Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill, NC, 27599, USA.
Division of Engineering, Faculty of Engineering, University of Fukui, Fukui, Japan.
Biosens Bioelectron. 2024 May 15;252:116092. doi: 10.1016/j.bios.2024.116092. Epub 2024 Feb 8.
This work presents the development of an enzyme fuel cell, termed "BioBattery", that utilizes multicopper oxidases as the anodic enzyme in a non-diffusion limited system. We evaluated various enzyme variants as the anode, including multicopper oxidase from Pyrobaculum aerophilum, laccase from Trametes versicolor, and bilirubin oxidase from Myrothecium verrucaria. Several combinations of cathodes were also examined, focusing on the reduction of oxygen as the primary electron acceptor. The optimal pairing used multicopper oxidase from Pyrobaculum aerophilum as the anode and amine reactive phenazine ethosulfate modified bovine serum albumin as the cathode. BioBattery was integrated with our previously developed BioCapacitor, proving capable of consistently powering a 470 μF capacitor, positioning it as a modular power source for wearable and implantable systems. This research work addresses and overcomes some of the fundamental limitations seen in enzyme fuel cells, where power and current are often limited by substrate accessibility to the active electrode surface. (152 words).
这项工作展示了一种酶燃料电池的开发,称为“BioBattery”,它在非扩散限制系统中使用多铜氧化酶作为阳极酶。我们评估了各种酶变体作为阳极,包括嗜热菌 Aerophilum 的多铜氧化酶、变色栓菌的漆酶和疣孢漆斑菌的胆红素氧化酶。还检查了几种阴极的组合,重点是将氧气还原为主要电子受体。最佳配对使用嗜热菌 Aerophilum 的多铜氧化酶作为阳极,胺反应性吩嗪乙硫酸酯修饰的牛血清白蛋白作为阴极。BioBattery 与我们之前开发的 BioCapacitor 集成,能够持续为 470 μF 的电容器供电,使其成为可穿戴和植入式系统的模块化电源。这项研究工作解决并克服了酶燃料电池中常见的一些基本限制,其中功率和电流通常受到活性电极表面对底物可及性的限制。(152 个单词)。