Xia Hong-Qi, Kitazumi Yuki, Shirai Osamu, Kano Kenji
Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University.
Anal Sci. 2017;33(7):839-844. doi: 10.2116/analsci.33.839.
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).
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)。