Enzymatic activity assay of D-hydantoinase by isothermal titration calorimetry. Determination of the thermodynamic activation parameters for the hydrolysis of several substrates |
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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 |
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Affiliation: | Dpto. Química Física, Bioquímica y Química Inorgánica, Universidad de Almería, Spain. |
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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. |
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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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