Intimate relation between cyclooxygenase and peroxidase activities of prostaglandin H synthase. Peroxidase reaction of ferulic acid and its influence on the reaction of arachidonic acid.

Abstract

The oxidation of ferulic acid by hydrogen peroxide catalyzed by prostaglandin H synthase follows a modified ping-pong irreversible mechanism, as is the case for classical peroxidases. The rate constant for the reaction of prostaglandin H synthase with hydrogen peroxide, determined from steady-state results, is (1.31 +/- 0.1) x 10(6) M-1 s-1, and for the reaction of prostaglandin H synthase-compound II with ferulic acid it is (5.5 +/- 0.3) x 10(6) M-1 s-1. Cyclooxygenase and peroxidase functions of prostaglandin H synthase were studied by comparing the initial rates of reaction of the cyclooxygenase substrate, arachidonic acid, and a peroxidase reducing substrate, ferulic acid, in mixtures of the two substrates. For both an equimolar ratio of arachidonic and ferulic acids and ferulic acid in excess of arachidonic acid a stimulation of the cyclooxygenase reaction is observed. The concentration of ferulic acid necessary to produce 50% stimulation of 0.2 mM arachidonic acid oxidation is 0.14 +/- 0.02 mM. A striking feature of our results is that prostaglandin H synthase catalyzes oxidation of the two substrates in a constant and fixed molar ratio of ferulic acid to arachidonic acid of 2:1, despite widely different starting concentrations. If arachidonic acid is in excess of ferulic acid, enzyme inactivation occurs. The results can be explained by an interconnected cyclooxygenase-peroxidase unbranched free radical mechanism in which arachidonic acid reacts with either the ferryl oxygen or the porphyrin pi-cation radical part of a conventional peroxidase compound I (a FeIV = O porphyrin pi-cation radical) and ferulic acid reacts with compound II (FeIV = O).(ABSTRACT TRUNCATED AT 250 WORDS)