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Polymer-supported electron transfer of PQQ-dependent glucose dehydrogenase at carbon nanotubes modified by electropolymerized polythiophene copolymers

机译:通过电聚合的聚噻吩共聚物改性的碳纳米管的PQQ依赖性葡萄糖脱氢酶的聚合物支持的电子转移

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The establishment of a polythiophene-supported electron transfer of PQQ-dependent glucose dehydrogenase (PQQ-GDH) at multiwalled carbon nanotubes is reported. For this purpose, thiol-functionalized MWCNTs are deposited on a gold electrode, which is further modified by on-top electropolymerization of different thiophene monomers. The enzyme is covalently bound to such an electrode by activating the carboxy groups of the polymer. The presence of the polythiophene copolymers allows for electrochemical wiring of PQQ-GDH that can subsequently transfer the electrons from the glucose oxidation to the electrode. Bioelectrocatalysis starts just at -0.2 V vs. Ag/AgCl and the anodic current reaches high values already at 0 V vs. Ag/AgCl. In order to improve the catalytic response, different parameters in the electropolymerization process are evaluated and buffer effects are investigated. The modified electrode surface is characterized by SEM-EDX, FTIR, UV-vis and XPS. The bioelectrocatalytic response towards increasing glucose concentrations is measured at 0 V vs. Ag/AgCl, showing a dynamic range extending from 1 mu M to 500 mM. (C) 2017 Elsevier Ltd. All rights reserved.
机译:报道了在多晶碳纳米管下建立了多噻吩支持的PQQ依赖性葡萄糖脱氢酶(PQQ-GDH)的电子传递。为此目的,将硫醇官能化的MWCNT沉积在金电极上,通过不同噻吩单体的顶部电聚合物进一步改性。通过激活聚合物的羧基与这种电极共价结合酶。聚噻吩共聚物的存在允许PQQ-GDH的电化学布线,其随后可以将电子从葡萄糖氧化转移到电极。生物电催化在-0.2V与Ag / AgCl和Ag / AgCl,阳极电流已经达到了0 V与Ag / AgCl的高值。为了改善催化反应,评估电聚合过程中的不同参数,并研究缓冲效应。改性电极表面的特征在于SEM-EDX,FTIR,UV-VI和XPS。在0V与Ag / AgCl下测量增加葡萄糖浓度的生物电催化反应,显示动态范围从1μm至500mm延伸。 (c)2017 Elsevier Ltd.保留所有权利。

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