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基于共固定化对羟基苯甲酸羟化酶和葡萄糖-6-磷酸脱氢酶的葡萄糖-6-磷酸生物传感器的研制。

Development of a glucose-6-phosphate biosensor based on coimmobilized p-hydroxybenzoate hydroxylase and glucose-6-phosphate dehydrogenase.

作者信息

Cui Yue, Barford John P, Renneberg Reinhard

机构信息

Department of Chemical Engineering and Department of Chemistry, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.

出版信息

Biosens Bioelectron. 2007 May 15;22(11):2754-8. doi: 10.1016/j.bios.2006.10.026. Epub 2006 Nov 29.

Abstract

This work reports the development of an amperometric glucose-6-phosphate biosensor by coimmobilizing p-hydroxybenzoate hydroxylase (HBH) and glucose-6-phosphate dehydrogenase (G6PDH) on a screen-printed electrode. The principle of the determination scheme is as follows: G6PDH catalyzes the specific dehydrogenation of glucose-6-phosphate by consuming NADP(+). The product, NADPH, initiates the irreversible the hydroxylation of p-hydroxybenzoate by HBH in the presence of oxygen to produce 3,4-dihydroxybenzoate, which results in a detectable signal due to its oxidation at the working electrode. The sensor shows a broad linear detection range between 2 microM and 1000 microM with a low detection limit of 1.2 microM. Also, it has a fast measuring time which can achieve 95% of the maximum current response in 20s after the addition of a given concentration of glucose-6-phosphate with a short recovery time (2 min).

摘要

这项工作报道了一种通过将对羟基苯甲酸羟化酶(HBH)和葡萄糖-6-磷酸脱氢酶(G6PDH)共固定在丝网印刷电极上而开发的安培型葡萄糖-6-磷酸生物传感器。测定方案的原理如下:G6PDH通过消耗NADP(+)催化葡萄糖-6-磷酸的特异性脱氢反应。产物NADPH在氧气存在下引发HBH对羟基苯甲酸的不可逆羟基化反应,生成3,4-二羟基苯甲酸,由于其在工作电极上的氧化而产生可检测信号。该传感器在2 microM至1000 microM之间具有较宽的线性检测范围,检测限低至1.2 microM。此外,它具有快速的测量时间,在加入给定浓度的葡萄糖-6-磷酸后20秒内可达到最大电流响应的95%,恢复时间短(2分钟)。

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