| Literature DB >> 26724953 |
Manel Ben Abdallah1,2, Fatma Karray3,4, Najla Mhiri1,5, Nan Mei2, Marianne Quéméneur2, Jean-Luc Cayol2, Gaël Erauso2,5, Jean-Luc Tholozan2, Didier Alazard1,2, Sami Sayadi1,5.
Abstract
Prokaryotic diversity was investigated in a Tunisian salt lake, Chott El Jerid, by quantitative real-time PCR, denaturing gradient gel electrophoresis (DGGE) fingerprinting methods targeting the 16S rRNA gene and culture-dependent methods. Two different samples S1-10 and S2-10 were taken from under the salt crust of Chott El Jerid in the dry season. DGGE analysis revealed that bacterial sequences were related to Firmicutes, Proteobacteria, unclassified bacteria, and Deinococcus-Thermus phyla. Anaerobic fermentative and sulfate-reducing bacteria were also detected in this ecosystem. Within the domain archaea, all sequences were affiliated to Euryarchaeota phylum. Quantitative real-time PCR showed that 16S rRNA gene copy numbers of bacteria was 5 × 10(6) DNA copies g(-1) whereas archaea varied between 5 × 10(5) and 10(6) DNA copies g(-1) in these samples. Eight anaerobic halophilic fermentative bacterial strains were isolated and affiliated with the species Halanaerobium alcaliphilum, Halanaerobium saccharolyticum, and Sporohalobacter salinus. These data showed an abundant and diverse microbial community detected in the hypersaline thalassohaline environment of Chott El Jerid.Entities:
Keywords: 16S rRNA; Anaerobic fermentative bacteria; Archaea; Bacteria; Hypersaline lake; Microbial diversity; PCR-DGGE; Quantitative PCR
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Year: 2016 PMID: 26724953 DOI: 10.1007/s00792-015-0805-7
Source DB: PubMed Journal: Extremophiles ISSN: 1431-0651 Impact factor: 2.395