Abstract
The energy conservation strategies of plants and animals are exceedingly homogeneous in comparison with those of bacterial cells. Among the wide variety of mechanisms that exist to provide energy and electrons to support bacterial life, the use of insoluble metallic elements as electron acceptors is one of the most interesting. The prevalence of metallic elements in the minerals that comprise soils and sediments raises the possibility that metal respiring organisms play a significant role in a variety of biogeochemical transformations. The environmental abundance of metals also inspires the hope that cells capable of coupling metal respiration to the oxidation of contaminant hydrocarbons can be captured, studied, and manipulated to enhance biodegradation processes. Indirect mechanisms of iron cycling may also play a role in hydrocarbon degradation. Biogenic Fe(II) bearing minerals such as magnetite, as well as reactive Fe(II) sorption on crystalline iron oxides, have also been shown to dechlorinate carbon tetrachloride and reduce nitroaromatic compounds. This protocol provides an overview of anaerobic culturing and specific techniques for the enrichment and isolation of metal respiring hydrocarbon oxidizers from environments of interest.
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References
Liu A, Garcia-Dominguez E, Rhine ED, Young LJ (2004) A novel arsenate respiring isolate that can utilize aromatic substrates. FEMS Microbiol Ecol 48(3):323–332
Villatoro-Monzón WR, Morales-Ibarria MG, Velázquez EK, RamÃrez-Saad H, Razo-Flores E (2008) Benzene biodegradation under anaerobic conditions coupled with metal oxides reduction. Water Air Soil Pollut 192(1–4):165–172
Holmes DE, Risso C, Smith JA, Lovley DR (2011) Anaerobic oxidation of benzene by the hyperthermophilic archaeon Ferroglobus placidus. Appl Environ Microbiol 77(17):5926–5933
Lovley D, Lonergan DJ (1990) Anaerobic oxidation of toluene, phenol, and para-cresol by the dissimilatory iron-reducing organism, GS-15. Appl Environ Microbiol 56:1858–1864
Coates JD, Bhupathiraju VK, Achenbach LA, McInerney MJ, Lovley DR (2001) Geobacter hydrogenophilus, Geobacter chapellei and Geobacter grbiciae, three new, strictly anaerobic, dissimilatory Fe(III)-reducers. Int J Syst Evol Microbiol 51:581–588
Kunapuli U, Jahn MK, Lueders T, Geyer R, Heipieper HJ, Meckenstock RU (2010) Desulfitobacterium aromaticivorans sp. nov. and Geobacter toluenoxydans sp. nov., iron-reducing bacteria capable of anaerobic degradation of monoaromatic hydrocarbons. Int J Syst Evol Microbiol 60(3):686–695
Zhang T, Bain TS, Nevin KP, Bartlett MA, Lovley DR (2012) Anaerobic benzene oxidation by Geobacter species. Appl Environ Microbiol 78(23):8304–8310
Zhou S, Yang G, Lu Q, Wu M (2014) Geobacter soli sp. nov., a dissimilatory Fe(III)-reducing bacterium isolated from forest soil. Int J Syst Evol Microbiol 64(Pt 11):3786–3791
Weelink SB, van Doesburg W, Saia FT, Rijpstra WIC, Roling WMF, Smidt H, Stams AJM (2009) A strictly anaerobic betaproteobacterium Georgfuchsia toluolica gen. nov., sp. nov. degrades aromatic compounds with Fe(III), Mn(IV) or nitrate as an electron acceptor. FEMS Microbiol Ecol 70(3):575–585
Kunapuli U, Lueders T, Meckenstock RU (2007) The use of stable isotope probing to identify key iron-reducing microorganisms involved in anaerobic benzene degradation. ISME J 1(7):643–653
Kleemann R, Meckenstock RU (2011) Anaerobic naphthalene degradation by Gram-positive, iron-reducing bacteria. FEMS Microbiol Ecol 78(3):488–496
Pilloni G, von Netzer F, Engel M, Lueders T (2011) Electron acceptor-dependent identification of key anaerobic toluene degraders at a tar-oil-contaminated aquifer by Pyro-SIP. FEMS Microbiol Ecol 78(1):165–175
Brileya K, Reysenbach AL (2014) The class Archaeoglobi. In: Rosenberg E et al (eds) The prokaryotes – other major lineages of bacteria and the archae. Springer, Berlin/Heidelberg, pp 545–577
Hafenbradl D, Keller M, Dirmeier R, Reinhard R, Roßnagel P, Burggraf S, Huber H, Stetter KO (1996) Ferroglobus placidus gen. nov., sp. nov., a novel hyperthermophilic archaeum that oxidizes Fe2+ at neutral pH under anoxic conditions. Arch Microbiol 166(5):308–314
Kashefi K, Tor JM, Holmes DE, Gaw van Praagh CV, Reysenbach AL, Lovley DR (2002) Geoglobus ahangari gen. nov., sp. nov., a novel hyperthermophilic archaeon capable of oxidizing organic acids and growing autotrophically on hydrogen with Fe(III) serving as the sole electron acceptor. Int J Syst Evol Microbiol 52(3):719–728
Slobodkina GB, Kolganova TV, Querellou J, Bonch-Osmolovskaya EA, Slobodkin AI (2009) Geoglobus acetivorans sp. nov., an iron(III)-reducing archaeon from a deep-sea hydrothermal vent. Int J Syst Evol Microbiol 59(11):2880–2883
Mardanov AV, Mardanov AJ, Slododkina GB, Slobodkin AI, Beletsky AV, Gavrilov SN, Kublanov IV, Bonch-Osmolovskaya EA, Skryabin KG, Ravin NV (2015) The Geoglobus acetivorans genome: Fe(III) reduction, acetate utilization, autotrophic growth, and degradation of aromatic compounds in a hyperthermophilic archaeon. Appl Environ Microbiol 81(3):1003–1012
Davidova I, Suflita J (2005) Enrichment and isolation of anaerobic hydrocarbon‚ degrading bacteria. Methods Enzymol 397:17–34
Balch WE, Fox GE, Magrum LJ, Woese CR, Wolfe RS (1979) Methanogens – reevaluation of a unique biological group. Microbiol Rev 43:260–296
Hungate RE (1969) A roll-tube method for cultivation of strict anaerobes. J Microbiol Methods 3B:117–132
Brezak J, Costilow R (1994) Physicochemical factors in growth. In: Gerhardt P (ed. in chief), Murray RGE, Wood WA, Krieg NR (eds) Methods for general and molecular bacteriology. American Society for Microbiology, Washington, DC
Widdel F (2016) Cultivation of anaerobic microorganisms with hydrocarbons as growth substrates. In: McGenity TJ, Timmis KN, Nogales B (eds) Hydrocarbon and lipid microbiology protocols. Springer protocols handbooks. doi: 10.1007/8623_2015_186
Rabus R, Nordhaus R, Ludwig W, Widdel F (1993) Complete oxidation of toluene under strictly anoxic conditions by a new sulfate-reducing bacterium. Appl Environ Microbiol 59:1444–1451
Fries MR, Zhou JH, Cheesanford J, Tiedje JM (1994) Isolation, characterization, and distribution of denitrifying toluene degraders from a variety of habitats. Appl Environ Microbiol 60:2802–2810
Coates JD, Chakraborty R, Lack JG, O’Connor SM, Cole KA, Bender KS, Achenbach LA (2001) Anaerobic benzene oxidation coupled to nitrate reduction in pure culture by two strains of Dechloromonas. Nature 411:1039–1043
Lovley DR, Woodward JC, Chapelle FH (1994) Stimulated anoxic biodegradation of aromatic-hydrocarbons using Fe(III) ligands. Nature 370:128–131
Lovley DR, Woodward JC (1996) Rapid anaerobic benzene oxidation with a variety of chelated Fe (III) forms. Rapid anaerobic benzene oxidation with a variety of chelated Fe (III) forms. Appl Environ Microbiol 62(1):288–291
Lovley DR, Woodward JC, Chapelle FH (1994) Nature stimulation of hydrocarbon degradation by Fe(III) chelation.pdf. Nature 370:128–131
Lovley D, Woodward J, Chapelle F (1996) Rapid anaerobic benzene oxidation with a variety of chelated Fe(III) forms. Appl Environ Microbiol 62(1):288–291
Cutting RS, Coker VS, Fellowes JW, Lloyd JR, Vaughan DJ (2009) Mineralogical and morphological constraints on the reduction of Fe(III) minerals by Geobacter sulfurreducens. Geochim Cosmochim Acta 73(14):4004–4022
Lentini CJ, Wankel SD, Hansel CM (2012) Enriched iron(III)-reducing bacterial communities are shaped by carbon substrate and iron oxide mineralogy. Front Microbiol 3:1–19
Anderson RT, Rooney-Varga JN, Gaw CV, Lovley DR (1998) Anaerobic benzene oxidation in the Fe(III) reduction zone of petroleum contaminated aquifers. Environ Sci Technol 32:1222–1229
Coates JD, Ellis DJ, Gaw CV, Lovley D (1999) Geothrix fermentans gen. nov., sp nov., a novel Fe(III)-reducing bacterium from a hydrocarbon-contaminated aquifer. Int J Syst Bacteriol 49:1615–1622
Cupples AM (2011) The use of nucleic acid based stable isotope probing to identify the microorganisms responsible for anaerobic benzene and toluene biodegradation. J Microbiol Methods 85(2):83–91
Lueders T (2015) DNA- and RNA-based stable isotope probing of hydrocarbon degraders. In: McGenity TJ, Timmis KN, Nogales B (eds) Hydrocarbon and lipid microbiology protocols. Springer, Heidelberg doi: 10.1007/8623_2015_74
Smith JA, Aklujkar M, Risso M, Leang C, Giloteaux L, Holmes DE (2015) Insight into mechanisms involved in Fe(III) respiration by the hyperthermophilic archaeon, Ferroglobus placidus. Appl Environ Microbiol 81(8):AEM.04038–14
Goto K, Taguchi S, Fukue Y, Ohta K (1977) Spectrophotometric determination of manganese with 1-(2-pyridylazo)-2-naphthol and a non-ionic surfactant. Talanta 24(12):752–753
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Williamson, A.J., Coates, J.D. (2016). Enrichment and Isolation of Metal Respiring Hydrocarbon Oxidizers. In: McGenity, T., Timmis, K., Nogales , B. (eds) Hydrocarbon and Lipid Microbiology Protocols. Springer Protocols Handbooks. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8623_2016_198
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DOI: https://doi.org/10.1007/8623_2016_198
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