Salinipyrone and Pacificanone Are Biosynthetic By-products of the Rosamicin Polyketide Synthase

被引:20
作者
Awakawa, Takayoshi [1 ,2 ]
Cruesemann, Max [1 ]
Munguia, Jason [3 ]
Ziemert, Nadine [1 ]
Nizet, Victor [3 ,4 ]
Fenical, William [1 ]
Moore, Bradley S. [1 ,4 ]
机构
[1] Univ Calif San Diego, Ctr Marine Biotechnol & Biomed, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[3] Univ Calif San Diego, Pediat, San Diego, CA 92093 USA
[4] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, San Diego, CA 92093 USA
关键词
biosynthesis; macrolide antibiotics; polyketide synthases; Salinispora; ACTINOMYCETE GENUS SALINISPORA; X-RAY CRYSTALLOGRAPHY; MACROLIDE ANTIBIOTICS; ABSOLUTE-CONFIGURATION; CYTOCHROME-P450; MYCINAMICINS; MACROLACTONE; DIVERSITY; MODEL; MYCG;
D O I
10.1002/cbic.201500177
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
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.
引用
收藏
页码:1443 / 1447
页数:5
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