首页> 美国卫生研究院文献>Journal of Bacteriology >Transcriptional control of the nuo operon which encodes the energy-conserving NADH dehydrogenase of Salmonella typhimurium.
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Transcriptional control of the nuo operon which encodes the energy-conserving NADH dehydrogenase of Salmonella typhimurium.

机译:nuo操纵子的转录控制该操纵子编码鼠伤寒沙门氏菌的节能NADH脱氢酶。

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摘要

The 14 nuo genes encode the subunits of the type I (energy-conserving) NADH dehydrogenase, a key component of the respiratory chain. Salmonella typhimurium, like Escherichia coli, has two enzymes that can oxidize NADH and transfer electrons to ubiquinone, but only the type I enzyme translocates protons across the membrane to generate a proton motive force. Cells with the type I enzyme are energetically more efficient; the role of the type II enzyme (encoded by ndh) is not established, but it may function like a relief valve to allow more rapid NADH recycling. Here, we have investigated transcription of the nuo gene cluster, primarily in S. typhimurium. Studies with polar insertion mutants demonstrate that these genes are arranged as a single, large operon that is expressed from a complex promoter region upstream of nuoA. The DNA sequence of the promoter region was determined, and primer extension analysis of nuo transcripts was used to map four major RNA 5' ends to this region. A set of lac operon fusions to various DNA segments from the nuo promoter region was also constructed. Analysis of these fusions confirmed the presence of at least two nuo promoters. Mutations in the global regulatory genes arcA, oxrA (fnr), crp, cya, and katF were tested for effects on expression of the nuo operon. However, none of the mutations tested had a large effect on expression of type I NADH dehydrogenase.
机译:这14个nuo基因编码I型(节能)NADH脱氢酶的亚基,NADH脱氢酶是呼吸链的关键组成部分。与大肠杆菌一样,鼠伤寒沙门氏菌也有两种酶,它们可以氧化NADH并将电子转移到泛醌,但是只有I型酶才能使质子跨膜移位,从而产生质子原动力。具有I型酶的细胞在能量上更有效。 II型酶(由ndh编码)的作用尚未确定,但它可能像安全阀一样起作用,以允许更快地回收NADH。在这里,我们研究了nuo基因簇的转录,主要是鼠伤寒沙门氏菌。极性插入突变体的研究表明,这些基因排列成单个大操纵子,从nuoA上游的复杂启动子区域表达。确定启动子区域的DNA序列,并使用nuo转录物的引物延伸分析将四个主要RNA 5'末端定位到该区域。还构建了一套从nuo启动子区域到各种DNA片段的lac操纵子融合体。这些融合的分析证实了至少两个nuo启动子的存在。测试了全球调控基因arcA,oxrA(fnr),crp,cya和katF中的突变对nuo操纵子表达的影响。但是,所测试的突变均未对I型NADH脱氢酶的表达产生较大影响。

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