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鉴定cbbBc为来自嗜糖假单胞菌的染色体cbb二氧化碳固定操纵子的另一个远端基因。

Identification of cbbBc as an additional distal gene of the chromosomal cbb CO2 fixation operon from Ralstonia eutropha.

作者信息

Bömmer D, Schäferjohann J, Bowien B

机构信息

Institut für Mikrobiologie, Georg-August-Universität Göttingen, Grisebachstrasse 8, D-37077 Göttingen, Germany.

出版信息

Arch Microbiol. 1996 Oct;166(4):245-51. doi: 10.1007/s002030050380.

Abstract

Ralstonia eutropha (formerly Alcaligenes eutrophus) strain H16 possesses two highly homologous cbb operons encoding most of the Calvin cycle enzymes. One copy of the operon is located on the chromosome, the other on the megaplasmid pHG1 of the organism. Sequence analysis of the region downstream of the presumptive 3'-terminal gene (cbbAc) of the chromosomal operon revealed the presence of an open reading frame comprising 2,274 bp. Evidence is presented that this open reading frame is an additional distal gene (designated cbbBc) of the operon. In contrast to the other genes of the operon, cbbBc is not duplicated in the plasmid-borne operon. The deduced amino acid sequence of the cbbBc product (757 residues, molecular mass 83.17 kDa) showed the highest similarity to the large catalytic subunits of various bacterial formate dehydrogenases (FDH), suggesting that cbbBc might represent a structural FDH gene of R. eutropha. However, the properties of a cbbBc mutant strain indicated that the potential gene product is not related to known FDH of the organism. Transcriptional analysis in the homologous host and heterologous expression in Escherichia coli demonstrated that cbbBc is an active gene, which apparently has no essential function in the autotrophic metabolism of R. eutropha. The gene is a novel member of cbb operons in autotrophic bacteria.

摘要

真养产碱杆菌(以前称为食酸产碱杆菌)H16菌株拥有两个高度同源的cbb操纵子,它们编码大部分卡尔文循环酶。该操纵子的一个拷贝位于染色体上,另一个位于该生物体的巨型质粒pHG1上。对染色体操纵子假定的3'-末端基因(cbbAc)下游区域的序列分析显示存在一个由2274 bp组成的开放阅读框。有证据表明这个开放阅读框是该操纵子的一个额外的远端基因(命名为cbbBc)。与该操纵子的其他基因不同,cbbBc在质粒携带的操纵子中没有重复。cbbBc产物的推导氨基酸序列(757个残基,分子量83.17 kDa)与各种细菌甲酸脱氢酶(FDH)的大催化亚基显示出最高的相似性,这表明cbbBc可能代表真养产碱杆菌的一个结构FDH基因。然而,cbbBc突变株的特性表明该潜在基因产物与该生物体已知的FDH无关。在同源宿主中的转录分析和在大肠杆菌中的异源表达表明cbbBc是一个活性基因,它显然在真养产碱杆菌的自养代谢中没有必需功能。该基因是自养细菌中cbb操纵子的一个新成员。

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