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Surface modifications for enhanced enzyme immobilization and improved electron transfer of PQQ-dependent glucose dehydrogenase anodes

机译:表面修饰可增强PQQ依赖性葡萄糖脱氢酶阳极的酶固定化并改善电子转移

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摘要

Pyrroloquinoline quinone dependent soluble glucose dehydrogenase (PQQ-sGDH) enzymatic MWCNT electrodes were p roduced using 1-pyrenecarboxylic acid (PCA) activated through carbodiimide functionalization and 1-Pyrenebutyric acid N-hydroxysuccinimide ester (PBSE) as tethering agents. At 600 mV potential, the current density generated by the activated-PCA tethered PQQ-sGDH anode was significantly greater than the current density generated by the untethered PQQ-sGDH and PBSE tethered anodes, and performance was nearly identical to the performance of a covalently bound PQQ-sGDH anode. A technique for covalently bonding heme-b (hemin), a natural quinohemoprotein porphyrin redox cofactor, to carbon nanotubes modified with arylamine groups is reported. The resulting performance of the covalently bound hemin PQQ-sGDH anode is considerably higher than that of any other PQQ-sGDH anodes tested. (C) 2015 Elsevier B.V. All rights reserved.
机译:吡咯并喹啉醌依赖性可溶性葡萄糖脱氢酶(PQQ-sGDH)酶促MWCNT电极是通过碳二亚胺官能化活化的1-吡啶甲酸(PCA)和1-Pyrenebutyric acid N-羟基琥珀酰亚胺酯(PBSE)作为束缚剂制备的。在600 mV电位下,活化的PCA系留的PQQ-sGDH阳极产生的电流密度显着大于未系留的PQQ-sGDH和PBSE系留的阳极产生的电流密度,其性能几乎与共价键合的性能相同PQQ-sGDH阳极。报道了一种将天然的喹诺酮蛋白卟啉氧化还原辅助因子血红素-b(血红素)与经芳基胺基修饰的碳纳米管共价键合的技术。共价结合的血红素PQQ-sGDH阳极的最终性能明显高于测试的任何其他PQQ-sGDH阳极。 (C)2015 Elsevier B.V.保留所有权利。

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