Literature DB >> 2169862

Proton electron-nuclear double-resonance spectra of molybdenum(V) in different reduced forms of xanthine oxidase.

B D Howes1, N M Pinhal, N A Turner, R C Bray, G Anger, A Ehrenberg, J B Raynor, D J Lowe.   

Abstract

Electron-nuclear double-resonance (ENDOR) spectra of protons coupled to molybdenum(V) in reduced xanthine oxidase samples have been recorded. Under appropriate conditions these protons may be studied without interference from protons coupled to reduced iron-sulfur centers. Spectra have been obtained for the molybdenum(V) species known as Rapid, Slow, Inhibited, and Desulfo Inhibited. Resonances corresponding to at least nine protons or sets of protons are observed for all four species, with coupling constants in the range 0.08-4 MHz. Most of these protons do not exchange when 2H2O is used as solvent. Additional protons giving couplings up to 40 MHz are also detected. These correspond to EPR-detectable protons studied in earlier work. The strongly coupled protons may be replaced by 2H, through appropriate use of 2H2O or of 2H-substituted substrates, with consequent disappearance of the 1H resonances. In most cases the corresponding 2H ENDOR features have also been observed. The nature of the various coupled protons is briefly discussed. Results permit specific conclusions to be drawn about the structures of the Inhibited and Desulfo Inhibited species. In particular, the data indicate that the aldehyde residue of the Inhibited species has been oxidized and that the four protons derived from the ethylene glycol molecule in the Desulfo Inhibited species are not all equivalent. Recent assignments [Edmondson, D.E., & D'Ardenne, S.C. (1989) Biochemistry 28, 5924-5930] of the weakly coupled protons in the latter species appear not to be soundly based. The possibility of obtaining more detailed structural information from the spectra is briefly considered.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1990        PMID: 2169862     DOI: 10.1021/bi00478a002

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  6 in total

1.  Multifrequency cw-EPR investigation of the catalytic molybdenum cofactor of polysulfide reductase from Wolinella succinogenes.

Authors:  Thomas Prisner; Sevdalina Lyubenova; Yener Atabay; Fraser MacMillan; Achim Kröger; Oliver Klimmek
Journal:  J Biol Inorg Chem       Date:  2003-01-17       Impact factor: 3.358

2.  Isotropic exchange interaction between Mo and the proximal FeS center in the xanthine oxidase family member aldehyde oxidoreductase from Desulfovibrio gigas on native and polyalcohol inhibited samples: an EPR and QM/MM study.

Authors:  María C Gómez; Nicolás I Neuman; Sergio D Dalosto; Pablo J González; José J G Moura; Alberto C Rizzi; Carlos D Brondino
Journal:  J Biol Inorg Chem       Date:  2014-10-25       Impact factor: 3.358

3.  The structure of formaldehyde-inhibited xanthine oxidase determined by 35 GHz 2H ENDOR spectroscopy.

Authors:  Muralidharan Shanmugam; Bo Zhang; Rebecca L McNaughton; R Adam Kinney; Russ Hille; Brian M Hoffman
Journal:  J Am Chem Soc       Date:  2010-10-13       Impact factor: 15.419

4.  Nitrite reduction by xanthine oxidase family enzymes: a new class of nitrite reductases.

Authors:  Luisa B Maia; José J G Moura
Journal:  J Biol Inorg Chem       Date:  2010-12-19       Impact factor: 3.358

5.  Spectroscopic and electronic structure studies probing covalency contributions to C-H bond activation and transition-state stabilization in xanthine oxidase.

Authors:  Joseph Sempombe; Benjamin Stein; Martin L Kirk
Journal:  Inorg Chem       Date:  2011-10-05       Impact factor: 5.165

6.  A structure-based catalytic mechanism for the xanthine oxidase family of molybdenum enzymes.

Authors:  R Huber; P Hof; R O Duarte; J J Moura; I Moura; M Y Liu; J LeGall; R Hille; M Archer; M J Romão
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-20       Impact factor: 11.205

  6 in total

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