Low-Denaturazing Glucose Oxidase Immobilization onto Graphite Electrodes by Incubation in Chitosan Solutions

Mireia Buaki-Sogó, Laura García-Carmona, M. Gil-Agusti, M. García-Pellicer, A. Quijano-López
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Abstract

In this work, glucose oxidase (GOx) has been immobilized onto graphite rod electrodes through an assisted-chitosan adsorption reaching an enzyme coverage of 4 nmol/cm2. The direct and irreversible single adsorption of the Flavine Adenine Dinucleotide (FAD) cofactor has been minimized by electrode incubation in a chitosan (CH) solution containing the enzyme GOx. Chitosan keeps the enzyme structure and conformation due to electrostatic interactions preventing FAD dissociation from the protein envelope. Using chitosan, both the redox cofactor FAD and the protein envelope remain in the active form as demonstrated by the electrochemistry studies and the enzymatic activity in the electrochemical oxidation of glucose up to a concentration of 20 mM. The application of the modified electrodes for energy harvesting delivered a power density of 119 µW/cm2 with a cell voltage of 0.3 V. Thus, chitosan presents a stabilizing effect for the enzyme conformation promoted by the confinement effect in the chitosan solution by electrostatic interactions. Additionally, it facilitated the electron transfer from the enzyme to the electrode due to the presence of embedded chitosan in the enzyme structure acting as an electrical wiring between the electrode and the enzyme (electron transfer rate constant 2.2 s−1). This method involves advantages compared with previously reported chitosan immobilization methods, not only due to good stability of the enzyme, but also to the simplicity of the procedure that can be carried out even for not qualified technicians which enable their easy implementation in industry.
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壳聚糖溶液中低变性葡萄糖氧化酶在石墨电极上的固定化
在这项工作中,葡萄糖氧化酶(GOx)通过壳聚糖的辅助吸附固定在石墨棒电极上,达到4 nmol/cm2的酶覆盖率。在含有GOx酶的壳聚糖(CH)溶液中进行电极孵育,使黄嘌呤腺嘌呤二核苷酸(FAD)辅因子的直接不可逆单吸附最小化。壳聚糖通过静电相互作用保持酶的结构和构象,防止FAD从蛋白包膜上解离。使用壳聚糖,电化学研究表明,氧化还原辅助因子FAD和蛋白质包膜都保持活性形式,并且在葡萄糖的电化学氧化中达到20 mM的酶活性。应用改性电极进行能量收集,在0.3 V的电池电压下,功率密度为119 μ W/cm2。由此可见,壳聚糖通过静电作用对壳聚糖溶液中的约束效应促进酶的构象具有稳定作用。此外,由于酶结构中嵌入的壳聚糖作为电极和酶之间的电线,它促进了电子从酶到电极的转移(电子转移速率常数为2.2 s−1)。与以往报道的壳聚糖固定化方法相比,该方法不仅具有良好的酶稳定性,而且操作简单,即使是不合格的技术人员也可以进行,使其易于在工业上实施。
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