@article {3135,
	title = {Sulfur oxidation to sulfate coupled with electron transfer to electrodes by Desulfuromonas strain TZ1.},
	journal = {Microbiology (Reading)},
	volume = {160},
	year = {2014},
	month = {2014 Jan},
	pages = {123-129},
	abstract = {<p>Microbial oxidation of elemental sulfur with an electrode serving as the electron acceptor is of interest because this may play an important role in the recovery of electrons from sulfidic wastes and for current production in marine benthic microbial fuel cells. Enrichments initiated with a marine sediment inoculum, with elemental sulfur as the electron donor and a positively poised (+300 mV versus Ag/AgCl) anode as the electron acceptor, yielded an anode biofilm with a diversity of micro-organisms, including Thiobacillus, Sulfurimonas, Pseudomonas, Clostridium and Desulfuromonas species. Further enrichment of the anode biofilm inoculum in medium with elemental sulfur as the electron donor and Fe(III) oxide as the electron acceptor, followed by isolation in solidified sulfur/Fe(III) medium yielded a strain of Desulfuromonas, designated strain TZ1. Strain TZ1 effectively oxidized elemental sulfur to sulfate with an anode serving as the sole electron acceptor, at rates faster than Desulfobulbus propionicus, the only other organism in pure culture previously shown to oxidize S{\textdegree} with current production. The abundance of Desulfuromonas species enriched on the anodes of marine benthic fuel cells has previously been interpreted as acetate oxidation driving current production, but the results presented here suggest that sulfur-driven current production is a likely alternative.</p>},
	keywords = {Bioelectric Energy Sources, Desulfuromonas, DNA, Bacterial, Electricity, Electrodes, Geologic Sediments, Molecular Sequence Data, Oxidation-Reduction, Sequence Analysis, DNA, Sulfates, Sulfur},
	issn = {1465-2080},
	doi = {10.1099/mic.0.069930-0},
	author = {Zhang, Tian and Bain, Timothy S and Barlett, Melissa A and Dar, Shabir A and Snoeyenbos-West, Oona L and Nevin, Kelly P and Lovley, Derek R}
}
@article {424,
	title = {Electrosynthesis of organic compounds from carbon dioxide is catalyzed by a diversity of acetogenic microorganisms.},
	journal = {Appl Environ Microbiol},
	volume = {77},
	year = {2011},
	month = {2011 May},
	pages = {2882-6},
	abstract = {Microbial electrosynthesis, a process in which microorganisms use electrons derived from electrodes to reduce carbon dioxide to multicarbon, extracellular organic compounds, is a potential strategy for capturing electrical energy in carbon-carbon bonds of readily stored and easily distributed products, such as transportation fuels. To date, only one organism, the acetogen Sporomusa ovata, has been shown to be capable of electrosynthesis. The purpose of this study was to determine if a wider range of microorganisms is capable of this process. Several other acetogenic bacteria, including two other Sporomusa species, Clostridium ljungdahlii, Clostridium aceticum, and Moorella thermoacetica, consumed current with the production of organic acids. In general acetate was the primary product, but 2-oxobutyrate and formate also were formed, with 2-oxobutyrate being the predominant identified product of electrosynthesis by C. aceticum. S. sphaeroides, C. ljungdahlii, and M. thermoacetica had high (>80\%) efficiencies of electrons consumed and recovered in identified products. The acetogen Acetobacterium woodii was unable to consume current. These results expand the known range of microorganisms capable of electrosynthesis, providing multiple options for the further optimization of this process.},
	keywords = {Acetobacterium, Carbon Dioxide, Clostridium, Electrodes, Electrons, Moorella, Organic Chemicals, Oxidation-Reduction, Veillonellaceae},
	issn = {1098-5336},
	doi = {10.1128/AEM.02642-10},
	author = {Nevin, Kelly P and Hensley, Sarah A and Franks, Ashley E and Summers, Zarath M and Ou, Jianhong and Woodard, Trevor L and Snoeyenbos-West, Oona L and Lovley, Derek R}
}
