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使用由顺序排列的L-谷氨酸脱氢酶和L-谷氨酸氧化酶组成的生物反应器通过化学发光法测定氨。

Use of a bioreactor consisting of sequentially aligned L-glutamate dehydrogenase and L-glutamate oxidase for the determination of ammonia by chemiluminescence.

作者信息

Murachi T, Tabata M

机构信息

Department of Clinical Science and Laboratory Medicine, Faculty of Medicine, Kyoto University, Japan.

出版信息

Biotechnol Appl Biochem. 1987 Aug;9(4):303-9. doi: 10.1111/j.1470-8744.1987.tb00479.x.

Abstract

A chemiluminometric method for the automated flow injection analysis of ammonia is described. The essence of the invention is the use of a bioreactor consisting of both immobilized L-glutamate dehydrogenase (GLDH) and L-glutamate oxidase (GLXD), which are sequentially aligned in this order in a minicolumn measuring 2.0 X 20 mm. The unidirectional constant flow of liquid through the column reactor minimizes the reversed diffusion of the solutes so that the following sequence of reactions is ensured. Thus, ammonia to be determined is first transformed by GLDH into L-glutamate, which then produces hydrogen peroxide by GLXD. Hydrogen peroxide in the effluent from the column is then determined by its chemiluminescence upon admixing with luminol and potassium ferricyanide. The present method gives linearity of the standard curve for ammonia up to 1.0 mM. It is at least 100 times more sensitive than the conventional method for ammonia assay using ultraviolet absorption measurement.

摘要

描述了一种用于氨的自动流动注射分析的化学发光法。本发明的核心是使用一种生物反应器,该反应器由固定化的L-谷氨酸脱氢酶(GLDH)和L-谷氨酸氧化酶(GLXD)组成,它们在一个2.0×20mm的微型柱中按此顺序依次排列。液体通过柱式反应器的单向恒定流动使溶质的反向扩散最小化,从而确保了以下反应顺序。因此,待测定的氨首先被GLDH转化为L-谷氨酸,然后L-谷氨酸由GLXD产生过氧化氢。然后,通过与鲁米诺和铁氰化钾混合后产生的化学发光来测定柱流出物中的过氧化氢。本方法给出的氨标准曲线线性范围可达1.0 mM。它比使用紫外吸收测量的传统氨测定方法至少灵敏100倍。

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