Ethanol generation, oxidation and energy production in a cooperative bioelectrochemical system
Integrating in situ biofuel production and energy conversion into a single system ensures the production of more robust networks as well as more renewable technologies. For this purpose, identifying and developing new biocatalysts is crucial. Herein, is reported a bioelectrochemical system consistin...
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Veröffentlicht in: | Bioelectrochemistry (Amsterdam, Netherlands) Netherlands), 2018-08, Vol.122, p.11-25 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Integrating in situ biofuel production and energy conversion into a single system ensures the production of more robust networks as well as more renewable technologies. For this purpose, identifying and developing new biocatalysts is crucial. Herein, is reported a bioelectrochemical system consisting of alcohol dehydrogenase (ADH) and Saccharomyces cerevisiae, wherein both function cooperatively for ethanol production and its bioelectrochemical oxidation. Here, it is shown that it is possible to produce ethanol and use it as a biofuel in a tandem manner. The strategy is to employ flexible carbon fibres (FCF) electrode that could adsorb both the enzyme and the yeast cells. Glucose is used as a substrate for the yeast for the production of ethanol, while the enzyme is used to catalyse the oxidation of ethanol to acetaldehyde. Regarding the generation of reliable electricity based on electrochemical systems, the biosystem proposed in this study operates at a low temperature and ethanol production is proportional to the generated current. With further optimisation of electrode design, we envision the use of the cooperative biofuel cell for energy conversion and management of organic compounds.
•A microbial-enzyme cooperative biofuel cell was designed.•Saccharomyces cerevisiae and alcohol dehydrogenase provided the biocatalysis.•Ethanol was produced by microbial fermentation of the glucose.•Ethanol bio-oxidation was carried out on carbon fibre electrode. |
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ISSN: | 1567-5394 1878-562X |
DOI: | 10.1016/j.bioelechem.2018.02.007 |