Abstract
A study of the kinetics of Mn2+ oxidation catalyzed by cell extracts of two bacterial isolates (E1, Pseudomonas III [new isolate] and E4, Citrobacter freundii) isolated from the core of manganese concretions from Greek soils is presented. The reaction velocity of Mn2+ oxidation was determined from the rate of consumption of Mn2+. The oxidation of Mn2+ was followed by measuring changes in Mn2+ concentration by activation analysis and by atomic absorption spectrophotometry. The reaction velocity was directly proportional to cell extract concentration when the reaction time was 1 h. At longer reaction times, the relationship deviated from linearity because substrate concentration became limiting. The rate of Mn2+ oxidation increased with the Mn2+ concentration. Analysis of the results by application of the integrated Michaelis equation for determining Michaelis constants and maximal velocities either in the presence (Km = 3.33 μmol/ml and Vmax = 1.25 μmol/ml·h) or in the absence of maleate buffer (Km = 2.52 μmol/ml and Vmax = 2.04 μmol/ml·h) indicated a strong affinity between the oxidizing system and manganese. All results in this study are consistent with an enzymatic manganese-oxidizing system and give an indication of the mechanism of biological Mn2+ oxidation in soil which differs from that in the marine environment.

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