首页> 外文期刊>Journal of Biochemical and Biophysical Methods >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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Enzymatic activity assay of D-hydantoinase by isothermal titration calorimetry. Determination of the thermodynamic activation parameters for the hydrolysis of several substrates.

机译:等温滴定热法测定D-乙内酰脲酶的酶活性。确定用于水解几种底物的热力学活化参数。

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摘要

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.
机译:通过监测反应过程中释放的热量,等温滴定热法(ITC)已用于测定具有多种底物的D-乙内酰脲酶(EC 3.5.2.2)的活性。该方法基于反应速率和所产生的热功率(热量/时间)之间的比例。在不同温度下进行的微量量热测定提供了催化速率常数对温度的依赖性。我们表明,ITC分析是一种非破坏性方法,可确定该反应的催化速率常数(kcat),米氏常数(KM),活化能和活化吉布斯能,焓和熵。

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