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Archaea diversity within a commercial biogas plant utilizing herbal biomass determined by 16S rDNA and mcr A analysis

2008; Oxford University Press; Volume: 105; Issue: 6 Linguagem: Inglês

10.1111/j.1365-2672.2008.03949.x

1365-2672

Edith Nettmann, Jean‐François Bergmann, K. Mundt, Bernd Linke, Michael Klocke,

Legume Nitrogen Fixing Symbiosis

The Archaea diversity was evaluated in an agricultural biogas plant supplied with cattle liquid manure and maize silage under mesophilic conditions.Two different genes (16S rRNA; methyl-coenzyme-M-reductase, MCR) targeted by three different PCR primer sets were selected and used for the construction of three clone libraries comprising between 104 and 118 clones. The clone libraries were analysed by restriction fragment polymorphism (RFLP). Between 11 and 31 operational taxonomic units (OTUs) were detected and assigned to orders Methanomicrobiales, Methanosarcinales and Methanobacteriales. Over 70% of all Archaea OTUs belong to the order Methanomicrobiales which mostly include hydrogenotrophic methanogens. Acetotrophic methanogens were detected in minor rates. Similar relative values were obtained by a quantitative real-time PCR analysis.The results implied that in this biogas plant the most of the methane formation resulted from the conversion of H(2) and CO(2).This study reports, for the first time, a molecular analysis of the archaeal community in this type of agricultural biogas plants. Therein the hydrogenotrophic methanogenesis seems to be the major pathway of methane formation. These results are in contrast with the common thesis that in biogas fermentations the primary substrate for methanogenesis is acetate.