Iterative polyketide biosynthesis by modular polyketide synthases in bacteria

被引:82
|
作者
Chen, Haotong [1 ]
Du, Liangcheng [1 ]
机构
[1] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
关键词
Biosynthesis; Natural products; Polyketides; Type I PKS; Iterative PKS; STREPTOMYCES VIRIDOCHROMOGENES TU57; POLYCYCLIC TETRAMATE MACROLACTAMS; SORANGIUM-CELLULOSUM SO-CE90; NATURAL-PRODUCT BIOSYNTHESIS; ANTITUMOR ANTIBIOTIC C-1027; POLYUNSATURATED FATTY-ACIDS; GENE-CLUSTER; ASSEMBLY-LINE; IKARUGAMYCIN BIOSYNTHESIS; LYSOBACTER-ENZYMOGENES;
D O I
10.1007/s00253-015-7093-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Modular polyketide synthases (type I PKSs) in bacteria are responsible for synthesizing a significant percentage of bioactive natural products. This group of synthases has a characteristic modular organization, and each module within a PKS carries out one cycle of polyketide chain elongation; thus each module is non-iterative in function. It was possible to predict the basic structure of a polyketide product from the module organization of the PKSs, since there generally existed a co-linearity between the number of modules and the number of chain elongations. However, more and more bacterial modular PKSs fail to conform to the canonical rules, and a particularly noteworthy group of non-canonical PKSs is the bacterial iterative type I PKSs. This review covers recent examples of iteratively used modular PKSs in bacteria. These non-canonical PKSs give rise to a large array of natural products with impressive structural diversity. The molecular mechanism behind the iterations is often unclear, presenting a new challenge to the rational engineering of these PKSs with the goal of generating new natural products. Structural elucidation of these synthase complexes and better understanding of potential PKS-PKS interactions as well as PKS-substrate recognition may provide new prospects and inspirations for the discovery and engineering of new bioactive polyketides.
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页码:541 / 557
页数:17
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