葡萄糖氧化酶
电子转移
纳米网
纳米技术
电极
胶体金
材料科学
噬菌体
化学工程
氧化还原
基质(水族馆)
胆红素氧化酶
化学
纳米颗粒
生物传感器
光化学
生物化学
无机化学
生物
物理化学
大肠杆菌
工程类
基因
石墨烯
生态学
作者
Rita A. Blaik,Esther H. Lan,Yu Huang,Bruce Dunn
出处
期刊:ACS Nano
[American Chemical Society]
日期:2015-11-23
卷期号:10 (1): 324-332
被引量:60
标识
DOI:10.1021/acsnano.5b04580
摘要
Glucose oxidase-based biofuel cells are a promising source of alternative energy for small device applications, but still face the challenge of achieving robust electrical contact between the redox enzymes and the current collector. This paper reports on the design of an electrode consisting of glucose oxidase covalently attached to gold nanoparticles that are assembled onto a genetically engineered M13 bacteriophage using EDC-NHS chemistry. The engineered phage is modified at the pIII protein to attach onto a gold substrate and serves as a high-surface-area template. The resulting "nanomesh" architecture exhibits direct electron transfer (DET) and achieves a higher peak current per unit area of 1.2 mA/cm2 compared to most other DET attachment schemes. The final enzyme surface coverage on the electrode was calculated to be approximately 4.74 × 10–8 mol/cm2, which is a significant improvement over most current glucose oxidase (GOx) DET attachment methods.
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