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Electrostatic effects in electron transfer reactions of [2Fe‐2S] ferredoxins with inorganic reagents
Author(s) -
Vidakovic Momcilo,
Germanas Juris P.
Publication year - 1996
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1002/pro.5560050905
Subject(s) - ferredoxin , electron transfer , ionic strength , anabaena , chemistry , reaction rate constant , kinetics , anabaena variabilis , ionic bonding , ion , aqueous solution , enzyme , biology , cyanobacteria , biochemistry , organic chemistry , physics , quantum mechanics , bacteria , genetics
The kinetics of electron transfer from the reduced [2Fe‐2S] ferredoxins from the cyanobacterium Anabaena 7120 and the protozoan Trichomonas vaginalis to select cobalt coordination compounds have been studied in order to gain insight into the mechanism of electron transfer and intrinsic reactivity of [2Fe‐2S] active sites. With tripositive cobalt complexes, reactions of both proteins displayed saturation kinetics; values of association constants of 12,900 and 1,400 M −1 and limiting rate constants of 7.6 and 3.5 s −1 were found for oxidation of T. vaginalis and Anabaena ferredoxins, respectively, by Co(NH 3 ) 6 3+ at room temperature and I = 0.1 M. An activation enthalpy of 12.1 kcal/mol and activation entropy of — 14.3 cal/mol K for oxidation of T. vaginalis ferredoxin by Co(NH 3 ) 6 3+ contrasted with corresponding values of 13.4 kcal/mol and — 10.5 cal/mol K for the Spirulina platensis protein, which is homologous to Anabaena ferredoxin. The dependence of the reaction rates on ionic strength were measured to probe the importance of electrostatics on the reactivity of the proteins. Analysis of the ionic strength dependence of the oxidation of the proteins by Co(NH 3 ) 6 3+ by the “parallel plate” model of Watkins et al. (1994, Protein Sci 3 :2104–2114) afforded values for active site charges of — 0.7 and — 1.1 and limiting rate constants at infinite ionic strength of 25,800 and 76 M −1 s −1 for T. vaginalis and Anabaena ferredoxins, respectively. These results suggest that the [2Fe‐2S] center of the protozoal ferredoxin is more accessible and adjacent to a less highly charged, more compact patch of negative charges than the photosynthetic protein.