenolone production, an integrative components pairing strategy was proposed for pairing the component sources and balancing the expression levels of CYP11A1, Adx, and AdR. Led by the above approaches, a 2344-fold improvement of pregnenolone titer was achieved at the shake flask level. Consequently, a highest reported pregnenolone titer of 78.0 mg/L in microbes was obtained in a 5 L bioreactor. Our study not only highlights the integrative components pairing of cytochrome P450scc as a general strategy for engineering other cytochrome P450s, but also provides a feasible and efficient platform of Y. lipolytica for other steroids production.
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