Abstract
The Na+-translocating nicotinamide adenine dinucleotide (NADH):quinine oxidoreductase (Na+–NQR) is a component of respiratory chain of various bacteria and it generates a redox-driven transmembrane electrochemical Na+ potential. It contains four different flavin prosthetic groups, including two flavin mononucleotide (FMN) residues covalently bound to the subunits NqrB and NqrC. Na+–NQR from Vibrio harveyi was poised at different redox potentials to prepare two samples, containing either both FMNNqrB and FMNNqrC or only FMNNqrB in a paramagnetic state. These two samples were comparatively studied using pulse electron paramagnetic resonance (EPR), electron-nuclear double resonance (ENDOR), and electron-electron double resonance (ELDOR) spectroscopy. The echo-detected EPR spectra and electron spin relaxation properties were very similar for flavin radicals in both samples. The splitting of the outer peaks in the proton ENDOR spectra, assigned to the C(8α) methyl protons, allows to identify both radicals as anionic flavosemiquinones. The mean interspin distance of 20.7 Å between these radicals was determined by pulse ELDOR experiment, which allows to estimate the edge-to-edge distance (r e) between these flavin centers as: 11.7 Å < r e < 20.7 Å. The direct electron transfer between FMNNqrB and FMNNqrC during the physiological turnover of the Na+–NQR complex is suggested.
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A.V. Bogachev, M.I. Verkhovsky, Biochemistry (Moscow) 70, 143–149 (2005)
W. Zhou, Y.V. Bertsova, B. Feng, P. Tsatsos, M.L. Verkhovskaya, R.B. Gennis, A.V. Bogachev, B. Barquera, Biochemistry 38, 16246–16252 (1999)
P.R. Rich, B. Meunier, F.B. Ward, FEBS Lett. 375, 5–10 (1995)
M. Hayashi, K. Hirai, T. Unemoto, FEBS Lett. 363, 75–77 (1995)
X.D. Pfenninger-Li, S.P. Albracht, R. van Belzen, P. Dimroth, Biochemistry 35, 6233–6242 (1996)
A.V. Bogachev, Y.V. Bertsova, B. Barquera, M.I. Verkhovsky, Biochemistry 40, 7318–7323 (2001)
M. Hayashi, Y. Nakayama, M. Yasui, M. Maeda, K. Furuishi, T. Unemoto, FEBS Lett. 488, 5–8 (2001)
O. Juárez, M.J. Nilges, P. Gillespie, J. Cotton, B. Barquera, J. Biol. Chem. 283, 33162–33167 (2008)
K. Turk, A. Puhar, F. Neese, E. Bill, G. Fritz, J. Steuber, J. Biol. Chem. 279, 21349–21355 (2004)
A.V. Bogachev, L.V. Kulik, D.A. Bloch, Y.V. Bertsova, M.S. Fadeeva, M.I. Verkhovsky, Biochemistry 48, 6291–6298 (2009)
A.V. Bogachev, D.A. Bloch, Y.V. Bertsova, M.I. Verkhovsky, Biochemistry 48, 6299–6304 (2009)
A.V. Bogachev, Y.V. Bertsova, E.K. Ruuge, M. Wikström, M.I. Verkhovsky, Biochim. Biophys. Acta 1556, 113–120 (2002)
B. Barquera, L. Ramirez-Silva, J.E. Morgan, M.J. Nilges, J. Biol. Chem. 281, 36482–36491 (2006)
A. Schweiger, G. Jeschke, Principles of Pulse Electron Paramagnetic Resonance (Oxford University Press, Oxford, 2001)
C. Gemperle, A. Schweiger, Chem. Rev. 91, 1481–1505 (1991)
A. Schnegg, A.A. Dubinskii, M.R. Fuchs, Yu.A. Grishin, E.P. Kirilina, W. Lubitz, M. Plato, A. Savitsky, K. Mobius, Appl. Magn. Reson. 31, 59–98 (2007)
S. Van Doorslaer, E. Vinck, Phys. Chem. Chem. Phys. 9, 4620–4638 (2008)
M. Pannier, S. Veit, A. Godt, G. Jeschke, H.W. Spiess, J. Magn. Reson. 142, 331–340 (2000)
S.A. Dzuba, Uspekhi Khimii 76, 752–767 (2007)
Y.D. Tsvetkov, A.D. Milov, A.G. Maryasov, Uspekhi Khimii 77, 515–550 (2008)
P.K. Smith, R.I. Krohn, G.T. Hermanson, A.K. Mallia, F.H. Gartner, M.D. Provenzano, E.K. Fujimoto, N.M. Goeke, B.J. Olson, D.C. Klenk, Anal. Biochem. 150, 76–85 (1985)
B. Barquera, J. Morgan, D. Lukoyanov, C.P. Scholes, R.B. Gennis, M.J. Nilges, J. Am. Chem. Soc. 125, 265–275 (2003)
G. Jeschke, V. Chechik, P. Ionita, A. Godt, H. Zimmermann, J. Banham, C.R. Timmel, D. Hilger, H. Jung, Appl. Magn. Reson. 30, 73–498 (2006)
O. Juárez, J.E. Morgan, B. Barquera, J. Biol. Chem. 284, 8963–8972 (2009)
D.E. Edmondson, Biochem. Soc. Trans. 13, 593–600 (1985)
S. Weber, K. Mobius, G. Richter, C.W.M. Kay, J. Am. Chem. Soc. 123, 3790–3798 (2001)
S. Weber, C.W.M. Kay, A. Bacher, G. Richter, R. Bittl, ChemPhysChem 6, 292–299 (2005)
C.W.M. Kay, C. Elsasser, R. Bittl, S.R. Farrell, C. Thorpe, J. Am. Chem. Soc. 128, 76–77 (2006)
A.J. Fielding, R.J. Usselman, N. Watmough, M. Slinkovic, F.E. Frerman, G.R. Eaton, S.S. Eaton, J. Magn. Reson. 190, 222–232 (2008)
A. Savitsky, A.A. Dubinskii, M. Flores, W. Lubitz, K. Mobius, J. Phys. Chem. B 111, 6245–6262 (2007)
L.V. Kulik, S.V. Paschenko, S.A. Dzuba, J. Magn. Reson. 159, 237–241 (2002)
Acknowledgments
The work was supported by the Russian Foundation for Basic Research (project nr. 07-04-00619), and by a grant of the President of the Russian Federation for scientific schools (project nr. NSh-551.2008.3). We are indebted to Prof. M. Verkhovsky for helpful discussions and for critical reading of the manuscript. We are thankful to Prof. S.A. Dzuba for continuous interest to this work.
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Kulik, L.V., Pivtsov, A.V. & Bogachev, A.V. Pulse EPR, ENDOR, and ELDOR Study of Anionic Flavin Radicals in Na+-Translocating NADH:Quinone Oxidoreductase. Appl Magn Reson 37, 353–361 (2010). https://doi.org/10.1007/s00723-009-0075-6
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DOI: https://doi.org/10.1007/s00723-009-0075-6