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本文引用的文献

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Consistent structure between bacterial and mitochondrial NADH:ubiquinone oxidoreductase (complex I).
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Characterization of the overproduced NADH dehydrogenase fragment of the NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli.来自大肠杆菌的烟酰胺腺嘌呤二核苷酸(NADH):泛醌氧化还原酶(复合体I)过量产生的NADH脱氢酶片段的特性分析。
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Modular evolution of the respiratory NADH:ubiquinone oxidoreductase and the origin of its modules.呼吸链NADH:泛醌氧化还原酶的模块化进化及其模块起源
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Alternative respiratory pathways of Escherichia coli: energetics and transcriptional regulation in response to electron acceptors.大肠杆菌的替代呼吸途径:响应电子受体的能量学与转录调控
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Buchnera aphidicola (endosymbiont of aphids) contains nuoC(D) genes that encode subunits of NADH dehydrogenase.
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Requirement for the proton-pumping NADH dehydrogenase I of Escherichia coli in respiration of NADH to fumarate and its bioenergetic implications.大肠杆菌质子泵NADH脱氢酶I在NADH呼吸生成延胡索酸过程中的需求及其生物能量学意义。
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The proton-translocating NADH-quinone oxidoreductase (NDH-1) of thermophilic bacterium Thermus thermophilus HB-8. Complete DNA sequence of the gene cluster and thermostable properties of the expressed NQO2 subunit.嗜热栖热菌HB-8的质子转运型NADH-醌氧化还原酶(NDH-1)。基因簇的完整DNA序列及所表达的NQO2亚基的热稳定特性。
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Flagellar assembly in Salmonella typhimurium.鼠伤寒沙门氏菌中的鞭毛组装
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O2 as the regulatory signal for FNR-dependent gene regulation in Escherichia coli.氧气作为大肠杆菌中FNR依赖性基因调控的调节信号。
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10
Expression and characterization of the flavoprotein subcomplex composed of 50-kDa (NQO1) and 25-kDa (NQO2) subunits of the proton-translocating NADH-quinone oxidoreductase of Paracoccus denitrificans.反硝化副球菌质子转运型NADH-醌氧化还原酶由50 kDa(NQO1)和25 kDa(NQO2)亚基组成的黄素蛋白亚复合物的表达与表征
J Biol Chem. 1996 Mar 8;271(10):5907-13. doi: 10.1074/jbc.271.10.5907.

对诺基因座的遗传分析,该基因座编码大肠杆菌中的质子转运型NADH脱氢酶。

Genetic analysis of the nuo locus, which encodes the proton-translocating NADH dehydrogenase in Escherichia coli.

作者信息

Falk-Krzesinski H J, Wolfe A J

机构信息

Department of Microbiology and Immunology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois 60153, USA.

出版信息

J Bacteriol. 1998 Mar;180(5):1174-84. doi: 10.1128/JB.180.5.1174-1184.1998.

DOI:10.1128/JB.180.5.1174-1184.1998
PMID:9495756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC107005/
Abstract

Complex I (EC 1.6.99.3) of the bacterium Escherichia coli is considered to be the minimal form of the type I NADH dehydrogenase, the first enzyme complex in the respiratory chain. Because of its small size and relative simplicity, the E. coli enzyme has become a model used to identify and characterize the mechanism(s) by which cells regulate the synthesis and assembly of this large respiratory complex. To begin dissecting the processes by which E. coli cells regulate the expression of nuo and the assembly of complex I, we undertook a genetic analysis of the nuo locus, which encodes the 14 Nuo subunits comprising E. coli complex I. Here we present the results of studies, performed on an isogenic collection of nuo mutants, that focus on the physiological, biochemical, and molecular consequences caused by the lack of or defects in several Nuo subunits. In particular, we present evidence that NuoG, a peripheral subunit, is essential for complex I function and that it plays a role in the regulation of nuo expression and/or the assembly of complex I.

摘要

大肠杆菌的复合体I(EC 1.6.99.3)被认为是I型NADH脱氢酶的最小形式,它是呼吸链中的首个酶复合体。由于其体积小且相对简单,大肠杆菌的这种酶已成为一种模型,用于识别和表征细胞调节这种大型呼吸复合体合成与组装的机制。为了开始剖析大肠杆菌细胞调节nuo表达和复合体I组装的过程,我们对nuo基因座进行了遗传分析,该基因座编码构成大肠杆菌复合体I的14个Nuo亚基。在此,我们展示了对一组同基因nuo突变体进行研究的结果,这些研究聚焦于几个Nuo亚基缺失或缺陷所导致的生理、生化和分子层面的后果。特别是,我们提供的证据表明,外周亚基NuoG对于复合体I的功能至关重要,并且它在nuo表达的调节和/或复合体I的组装中发挥作用。