Abstract
Generation of a membrane potential in the respiratory chain-deficient particles of beef heart mitochondria has been studied. For detection of membrane potential, phenyl dicarbaundecaborane (PCB−,) and anilinonaphthalene sulphonate (ANS−) probes were used. The respiratory chain-deficient submitochondrial particles were prepared after Arion and Racker (E-SMP), the procedure including complete disappearance of membrane structures and subsequent reconstitution of membrane vesicles as judged by the electron microscopy study. E-SMP were found to be deficient in cytochromesa,a 3 and transhydrogenase, the cytochromeb,c 1 andc content being lowered. Addition of NADH, succinate and tetramethyl-p-phenylenediamine+ascorbate did not induce either any oxygen consumption or membrane potential formation. Treatment of E-SMP with NADPH+NAD+ or with NADH+CoQ0 did not entail generation of membrane potential, in contrast to that of parent, “pyrophosphate” submitochondrial particles (PP-SMP).
E-SMP displayed an oligomycin-sensitive ATPase activity which could be increased by reconstitution of E-SMP with coupling factor F1. Addition of ATP resulted in an uptake of PCB− and enhancement of ANS− fluorescence, the facts testifying to the formation of the membrane potential with “plus” inside E-SMP. Membrane potential formation was arrested by oligomycin, rutamycin, and uncouplers. Addition of respiratory chain inhibitors (antimycin+rotenone+ cyanide), complete reduction of respiratory carriers by dithionite and oxidation by ferricyanide were without effect on ATP-supported formation of membrane potential in E-SMP. It was concluded that utilization of ATP energy for the membrane potential generation does not depend on the state of the respiratory carriers and can be demonstrated under the conditions when none of redox chain coupling sites were functioning.
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Abbreviations
- PCB− :
-
phenyl dicarbaundecaborane
- ANS− :
-
anilinonaphthalene sulfonate
- E-SMP:
-
the respiratory chain-deficient submitochondrial particles
- PP-SMP:
-
“pyrophosphate” submitochondrial particles
References
P. Mitchell,Chemiosmotic Coupling in Oxidative and Photosynthetic Phosphorylation, glynn Res. Ltd., Bodmin, 1966.
J. B. Chappell and A. R. Crofts,Biochem. J., 95 (1965) 393.
P. Hinkle and P. Mitchell,J. Bioenergetics, 1 (1970) 45.
V. P. Skulachev,FEBS Letters, 11 (1970) 301.
A. E. Dontsov, L. L. Grinius, A. A. Jasaitis, I. I. Severina and V. P. Skulachev,J. Bioenergetics, 3 (1972).
E. Racker,Proc. Natl. Acad. Sci. U.S.A., 48 (1962) 1659.
W. J. Arion and E. Racker,J. Biol. Chem., 245 (1970) 5186.
L. L. Grinius, A. A. Jasaitis, Yu. P. Kadziauskas, E. A. Liberman, V. P. Skulachev, V. P. Topali, L. M. Tsofina and M. A. Vladimirova,Biochim. Biophys. Acta, 216 (1970) 1.
A. A. Jasaitis, V. V. Kuliene and V. P. Skulachev,Biochim. Biophys. Acta, 234 (1971) 177.
L. L. Grinius, T. I. Guds and V. P. Skulachev,J. Bioenergetics, 2 (1971) 101.
M. Gutman, M. Mayr, R. Oltzik and T. P. Singer,Biochim. Biophys. Res. Commun., 41 (1970) 40.
M. Klingenberg and P. Schollmeyer, in:Intracellular Respiration: Phosphorylating and Non-Phosphorylating Oxidation Reactions, Proc. 5th Internat. Congress of Biochemistry, Pergamon Press, Oxford-London-New York-Paris, 1963, Vol. 5, p. 46.
G. S. P. Groot, L. Kovač and G. Schatz,Proc. Natl. Acad. Sci. U.S.A., 68 (1971) 308.
R. S. Cockrell, E. J. Harris and B. C. Pressman,Nature, 215 (1967) 1487.
V. P. Skulachev,J. Bioenergetics, 3 (1972).
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Jasaitis, A.A., Severina, I.I., Skulachev, V.P. et al. A study on the mechanism of energy coupling in the redox chain. J Bioenerg Biomembr 3, 388–396 (1972). https://doi.org/10.1007/BF01516077
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DOI: https://doi.org/10.1007/BF01516077