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  Retrieval of first genome data for rice cluster I methanogens by a combination of cultivation and molecular techniques

Erkel, C., Kemnitz, D., Kube, M., Ricke, P., Chin, K., Dedysh, S., et al. (2005). Retrieval of first genome data for rice cluster I methanogens by a combination of cultivation and molecular techniques. FEMS Microbiology Ecology, 53, 187-204. doi:10.1016/j.femsec.2004.12.004.

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 Creators:
Erkel, C.1, Author           
Kemnitz, D.1, Author           
Kube, M.1, Author           
Ricke, P.1, Author           
Chin, K.1, Author           
Dedysh, S.1, Author           
Reinhardt, R., Author
Conrad, R.2, Author           
Liesack, W.3, Author           
Affiliations:
1Department of Biogeochemistry, Alumni, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266312              
2Emeriti Methanogenic Degradation and Microbial Metabolism of Trace Gases, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266290              
3Department-Independent Research Group Methanotrophic Bacteria, and Environmental Genomics/Transcriptomics, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266274              

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Free keywords: Methanogens; Rice cluster I; Metagenomics; rrn Operons; Informational genes; Phylogeny
 Abstract: We report first insights into a representative genome of rice cluster I (RC-I), a major group of as-yet uncultured methanogens. The starting point of our study was the methanogenic consortium MRE50 that had been stably maintained for 3 years by consecutive transfers to fresh medium and anaerobic incubation at 50 °C. Process-oriented measurements provided evidence for hydrogenotrophic CO2-reducing methanogenesis. Assessment of the diversity of consortium MRE50 suggested members of the families Thermoanaerobacteriaceae and Clostridiaceae to constitute the major bacterial component, while the archaeal population was represented entirely by RC-I. The RC-I population amounted to more than 50% of total cells, as concluded from fluorescence in situ hybridization using specific probes for either Bacteria or Archaea. The high enrichment status of RC-I prompted construction of a large insert fosmid library from consortium MRE50. Comparative sequence analysis of internal transcribed spacer (ITS) regions revealed that three different RC-I rrn operon variants were present in the fosmid library. Three, approximately 40-kb genomic fragments, each representative for one of the three different rrn operon variants, were recovered and sequenced. Computational analysis of the sequence data resulted in two major findings: (i) consortium MRE50 most likely harbours only a single RC-I genotype, which is characterized by multiple rrn operon copies; (ii) seven genes were identified to possess a strong phylogenetic signal (eIF2a, dnaG, priA, pcrA, gatD, gatE, and a gene encoding a putative RNA-binding protein). Trees exemplarily computed for the deduced amino acid sequences of eIF2a, dnaG, and priA corroborated a specific phylogenetic association of RC-I with the Methanosarcinales.

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Language(s): eng - English
 Dates: 2005
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 233104
DOI: 10.1016/j.femsec.2004.12.004
 Degree: -

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Title: FEMS Microbiology Ecology
Source Genre: Journal
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Pages: - Volume / Issue: 53 Sequence Number: - Start / End Page: 187 - 204 Identifier: -