Literature DB >> 8526521

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

R E Hodson1, W A Dustman, R P Garg, M A Moran.   

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.

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Year:  1995        PMID: 8526521      PMCID: PMC167714          DOI: 10.1128/aem.61.11.4074-4082.1995

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  22 in total

1.  Adaptation of model genetically engineered microorganisms to lake water: growth rate enhancements and plasmid loss.

Authors:  P A Sobecky; M A Schell; M A Moran; R E Hodson
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

2.  Identification of Whole Fixed Bacterial Cells with Nonradioactive 23S rRNA-Targeted Polynucleotide Probes.

Authors:  K Trebesius; R Amann; W Ludwig; K Mühlegger; K H Schleifer
Journal:  Appl Environ Microbiol       Date:  1994-09       Impact factor: 4.792

3.  Phylogenetic stains: ribosomal RNA-based probes for the identification of single cells.

Authors:  E F DeLong; G S Wickham; N R Pace
Journal:  Science       Date:  1989-03-10       Impact factor: 47.728

4.  Primed in situ DNA amplification (PIDA).

Authors:  R B Moss; M A Kaliner
Journal:  J Clin Lab Anal       Date:  1994       Impact factor: 2.352

5.  In situ identification of bacteria in drinking water and adjoining biofilms by hybridization with 16S and 23S rRNA-directed fluorescent oligonucleotide probes.

Authors:  W Manz; U Szewzyk; P Ericsson; R Amann; K H Schleifer; T A Stenström
Journal:  Appl Environ Microbiol       Date:  1993-07       Impact factor: 4.792

6.  In situ polymerase chain reaction: localization of HSV-2 DNA sequences in infections of the nervous system.

Authors:  P Gressens; J R Martin
Journal:  J Virol Methods       Date:  1994-01       Impact factor: 2.014

7.  Transcriptional control of the nah and sal hydrocarbon-degradation operons by the nahR gene product.

Authors:  M A Schell
Journal:  Gene       Date:  1985       Impact factor: 3.688

8.  Detection of micro-organisms in soil after in situ hybridization with rRNA-targeted, fluorescently labelled oligonucleotides.

Authors:  D Hahn; R I Amann; W Ludwig; A D Akkermans; K H Schleifer
Journal:  J Gen Microbiol       Date:  1992-05

9.  Leucine incorporation and its potential as a measure of protein synthesis by bacteria in natural aquatic systems.

Authors:  D Kirchman; E K'nees; R Hodson
Journal:  Appl Environ Microbiol       Date:  1985-03       Impact factor: 4.792

10.  Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.

Authors:  G Ditta; S Stanfield; D Corbin; D R Helinski
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

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  31 in total

1.  In situ reverse transcription-PCR for monitoring gene expression in individual Methanosarcina mazei S-6 cells.

Authors:  M Lange; T Tolker-Nielsen; S Molin; B K Ahring
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

Review 2.  Measurement of bacterial gene expression in vivo.

Authors:  I Hautefort; J C Hinton
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-05-29       Impact factor: 6.237

3.  Monitoring of Ralstonia eutropha KT1 in groundwater in an experimental bioaugmentation field by in situ PCR.

Authors:  Katsuji Tani; Masahiro Muneta; Kanji Nakamura; Katsutoshi Shibuya; Masao Nasu
Journal:  Appl Environ Microbiol       Date:  2002-01       Impact factor: 4.792

4.  Bromodeoxyuridine (BrdU) labeling and subsequent fluorescence activated cell sorting for culture-independent identification of dissolved organic carbon-degrading bacterioplankton.

Authors:  Steven Robbins; Jisha Jacob; Xinxin Lu; Mary Ann Moran; Xiaozhen Mou
Journal:  J Vis Exp       Date:  2011-09-10       Impact factor: 1.355

5.  Dynamics of microcystin-degrading bacteria in mucilage of Microcystis.

Authors:  T Maruyama; K Kato; A Yokoyama; T Tanaka; A Hiraishi; H D Park
Journal:  Microb Ecol       Date:  2003-08       Impact factor: 4.552

6.  Culture-independent analysis of fecal enterobacteria in environmental samples by single-cell mRNA profiling.

Authors:  Han Chen; Gomathinayagam Ponniah; Nancy Salonen; Paul Blum
Journal:  Appl Environ Microbiol       Date:  2004-08       Impact factor: 4.792

Review 7.  Single-cell microbiology: tools, technologies, and applications.

Authors:  Byron F Brehm-Stecher; Eric A Johnson
Journal:  Microbiol Mol Biol Rev       Date:  2004-09       Impact factor: 11.056

8.  Improved sensitivity of whole-cell hybridization by the combination of horseradish peroxidase-labeled oligonucleotides and tyramide signal amplification.

Authors:  W Schönhuber; B Fuchs; S Juretschko; R Amann
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

9.  Use of green fluorescent protein to tag and investigate gene expression in marine bacteria.

Authors:  S Stretton; S Techkarnjanaruk; A M McLennan; A E Goodman
Journal:  Appl Environ Microbiol       Date:  1998-07       Impact factor: 4.792

10.  In situ reverse transcription, an approach to characterize genetic diversity and activities of prokaryotes.

Authors:  F Chen; J M Gonzalez; W A Dustman; M A Moran; R E Hodson
Journal:  Appl Environ Microbiol       Date:  1997-12       Impact factor: 4.792

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