Abstract
Obtaining information on the genetic capabilities and phylogenetic affinities of individual prokaryotic cells within natural communities is a high priority in the fields of microbial ecology, microbial biogeochemistry, and applied microbiology, among others. A method for prokaryotic in situ PCR (PI-PCR), a technique which will allow single cells within complex mixtures to be identified and characterized genetically, is presented here. The method involves amplification of specific nuclei acid sequences inside intact prokaryotic cells followed by color or fluorescence detection of the localized PCR product via bright-field or epifluorescence microscopy. Prokaryotic DNA and mRNA were both used successfully as targets for PI-PCR. We demonstrate the use of PI-PCR to identify nahA-positive cells in mixtures of bacterial isolates and in model marine bacterial communities.
MeSH Terms
Base Sequence
Cell Membrane Permeability
DNA Primers/genetics
DNA, Bacterial/genetics
Ecosystem
Escherichia coli/genetics
Genes, Bacterial
Marine Biology
Models, Biological
Molecular Sequence Data
Polymerase Chain Reaction/methods
Prokaryotic Cells
Pseudomonas aeruginosa/genetics
Pseudomonas putida/genetics
Chemicals
DNA Primers
DNA, Bacterial
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hodson R E
Department of Marine Sciences, University of Georgia, Athens 30602-2206, USA.
Dustman W A
Garg R P
Moran M A
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