Journal
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 92, Issue 5, Pages 1083-1093Publisher
SPRINGER
DOI: 10.1007/s00253-011-3583-x
Keywords
Desulfovibrio G11; MEC; Hydrogen; Exocellular electron transfer; Sulfate-reducing bacteria
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Funding
- Wetsus and the Chemical Sciences Division of the Netherlands Organisation for Scientific Research [CW-TOP 700.55.343]
- Dutch Ministry of Economic Affairs
- European Union Regional Development
- province of Friesland
- City of Leeuwarden
- EZ/Kompas program of the Samenwerkingsverband Noord-Nederland.
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The microbial electrolysis cell (MEC) is a promising system for hydrogen production. Still, expensive catalysts such as platinum are needed for efficient hydrogen evolution at the cathode. Recently, the possibility to use a biocathode as an alternative for platinum was shown. The microorganisms involved in hydrogen evolution in such systems are not yet identified. We analyzed the microbial community of a mixed culture biocathode that was enriched in an MEC bioanode. This biocathode produced 1.1 A m(-2) and 0.63 m(3) H-2 m(-3) cathode liquid volume per day. The bacterial population consisted of 46% Proteobacteria, 25% Firmicutes, 17% Bacteroidetes, and 12% related to other phyla. The dominant ribotype belonged to the species Desulfovibrio vulgaris. The second major ribotype cluster constituted a novel taxonomic group at the genus level, clustering within uncultured Firmicutes. The third cluster belonged to uncultured Bacteroidetes and grouped in a taxonomic group from which only clones were described before; most of these clones originated from soil samples. The identified novel taxonomic groups developed under environmentally unusual conditions, and this may point to properties that have not been considered before. A pure culture of Desulfovibrio strain G11 inoculated in a cathode of an MEC led to a current development from 0.17 to 0.76 A m(-2) in 9 days, and hydrogen gas formation was observed. On the basis of the known characteristics of Desulfovibrio spp., including its ability to produce hydrogen, we propose a mechanism for hydrogen evolution through Desulfovibrio spp. in a biocathode system.
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