The chromosome of Streptomyces coelicolor A3(2), a model organism for the genus Streptomyces, contains a cryptic type I polyketide synthase (PKS) gene cluster which was revealed when the genome was sequenced. The ca. 54-kb cluster contains three large genes, cpkA, cpkB and cpkC, encoding the PKS subunits. In silico analysis showed that the synthase consists of a loading module, five extension modules and a unique reductase as a terminal domain instead of a typical thioesterase. All acyltransferase domains are specific for a malonyl extender, and have a B-type ketoreductase. Tailoring and regulatory genes were also identified within the gene cluster. Surprisingly, some genes show high similarity to primary metabolite genes not commonly identified in any antibiotic biosynthesis cluster. Using western blot analysis with a PKS subunit (CpkC) antibody, CpkC was shown to be expressed in S. coelicolor at transition phase. Disruption of cpkC gave no obvious phenotype.

译文

链霉菌属链霉菌A3(2) 的染色体是链霉菌属的模式生物,包含一个隐秘的I型聚酮化合物合酶 (PKS) 基因簇,该基因簇在基因组测序时被揭示。ca。54kb簇包含三个大基因,cpkA,cpkB和cpkC,编码PKS亚基。在计算机分析中,合酶由一个加载模块,五个延伸模块和一个独特的还原酶组成,作为末端结构域,而不是典型的硫酯酶。所有酰基转移酶结构域都对丙二酰延伸剂具有特异性,并且具有b型酮还原酶。在基因簇中还鉴定了定制和调节基因。令人惊讶的是,一些基因与在任何抗生素生物合成簇中不常见的初级代谢物基因显示出高度相似性。使用带有PKS亚基 (CpkC) 抗体的蛋白质印迹分析,显示CpkC在过渡期在coelicolor中表达。cpkC的破坏没有明显的表型。

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