Biosynthesis-based artificial evolution of microbial natural products

被引:6
|
作者
Lin, Zhi [1 ]
Chen, Dandan [2 ]
Liu, Wen [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
[2] Huzhou Ctr Biosynthet Innovat, Huzhou 313000, Peoples R China
基金
中国国家自然科学基金;
关键词
biosynthesis; artificial evolution; RiPPs; NRPS; PKS; enzymatic diversity; ERYTHROMYCIN POLYKETIDE SYNTHASE; GLYCOSYLTRANSFERASE-CATALYZED REACTIONS; CROTONYL-COA CARBOXYLASE/REDUCTASE; NONRIBOSOMAL PEPTIDE ANTIBIOTICS; PREPEPTIDE GENE REPLACEMENT; THIOPEPTIDE ANTIBIOTICS; EXTENDER UNITS; MUTATIONAL BIOSYNTHESIS; ACYLTRANSFERASE DOMAIN; SUBSTRATE-SPECIFICITY;
D O I
10.1007/s11426-016-0062-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Natural products are often secondary metabolites in living organisms with a wide variety of biological activities. The diversification of their structures, aiming to the search for biologically active small molecules by expanding chemical and functional spaces, is a major area of current interest in synthetic chemistry. However, developing synthetic accessibility and efficiency often faces challenges associated with structural complexity. Synthetic biology has recently emerged and is promising to accomplish complex molecules; by contrast, the application to structural diversification of natural products relies on the understanding, development and utilization of compatible biosynthetic machinery. Here, we review the strategies primarily concerning the artificial evolution of microbial natural products whose biosynthesis features template enzymology, including ribosomally synthesized and post-translationally modified peptides as well as the assembly line-resultant polyketides, non-ribosomal peptides and hybrids. The establishment of these approaches largely facilitates the expansion of the molecular diversity and utility through bioengineering at different stages/levels of biosynthetic pathways.
引用
收藏
页码:1175 / 1187
页数:13
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