Crouzet J, Levy-Schil S, Cameron B, Cauchois L, Rigault S, Rouyez M C, Blanche F, Debussche L, Thibaut D
Unité de Biologie Moléculaire, Institut des Biotechnologies, Vitry-sur-Seine, France.
J Bacteriol. 1991 Oct;173(19):6074-87. doi: 10.1128/jb.173.19.6074-6087.1991.
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.
一段携带反硝化假单胞菌钴胺素(cob)基因的13.1千碱基对(kb)DNA片段已被测序。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,分别命名为cobN至cobQ以及cobW。基于纯化的Cob蛋白的氨基末端序列和分子量的相似性,CobQ被鉴定为钴啉酸合酶,CobP被鉴定为一种具有钴胺酰胺激酶和钴胺酰胺磷酸鸟苷基转移酶活性的双功能酶,CobO被鉴定为钴胺素(I)腺苷转移酶。推测CobN在钴插入反应中起作用。在13.1 kb片段上鉴定出另外四个开放阅读框,但它们的染色体失活并未导致钴胺素缺陷型表型。