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Steady state kinetic theory model calculations

Chemistry of High Energy Atomic Fluorine Steady State Kinetic Theory Model Calculations for the + H2 Reaction m... [Pg.314]

Yang and Schulz also formulated a treatment of coupled enzyme reaction kinetics that does not assume an irreversible first reaction. The validity of their theory is confirmed by a model system consisting of enoyl-CoA hydratase (EC 4.2.1.17) and 3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35) with 2,4-decadienoyl coenzyme A as a substrate. Unlike the conventional theory, their approach was found to be indispensible for coupled enzyme systems characterized by a first reaction with a small equilibrium constant and/or wherein the coupling enzyme concentration is higher than that of the intermediate. Equations based on their theory can allow one to calculate steady-state velocities of coupled enzyme reactions and to predict the time course of coupled enzyme reactions during the pre-steady state. [Pg.174]


See other pages where Steady state kinetic theory model calculations is mentioned: [Pg.8]    [Pg.164]    [Pg.320]    [Pg.239]    [Pg.332]    [Pg.242]    [Pg.376]    [Pg.453]    [Pg.4086]    [Pg.241]    [Pg.838]    [Pg.308]    [Pg.4085]    [Pg.332]    [Pg.241]    [Pg.315]    [Pg.43]    [Pg.20]    [Pg.292]   


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Kinetic theory 492 kinetics

Kinetics theory

Model calculations

Model theory

Modeling steady-state

Steady state calculations

Steady state kinetic

Steady state kinetics

Steady state theory model calculations

Steady-state kinetic model

Steady-state theory

Theory calculation

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