首页> 美国卫生研究院文献>Journal of Bacteriology >Nucleotide sequence and genetic analysis of a 13.1-kilobase-pair Pseudomonas denitrificans DNA fragment containing five cob genes and identification of structural genes encoding Cob(I)alamin adenosyltransferase cobyric acid synthase and bifunctional cobinamide kinase-cobinamide phosphate guanylyltransferase.
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Nucleotide sequence and genetic analysis of a 13.1-kilobase-pair Pseudomonas denitrificans DNA fragment containing five cob genes and identification of structural genes encoding Cob(I)alamin adenosyltransferase cobyric acid synthase and bifunctional cobinamide kinase-cobinamide phosphate guanylyltransferase.

机译:含有五个cob基因的13.1千碱基对反硝化假单胞菌DNA片段的核苷酸序列和遗传分析以及鉴定编码Cob(I)alamin腺苷基转移酶cobyric酸合酶和双功能cobinamide激酶-cobinamide磷酸胍基转移酶的结构基因。

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摘要

A 13.1-kb DNA fragment carrying Pseudomonas denitrificans cob genes has been sequenced. The nucleotide sequence and genetic analysis revealed that this fragment contained five different cob genes named cobN to cobQ and cobW. Based on the similarity of NH2-terminal sequences and molecular weights of the purified Cob proteins, CobQ was identified as cobyric acid synthase, CobP was identified as a bifunctional enzyme exhibiting both cobinamide kinase and cobinamide phosphate guanylyltransferase activities, and CobO was identified as cob(I)alamin adenosyltransferase. CobN is proposed to play a role in cobalt insertion reactions. Four other open reading frames were identified on the 13.1-kb fragment, but their chromosomal inactivation did not lead to a cobalamin-minus phenotype.
机译:携带反硝化假单胞菌cob基因的13.1kb DNA片段已测序。核苷酸序列和遗传分析表明,该片段包含五个不同的cob基因,分别名为cobN至cobQ和cobW。根据NH2末端序列的相似性和纯化的Cob蛋白的分子量,将CobQ鉴定为cobyric acid合酶,将CobP鉴定为同时具有cobinamide激酶和cobinamide磷酸鸟苷转移酶活性的双功能酶,并将CobO鉴定为cob( I)丙氨酸腺苷基转移酶。有人建议CobN在钴插入反应中起作用。在13.1kb的片段上鉴定出其他四个开放阅读框,但它们的染色体失活并未导致钴胺素-负表型。

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