聚酮合酶
聚酮
生物合成
基因簇
生物
突变
天然产物
计算生物学
酶
基因
生物化学
突变
作者
Takayoshi Awakawa,Max Crüsemann,Jason Munguia,Nadine Ziemert,Victor Nizet,William Fenical,Bradley S. Moore
出处
期刊:ChemBioChem
[Wiley]
日期:2015-04-30
卷期号:16 (10): 1443-1447
被引量:25
标识
DOI:10.1002/cbic.201500177
摘要
Salinipyrones and pacificanones are structurally related polyketides from Salinispora pacifica CNS-237 that are proposed to arise from the same modular polyketide synthase (PKS) assembly line. Genome sequencing revealed a large macrolide PKS gene cluster that codes for the biosynthesis of rosamicin A and a series of new macrolide antibiotics. Mutagenesis experiments unexpectedly correlated salinipyrone and pacificanone biosynthesis to the rosamicin octamodule Spr PKS. Remarkably, this bifurcated polyketide pathway illuminates a series of enzymatic domain- and module-skipping reactions that give rise to natural polyketide product diversity. Our findings enlarge the growing knowledge of polyketide biochemistry and illuminate potential challenges in PKS bioengineering.
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