Falk-Krzesinski H J, Wolfe A J
Department of Microbiology and Immunology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois 60153, USA.
J Bacteriol. 1998 Mar;180(5):1174-84. doi: 10.1128/JB.180.5.1174-1184.1998.
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.
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。