首页> 外文OA文献 >Cloning, sequencing, and analysis of the griseusin polyketide synthase gene cluster from Streptomyces griseus.
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Cloning, sequencing, and analysis of the griseusin polyketide synthase gene cluster from Streptomyces griseus.

机译:灰链霉菌的灰霉菌素聚酮化合物合酶基因簇的克隆,测序和分析。

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摘要

A fragment of DNA was cloned from the Streptomyces griseus K-63 genome by using genes (act) for the actinorhodin polyketide synthase (PKS) of Streptomyces coelicolor as a probe. Sequencing of a 5.4-kb segment of the cloned DNA revealed a set of five gris open reading frames (ORFs), corresponding to the act PKS genes, in the following order: ORF1 for a ketosynthase, ORF2 for a chain length-determining factor, ORF3 for an acyl carrier protein, ORF5 for a ketoreductase, and ORF4 for a cyclase-dehydrase. Replacement of the gris genes with a marker gene in the S. griseus genome by using a single-stranded suicide vector propagated in Escherichia coli resulted in loss of the ability to produce griseusins A and B, showing that the five gris genes do indeed encode the type II griseusin PKS. These genes, encoding a PKS that is programmed differently from those for other aromatic PKSs so far available, will provide further valuable material for analysis of the programming mechanism by the construction and analysis of strains carrying hybrid PKS.
机译:通过使用天蓝色链霉菌的放线菌丝蛋白聚酮化合物合酶(PKS)的基因(act)作为探针,从灰链霉菌K-63基因组中克隆了DNA片段。对克隆的DNA的5.4-kb片段进行测序,揭示了一组五个gris开放阅读框(ORF),分别对应于act PKS基因,其顺序如下:ORF1为酮合成酶,ORF2为链长决定因子,酰基载体蛋白为ORF3,酮还原酶为ORF5,环化酶脱水酶为ORF4。通过使用在大肠杆菌中繁殖的单链自杀载体,用灰链霉菌基因组中的标记基因替换gris基因,导致丧失生产灰霉菌素A和B的能力,这表明这五个gris基因确实编码了II型灰黄霉素PKS。这些编码PKS的基因与迄今为止可用的其他芳香族PKS的编程方式不同,这些基因将通过构建和分析携带杂交PKS的菌株为编程机制分析提供更多有价值的材料。

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