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使用与多酶系统共固定的细菌荧光素酶对各种代谢物进行生物发光微量测定。

Bioluminescent microassay of various metabolites using bacterial luciferase co-immobilized with multienzyme systems.

作者信息

Ugarova N N, Lebedeva O V, Frumkina I G

机构信息

Chemistry Department, Lomonosov Moscow State University, USSR.

出版信息

Anal Biochem. 1988 Sep;173(2):221-7. doi: 10.1016/0003-2697(88)90182-0.

Abstract

Co-immobilization methods have been developed for a bienzymatic system of luminescent Beneckea harveyi bacteria with formate dehydrogenase, glucose-6-phosphate dehydrogenase, and phosphoglucomutase. Bioluminescent assays have been devised for NADH, NAD, FMN, glucose 6-phosphate, and glucose 1-phosphate using the co-immobilized enzyme preparation. The lowest detection limits were in the picomole range with the bacterial extract and in the femtomole range with the partially purified enzymes, bacterial luciferase, and NADH:FMN oxidoreductase.

摘要

已经开发出共固定化方法,用于发光哈维贝内克氏菌(Beneckea harveyi bacteria)与甲酸脱氢酶、葡萄糖-6-磷酸脱氢酶和磷酸葡萄糖变位酶的双酶系统。使用共固定化酶制剂设计了针对NADH、NAD、FMN、葡萄糖6-磷酸和葡萄糖1-磷酸的生物发光测定法。细菌提取物的最低检测限在皮摩尔范围内,部分纯化的酶、细菌荧光素酶和NADH:FMN氧化还原酶的最低检测限在飞摩尔范围内。

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