Leif H, Sled V D, Ohnishi T, Weiss H, Friedrich T
Institut für Biochemie, Heinrich-Heine-Universität Düsseldorf, Germany.
Eur J Biochem. 1995 Jun 1;230(2):538-48. doi: 10.1111/j.1432-1033.1995.tb20594.x.
The proton-translocating NADH:ubiquinone oxidoreductase (complex I) was isolated from Escherichia coli by chromatographic steps performed in the presence of an alkylglucoside detergent at pH 6.0. The complex is obtained in a monodisperse state with a molecular mass of approximately 550,000 Da and is composed of 14 subunits. The subunits were assigned to the 14 genes of the nuo operon, partly based on their N-terminal sequences and partly on their apparent molecular masses. The preparation contains one noncovalently bound FMN/molecule. At least two binuclear (N1b and N1c) and three tetranuclear (N2, N3 and N4) iron-sulfur clusters were detected by EPR in the preparation when reduced with NADH. Their EPR characteristics remained mostly unaltered during the isolation process. After reconstitution in phospholipid membranes, the preparation catalyses piericidin-A-sensitive electron transfer from NADH to ubiquinone-2 with Km values similar to those of complex I in cytoplasmic membranes but with only 10% of the Vmax value. The isolated complex I was cleaved into three fragments when the pH was raised from 6.0 to 7.5 and the detergent exchanged to Triton X-100. One of these fragments is a water-soluble NADH dehydrogenase fragment which is composed of three subunits bearing at least four iron-sulfur clusters (N1b, N1c, N3 and N4) that can be reduced with NADH, one of them bearing FMN. The second, amphipathic, fragment, which is presumed to connect the NADH dehydrogenase fragment with the membrane, contains four subunits and at least one EPR-detectable iron-sulfur cluster whose spectral properties are reminiscent of the eucaryotic cluster N2. The third membrane fragment is composed of seven homologues of the mitochondrially encoded subunits of the eucaryotic complex I. This subunit arrangement coincidences to some extent with the order of the genes on the nuo operon. A topological model of the E. coli complex I is proposed.
质子转运型NADH:泛醌氧化还原酶(复合体I)是在pH 6.0条件下,于烷基葡糖苷去污剂存在的情况下,通过色谱步骤从大肠杆菌中分离得到的。该复合体以单分散状态获得,分子量约为550,000道尔顿,由14个亚基组成。这些亚基部分基于其N端序列,部分基于其表观分子量,被分配到nuo操纵子的14个基因中。该制剂含有一个非共价结合的FMN/分子。当用NADH还原时,通过电子顺磁共振(EPR)在制剂中检测到至少两个双核(N1b和N1c)和三个四核(N2、N3和N4)铁硫簇。它们的EPR特征在分离过程中大多保持不变。在磷脂膜中重构后,该制剂催化对杀粉蝶菌素A敏感的电子从NADH转移到泛醌-2,其米氏常数(Km)值与细胞质膜中复合体I的相似,但最大反应速度(Vmax)值仅为其10%。当pH从6.0升高到7.5且去污剂换成Triton X-100时,分离得到的复合体I被切割成三个片段。其中一个片段是水溶性NADH脱氢酶片段,由三个亚基组成,带有至少四个可被NADH还原的铁硫簇(N1b、N1c、N3和N4),其中一个带有FMN。第二个片段具有两亲性,推测用于将NADH脱氢酶片段与膜连接,它包含四个亚基和至少一个EPR可检测的铁硫簇(其光谱特性让人联想到真核生物的簇N2)。第三个膜片段由真核生物复合体I线粒体编码亚基的七个同源物组成。这种亚基排列在一定程度上与nuo操纵子上基因的顺序一致。提出了大肠杆菌复合体I的拓扑模型。