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Direct Electron Transfer at a Glucose Oxidase– Chitosan-Modified Vulcan Carbon Paste Electrode for Electrochemical Biosensing of Glucose

机译:葡萄糖氧化酶-壳聚糖修饰的Vulcan碳糊电极上的直接电子转移,用于葡萄糖的电化学生物传感

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摘要

This article describes the investigation of direct electron transfer (DET) between glucose oxidase (GOD) and the electrode materials in an enzyme-catalyzed reaction for the development of improved bioelectrocatalytic system. The GOD pedestal electrochemical reaction takes place by means of DET in a tailored Vulcan carbon paste electrode surfaces with GOD and chitosan (CS), allowing efficient electron transfer between the electrode and enzyme. The key understanding of the stability, biocatalytic activity, selectivity, and redox properties of these enzyme-based glucose biosensors is studied without using any reagents, and the properties are characterized using electrochemical techniques like cyclic voltammogram, amperometry, and electrochemical impedance spectroscopy. Furthermore, the interaction between the enzyme and the electrode surface is studied using ultraviolet–visible (UV– Vis) and Fourier transform infrared (FTIR) spectroscopy. The present glucose biosensor exhibited better linearity, limit of detection (LOD=0.37±0.02 mol/L) and a Michaelis–Menten constant of 0.40±0.01 mol/L. The proposed enzyme electrode exhibited excellent sensitivity, selectivity, reproducibility, and stability. This provides a simple "reagent-less" approach and efficient platform for the direct electrochemistry of GOD and developing novel bioelectrocatalytic systems.
机译:本文介绍了葡萄糖氧化酶(GOD)与电极材料之间在酶催化反应中直接电子转移(DET)的研究,以开发改进的生物电催化系统。 GOD基座电化学反应通过DET在具有GOD和壳聚糖(CS)的定制Vulcan碳糊电极表面上进行,从而实现了电极与酶之间的有效电子转移。在不使用任何试剂的情况下,研究了对这些基于酶的葡萄糖生物传感器的稳定性,生物催化活性,选择性和氧化还原特性的关键理解,并使用循环伏安图,安培法和电化学阻抗谱等电化学技术对特性进行了表征。此外,使用紫外可见(UV-Vis)和傅里叶变换红外(FTIR)光谱研究了酶与电极表面之间的相互作用。目前的葡萄糖生物传感器表现出更好的线性度,检测极限(LOD = 0.37±0.02 mol / L)和米氏-门腾常数为0.40±0.01 mol / L。提出的酶电极表现出优异的灵敏度,选择性,可再现性和稳定性。这为GOD的直接电化学和开发新型生物电催化系统提供了一个简单的“无试剂”方法和高效平台。

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