@article {3109,
	title = {Enhancing syntrophic metabolism in up-flow anaerobic sludge blanket reactors with conductive carbon materials.},
	journal = {Bioresour Technol},
	volume = {191},
	year = {2015},
	month = {2015 Sep},
	pages = {140-5},
	abstract = {<p>Syntrophic metabolism of alcohols and fatty acids is a critical step in anaerobic digestion, which if enhanced can better stabilize the process and enable shorter retention times. Direct interspecies electron transfer (DIET) has recently been recognized as an alternative route to hydrogen interspecies transfer as a mechanism for interspecies syntrophic electron exchange. Therefore, the possibility of accelerating syntrophic metabolism of ethanol in up-flow anaerobic sludge blanket (UASB) reactors by incorporating conductive materials in reactor design was investigated. Graphite, biochar, and carbon cloth all immediately enhanced methane production and COD removal. As the hydraulic retention time was decreased the increased effectiveness of treatment in reactors with conductive materials increased versus the control reactor. When these conductive materials were removed from the reactors rates of syntrophic metabolism declined to rates comparable to the control reactor. These results suggest that incorporating conductive materials in the design of UASB reactors may enhance digester effectiveness.</p>},
	keywords = {Anaerobiosis, Bioreactors, Carbon, Charcoal, Electron Transport, Graphite, Hydrogen, Methane, Sewage, Waste Disposal, Fluid},
	issn = {1873-2976},
	doi = {10.1016/j.biortech.2015.05.007},
	author = {Zhao, Zhiqiang and Zhang, Yaobin and Woodard, T L and Nevin, K P and Lovley, D R}
}
@article {599,
	title = {Anaerobic degradation of methyl tert-butyl ether (MTBE) and tert-butyl alcohol (TBA).},
	journal = {Environ Sci Technol},
	volume = {35},
	year = {2001},
	month = {2001 May 1},
	pages = {1785-90},
	abstract = {The potential for anaerobic degradation of methyl tert-butyl ether (MTBE) and tert-butyl alcohol (TBA) was investigated in laboratory incubations of sediments from a petroleum-contaminated aquifer and in aquatic sediments. The addition of humic substances (HS) stimulated the anaerobic degradation of MTBE in aquifer sediments in which Fe(III) was available as an electron acceptor. This is attributed to the fact that HS and other extracellular quinones can stimulate the activity of Fe(III)-reducing microorganisms by acting as an electron shuttle between Fe(III)-reducing microorganisms and insoluble Fe(III) oxides. MTBE was not degraded in aquifer sediments without Fe(III) and HS. [14C]-MTBE added to aquatic sediments adapted for anaerobic MTBE degradation was converted to 14CO2 in the presence or absence of HS or the HS analog, anthraquione-2,6-disulfonate. Unamended aquatic sediments produced 14CH4 as well as 14CO2 from [14C]-MTBE. The aquatic sediments also rapidly consumed TBA under anaerobic conditions and converted [14C]-TBA to 14CH4 and 14CO2. An adaptation period of ca. 250-300 days was required prior to the most rapid anaerobic MTBE degradation in both sediment types, whereas TBA was metabolized in the aquatic sediments without a lag. These results demonstrate that, under the appropriate conditions, MTBE and TBA can be degraded in the absence of oxygen. This suggests that it may be possible to design strategies for the anaerobic remediation of MTBE in petroleum-contaminated subsurface environments.},
	keywords = {Anaerobiosis, Biodegradation, Environmental, Carbon Dioxide, Geologic Sediments, Methane, Methyl Ethers, tert-Butyl Alcohol, Water Pollutants, Chemical},
	issn = {0013-936X},
	author = {Finneran, K T and Lovley, D R}
}
@article {591,
	title = {Bioremediation. Anaerobes to the rescue.},
	journal = {Science},
	volume = {293},
	year = {2001},
	month = {2001 Aug 24},
	pages = {1444-6},
	keywords = {Bacteria, Aerobic, Bacteria, Anaerobic, Biodegradation, Environmental, Euryarchaeota, Ferric Compounds, Genome, Archaeal, Genome, Bacterial, Hydrocarbons, Aromatic, Hydrocarbons, Chlorinated, Metals, Methane, Nitrates, Oxidation-Reduction, Oxygen, Soil Microbiology, Sulfates, Sulfur-Reducing Bacteria, Water Pollutants, Chemical},
	issn = {0036-8075},
	doi = {10.1126/science.1063294},
	author = {Lovley, D R}
}
@article {612,
	title = {Hexadecane decay by methanogenesis.},
	journal = {Nature},
	volume = {404},
	year = {2000},
	month = {2000 Apr 13},
	pages = {722-3},
	keywords = {Alkanes, Anaerobiosis, Bacteria, Biodegradation, Environmental, Geologic Sediments, Methane, Petroleum},
	issn = {0028-0836},
	doi = {10.1038/35008145},
	author = {Anderson, R T and Lovley, D R}
}
@article {643,
	title = {Stimulated anoxic biodegradation of aromatic hydrocarbons using Fe(III) ligands.},
	journal = {Nature},
	volume = {370},
	year = {1994},
	month = {1994 Jul 14},
	pages = {128-31},
	abstract = {Contamination of ground waters with water-soluble aromatic hydrocarbons, common components of petroleum pollution, often produces anoxic conditions under which microbial degradation of the aromatics is slow. Oxygen is often added to contaminated ground water to stimulate biodegradation, but this can be technically difficult and expensive. Insoluble Fe(III) oxides, which are generally abundant in shallow aquifers, are alternative potential oxidants, but are difficult for microorganisms to access. Here we report that adding organic ligands that bind to Fe(III) dramatically increases its bioavailability, and that in the presence of these ligands, rates of degradation of aromatic hydrocarbons in anoxic aquifer sediments are comparable to those in oxic sediments. We find that even benzene, which is notoriously refractory in the absence of oxygen, can be rapidly degraded. Our results suggest that increasing the bioavailability of Fe(III) by adding suitable ligands provides a potential alternative to oxygen addition for the bioremediation of petroleum-contaminated aquifers.},
	keywords = {Benzene, Biodegradation, Environmental, Ferric Compounds, Hydrocarbons, Ligands, Methane, Nitrilotriacetic Acid, Oxidation-Reduction, Toluene, Water Pollutants, Chemical},
	issn = {0028-0836},
	doi = {10.1038/370128a0},
	author = {Lovley, D R and Woodward, J C and Chapelle, F H}
}
@article {669,
	title = {Identification of methyl coenzyme M as an intermediate in methanogenesis from acetate in Methanosarcina spp.},
	journal = {J Bacteriol},
	volume = {160},
	year = {1984},
	month = {1984 Nov},
	pages = {521-5},
	abstract = {The transfer of the methyl group of acetate to coenzyme M (2-mercaptoethanesulfonic acid; HS-CoM) during the metabolism of acetate to methane was investigated in cultures of Methanosarcina strain TM-1. The organism metabolized CD3COO- to 83\% CD3H and 17\% CD2H2 and produced no CDH3 or CH4. The isotopic composition of coenzyme M in cells grown on CD3COO- was analyzed with a novel gas chromatography-mass spectrometry technique. The cells contained CD3-D-CoM and CD2H-S-CoM) in a proportion similar to that of CD3H to CD2H2. These results, in conjunction with a report (J.K. Nelson and J.G. Ferry, J. Bacteriol. 160:526-532, 1984) that extracts of acetate-grown strain TM-1 contain high levels of CH3-S-CoM methylreductase, indicate that CH3-S-CoM is an intermediate in the metabolism of acetate to methane in this organism.},
	keywords = {Acetates, Deuterium, Euryarchaeota, Gas Chromatography-Mass Spectrometry, Mercaptoethanol, Mesna, Methane, Methylation},
	issn = {0021-9193},
	author = {Lovley, D R and White, R H and Ferry, J G}
}
