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|Title:||Enzymatic fuel cells with an oxygen resistant variant of pyranose-2-oxidase as anode biocatalyst|
Eileen Hao Yu
Vidyasirimedhi Institute of Science and Technology
Newcastle University, United Kingdom
Bilecik Şeyh Edebali University
|Keywords:||Biochemistry, Genetics and Molecular Biology;Chemistry;Engineering|
|Citation:||Biosensors and Bioelectronics. Vol.107, (2018), 17-25|
|Abstract:||© 2018 In enzymatic fuel cells (EnFCs), hydrogen peroxide formation is one of the main problems when enzymes, such as, glucose oxidase (GOx) is used due to the conversion of oxygen to hydrogen peroxide in the catalytic reaction. To address this problem, we here report the first demonstration of an EnFC using a variant of pyranose-2-oxidase (P2O-T169G) which has been shown to have low activity towards oxygen. A simple and biocompatible immobilisation approach incorporating multi-walled-carbon nanotubes within ferrocene (Fc)-Nafion film was implemented to construct EnFCs. Successful immobilisation of the enzymes was demonstrated showing 3.2 and 1.7-fold higher current than when P2O-T169G and GOx were used in solution, respectively. P2O-T169G showed 25% higher power output (maximum power density value of 8.45 ± 1.6 μW cm−2) and better stability than GOx in aerated glucose solutions. P2O-T169G maintained > 70% of its initial current whereas GOx lost activity > 90% during the first hour of 12 h operation at 0.15 V (vs Ag/Ag+). A different fuel cell configuration using gas-diffusion cathode and carbon paper electrodes were used to improve the power output of the fuel cell to 29.8 ± 6.1 µW cm−2. This study suggests that P2O-T169G with low oxygen activity could be a promising anode biocatalyst for EnFC applications.|
|Appears in Collections:||Scopus 2018|
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