Literature DB >> 171646

Interaction of ubisemiquinone with a paramagnetic component in heart tissue.

F J Ruzicka, H Beinert, K L Schepler, W R Dunham, R H Sands.   

Abstract

The origin of most of the electron paramagnetic resonances obtained at low temperature and low microwave power from heart tissue and subcellular fractions derived therefrom is now understood. A signal that emerges on partial reduction with characteristic lines at 3227 G (0.3227 tesla) and 3309 G (0.3309 tesla) (at 9.2 GHz) and disappears again on full reduction has remained unidentified. According to its behavior on oxidation-reduction, the substance giving rise to this signal has the properties of a two-electron acceptor. The signal is strongly dependent on temperature and can only be well resolved at less than 20 degrees K. It is readily elicited in submitochondrial particles by partial reduction, but has not been observed in submitochondrial particles from which ubiquinone has been removed by pentane extraction. When ubiquinone is reincorporated into extracted submitochondrial particles, the signal is again easily produced by partial reduction. Electron paramagnetic resonance spectra of partially reduced submitochondrial particles recorded at 34 GHz show lines centered about g approximately 2 with the same separation (approximately 82 G; approximately 0.0082 tesla) as do 9.2 GHz spectra, whereas no lines are detected with a separation of approximately 82 X 34/9.2 G (0.0082 X 34/9.2 tesla). We suggest, on the basis of these observations, that the unidentified signal arises from an interaction of ubisemiquinone and a second paramagnetic species. Three obvious choices exist concerning this second species: ubisemiquinone, flavin semiquinone, or an iorn-sulfur center. It is not possible without much additional information to decide between these possibilities. Since we have never observed the signal in the absence of the membrane-bound, high-potential type iron-sulfur protein, we have considered involvement of this species in the interaction. However, according to computer simulations of the observed electron paramagnetic resonance spectra, which yield best fits for semiquinone-semiquinone interaction, the possibility that ubi- or flavin semiquinone is the interaction partner appears more likely at this time. The interaction appears to be of the magnetic dipole-dipole type, but it is not certain whether there is also a contribution from spin exchange coupling. If it is assumed that the signal is due to magnetic dipole-dipole interaction, the distance of the partners is less than or equal to 7.7 A.

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Year:  1975        PMID: 171646      PMCID: PMC432883          DOI: 10.1073/pnas.72.8.2886

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  10 in total

1.  Studies on the electron transfer system. IV. The electron transfer particle.

Authors:  F L CRANE; J L GLENN; D E GREEN
Journal:  Biochim Biophys Acta       Date:  1956-12

2.  The electron paramagnetic resonance of oxidized clostridial ferredoxins.

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Journal:  Biochem Biophys Res Commun       Date:  1974-07-10       Impact factor: 3.575

3.  On the nature of the spin coupling between the iron-sulfur clusters in the eight-iron ferredoxins.

Authors:  R Mathews; S Charlton; R H Sands; G Palmer
Journal:  J Biol Chem       Date:  1974-07-10       Impact factor: 5.157

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5.  EPR studies by 57Fe isotopic substitution on the nature of an unknown electron acceptor in Azotobacter vinelandii phosphorylating particles.

Authors:  D V Dervartanian; T V Morgan; R V Brantner
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6.  Electron paramagnetic resonance-detectable electron acceptors in beef heart mitochondria. Ubihydroquinone-cytochrome c reductase segment of the electron transfer system and complex mitochondrial fragments.

Authors:  N R Orme-Johnson; R E Hansen; H Beinert
Journal:  J Biol Chem       Date:  1974-03-25       Impact factor: 5.157

7.  EPR detectable electron acceptors in submitochondrial particles from beef heart with special reference to the iron-sulfur components of DPNH-ubiquinone reductase.

Authors:  N R Orme-Johnson; W H Orme-Johnson; R E Hansen; H Beinert; Y Hatefi
Journal:  Biochem Biophys Res Commun       Date:  1971-07-16       Impact factor: 3.575

8.  Electron spin resonance measurement on ubiquinone-depleted and ubiquinone-replenished submitochondrial particles.

Authors:  D Bäckström; B Norling; A Ehrenberg; L Ernster
Journal:  Biochim Biophys Acta       Date:  1970-01-13

9.  On the role of ubiquinone in mitochondria. II. Redox reactions of ubiquinone under the control of oxidative phosphorylation.

Authors:  A Kröger; M Klingenberg
Journal:  Biochem Z       Date:  1966-06-07

10.  Studies with ubiquinone-depleted submitochondrial particles. Quantitative incorporation of small amounts of ubiquinone and its effects on the NADH and succinate oxidase activities.

Authors:  B Norling; E Glazek; B D Nelson; L Ernster
Journal:  Eur J Biochem       Date:  1974-09-16
  10 in total
  16 in total

Review 1.  The quinone-binding and catalytic site of complex II.

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2.  Saccharomyces cerevisiae coq10 null mutants are responsive to antimycin A.

Authors:  Cleverson Busso; Erich B Tahara; Renata Ogusucu; Ohara Augusto; Jose Ribamar Ferreira-Junior; Alexander Tzagoloff; Alicia J Kowaltowski; Mario H Barros
Journal:  FEBS J       Date:  2010-09-28       Impact factor: 5.542

3.  Magnetic coupling of the molybdenum and iron-sulphur centres in xanthine oxidase and xanthine dehydrogenases.

Authors:  D J Lowe; R C Bray
Journal:  Biochem J       Date:  1978-03-01       Impact factor: 3.857

4.  Oxidation of reduced menaquinone by the fumarate reductase complex in Escherichia coli requires the hydrophobic FrdD peptide.

Authors:  G Cecchini; C R Thompson; B A Ackrell; D J Westenberg; N Dean; R P Gunsalus
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

5.  Reappraisal of the e.p.r. signals in (post)-ischaemic cardiac tissue.

Authors:  A M van der Kraaij; J F Koster; W R Hagen
Journal:  Biochem J       Date:  1989-12-15       Impact factor: 3.857

6.  Iron-sulphur centres in mitochondria from Arum maculatum spadix with very high rates of cyanide-resistant respiration.

Authors:  R Cammack; J M Palmer
Journal:  Biochem J       Date:  1977-09-15       Impact factor: 3.857

7.  Surface localization of sites of reduction of nitroxide spin-labeled molecules in mitochondria.

Authors:  A T Quintanilha; L Packer
Journal:  Proc Natl Acad Sci U S A       Date:  1977-02       Impact factor: 11.205

8.  The probable site of action of thenolytrifluoracetone on the respiratory chain.

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Journal:  Biochem J       Date:  1977-06-15       Impact factor: 3.857

9.  Computationally modeling mammalian succinate dehydrogenase kinetics identifies the origins and primary determinants of ROS production.

Authors:  Neeraj Manhas; Quynh V Duong; Pilhwa Lee; Joshua D Richardson; John D Robertson; Michael A Moxley; Jason N Bazil
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Review 10.  Defining a direction: electron transfer and catalysis in Escherichia coli complex II enzymes.

Authors:  Elena Maklashina; Gary Cecchini; Sergei A Dikanov
Journal:  Biochim Biophys Acta       Date:  2013-02-08
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