Turkish Journal of Biology
In order to elucidate the kinetic mechanism of human erythrocyte catalase a well-known substrate, H_2O_2 and inhibitor azide were used. The catalase-mediated conversion of H_2O_2 to H_2O and O_2, in the presence and absence of azide, was studied in 50 mM phosphate buffer pH 7.0 at 37 ºC under conditions where the peroxidation side reaction (RH_2 + H_2O_2 R + 2H_2O) is negligible ([H_2O_2] =< 25 mM; assay time, 10 s). The kinetics conformed to the Michaelis-Menten model. Lineweaver-Burk plots for H_2O_2 at different fixed concentrations of azide were linear and intersected on the abscissa indicating a noncompetitive or irreversible type of inhibition. To identify the inhibition type Vm vs. [E] plots were constructed at different [N_3-]. The plots were linear and converged at the origin, indicating that N_3- is a noncompetitive inhibitor. Using a non-linear curve-fitting program, the kinetic parameters were calculated. The K_m value for H_2O_2, and the K_i value for azide were found to be 10.97 ± 1.46 mM and 1.107 ± 0.093 µM, respectively.
Human erythrocytes, catalase, substrate kinetics, azide inhibition
AKSOY, YASEMİN; BALK, MEVHİBE; ÖĞÜŞ, HAMDİ; and ÖZER, NAZMİ (2004) "The Mechanism of Inhibition of Human Erythrocyte Catalase by Azide," Turkish Journal of Biology: Vol. 28: No. 2, Article 2. Available at: https://journals.tubitak.gov.tr/biology/vol28/iss2/2