Hofmeister specific-ion effects on enzyme activity and buffer pH: Horseradish peroxidase in citrate buffer
Date
2006
Authors
Bauduin, Pierre
Nohmie, Fawaz
Touraud, Didier
Neueder, Roland
Kunz, Werner
Ninham, Barry
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Elsevier
Abstract
Salt addition to enzymes in buffer always induce the problem of the respective influences of electrostatic interactions and anion specificity on buffer pH and enzyme kinetics. In the present paper the influence of some sodium salts (Na2SO4, NaCl, NaBr and NaNO3) on the pH of a citrate buffer (c = 0.025 M), and on the catalytic constants of horseradish peroxidase (HRP) is studied. First, the pH changes due to the presence of salts in the buffer are examined; second, catalytic constants, KmABTS, VmaxABTS and V maxABTS/KmABTS, are studied as a function of pH in buffer with and without added salt, at various salt concentrations and different pH values due to the salt additions. With a simple electrostatic model, it is possible to show that the glass electrode yields reasonable pH values even in the presence of fairly high 1 : 1 salt concentrations. For the catalytic efficiency, VmaxABTS/KmABTS, a Hofmeister series is found with opposite deviations from the pure pH effect for salting-in and salting-out ions over a large range of salt concentrations. This usual Hofmeister series is a consequence of three, for the moment inseparable salt concentration and specific ion-induced phenomena: global bulk effects, local active site effects and surface effects.
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Keywords: Catalyst activity; Concentration (process); Electrostatics; Enzyme kinetics; pH effects; Salts; Surface properties; Hofmeister effectsd; Horseradish peroxidase; Ion specificity; Ionization Electrostatics; Enzyme kinetics; Hofmeister effects; Horseradish peroxidase; Ion specificity
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Source
Journal of Molecular Liquids
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Journal article
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2037-12-31
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