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用于L-谷氨酸生物燃料阳极的电极表面多酶反应设计。

Design of a multi-enzyme reaction on an electrode surface for an L-glutamate biofuel anode.

作者信息

Sakamoto Hiroaki, Komatsu Tomohiro, Yamasaki Koji, Satomura Takenori, Suye Shin-Ichiro

机构信息

Tenure-Track Program for Innovation Research, University of Fukui, Fukui, Japan.

Department of Frontier Fiber Technology and Science, Graduate School of Engineering, University of Fukui, Bunkyo 3-9-1, Fukui, 910-8507, Japan.

出版信息

Biotechnol Lett. 2017 Feb;39(2):235-240. doi: 10.1007/s10529-016-2237-6. Epub 2016 Oct 19.

Abstract

OBJECTIVES

To design and construct a novel bio-anode electrode based on the oxidation of glutamic acid to produce 2-oxoglutarate, generating two electrons from NADH.

RESULTS

Efficient enzyme reaction and electron transfer were observed owing to immobilization of the two enzymes using a mixed self-assembled monolayer. The ratio of the immobilized enzymes was an important factor affecting the efficiency of the system; thus, we quantified the amounts of immobilized enzyme using a quartz crystal microbalance to further evaluate the electrochemical reaction. The electrochemical reaction proceeded efficiently when approximately equimolar amounts of the enzyme were on the electrode. The largest oxidation peak current increase (171 nA) was observed under these conditions.

CONCLUSION

Efficient multi-enzyme reaction on the electrode surface has been achieved which is applicable for biofuel cell application.

摘要

目的

设计并构建一种新型生物阳极电极,该电极基于谷氨酸氧化生成2-氧代戊二酸,从烟酰胺腺嘌呤二核苷酸(NADH)产生两个电子。

结果

由于使用混合自组装单分子层固定两种酶,观察到了高效的酶反应和电子转移。固定化酶的比例是影响系统效率的重要因素;因此,我们使用石英晶体微天平对固定化酶的量进行定量,以进一步评估电化学反应。当电极上的酶量近似等摩尔时,电化学反应高效进行。在这些条件下观察到最大氧化峰电流增加(171 nA)。

结论

已在电极表面实现了高效的多酶反应,该反应适用于生物燃料电池应用。

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