Applied and Environmental Microbiology · 2006 · 143 citations · 58 references
Life SciencesMicrobiologyMolecular BiologyMetabolismMicrobial EcologyMicrobial Metabolism16S Ribosomal Ribonucleic Acid AnalysisBacterial MetabolismMicrobial Community ProfilingMicrobial DiversityMicrobial Sulfur CyclingSulfur MetabolismMicrobial Sulfur MetabolismSulfate-reducing BacteriaSulfate-reducing BioreactorsSulfate-reducing MicroorganismsSulfur Cycling BacteriaSulfur-metabolizing MicroorganismsSulfur-oxidizing BacteriaSulfur-reducing Bioreactors
Here we describe the diversity and activity of sulfate-reducing bacteria (SRB) in sulfidogenic bioreactors by using the simultaneous analysis of PCR products obtained from DNA and RNA of the 16S rRNA and dissimilatory sulfite reductase (dsrAB) genes. We subsequently analyzed the amplified gene fragments by using denaturing gradient gel electrophoresis (DGGE). We observed fewer bands in the RNA-based DGGE profiles than in the DNA-based profiles, indicating marked differences in the populations present and in those that were metabolically active at the time of sampling. Comparative sequence analyses of the bands obtained from rRNA and dsrB DGGE profiles were congruent, revealing the same SRB populations. Bioreactors that received either ethanol or isopropanol as an energy source showed the presence of SRB affiliated with Desulfobulbus rhabdoformis and/or Desulfovibrio sulfodismutans, as well as SRB related to the acetate-oxidizing Desulfobacca acetoxidans. The reactor that received wastewater containing a diverse mixture of organic compounds showed the presence of nutritionally versatile SRB affiliated with Desulfosarcina variabilis and another acetate-oxidizing SRB, affiliated with Desulfoarculus baarsii. In addition to DGGE analysis, we performed whole-cell hybridization with fluorescently labeled oligonucleotide probes to estimate the relative abundances of the dominant sulfate-reducing bacterial populations. Desulfobacca acetoxidans-like populations were most dominant (50 to 60%) relative to the total SRB communities, followed by Desulfovibrio-like populations (30 to 40%), and Desulfobulbus-like populations (15 to 20%). This study is the first to identify metabolically active SRB in sulfidogenic bioreactors by using the functional gene dsrAB as a molecular marker. The same approach can also be used to infer the ecological role of coexisting SRB in other habitats.
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Gerard Muyzer, Ellen C. de Waal, André G. Uitterlinden · Applied and Environmental Microbiology · 1993 · 11.5K citations · Full text
ARB: a software environment for sequence data
Wolfgang Ludwig · Nucleic Acids Research · 2004 · 6.8K citations · Full text