Community Structure, Cellular rRNA Content, and Activity of Sulfate-Reducing Bacteria in Marine Arctic Sediments
- 1 August 2000
- journal article
- research article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 66 (8) , 3592-3602
- https://doi.org/10.1128/aem.66.8.3592-3602.2000
Abstract
The community structure of sulfate-reducing bacteria (SRB) of a marine Arctic sediment (Smeerenburgfjorden, Svalbard) was characterized by both fluorescence in situ hybridization (FISH) and rRNA slot blot hybridization by using group- and genus-specific 16S rRNA-targeted oligonucleotide probes. The SRB community was dominated by members of the Desulfosarcina-Desulfococcus group. This group accounted for up to 73% of the SRB detected and up to 70% of the SRB rRNA detected. The predominance was shown to be a common feature for different stations along the coast of Svalbard. In a top-to-bottom approach we aimed to further resolve the composition of this large group of SRB by using probes for cultivated genera. While this approach failed, directed cloning of probe-targeted genes encoding 16S rRNA was successful and resulted in sequences which were all affiliated with the Desulfosarcina-Desulfococcus group. A group of clone sequences (group SVAL1) most closely related toDesulfosarcina variabilis (91.2% sequence similarity) was dominant and was shown to be most abundant in situ, accounting for up to 54.8% of the total SRB detected. A comparison of the two methods used for quantification showed that FISH and rRNA slot blot hybridization gave comparable results. Furthermore, a combination of the two methods allowed us to calculate specific cellular rRNA contents with respect to localization in the sediment profile. The rRNA contents of Desulfosarcina-Desulfococcus cells were highest in the first 5 mm of the sediment (0.9 and 1.4 fg, respectively) and decreased steeply with depth, indicating that maximal metabolic activity occurred close to the surface. Based on SRB cell numbers, cellular sulfate reduction rates were calculated. The rates were highest in the surface layer (0.14 fmol cell−1day−1), decreased by a factor of 3 within the first 2 cm, and were relatively constant in deeper layers.Keywords
This publication has 96 references indexed in Scilit:
- Process measurement and phylogenetic analysis of the sulfate reducing bacterial communities of two contrasting benthic sites in the upper estuary of the Great Ouse, Norfolk, UKFEMS Microbiology Ecology, 2006
- Anaerobic oxidation of thiosulfate to tetrathionate by obligately heterotrophic bacteria, belonging to the Pseudomonas stutzeri groupFEMS Microbiology Ecology, 1999
- Strategies of sulfate-reducing bacteria to escape oxygen stress in a cyanobacterial matFEMS Microbiology Ecology, 1998
- Abundance and spatial organization of Gram-negative sulfate-reducing bacteria in activated sludge investigated by in situ probing with specific 16S rRNA targeted oligonucleotidesFEMS Microbiology Ecology, 1998
- Abundance and spatial organization of Gram-negative sulfate-reducing bacteria in activated sludge investigated by in situ probing with specific 16S rRNA targeted oligonucleotidesFEMS Microbiology Ecology, 1998
- Temperature dependence and rates of sulfate reduction in cold sediments of svalbard, arctic oceanGeomicrobiology Journal, 1998
- Process measurement and phylogenetic analysis of the sulfate reducing bacterial communities of two contrasting benthic sites in the upper estuary of the Great Ouse, Norfolk, UKFEMS Microbiology Ecology, 1997
- Use of 16S rRNA-targeted oligonucleotide probes to investigate the occurrence and selection of sulfate-reducing bacteria in response to nutrient addition to sediment slurry microcosms from a Japanese estuaryFEMS Microbiology Ecology, 1997
- Use of 16S rRNA-targeted oligonucleotide probes to investigate the occurrence and selection of sulfate-reducing bacteria in response to nutrient addition to sediment slurry microcosms from a Japanese estuaryFEMS Microbiology Ecology, 1997
- Aerobic respiration in sulfate-reducing bacteriaFEMS Microbiology Letters, 1990