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Enzymatic activity assay of D-hydantoinase by isothermal titration calorimetry. Determination of the thermodynamic activation parameters for the hydrolysis of several substrates
Authors:Andújar-Sánchez Montserrat  Las Heras-Vázquez Francisco Javier  Clemente-Jiménez Josefa María  Martínez-Rodríguez Sergio  Camara-Artigas Ana  Rodríguez-Vico Felipe  Jara-Pérez Vicente
Affiliation:Dpto. Química Física, Bioquímica y Química Inorgánica, Universidad de Almería, Spain.
Abstract:Isothermal titration calorimetry (ITC) has been applied to the determination of the activity of D-hydantoinase (EC 3.5.2.2) with several substrates by monitoring the heat released during the reaction. The method is based on the proportionality between the reaction rate and the thermal power (heat/time) generated. Microcalorimetric assays carried out at different temperatures provided the dependence of the catalytic rate constant on temperature. We show that ITC assay is a nondestructive method that allows the determination of the catalytic rate constant (kcat), Michaelis constant (KM), activation energy and activation Gibbs energy, enthalpy and entropy of this reaction.
Keywords:ITC, Isothermal titration calorimetry   kcat, catalytic rate constant   KM, Michaelis constant   Ea, activation energy   LB, Luria Bertani   ΔHm, molar enthalpy
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