首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Mutants defective in the energy-conserving NADH dehydrogenase of Salmonella typhimurium identified by a decrease in energy-dependent proteolysis after carbon starvation.
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Mutants defective in the energy-conserving NADH dehydrogenase of Salmonella typhimurium identified by a decrease in energy-dependent proteolysis after carbon starvation.

机译:鼠伤寒沙门氏菌的节能NADH脱氢酶中有缺陷的突变体通过碳饥饿后能量依赖性蛋白水解的减少而鉴定。

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摘要

NADH dehydrogenase is the first component of the respiratory chain. It transfers electrons from NADH to ubiquinone and concomitantly establishes a proton motive force across the membrane. Salmonella typhimurium mutants defective in this enzyme were isolated in a screen for strains with increased expression of beta-galactosidase from a hemA-lacZ protein fusion. This unexpected phenotype results from stabilization of the hybrid protein during carbon starvation and is apparently due to an energy requirement for proteolytic attack. Sequence analysis of DNA fragments cloned from an insertion mutant indicates that S. typhimurium has a large cluster of genes encoding the energy-conserving NADH dehydrogenase, similar to one recently described in Paracoccus denitrificans. These findings establish the potential for genetic analysis of a complex enzyme whose function, especially in proton efflux, is poorly understood.
机译:NADH脱氢酶是呼吸链的第一部分。它将电子从NADH转移到泛醌,并随之在整个膜上建立质子原动力。在筛选中,从hemA-lacZ蛋白融合体中筛选出具有增加的β-半乳糖苷酶表达的菌株,从而筛选出该酶中有缺陷的鼠伤寒沙门氏菌突变体。这种出乎意料的表型是由于碳饥饿期间杂合蛋白的稳定而产生的,显然是由于蛋白水解攻击需要能量。从插入突变体克隆的DNA片段的序列分析表明,鼠伤寒沙门氏菌具有编码节能NADH脱氢酶的大量基因簇,类似于最近在反硝化副球菌中描述的一种。这些发现建立了对复杂酶进行遗传分析的潜力,该酶的功能(尤其是质子外排)的功能尚不清楚。

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