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基因证据表明基因fdhD和fdhE不控制大肠杆菌K-12中甲酸脱氢酶-N的合成。

Genetic evidence that genes fdhD and fdhE do not control synthesis of formate dehydrogenase-N in Escherichia coli K-12.

作者信息

Stewart V, Lin J T, Berg B L

机构信息

Section of Microbiology, Cornell University, Ithaca, New York 14853-8101.

出版信息

J Bacteriol. 1991 Jul;173(14):4417-23. doi: 10.1128/jb.173.14.4417-4423.1991.

Abstract

Enterobacteria synthesize two formate dehydrogenases, formate dehydrogenase-N (encoded by fdnGHI) and formate dehydrogenase H (encoded by fdhF). Previous work has identified two rha-linked Salmonella typhimurium genes, fdnB and fdnC, which are required primarily for formate dehydrogenase-N activity. Analogous mutants, termed fdhD and fdhE, have been isolated in Escherichia coli. We used gene fusions between fdnG, the structural gene for the large subunit of formate dehydrogenase-N, and lacZ, the structural gene for beta-galactosidase, to examine E. coli fdnGHI operon expression in fdhD and fdhE insertion mutants. Expression of the phi (fdnG-lacZ) gene fusions was little affected by these insertions, suggesting that fdhD and fdhE do not control transcription or UGA decoding of the formate dehydrogenase-N structural genes. Our complementation tests, with cloned E. coli fdhD and fdhE genes, indicate that the S. typhimurium fdnC and fdnB genes are functionally homologous to the E. coli fdhD and fdhE genes, respectively.

摘要

肠杆菌合成两种甲酸脱氢酶,即甲酸脱氢酶 -N(由fdnGHI编码)和甲酸脱氢酶H(由fdhF编码)。先前的研究已经鉴定出两个与rha相连的鼠伤寒沙门氏菌基因,fdnB和fdnC,它们主要是甲酸脱氢酶 -N活性所必需的。在大肠杆菌中已经分离出类似的突变体,称为fdhD和fdhE。我们利用甲酸脱氢酶 -N大亚基的结构基因fdnG与β-半乳糖苷酶的结构基因lacZ之间的基因融合,来检测fdhD和fdhE插入突变体中大肠杆菌fdnGHI操纵子的表达。这些插入对phi(fdnG - lacZ)基因融合的表达影响很小,这表明fdhD和fdhE并不控制甲酸脱氢酶 -N结构基因的转录或UGA解码。我们用克隆的大肠杆菌fdhD和fdhE基因进行的互补试验表明,鼠伤寒沙门氏菌的fdnC和fdnB基因分别与大肠杆菌的fdhD和fdhE基因功能同源。

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Mutants of Escherichia coli specifically deficient in respiratory formate dehydrogenase activity.
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