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介孔碳电极上辣根过氧化物酶的直接电子转移型生物电催化及其在基于双酶体系的葡萄糖测定中的应用。

Direct Electron Transfer-type Bioelectrocatalysis of Peroxidase at Mesoporous Carbon Electrodes and Its Application for Glucose Determination Based on Bienzyme System.

作者信息

Xia Hong-Qi, Kitazumi Yuki, Shirai Osamu, Kano Kenji

机构信息

Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University.

出版信息

Anal Sci. 2017;33(7):839-844. doi: 10.2116/analsci.33.839.

Abstract

Non-catalytic direct electron transfer (DET) signal of Compound I of horseradish peroxidase (POD) was first detected at 0.7 V on POD/carbon nanotube mixture-modified electrodes. Excellent performance of DET-type bioelectrocatalysis was achieved with POD immobilized with glutaraldehyde on Ketjen Black (KB)-modified electrodes for HO reduction with an onset potential of 0.65 V (vs. Ag | AgCl | sat. KCl) without any electrode surface modification. The POD-immobilized KB electrode was found to be suitable for detecting HO with a low detection limit (0.1 μM at S/N = 3) at -0.1 V. By co-immobilizing glucose oxidase (GOD) and POD on the KB-modified electrode, a bienzyme electrode was constructed to couple the oxidase reaction of GOD with the DET-type bioelectrocatalytic reduction of HO by POD. The amperometric detection of glucose was performed with a high sensitivity (0.33 ± 0.01 μA cm μM) and a low detection limit (2 μM at S/N = 3).

摘要

在辣根过氧化物酶(POD)/碳纳米管混合物修饰电极上,首先在0.7 V处检测到了POD化合物I的非催化直接电子转移(DET)信号。通过戊二醛将POD固定在科琴黑(KB)修饰电极上,在没有任何电极表面修饰的情况下,实现了用于HO还原的DET型生物电催化的优异性能,起始电位为0.65 V(相对于Ag | AgCl |饱和KCl)。发现固定有POD的KB电极适用于在-0.1 V下检测HO,检测限低(S/N = 3时为0.1 μM)。通过将葡萄糖氧化酶(GOD)和POD共固定在KB修饰电极上,构建了一种双酶电极,以将GOD的氧化酶反应与POD对HO的DET型生物电催化还原偶联起来。葡萄糖的安培检测具有高灵敏度(0.33±0.01 μA cm μM)和低检测限(S/N = 3时为2 μM)。

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