Expansion of chemical space for natural products by uncommon P450 reactions

被引:152
作者
Zhang, Xingwang [1 ]
Li, Shengying [1 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Shandong Prov Key Lab Synthet Biol, CAS Key Lab Biofuels, Qingdao 266101, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
FLAVIOLIN SUBSTRATE MOLECULES; STREPTOMYCES-COELICOLOR A3(2); TROPANE ALKALOID BIOSYNTHESIS; FATTY-ACID DECARBOXYLASE; PHENOL COUPLING REACTION; CYTOCHROME-P450; MONOOXYGENASE; MULTIFUNCTIONAL CYTOCHROME-P450; VANCOMYCIN BIOSYNTHESIS; COMBINATORIAL BIOSYNTHESIS; POLYKETIDE SYNTHASE;
D O I
10.1039/c7np00028f
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
C Cytochrome P450 enzymes (P450s) are the most versatile biocatalysts in nature. The catalytic competence of these extraordinary hemoproteins is broadly harnessed by numerous chemical defenders such as bacteria, fungi, and plants for the generation of diverse and complex natural products. Rather than the common tailoring reactions (e.g. hydroxylation and epoxidation) mediated by the majority of biosynthetic P450s, in this review, we will focus on the unusual P450 enzymes in relation to new chemistry, skeleton construction, and structure re-shaping via their own unique catalytic power or the intriguing protein-protein interactions between P450s and other proteins. These uncommon P450 reactions lead to a higher level of chemical space expansion for natural products, through which a broader spectrum of bioactivities can be gained by the host organisms.
引用
收藏
页码:1061 / 1089
页数:29
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