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Pyrene hydrogel for promoting direct bioelectrochemistry: ATP-independent electroenzymatic reduction of N2†
Chemical Science ( IF 8.4 ) Pub Date : 2018-05-14 00:00:00 , DOI: 10.1039/c8sc01638k
David P. Hickey 1, 2, 3, 4 , Koun Lim 1, 2, 3, 4 , Rong Cai 1, 2, 3, 4 , Ashlea R. Patterson 1, 2, 3, 4 , Mengwei Yuan 1, 2, 3, 4 , Selmihan Sahin 1, 1, 2, 3, 4 , Sofiene Abdellaoui 1, 2, 3, 4 , Shelley D. Minteer 1, 2, 3, 4
Affiliation  

Enzymatic bioelectrocatalysis often requires an artificial redox mediator to observe significant electron transfer rates. The use of such mediators can add a substantial overpotential and obfuscate the protein's native kinetics, which limits the voltage of a biofuel cell and alters the analytical performance of biosensors. Herein, we describe a material for facilitating direct electrochemical communication with redox proteins based on a novel pyrene-modified linear poly(ethyleneimine). This method was applied for promoting direct bioelectrocatalytic reduction of O2 by laccase and, by immobilizing the catalytic subunit of nitrogenase (MoFe protein), to demonstrate the ATP-independent direct electroenzymatic reduction of N2 to NH3.

中文翻译:

用于促进直接生物电化学的水凝胶:不依赖ATP的电酶还原N 2

酶促生物电催化通常需要人工氧化还原介体来观察显着的电子转移速率。此类介体的使用可能会增加大量的过电位并混淆蛋白质的天然动力学,从而限制了生物燃料电池的电压并改变了生物传感器的分析性能。在本文中,我们描述了一种基于新型-修饰的线性聚(乙烯亚胺)的材料,以促进与氧化还原蛋白的直接电化学通讯。该方法用于通过漆酶促进O 2的直接生物电催化还原,并通过固定固氮酶(MoFe蛋白)的催化亚基,证明N 2不依赖于ATP的直接电催化还原为NH 3
更新日期:2018-05-14
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