Kinetic isotope effect of prostaglandin H synthase exhibits inverted temperature dependence

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Abstract

Conversion of arachidonic acid to prostaglandin G2/H2 catalyzed by prostaglandin H synthase (PGHS) is proposed to involve initial transfer of the C13 pro-(S) hydrogen atom from arachidonate to the Tyr385 radical in PGHS, followed by insertion of two oxygen molecules and several chemical bond rearrangements. The initial hydrogen-transfer was recently concluded to be a rate-limiting step in cyclooxygenase catalysis based on the observed intrinsic deuterium kinetic isotope effect values (Dkcat). In the present study, we have found that Dkcat values of both PGHS-1 and -2 show an unusual increase with temperatures in the range of 288-310 K, exhibiting an inverted temperature dependence. The value of lnDkcat, however, decreased linearly with 1/T, consistent with a typical Arrhenius relationship. © 2014 by the authors; licensee MDPI, Basel, Switzerland.

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Wu, G., Kulmacz, R. J., & Tsai, A. L. (2014). Kinetic isotope effect of prostaglandin H synthase exhibits inverted temperature dependence. Catalysts, 4(2), 174–185. https://doi.org/10.3390/catal4020174

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