Type III polyketide synthase β-ketoacyl-ACP starter unit and ethylmalonyl-CoA extender unit selectivity discovered by Streptomyces coelicolor genome mining

被引:125
作者
Song, Lijiang
Barona-Gomez, Francisco
Corre, Christophe
Xiang, Longkuan
Udwary, Daniel W.
Austin, Michael B.
Noel, Joseph P.
Moore, Bradley S.
Challis, Gregory L. [1 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[2] Univ Calif San Diego, Scripps Inst Oceanog, San Diego, CA 92093 USA
[3] Howard Hughes Med Inst, Salk Inst Biol Studies, San Diego, CA 92186 USA
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1021/ja065247w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyketide synthases (PKSs) are involved in the biosynthesis of many important natural products. In bacteria, type III PKSs typically catalyze iterative decarboxylation and condensation reactions of malonyl-CoA building blocks in the biosynthesis of polyhydroxyaromatic products. Here it is shown that Gcs, a type III PKS encoded by the sco7221 ORF of the bacterium Streptomyces coelicolor, is required for biosynthesis of the germicidin family of 3,6-dialkyl-4-hydroxypyran-2-one natural products. Evidence consistent with Gcs-catalyzed elongation of specific β-ketoacyl-ACP products of the fatty acid synthase FabH with ethyl- or methylmalonyl-CoA in the biosynthesis of germicidins is presented. Selectivity for β-ketoacyl-ACP starter units and ethylmalonyl-CoA as an extender unit is unprecedented for type III PKSs, suggesting these enzymes may be capable of utilizing a far wider range of starter and extender units for natural product assembly than believed until now. Copyright © 2006 American Chemical Society.
引用
收藏
页码:14754 / 14755
页数:2
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