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A general method for the analysis of random bisubstrate enzyme mechanisms
Authors:Vladimir?Leskovac  author-information"  >  author-information__contact u-icon-before"  >  mailto:leskovac@neobee.net"   title="  leskovac@neobee.net"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Svetlana?Trivi?,Draginja?Peri?in,Julijan?Kandra?
Affiliation:(1) Faculty of Technology, Bulevar Cara Lazara 1, 21000 Novi Sad, Yugoslavia;(2) Faculty of Science, Bulevar Cara Lazara 1, 21000 Novi Sad, Yugoslavia;(3) Faculty of Agriculture, Bulevar Cara Lazara 1, 21000 Novi Sad, Yugoslavia
Abstract:In the present communication, a general method for the kinetic analysis of random bisubstrate mechanisms is described. The method comprises a stepwise application of the following kinetic and ligand-binding experiments: determination of steady-state kinetic constants, product inhibition patterns, maximum rate relationships, application of alternate substrates, application of dead-end inhibitors, direct binding of substrates, kinetic isotope effects, and isotope exchange studies. This general method was applied to a practical example: a yeast alcohol dehydrogenase-catalyzed oxidation of 2-propanol by NAD+ at pH 7.0, 25°C. It was found that this fully reversible reaction proceeds by a steady-state random Bi-Bi mechanism, whereby both dead-end complexes are formed.
Keywords:Yeast alcohol dehydrogenase  Kinetic mechanism of action
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