Wiring of bilirubin oxidases with redox polymers on gas diffusion electrodes for increased stability of self-powered biofuel cells-based glucose sensing

•A glucose oxygen biofuel cell/glucose sensor with a non-limiting biocathode.•Three types of bilirubin oxidase were evaluated in direct and mediated electron transfer.•The bilirubin oxidase from Magnaporthe oryzae (Mo-BOD) showed the highest oxygen reduction current. A new redox polymer/bilirubin ox...

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Veröffentlicht in:Bioelectrochemistry (Amsterdam, Netherlands) Netherlands), 2023-02, Vol.149, p.108314-108314, Article 108314
Hauptverfasser: Becker, Jana M., Lielpetere, Anna, Szczesny, Julian, Bichon, Sabrina, Gounel, Sébastien, Mano, Nicolas, Schuhmann, Wolfgang
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Sprache:eng
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Zusammenfassung:•A glucose oxygen biofuel cell/glucose sensor with a non-limiting biocathode.•Three types of bilirubin oxidase were evaluated in direct and mediated electron transfer.•The bilirubin oxidase from Magnaporthe oryzae (Mo-BOD) showed the highest oxygen reduction current. A new redox polymer/bilirubin oxidase (BOD)-based gas diffusion electrode was designed to be implemented as the non-current and non-stability limiting biocathode in a glucose/O2 biofuel cell that acts as a self-powered glucose biosensor. For the proof-of-concept, a bioanode comprising the Os-complex modified redox polymer P(VI-co-AA)-[Os(bpy)2Cl]Cl and FAD-dependent glucose dehydrogenase to oxidize the analyte was used. In order to develop an optimal O2-reducing biocathode for the biofuel cell Mv-BOD as well as Bp-BOD and Mo-BOD have been tested in gas diffusion electrodes in direct electron transfer as well as in mediated electron transfer immobilized in the Os-complex modified redox polymer P(VI-co-AA)-[Os(diCl-bpy)2]Cl2. The resulting biofuel cell exhibits a glucose-dependent current and power output in the concentration region between 1 and 10 mM. To create a more realistic test environment, the performance and long-term stability of the biofuel cell-based self-powered glucose biosensor has been investigated in a flow-through cell design.
ISSN:1567-5394
1878-562X
DOI:10.1016/j.bioelechem.2022.108314