Medical Research Council Mitochondrial Biology Unit, Wellcome Trust/MRC Building, Cambridge, UK.
FEBS Lett. 2011 Jul 21;585(14):2318-22. doi: 10.1016/j.febslet.2011.05.065. Epub 2011 Jun 12.
The flavin mononucleotide in complex I (NADH:ubiquinone oxidoreductase) catalyzes NADH oxidation, O(2) reduction to superoxide, and the reduction of several 'artificial' electron acceptors. Here, we show that the positively-charged electron acceptors paraquat and hexaammineruthenium(III) react with the nucleotide-bound reduced flavin in complex I, by an unusual ternary mechanism. NADH, ATP, ADP and ADP-ribose stimulate the reactions, indicating that the positively-charged acceptors interact with their negatively-charged phosphates. Our mechanism for paraquat reduction defines a new mechanism for superoxide production by complex I (by redox cycling); in contrast to direct O(2) reduction the rate is stimulated, not inhibited, by high NADH concentrations.
复合物 I(NADH:泛醌氧化还原酶)中的黄素单核苷酸催化 NADH 氧化、O2 还原为超氧化物以及几种“人工”电子受体的还原。在这里,我们表明,带正电荷的电子受体百草枯和六氨合钌(III)通过不寻常的三元机制与复合物 I 中结合核苷酸的还原黄素反应。NADH、ATP、ADP 和 ADP-核糖刺激反应,表明带正电荷的受体与它们带负电荷的磷酸根相互作用。我们的百草枯还原机制定义了复合物 I 通过氧化还原循环产生超氧化物的新机制(与直接 O2 还原相反,该速率受高 NADH 浓度的刺激而不是抑制)。