The effect of cobalt ions (Co²⁺) on horseradish peroxidase (HRP) was studied in vitro by enzymatic activity assay, electronic absorption spectra, intrinsic fluorescence spectra and 8-anilo-1-naphthalenesulfonate(ANS)-binding fluorescence spectra. Co²⁺ at concentrations below 0.1 mM mildly increased the HRP activity, whereas higher concentrations of Co²⁺ significantly inactivated HRP in a time and concentration-dependent manner. Steady-state kinetic studies show that Co²⁺ was a noncompetitive inhibitor of o-dianisidine oxidation by HRP. The K_i value dropped as the incubation time increased. Furthermore, Co²⁺ was found to be an uncompetitive inhibitor of H₂O₂. These results suggested that Co²⁺ would slowly bind to the enzyme and progressively induce conformational changes. Spectroscopic analysis showed that even for high Co²⁺ concentrations, the structure of HRP as a whole only changed slightly; however, there were significant conformational changes near or in the active site of HRP. Based on the above results, we suggest that Co²⁺ may bind with some amino acids near or in the active site of HRP and the conformational changes of HRP induced by such binding should be the main reason for activation and inactivation effect of Co²⁺. The potential binding sites of Co²⁺ were also proposed.

Key words: Horseradish peroxidase; Cobalt ions; Activation; Inactivation; and Active site.