Reactions of the flavin mononucleotide in complex I: a combined mechanism describes NADH oxidation coupled to the reduction of APAD+, ferricyanide, or molecular oxygen
- PMID: 19899808
- DOI: 10.1021/bi901706w
Reactions of the flavin mononucleotide in complex I: a combined mechanism describes NADH oxidation coupled to the reduction of APAD+, ferricyanide, or molecular oxygen
Abstract
NADH:ubiquinone oxidoreductase (complex I) is a complicated respiratory chain enzyme that conserves the energy from NADH oxidation, coupled to ubiquinone reduction, as a proton motive force across the mitochondrial inner membrane. Alternatively, NADH oxidation, by the flavin mononucleotide in complex I, can be coupled to the reduction of hydrophilic electron acceptors, in non-energy-transducing reactions. The reduction of molecular oxygen and hydrophilic quinones leads to the production of reactive oxygen species, the reduction of nicotinamide nucleotides leads to transhydrogenation, and "artificial" electron acceptors are widely used to study the mechanism of NADH oxidation. Here, we use a combined modeling strategy to accurately describe data from three flavin-linked electron acceptors (molecular oxygen, APAD(+), and ferricyanide), in the presence and absence of a competitive inhibitor, ADP-ribose. Our combined ping-pong (or ping-pong-pong) mechanism comprises the Michaelis-Menten equation for the reactions of NADH and APAD(+), simple dissociation constants for nonproductive nucleotide-enzyme complexes (defined for specific flavin oxidation states), and second-order rate constants for the reactions of ferricyanide and oxygen. The NADH-dependent parameters are independent of the identity of the electron acceptor. In contrast, a further flavin-linked acceptor, hexaammineruthenium(III), does not obey ping-pong-pong kinetics, and alternative sites for its reaction are discussed. Our analysis provides kinetic and thermodynamic information about the reactions of the flavin active site in complex I that is relevant to understanding the physiologically relevant mechanisms of NADH oxidation and superoxide formation.
Similar articles
-
Investigation of NADH binding, hydride transfer, and NAD(+) dissociation during NADH oxidation by mitochondrial complex I using modified nicotinamide nucleotides.Biochemistry. 2013 Jun 11;52(23):4048-55. doi: 10.1021/bi3016873. Epub 2013 May 30. Biochemistry. 2013. PMID: 23683271 Free PMC article.
-
Transhydrogenation reactions catalyzed by mitochondrial NADH-ubiquinone oxidoreductase (Complex I).Biochemistry. 2007 Dec 11;46(49):14250-8. doi: 10.1021/bi7017915. Epub 2007 Nov 15. Biochemistry. 2007. PMID: 18001142
-
Reduction of hydrophilic ubiquinones by the flavin in mitochondrial NADH:ubiquinone oxidoreductase (Complex I) and production of reactive oxygen species.Biochemistry. 2009 Mar 10;48(9):2053-62. doi: 10.1021/bi802282h. Biochemistry. 2009. PMID: 19220002 Free PMC article.
-
The ins and outs of the flavin mononucleotide cofactor of respiratory complex I.IUBMB Life. 2022 Jul;74(7):629-644. doi: 10.1002/iub.2600. Epub 2022 Feb 14. IUBMB Life. 2022. PMID: 35166025 Review.
-
Energy conversion, redox catalysis and generation of reactive oxygen species by respiratory complex I.Biochim Biophys Acta. 2016 Jul;1857(7):872-83. doi: 10.1016/j.bbabio.2015.12.009. Epub 2015 Dec 22. Biochim Biophys Acta. 2016. PMID: 26721206 Free PMC article. Review.
Cited by
-
Cytoprotective Effects of Dinitrosyl Iron Complexes on Viability of Human Fibroblasts and Cardiomyocytes.Front Pharmacol. 2019 Nov 11;10:1277. doi: 10.3389/fphar.2019.01277. eCollection 2019. Front Pharmacol. 2019. PMID: 31780929 Free PMC article.
-
Characterization of clinically identified mutations in NDUFV1, the flavin-binding subunit of respiratory complex I, using a yeast model system.Hum Mol Genet. 2015 Nov 15;24(22):6350-60. doi: 10.1093/hmg/ddv344. Epub 2015 Sep 7. Hum Mol Genet. 2015. PMID: 26345448 Free PMC article.
-
Reaction mechanism of single subunit NADH-ubiquinone oxidoreductase (Ndi1) from Saccharomyces cerevisiae: evidence for a ternary complex mechanism.J Biol Chem. 2011 Mar 18;286(11):9287-97. doi: 10.1074/jbc.M110.175547. Epub 2011 Jan 10. J Biol Chem. 2011. PMID: 21220430 Free PMC article.
-
Superoxide is produced by the reduced flavin in mitochondrial complex I: a single, unified mechanism that applies during both forward and reverse electron transfer.J Biol Chem. 2011 May 20;286(20):18056-65. doi: 10.1074/jbc.M110.186841. Epub 2011 Mar 10. J Biol Chem. 2011. PMID: 21393237 Free PMC article.
-
Control of mitochondrial superoxide production by reverse electron transport at complex I.J Biol Chem. 2018 Jun 22;293(25):9869-9879. doi: 10.1074/jbc.RA118.003647. Epub 2018 May 9. J Biol Chem. 2018. PMID: 29743240 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources