Biochemistry · 1976 · 65 citations · 33 references
Natural SciencesBiochemistryChemistryChemical KineticsInorganic ChemistryOrganic ChemistryBiophysical KineticsElectrochemical KineticsEnzyme KineticsMichaelis-menten KineticsElectron TransferElectron Transfer DynamicsElectron Transfer KineticsElectron Transfer RatesElectron Transfer ThermodynamicsHeterogeneous Electron TransferKinetic Relationships
The electron transfer reaction between the "blue" single copper protein azurin (from Pseudomonas aeruginosa) and the hexacyanoiron (II/III) couple has been studied. Equilibrium constants for the reduction of azurin were measured spectrophotometrically in the temperature range 5-33 degrees C (K = 1.1 X 10(-2) at 25 degrees C, deltaH degrees = 10.9 kcal/mol, 0.1 M potassium phosphate, pH 7.0, I = 0.22). The enthalpy change was also determined by microcalorimetry and from the analysis of chemical relaxation amplitudes. Following a temperature-jump perturbation of this equilibrium, only a single relaxation was observed. The reciprocal of the relaxation time increased linearly as oxidized azurin was reacted with increasing amounts of ferrocyanide, yet reached saturation when reduced azurin was titrated with ferricyanide. This behavior as well as the analysis of the relaxation amplitudes led to the following scheme for this system: see article. At 25 degrees C the rate constants for the electron transfer were k+3=6.4s-1 and k-3=45s-1, the association constants K1=54 M-1 and K2-1=610 M-1. The activation and overall thermodynamic parameters as well as the individual thermodynamic values for the different steps were combined to construct a self-consistent energy profile for the reaction.
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Environment of copper in Pseudomonas fluorescens Azurin: fluorometric approach
Alessandro Finazzi‐Agrò, Giuseppe Rotilio, Luciana Avigliano et al. · Biochemistry · 1970 · 157 citations