%0 Journal Article
%T The Sulfate-Rich and Extreme Saline Sediment of the Ephemeral Tirez Lagoon: A Biotope for Acetoclastic Sulfate-Reducing Bacteria and Hydrogenotrophic Methanogenic Archaea
%A Lilia Montoya
%A Irma Lozada-Ch¨¢vez
%A Ricardo Amils
%A Nuria Rodriguez
%A Irma Mar¨ªn
%J International Journal of Microbiology
%D 2011
%I Hindawi Publishing Corporation
%R 10.1155/2011/753758
%X Our goal was to examine the composition of methanogenic archaea (MA) and sulfate-reducing (SRP) and sulfur-oxidizing (SOP) prokaryotes in the extreme athalassohaline and particularly sulfate-rich sediment of Tirez Lagoon (Spain). Thus, adenosine- -phosphosulfate (APS) reductase ¦Á (aprA) and methyl coenzyme M reductase ¦Á (mcrA) gene markers were amplified given that both enzymes are specific for SRP, SOP, and MA, respectively. Anaerobic populations sampled at different depths in flooded and dry seasons from the anoxic sediment were compared qualitatively via denaturing gradient gel electrophoresis (DGGE) fingerprint analysis. Phylogenetic analyses allowed the detection of SRP belonging to Desulfobacteraceae, Desulfohalobiaceae, and Peptococcaceae in £¿-proteobacteria and Firmicutes and SOP belonging to Chromatiales/Thiotrichales clade and Ectothiorhodospiraceae in ¦Ã-proteobacteria as well as MA belonging to methylotrophic species in Methanosarcinaceae and one hydrogenotrophic species in Methanomicrobiaceae. We also estimated amino acid composition, GC content, and preferential codon usage for the AprA and McrA sequences from halophiles, nonhalophiles, and Tirez phylotypes. Even though our results cannot be currently conclusive regarding the halotolerant strategies carried out by Tirez phylotypes, we discuss the possibility of a plausible ¡°salt-in¡± signal in SRP and SOP as well as of a speculative complementary haloadaptation between salt-in and salt-out strategies in MA. 1. Introduction Molecular oxygen is found only in those biotopes that harbor organisms carrying out oxygenic photosynthesis. In oxygen-deficient systems, the nature of the redox couple and concentrations of electron acceptor/donor determine the succession of dissimilatory metabolisms due to thermodynamic conditions [1]. For a given substrate and under standard conditions, the aerobic dissimilatory metabolisms provide about one order of magnitude more energy than the anaerobic ones, for example, glucose respiration ( £¿kJ/mol) versus glucose fermentation ( £¿kJ/mol) [2]. Therefore, in sedimentary environments oxygen is exhausted at deeper layers and the dissimilatory metabolisms are anaerobic as a result. Anaerobic microorganisms are of interest in extreme environments because environmental parameters such as temperature and salinity regulate the rates of organic matter remineralization [3]. Extreme halophilic microorganisms require at least 15% NaCl and tolerate up to 35% NaCl. Interestingly, the low activity of water and the expense on biosynthesis only select heterotrophs and strict
%U http://www.hindawi.com/journals/ijmicro/2011/753758/