4
Views
9
CrossRef citations to date
0
Altmetric
Original Article

Ubiquinones: Stereochemistry and Biological Implications

, , &
Pages 105-118 | Published online: 09 Jul 2009

References

  • Baccarini‐Melandri A., Melandri B. A. A role for ubiquinone‐10 in the B–C2 segment of the photosynthetic bacterial electron transport chain. FEBS Lett. 1977; 80(2)459–464
  • Barfield M., Spear R. J., Sternhell S. Allylic interproton spin‐spin coupling. Chem. Rev. 1976; 76: 593–624
  • Bashford C. L., Prince R. C., Takamiya K. I., Dutton P. L. Electrogenic events in the ubiquinone‐cytochrome B/C2 oxidoreductase of rhodopseudomonas sphaeroides. Biochim. Biophys. Acta 1979; 545(2)223–235
  • Breitmaier E., Voelter W. 13C‐NMR spectroscopy of organic compounds. 13C‐NMR Spectroscopy. Verlag Chemie, Weinheim 1974; 119–194
  • Emsley J. W., Feeney J., Sutcliffe L. H. Theoretical calculations of spin‐spin coupling constants of simple molecules. High Resolution NMR Spectroscopy. Pergamon Press, Oxford 1965; 160–191
  • Formacek V., Desnoier L., Kellerhals M. P., Keller T., Clerc J. T. 13C Data Bank. Bruker Physic Karlsruhe. 1976
  • Fowler L. R., Richardson S. H. Studies on the electron transfer system L. On the mechanism of reconstitution of the mitochondrial electron transfer system. J. Biol. Chem. 1963; 238: 456–463
  • Gutman M., Coles C. J., Singer T. P., Casida J. E. On the functional organization of the respiratory chain at the dehydrodenase coenzyme Q junction. Biochemistry 1971; 10: 2036–2043
  • Hatefy Y., Haavik A. G., Fowler L. R., Griffiths D. E. Studies on the electron transfer system. XLII Reconstitution of the electron transfer system. J. Biol. Chem. 1962; 237: 2661–2669
  • Hatefy Y. Coenzyme Q (Ubiquinone). Adv. Enzymol. 1963; 25: 275–328
  • Futami A., Murt E., Hauska G. The permeability of quinones through membranes. Biochim. Biophys. Acta 1979; 547: 583–593
  • Jackman L. M., Sternhell S. Spin‐Spin coupling. Application of NMR Spectroscopy in Organic Chemistry. Pergamon Press, Oxford 1969; 269–322
  • Johnson L. F., Jankowski W. C. Carbon 13 NMR Spectra. Wiley Int., New York 1972
  • Kröger A., Klingenberg M. The kinetics of the redox reaction of ubiquinones related to electron‐transport activity in the respiratory chain. Eur. J. Biochem. 1973; 34: 358–368
  • Lenaz G., Daves G. D., Jr., Folkers K. Organic structurals specificity and sites of coenzyme Q in succinoxidase and DPNH‐oxidase systems. Arch. Biochem. Biophys. 1968; 123: 539–550
  • Lenaz G., Pasquali P., Bertoli E., Parenti‐Castelli G., Folkers K. The inhibition of NADH oxidase by the low homologs of coenzyme Q. Arch. Biochem. Biophys. 1975; 169: 217–226
  • Lenaz G., Mascarello S., Landi L., Cabrini L., Pasquali P., Parenti‐Castelli G., Sechi A. M., Bertoli E. Membrane Bioenergetics. North Holland, Amsterdam 1977; 189–198
  • Lenaz G., Landi L., Cabrini L., Pasquali P., Sechi A. M., Ozawa T. On the sidedness of the ubiquinone redox cycle. Kinetic studies in mitochondrial membranes. Biochem. Biophys. Res. Commun. 1978; 85: 1047–1053
  • Mitchell P. Possible molecular mechanisms of proton‐motive function of cytochrome system. J. Theor. Biol. 1976; 62: 327–368
  • Masotti L., Spisni C., Ramponi C., Sartor G., Pasquali‐Ronchetti I., Boicelli C. A. Conformational and functional studies on CoQ. Ital. J. Biochem. 1978; 27: 262–264
  • Nelson B. D., Norling B., Persson B., Ernster L. Effect of thenoyltrifluoroacetone on the interaction of succinate dehydrogenase and cytochrome b in ubiquinone depleted submitochondrial particles. Biochem. Biophys. Res. Commun. 1971; 44: 1312–1320
  • Nelson B. D., Norling B., Persson B., Ernster L. Effects of certain iron‐chelators and antibiotics on the interaction of succinate dehydrogenase and cytochrome b in ubiquinone‐depleted submitochondrial particles. Biochem. Biophys. Res. Commun. 1971; 44: 1321–1329
  • Nelson B. D., Norling B., Persson B., Ernster L. Influence of ubiquinone on the rate of antimycin binding to submitochondrial particles. Biochim. Biophys. Acta 1972; 267: 205–210
  • Rodd's Chemistry of Carbon Compounds. Benzoquinones and related compounds, S. Coffey. Elsevier‐Sequoia Ed., AmsterdamThe Netherlands 1977; Vol. IIIb: 1–166
  • Sauders J. K. M., Hanson S. W., Williams D. H. Paramagnetic shift reagents: the nature of the interactions. J. Am. Chem. Soc. 1972; 94: 5325–5335
  • Sato M., Yamada K., Ozawa H. Rhodoquinone specificity in the reactivation of succinoxidase activity of acetone‐extracted ascaris mitochondria. Biochem. Biophys. Res. Commun. 1972; 46: 578–582
  • Sievers R. E. Structural elucidation of natural products. NMR Shift Reagents. Academic Press, New York 1973; 99–127
  • Spisni A., Masotti L., Lenaz G., Bertoli E., Pedulli G. F., Zannoni C. Interactions between ubiquinones and phospholipid bilayers. Arch. Biochem. Biophys. 1978; 190: 454–458
  • Spisni A., Sartor G., Lenaz G., Masotti L. Effect of CoQ homologues on the fluidity of phospholipid bilayers as studied by fluorescence polarization of perylene. Membrane Biochemistry 1981, in press
  • Stothers J. B. Structural and stereochemical application. Carbon 13 NMR Spectroscopy. Academic Press, New York 1972; 451–457
  • Wehrly F. W., Wirthlin T. The spectral parameters. Interpretation of Carbon 13 NMR Spectra. Heyden, London 1976; 22–63
  • Wilcznskj J. J., Daves G. D., Jr., Folkers K. Structure determination of ubiquinones analogs by solvent shifts in nuclear magnetic resonance spectra. J. Am. Chem. Soc. 1978; 90: 5593–5598

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.