Abstract
The community structure of bacterioplankton in meromictic Lake Saelenvannet was examined by PCR amplification of the V3 region of 16S rRNA from microbial communities recovered from various depths in the water column. Two different primer sets were used, one for amplification of DNA from the domain Bacteria and another specific for DNA from the domain Archaea. Amplified DNA fragments were resolved by denaturing gradient gel electrophoresis (DGGE), and the resulting profiles were reproducible and specific for the communities from different depths. Bacterial diversity estimated from the number and intensity of specific fragments in DGGE profiles decreased with depth. The reverse was true for the Archaea, with the diversity increasing with depth. Hybridization of DGGE profiles with oligonucleotide probes specific for phylogenetic groups of microorganisms showed the presence of both sulfate-reducing bacteria and methanogens throughout the water column, but they appeared to be most abundant below the chemocline. Several dominant fragments in the DGGE profiles were excised and sequenced. Among the dominant populations were representatives related to Chlorobium phaeovibrioides, chloroplasts from eukaryotic algae, and unidentified Archaea.
MeSH Terms
Animals
Bacteria/genetics,isolation & purification
Base Sequence
DNA Primers/genetics
DNA, Bacterial/genetics
DNA, Ribosomal/genetics
Ecosystem
Fresh Water/microbiology
Genetic Variation
Marine Biology
Molecular Sequence Data
Norway
Plankton/genetics,isolation & purification
Polymerase Chain Reaction
RNA, Bacterial/genetics
RNA, Ribosomal, 16S/genetics
Species Specificity
Time Factors
Chemicals
DNA Primers
DNA, Bacterial
DNA, Ribosomal
RNA, Bacterial
RNA, Ribosomal, 16S
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Forney L
Daae F L
Torsvik V
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