Enzymatic nitrate assay by a kinetic method employing Escherichia coli nitrate reductase.

J Schild, J H Klemme
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引用次数: 5

Abstract

An enzymatic assay system for nitrate employing the membrane-bound nitrate reductase (EC 1.7.99.4) of E. coli is described. Contrary to previous enzymatic assay systems, the present method is a kinetic one, i.e. the substrate, nitrate, is assayed by measuring the reaction rate of the nitrate reductase-catalyzed reaction. Based on the observation that the nitrate reductase-catalyzed reaction obeys pseudo-first order kinetics, a test system is described allowing the assay of nitrate at a concentration as low as 1 ppm. The relatively high Michaelis-Menten constant for nitrate (0.3 mM) of the E. coli nitrate reductase favours nitrate assay by the kinetic method.

用大肠杆菌硝酸还原酶动力学法测定硝酸盐。
描述了一种利用大肠杆菌的膜结合硝酸盐还原酶(EC 1.7.99.4)的硝酸盐酶测定系统。与以前的酶分析系统相反,本方法是一种动力学方法,即通过测量硝酸还原酶催化反应的反应速率来测定底物硝酸盐。基于对硝酸还原酶催化反应服从准一级动力学的观察,描述了一种测试系统,允许在低至1ppm的浓度下测定硝酸盐。大肠杆菌硝酸盐还原酶的Michaelis-Menten常数较高(0.3 mM),有利于用动力学法测定硝酸盐。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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