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PMID: 8526521 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

In situ PCR for visualization of microscale distribution of specific genes and gene products in prokaryotic communities.

Applied and environmental microbiology ·Vol. 61 ·No. 11 ·1995-11-00 ·Pages 4074-82

Hodson RE, Dustman WA, Garg RP, Moran MA

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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Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1995-11-00
Pages
4074-82
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC167714
Subset
IM
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