Abstract
Confocal laser scanning microscopy, using fluorescently labelled oligonucleotide probes targeting the 16S rRNA of different physiological groups of methanogens, was used to identify which methanogenic genera were present and to describe their in situ spatial locations in samples taken at different depths from blanket peat bog cores. Total bacterial DNA was also extracted and purified from the samples and used as template for amplification of 16S rRNA and regions of methyl CoM reductase-encoding genes using the polymerase chain reaction, as well as for oligonucleotide hybridisation experiments. These techniques, used in concert, demonstrated that methanogens of several physiological groups were present in highest numbers in the mid regions of 25 cm deep peat cores. Some discrepancies were apparent in the findings of the microscopic and molecular methods, though these may be partially accounted for by the different sensitivities of the techniques employed. The combined approaches used in this study gave an insight into the diversity and distribution of methanogens in peat environments not possible using molecular ecological methods alone.
Original language | English |
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Pages (from-to) | 275-281 |
Number of pages | 0 |
Journal | FEMS Microbiol Lett |
Volume | 193 |
Issue number | 2 |
DOIs | |
Publication status | Published - 15 Dec 2000 |
Keywords
- DNA
- Archaeal
- Bacterial
- Ecosystem
- Euryarchaeota
- In Situ Hybridization
- Fluorescence
- Microscopy
- Confocal
- Oligonucleotide Probes
- Oxidoreductases
- Polymerase Chain Reaction
- RNA
- Ribosomal
- 16S
- Soil Microbiology