Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1977 Jun 15;164(3):699–704. doi: 10.1042/bj1640699

Studies of energy-linked reactions. Inhibition of oxidative phosphorylation by DL-8-methyldihydrolipoate.

D E Griffiths, K Cain, R L Hyams
PMCID: PMC1164849  PMID: 142482

Abstract

1. DL-8-Methyldihydrolipoate was shown to be a potent inhibitor of mitochondrial oxidative phosphorylation and ATP-driven energy-linked reactions. 2. ADP-stimulated respiration utilizing pyruvate + malate and succinate in both ox heart and rat liver mitochondria is inhibited; oxidative phosphorylation using pyruvate + malate, succinate and ascorbate + NNN'N'-tetramethyl-p-phenylenediamine as substrates is also inhibited; uncoupler-stimulated respiration is unaffected regardless of the substrate used. 3. Mitochondrial oligomycin-sensitive adenosine triphosphatase is inhibited in both the membrane-bound form and the purified detergent-dispersed preparation. 4. ATP-driven transhydrogenase and the ATP-driven energy-linked reduction of NAD+ by succinate in ox heart submitochondrial particles are inhibited, whereas the respiratory-chain-driven transhydrogenase is unaffected. 5. DL-8-Methyl-lipoate has no immediate effect on the above reactions, demonstrating the requirement for the reduced form for inhibition. 6. The inhibitory properties of DL-8-methyldihydrolipoate are analogous to those of oligomycin and provide further evidence of a role for lipoic acid in oxidative phosphorylation.

Full text

PDF
699

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Griffiths D. E., Houghton R. L. Studies on energy-linked reactions: modified mitochondrial ATPase of oligomycin-resistant mutants of Saccharomyces cerevisiae. Eur J Biochem. 1974 Jul 1;46(1):157–167. doi: 10.1111/j.1432-1033.1974.tb03608.x. [DOI] [PubMed] [Google Scholar]
  2. Griffiths D. E., Roberton A. M. Energy-linked reactions in mitochondria. Studies on the reduction of NAD+ by succinate. Biochim Biophys Acta. 1966 Jan 11;113(1):13–26. doi: 10.1016/s0926-6593(66)80116-9. [DOI] [PubMed] [Google Scholar]
  3. Griffiths D. E., Roberton A. M. Energy-linked reactions in mitochondria: studies on the mechanism of the energy-linked transhydrogenase reaction. Biochim Biophys Acta. 1966 Jun 15;118(3):453–464. doi: 10.1016/s0926-6593(66)80089-9. [DOI] [PubMed] [Google Scholar]
  4. Griffiths D. E. Studies of energy-linked reactions. Net synthesis of adenosine triphosphate by isolated adenosine triphosphate synthase preparations: a role for lipoic acid and unsaturated fatty acids. Biochem J. 1976 Dec 15;160(3):809–812. doi: 10.1042/bj1600809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hatefi Y., Stiggall D. L., Galante Y., Hanstein W. G. Mitochondrial ATP-Pi exchange complex. Biochem Biophys Res Commun. 1974 Nov 6;61(1):313–321. doi: 10.1016/0006-291x(74)90568-3. [DOI] [PubMed] [Google Scholar]
  6. REED L. J. The chemistry and function of lipoic acid. Adv Enzymol Relat Subj Biochem. 1957;18:319–347. doi: 10.1002/9780470122631.ch8. [DOI] [PubMed] [Google Scholar]
  7. STOKSTAD E. L. Discussion: biological activities of analogues and derivatives of thioctic acid. Fed Proc. 1954 Sep;13(3):712–714. [PubMed] [Google Scholar]
  8. Schmidt U., Grafen P., Altland K., Goedde H. W. Biochemistry and chemistry of lipoic acids. Adv Enzymol Relat Areas Mol Biol. 1969;32:423–469. doi: 10.1002/9780470122778.ch10. [DOI] [PubMed] [Google Scholar]
  9. Serrano R., Kanner B. I., Racker E. Purification and properties of the proton-translocating adenosine triphosphatase complex of bovine heart mitochondria. J Biol Chem. 1976 Apr 25;251(8):2453–2461. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES