首页> 外文期刊>Antimicrobial agents and chemotherapy. >Molecular Cloning, Sequence Analysis, and Heterologous Expression of the Phosphinothricin Tripeptide Biosynthetic Gene Cluster from Streptomyces viridochromogenes DSM 40736.
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Molecular Cloning, Sequence Analysis, and Heterologous Expression of the Phosphinothricin Tripeptide Biosynthetic Gene Cluster from Streptomyces viridochromogenes DSM 40736.

机译:绿链霉菌DSM 40736的磷脂酰三肽生物合成基因簇的分子克隆,序列分析和异源表达

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摘要

A fosmid library from genomic DNA of Streptomyces viridochromogenes DSM 40736 was constructed and screened for the presence of genes known to be involved in the biosynthesis of phosphinothricin tripeptide (PTT). Eight positives were identified, one of which was able to confer PTT biosynthetic capability upon Streptomyces lividans after integration of the fosmid into the chromosome of this heterologous host. Sequence analysis of the 40,241-bp fosmid insert revealed 29 complete open reading frames (ORFs). Deletion analysis demonstrated that a minimum set of 24 ORFs were required for PTT production in the heterologous host. Sequence analysis revealed that most of these PTT genes have been previously identified in either S. viridochromogenes or S. hygroscopicus (or both), although only 11 out of 24 of these ORFs have experimentally defined functions. Three previously unknown genes within the cluster were identified and are likely to have roles in the stepwise production of phosphonoformate from phosphonoacetaldehyde. This is the first report detailing the entire PTT gene cluster from any producing streptomycete.
机译:从病毒链霉菌DSM 40736的基因组DNA构建了一个fosmid文库,并筛选了已知与膦丝菌素三肽(PTT)的生物合成有关的基因的存在。鉴定出八种阳性,其中一种能够在将化纤溶质整合到该异源宿主的染色体中后赋予青紫链霉菌PTT生物合成能力。对40,241-bp的fosmid插入片段进行序列分析,发现29个完整的开放阅读框(ORF)。缺失分析表明,在异源宿主中生产PTT至少需要24组ORF。序列分析显示,虽然这些ORF中只有11个具有实验定义的功能,但大多数PTT基因先前已在病毒链霉菌或吸水链霉菌(或两者中)中鉴定出。确定了簇中三个以前未知的基因,这些基因可能在从膦酰乙醛逐步生产膦酸酯的过程中起作用。这是第一份报告,详细介绍了任何产链霉菌的整个PTT基因簇。

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