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大肠杆菌甲酸氢化酶的遗传调控:fhlA基因产物作为新调控基因fhlB转录激活因子的作用。

Genetic regulation of formate hydrogenlyase of Escherichia coli: role of the fhlA gene product as a transcriptional activator for a new regulatory gene, fhlB.

作者信息

Maupin J A, Shanmugam K T

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville 32611.

出版信息

J Bacteriol. 1990 Sep;172(9):4798-806. doi: 10.1128/jb.172.9.4798-4806.1990.

Abstract

A new gene whose product is required for the production of formate hydrogenlyase (FHL) has been identified in Escherichia coli. This gene, termed fhlB, maps between the frdA (94.4 min) and argI (96.6 min) genes on the E. coli chromosome and is transcribed in a clockwise direction toward argI. Biochemical analysis of an FhlB- mutant, strain SE-2011 [phi(fhlB-lacZ+)], revealed that the mutant lacks formate dehydrogenase activity associated with FHL (FDH-H) and hydrogenase activity. As a result of these defects, fermentative hydrogen production and hydrogen uptake reactions were undetectable in strain SE-2011. Fumarate reductase activity of this mutant was also reduced to about 15% of the levels of the parent (strain MC4100), and strain SE-2011 did not produce succinate as a fermentation end product. Regulation of expression of the fhlB gene, studied as production of beta-galactosidase activity by strain SE-2011, revealed that the operon is expressed at low levels under aerobic conditions. Under anaerobic growth conditions, this activity increased by two- to threefold. Addition of formate enhanced the differential rate of synthesis of the fhlB gene product to as high as 130 U of beta-galactosidase specific activity per microgram of cell protein, but only under anaerobic conditions. Formate-dependent expression of phi(fhlB-lacZ+) required the sigma 54 subunit of RNA polymerase and the fhlA gene product. The concentration of formate required for maximum expression of the fhlB gene was about 15 mM; this value decreased to about 3 mM in the presence of plasmid pSE-133, which carries the fhlA gene in a multicopy plasmid. DNA sequence analysis of the fhlA gene showed that the FhlA protein is 686 amino acids long and has an anhydrous molecular weight of 78,086. On the basis of sequence homology with other transcriptional activators such as NtrC, HydG, and Klebsiella pneumoniae NifA proteins, the FhlA protein was deduced to be a transcriptional activator controlling the production of FHL. It is proposed that formate interacts with the FhlA protein and that this active complex initiates transcription of the fhlB gene. The FhlA and FhlB proteins act as a cascade in regulating the production of FDH-H and the FHL-linked hydrogenase and ultimately the production of FHL and fermentative hydrogen.

摘要

在大肠杆菌中已鉴定出一种新基因,其产物是甲酸氢解酶(FHL)产生所必需的。该基因称为fhlB,位于大肠杆菌染色体上的frdA(94.4分钟)和argI(96.6分钟)基因之间,并以顺时针方向朝向argI转录。对FhlB -突变体菌株SE - 2011 [phi(fhlB - lacZ+)]进行的生化分析表明,该突变体缺乏与FHL相关的甲酸脱氢酶活性(FDH - H)和氢化酶活性。由于这些缺陷,在菌株SE - 2011中未检测到发酵产氢和氢摄取反应。该突变体的延胡索酸还原酶活性也降至亲本(菌株MC4100)水平的约15%,并且菌株SE - 2011不产生琥珀酸作为发酵终产物。以菌株SE - 2011产生β -半乳糖苷酶活性来研究fhlB基因的表达调控,结果表明该操纵子在有氧条件下低水平表达。在厌氧生长条件下,该活性增加了两到三倍。添加甲酸可将fhlB基因产物的差异合成速率提高至每微克细胞蛋白高达130 U的β -半乳糖苷酶比活性,但仅在厌氧条件下。phi(fhlB - lacZ+)的甲酸依赖性表达需要RNA聚合酶的σ54亚基和fhlA基因产物。fhlB基因最大表达所需的甲酸浓度约为15 mM;在携带多拷贝质粒中fhlA基因的质粒pSE - 133存在下,该值降至约3 mM。fhlA基因的DNA序列分析表明,FhlA蛋白长686个氨基酸,无水分子量为78,086。基于与其他转录激活因子如NtrC、HydG和肺炎克雷伯菌NifA蛋白的序列同源性,推断FhlA蛋白是控制FHL产生的转录激活因子。有人提出,甲酸与FhlA蛋白相互作用,并且这种活性复合物启动fhlB基因的转录。FhlA和FhlB蛋白在调节FDH - H和FHL相关氢化酶的产生以及最终FHL和发酵产氢的过程中起级联作用。

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