Formulation of a Universal First-Order Rate Constant for Enzymatic Reactions

  • IMOTO Taiji
    Emeritus Professor, Graduate School of Pharmaceutical Sciences, Kyushu University

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It is a common practice to employ kcat[E]0/Km as a first-order rate constant for the analysis of an enzymatic reaction, where [E]0 is the total enzyme concentration. I describe in this report a serious shortcoming in analyzing enzymatic reactions when kcat[E]0/Km is employed and show that kcat[E]0/Km can only be applied under very limited conditions. I consequently propose the use of a more universal first-order rate constant, kcat[ES]K/[S]0, where [ES]K is the initial equilibrium concentration of the ES-complex derived from [E]0, [S]0 and Km. Employing kcat[ES]K/[S]0 as the first-order rate constant enables all enzymatic reactions to be reasonably simulated under a wide range of conditions, and the catalytic and binding contributions to the rate constant of any enzyme can be determined under any and all conditions.

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