聚酮
同色链霉菌
生物合成
化学
聚酮合酶
酰基载体蛋白
生物化学
立体化学
链霉菌
酶
ATP合酶
脱羧
细菌
基因
生物
遗传学
催化作用
突变体
作者
Lijiang Song,Francisco Barona‐Gómez,Christophe Corre,Longkuan Xiang,Daniel W. Udwary,M.B. Austin,Joseph P. Noel,Bradley S. Moore,Gregory L. Challis
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.
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