Abstract

The relationship between the steady-state level of membrane potential (delta psi) and the rates of energy production and consumption has been studied in mitochondria and submitochondrial particles. The energy-linked reactions investigated were oxidative phosphorylation (with NADH, succinate, and beta-hydroxybutyrate as respiratory substrates) and nucleoside triphosphate-driven transhydrogenation from NADH to NADP and uphill electron transfer from succinate to NAD. Results have shown the following. 1) Attenuation of the rates of the energy-producing reactions results in a parallel change in the rates of the energy-consuming reactions with little or no change in the magnitude of steady-state delta psi. 2) At low rates of energy production and consumption, steady-state delta psi decreases. However, this is due largely to the energy leak of the system which lowers static-head delta psi when the rate of energy production is slow. 3) When the rate of energy production and static-head delta psi are held constant, and the rate of energy consumption is diminished by partial inhibition or the use of suboptimal conditions (e.g. subsaturating substrate concentrations), then even a small decrease in the rate of energy consumption results in an upward adjustment of the level of steady-state delta psi. The lower the rate of energy input, the greater the upward adjustment of steady-state delta psi upon suppression of the rate of energy consumption. 4) The above results have been discussed with regard to the role of bulk-phase delta mu H+ or delta psi in the mitochondrial energy transfer reactions.

Highlights

  • The relationship between the steady-state level of source to sink as the transmembrane electrochemical potenmembrane potential (A$) and the ratesof energy pro- tial of protons (A/;H+) via the aqueous phase that surrounds duction and consumption has been studied in mitochon- the energy transducing membranes [1,5]

  • The energy- this model, protonic energy wouldbedelocalized over the linked reactions investigated were oxidative phospho- entire membrane, which must be in the form of a closed rylation

  • The oxidation rates of NADH and [38,39,40].The latter is apparent from the drop in static-head p-hydroxybutyrate were suppressed by addition to the assay A$ when the rate of energy input was suppressed to very low of increasing amounts of Seconal, which inhibits electron levels

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Summary

Studies on the Mechanism of Oxidative Phosphorylation

From the Division of Biochemistry,Department of Basic and Clinical Research,Scripps Clinic and Research Foundation, ”. 2) At lowrates of energy reasons for the proposed alternatives to the chemiosmotic production and consumption, steady-state A+ de- model of proton transfer have been discussed in excellent creases. This isdue largely to the energy leak recent reviews [7,8,9, 11, 13,14,15] and cannot be detailed here. Steadystate A$ does respond to changes inthe rates of energy input and outflow, and its magnitude appears to depend o n the relative magnitudes of these tworates

MATERIALS ANDMETHODS
RESULTS
MechanismPhoof sOphxiodraytliavteion
Oxidatlve Phosphorylation Activity
Tnnshydragenaso Activity m l nd NADP nducdhninltngl
DISCUSSION
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