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Methanogen genotypes involved in methane formation during anaerobic decomposition of Microcystis blooms at different temperatures

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Abstract

The main goal of this work was to determine which methanogens were present during the anaerobic degradation of Microcystis biomass in the water columns of freshwater lakes. Simulation experiments were performed in which 30 ml Microcystis slurries were anaerobically incubated in 60 ml airtight bottles at three temperatures (15, 25, and 35 °C) for over 90 days. The production of CH4 was monitored, and the methanogenic community was analyzed by cloning and sequencing the mcrA genes in samples incubated at the three different temperatures. In total, four clusters were detected at different temperatures by phylogenetic analysis of mcrA genes; these included members of Methanomicrobiales, Methanobacteriaceae, and Methanosarcina. An apparent linkage between temperature and phylogeny of the methanogenic community was observed: Methanomicrobiales and Methanobacteriaceae dominated the incubation system at the lower temperatures of 15 and 25 °C, whereas Methanosarcina prevailed at 35 °C. The dominance of these hydrogenotrophic methanogens suggested that, at least at lower temperatures, H2 and CO2 might be the primary substrates for CH4 production during Microcystis anaerobic decomposition.

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References

  • Bastviken D, Tranvik LJ, Downing JA et al (2011) Freshwater methane emissions offset the continental carbon sink. Science 331:50

    Article  CAS  Google Scholar 

  • Bokranz M, Bäumner G, Allmansberger R et al (1988) Cloning and characterization of the methyl coenzyme M reductase genes from Methanobacterium thermoautotrophicum. J Bacteriol 170:568–577

    CAS  Google Scholar 

  • Castro H, Ogram A, Reddy KR (2004) Phylogenetic characterization of methanogenic assemblages in eutrophic and oligotrophic areas of the Florida Everglades. Appl Environ Microbiol 70:6559–6568

    Article  CAS  Google Scholar 

  • Chao A, Chazdon RL, Colwell RK et al (2005) A new statistical approach for assessing similarity of species composition with incidence and abundance data. Ecol Lett 8:148–159

    Article  Google Scholar 

  • Chen Y, Qin B, Teubner K et al (2003) Long-term dynamics of phytoplankton assemblages: Microcystis-domination in Lake Taihu, a large shallow lake in China. J Plankton Res 25:445–453

    Article  Google Scholar 

  • Conrad R, Claus P (2009) Characterization of stable isotope fractionation during methane production in the sediment of a eutrophic lake, Lake Dagow, Germany. Limnol Oceanogr 54:457–471

    Article  CAS  Google Scholar 

  • Grossart H-P, Frindte K, Dziallas C et al (2011) Microbial methane production in oxygenated water column of an oligotrophic lake. Proc Natl Acad Sci USA 108:19657–19661

    Article  CAS  Google Scholar 

  • Groβkopf R, Janssen PH, Liesack W (1998) Diversity and structure of the methanogenic community in anoxic rice paddy soil microcosms as examined by cultivation and direct 16S rRNA gene sequence retrieval. Appl Environ Microbiol 64:960–969

    Google Scholar 

  • Hales B, Edwards C, Ritchie D et al (1996) Isolation and identification of methanogen-specific DNA from blanket bog peat by PCR amplification and sequence analysis. Appl Environ Microbiol 62:668–675

    CAS  Google Scholar 

  • Hallam SJ, Girguis PR, Preston CM et al (2003) Identification of methyl coenzyme M reductase a (mcrA) genes associated with methane-oxidizing archaea. Appl Environ Microbiol 69:5483–5491

    Article  CAS  Google Scholar 

  • Høj L, Olsen RA, Torsvik VL (2008) Effects of temperature on the diversity and community structure of known methanogenic groups and other archaea in high Arctic peat. ISME J 2:37–48

    Article  Google Scholar 

  • Larkin MA, Blackshields G, Brown NP et al (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–2948

    Article  CAS  Google Scholar 

  • Li H, Xing P, Chen M et al (2011) Short-term bacterial community composition dynamics in response to accumulation and breakdown of Microcystis blooms. Water Res 43:1702–1710

    Article  Google Scholar 

  • Lovley DR, Ferry JG (1985) Production and consumption of H2 during growth of Methanosarcina spp. on acetate. Appl Environ Microbiol 49:247–249

    CAS  Google Scholar 

  • Luton PE, Wayne JM, Sharp RJ et al (2002) The mcrA gene as an alternative to 16S rRNA in the phylogenetic analysis of methanogen populations in landfill. Microbiology 148:3521–3530

    CAS  Google Scholar 

  • Paerl HW, Huisman J (2008) Blooms like it hot. Science 320:57–58

    Article  CAS  Google Scholar 

  • Schloss PD, Handelsman J (2005) Introducing DOTUR, a computer program for defining operational taxonomic units and estimating species richness. Appl Environ Microbiol 71:1501–1506

    Article  CAS  Google Scholar 

  • Schnürer A, Schink B, Svensson BH (1996) Clostridium ultunense sp. nov., a mesophilic bacterium oxidizing acetate in syntrophic association with a hydrogenotrophic methanogenic bacterium. Int J Syst Bacteriol 46:1145–1152

    Article  Google Scholar 

  • Schwarz JIK, Eckert W, Conrad R (2008) Response of the methanogenic microbial community of a profundal lake sediment (Lake Kinneret, Israel) to algal deposition. Limnol Oceanogr 53:113–121

    Article  CAS  Google Scholar 

  • Springer E, Sachs MS, Woese CR et al (1995) Partial gene-sequences for the A subunit of methyl-coenzyme M reductase (mcrI) as a phylogenetic tool for the family Methanosarcinaceae. Int J Syst Bacteriol 45:554–559

    Article  CAS  Google Scholar 

  • Steinberg LM, Regan JM (2008) Phylogenetic comparison of the methanogenic communities from an acidic, oligotrophic fen and an anaerobic digester treating municipal wastewater sludge. Appl Environ Microbiol 74:6663–6671

    Article  CAS  Google Scholar 

  • Steinberg LM, Regan JM (2009) mcrA-targeted real-time quantitative PCR method to examine methanogen communities. Appl Environ Microbiol 75:4435

    Article  CAS  Google Scholar 

  • Tamura K, Dudley J, Nei M et al (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599

    Article  CAS  Google Scholar 

  • Wang H, Lu J, Wang W et al (2006) Methane fluxes from the littoral zone of hypereutrophic Taihu lake China. J Geophys Res 111:D17109

    Article  Google Scholar 

  • Xing P, Guo L, Tian W et al (2011) Novel Clostridium populations involved in the anaerobic degradation of Microcystis blooms. ISME J 5:792–800

    Article  CAS  Google Scholar 

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Acknowledgments

We thank Xing Jin and Chengsheng Long for their assistance in conducting the entire experiment. This work was supported by the National Basic Research Program of China (973 program) (No. 2008CB418104) and the National Natural Science Foundation of China (No. 31000241).

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Correspondence to Peng Xing.

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Xing, P., Zheng, J., Li, H. et al. Methanogen genotypes involved in methane formation during anaerobic decomposition of Microcystis blooms at different temperatures. World J Microbiol Biotechnol 29, 373–377 (2013). https://doi.org/10.1007/s11274-012-1191-2

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