Fig. 4.
Fig. 4. Determination of GPO and catalase activity in a mixture of purified enzymes. (A) After the addition of enzyme mixture (GPO, 0.01 U/mL; catalase, kcat = 0.034 s−1) only the catalase-mediated H2O2 decay is observed. (B) Inhibition of catalase by 1 mmol/L NaN3 . (C) Second addition of 10−5 mol/L H2O2 shows complete inhibition of catalase. (D) Addition of 2 mmol/L GSH and recalibration of the measuring system (see Mueller et al25 ). (E) The GPO-mediated decomposition of H2O2 is observed after the addition of 10−4 mol/L H2O2 . These experiments were performed with GPO activities higher than those in erythrocytes with respect to catalase to improve the kinetic characterization of both enzymes.

Determination of GPO and catalase activity in a mixture of purified enzymes. (A) After the addition of enzyme mixture (GPO, 0.01 U/mL; catalase, kcat = 0.034 s−1) only the catalase-mediated H2O2 decay is observed. (B) Inhibition of catalase by 1 mmol/L NaN3 . (C) Second addition of 10−5 mol/L H2O2 shows complete inhibition of catalase. (D) Addition of 2 mmol/L GSH and recalibration of the measuring system (see Mueller et al25 ). (E) The GPO-mediated decomposition of H2O2 is observed after the addition of 10−4 mol/L H2O2 . These experiments were performed with GPO activities higher than those in erythrocytes with respect to catalase to improve the kinetic characterization of both enzymes.

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