Literature DB >> 6295464

Transient kinetics of electron transfer reactions of flavodoxin: ionic strength dependence of semiquinone oxidation by cytochrome c, ferricyanide, and ferric ethylenediaminetetraacetic acid and computer modeling of reaction complexes.

R P Simondsen, P C Weber, F R Salemme, G Tollin.   

Abstract

Electron transfer reactions between Clostridum pasteurianum flavodoxin semiquinone and various oxidants [horse heart cytochrome c, ferricyanide, and ferric ethylenediaminetetraacetic [horse heart cytochrome c, ferricyanide, and ferric ethylenediaminetetraacetic acid (EDTA)] have been studied as a function of ionic strength by using stopped-flow spectrophotometry. The cytochrome c reaction is complicated by the existence of two cytochrome species which react at different rates and whose relative concentrations are ionic strength dependent. Only the faster of these two reactions is considered here. At low ionic strength, complex formation between cytochrome c and flavodoxin is indicated by a leveling off of the pseudo-first-order rate constant at high cytochrome c concentration. This is not observed for either ferricyanide or ferric EDTA. For cytochrome c, the rate and association constants for complex formation were found to increase with decreasing ionic strength, consistent with negative charges on flavodoxin interacting with the positively charged cytochrome electron transfer site. Both ferricyanide and ferric EDTA are negatively charged oxidants, and the rate data respond to ionic strength changes as would be predicted for reactants of the same charge sign. These results demonstrate that electrostatic interactions involving negatively charged groups are important in orienting flavodoxin with respect to oxidants during electron transfer. We have also carried out computer modeling studies of putative complexes of flavodoxin with cytochrome c and ferricyanide, which relate their structural properties to both the observed kinetic behavior and some more general features of physiological electron transfer processes. The results of this study are consistent with the ionic strength behavior described above.

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Year:  1982        PMID: 6295464     DOI: 10.1021/bi00268a008

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


  15 in total

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3.  Electrostatic forces involved in orienting Anabaena ferredoxin during binding to Anabaena ferredoxin:NADP+ reductase: site-specific mutagenesis, transient kinetic measurements, and electrostatic surface potentials.

Authors:  J K Hurley; J T Hazzard; M Martínez-Júlvez; M Medina; C Gómez-Moreno; G Tollin
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4.  Use of flavin photochemistry to probe intraprotein and interprotein electron transfer mechanisms.

Authors:  G Tollin
Journal:  J Bioenerg Biomembr       Date:  1995-06       Impact factor: 2.945

Review 5.  Experimental and theoretical analysis of the interaction between cytochrome c and cytochrome b5.

Authors:  A G Mauk; M R Mauk; G R Moore; S H Northrup
Journal:  J Bioenerg Biomembr       Date:  1995-06       Impact factor: 2.945

6.  Identification of redox partners and development of a novel chimeric bacterial nitric oxide synthase for structure activity analyses.

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Journal:  J Biol Chem       Date:  2014-09-06       Impact factor: 5.157

7.  Electrostatic influence on energetics of electron transfer reactions.

Authors:  D C Rees
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

8.  Three-dimensional structure of flavocytochrome b2 from baker's yeast at 3.0-A resolution.

Authors:  Z X Xia; N Shamala; P H Bethge; L W Lim; H D Bellamy; N H Xuong; F Lederer; F S Mathews
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205

9.  A "parallel plate" electrostatic model for bimolecular rate constants applied to electron transfer proteins.

Authors:  J A Watkins; M A Cusanovich; T E Meyer; G Tollin
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

10.  Possible role of a short extra loop of the long-chain flavodoxin from Azotobacter chroococcum in electron transfer to nitrogenase: complete 1H, 15N and 13C backbone assignments and secondary solution structure of the flavodoxin.

Authors:  S Peelen; S Wijmenga; P J Erbel; R L Robson; R R Eady; J Vervoort
Journal:  J Biomol NMR       Date:  1996-06       Impact factor: 2.835

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