PMID- 10919825 OWN - NLM STAT- MEDLINE DCOM- 20010104 LR - 20210526 IS - 0099-2240 (Print) IS - 1098-5336 (Electronic) IS - 0099-2240 (Linking) VI - 66 IP - 8 DP - 2000 Aug TI - Community structure, cellular rRNA content, and activity of sulfate-reducing bacteria in marine arctic sediments. PG - 3592-602 AB - 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 to Desulfosarcina 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(-1) day(-1)), decreased by a factor of 3 within the first 2 cm, and were relatively constant in deeper layers. FAU - Ravenschlag, K AU - Ravenschlag K AD - Molecular Ecology Group, Max Planck Institute for Marine Microbiology, 28359 Bremen, Germany. FAU - Sahm, K AU - Sahm K FAU - Knoblauch, C AU - Knoblauch C FAU - Jorgensen, B B AU - Jorgensen BB FAU - Amann, R AU - Amann R LA - eng SI - GENBANK/AF233491 SI - GENBANK/AF233492 SI - GENBANK/AF233493 SI - GENBANK/AF233494 SI - GENBANK/AF233495 SI - GENBANK/AF233496 SI - GENBANK/AF233497 SI - GENBANK/AF233498 SI - GENBANK/AF233499 SI - GENBANK/AF233500 PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Appl Environ Microbiol JT - Applied and environmental microbiology JID - 7605801 RN - 0 (DNA, Bacterial) RN - 0 (DNA, Ribosomal) RN - 0 (RNA, Bacterial) RN - 0 (RNA, Ribosomal, 16S) RN - 0 (Sulfates) SB - IM MH - Arctic Regions MH - DNA, Bacterial/analysis/genetics MH - DNA, Ribosomal/analysis/genetics MH - *Ecosystem MH - Fermentation MH - Genes, rRNA MH - Geologic Sediments/*microbiology MH - In Situ Hybridization, Fluorescence MH - Molecular Sequence Data MH - Nucleic Acid Hybridization MH - Oxidation-Reduction MH - Phylogeny MH - Polymerase Chain Reaction MH - RNA, Bacterial/analysis MH - RNA, Ribosomal, 16S/*analysis/genetics MH - Sulfates/*metabolism MH - Sulfur-Reducing Bacteria/chemistry/genetics/*isolation & purification/metabolism PMC - PMC92189 EDAT- 2000/08/05 11:00 MHDA- 2001/02/28 10:01 PMCR- 2000/08/01 CRDT- 2000/08/05 11:00 PHST- 2000/08/05 11:00 [pubmed] PHST- 2001/02/28 10:01 [medline] PHST- 2000/08/05 11:00 [entrez] PHST- 2000/08/01 00:00 [pmc-release] AID - 0372 [pii] AID - 10.1128/AEM.66.8.3592-3602.2000 [doi] PST - ppublish SO - Appl Environ Microbiol. 2000 Aug;66(8):3592-602. doi: 10.1128/AEM.66.8.3592-3602.2000.