The upper and lower limits of the mechanistic stoichiometry of mitochondrial oxidative phosphorylation. Stoichiometry of oxidative phosphorylation
- 1 July 1986
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 158 (2), 315-322
- https://doi.org/10.1111/j.1432-1033.1986.tb09753.x
Abstract
Determination of the intrinsic or mechanistic P/O ratio of oxidative phosphorylation is difficult because of the unknown magnitude of leak fluxes. Applying a new approach developed to overcome this problem (see our preceding paper in this journal), the relationships between the rate of O2 uptake [(JO)3], the net rate of phosphorylation (JP), the P/O ratio, and the respiratory control ratio (RCR) have been determined in rat liver mitochondria when the rate of phosphorylation was systematically varied by three specific means. (a) When phosphorylation is titrated with carboxyatractyloside, linear relationships are observed between JP and (JO)3. These data indicate that the upper limit of the mechanistic P/O ratio is 1.80 for succinate and 2.90 for 3‐hydroxybutyrate oxidation. (b) Titration with malonate or antimycin yields linear relationships between JP and (JO)3. These data give the lower limit of the mechanistic P/O ratio of 1.63 for succinate and 2.66 for 3‐hydroxybutyrate oxidation. (c) Titration with a protonophore yields linear relationships between JP, (JO)3, and (JO)4 and between P/O and 1/RCR. Extrapolation of the P/O ratio to 1/RCR = 0 yields P/O ratios of 1.75 for succinate and 2.73 for 3‐hydroxybutyrate oxidation which must be equal to or greater than the mechanistic stoichiometry. When published values for the H+/O and H+/ATP ejection ratios are taken into consideration, these measurements suggest that the mechanistic P/O ratio is 1.75 for succinate oxidation and 2.75 for NADH oxidation.This publication has 50 references indexed in Scilit:
- The H+/O ratio of proton translocation linked to the oxidation of succinate by mitochondriaFEBS Letters, 1985
- Thermodynamic limits to the stoichiometry of H+ pumping by mitochondrial cytochrome oxidaseFEBS Letters, 1985
- A minimal hypothesis for membrane-linked free-energy transduction: The role of independent, small coupling unitsBiochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics, 1984
- The H+/O ratio of proton translocation linked to the oxidation of succinate by mitochondriaFEBS Letters, 1984
- Thermodynamics of reverse electron transfer across site 1: ATP/2e− is greater than oneBiochemical and Biophysical Research Communications, 1984
- Proton-pumping cytochrome c oxidaseBiochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics, 1979
- Proton translocation quotient for the adenosine triphosphatase of rat liver mitochondriaFEBS Letters, 1973
- Proton Translocation Coupled to ATP Hydrolysis in Rat Liver MitochondriaEuropean Journal of Biochemistry, 1968
- Studies on bacterial photophosphorylation IV. On the maximum amount of delayed photophosphorylation induced by a single flashBiochimica et Biophysica Acta, 1962
- Note on spectrophotometric determination of proteins in dilute solutionsBiochimica et Biophysica Acta, 1960