Literature DB >> 7952328

Fluorescent Pseudomonas species categorized by using polymerase chain reaction (PCR)/restriction fragment analysis of 16S rDNA.

G Laguerre1, L Rigottier-Gois, P Lemanceau.   

Abstract

A rapid procedure for the identification of fluorescent pseudomonads, based on the polymerase chain reaction (PCR) and restriction fragment analysis of 16S rDNA genes is described. Thirty-one strains belonging to 10 different Pseudomonas species of the Pseudomonas fluorescens rRNA branch were characterized. Amplified rDNA was digested with 13 different restriction endonucleases. The combined data from restriction analysis enabled the definition of 17 different 16S rDNA genotypes. All type strains belonging to different species were differentiated. The good correlation between grouping obtained using restriction analysis with other molecular classification criteria demonstrates the value of the described method to characterize rapidly fluorescent Pseudomonas strains at the species level.

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Year:  1994        PMID: 7952328     DOI: 10.1111/j.1365-294x.1994.tb00126.x

Source DB:  PubMed          Journal:  Mol Ecol        ISSN: 0962-1083            Impact factor:   6.185


  12 in total

1.  Comparative genetic diversity of the narG, nosZ, and 16S rRNA genes in fluorescent pseudomonads.

Authors:  Sandrine Delorme; Laurent Philippot; Veronique Edel-Hermann; Chrystel Deulvot; Christophe Mougel; Philippe Lemanceau
Journal:  Appl Environ Microbiol       Date:  2003-02       Impact factor: 4.792

2.  The composition of fluorescent pseudomonad populations associated with roots is influenced by plant and soil type.

Authors:  X Latour; T Corberand; G Laguerre; F Allard; P Lemanceau
Journal:  Appl Environ Microbiol       Date:  1996-07       Impact factor: 4.792

3.  Assessment of genetic and functional relationship of antagonistic fluorescent pseudomonads of rice rhizosphere by repetitive sequence, protein coding sequence and functional gene analyses.

Authors:  Jayakumar Pathma; Niraikulam Ayyadurai; Natarajan Sakthivel
Journal:  J Microbiol       Date:  2011-01-09       Impact factor: 3.422

4.  Bacteria associated with hazelnut (Corylus avellana L.) decline are of two groups: Pseudomonas avellanae and strains resembling P. syringae pv. syringae.

Authors:  Marco Scortichini; Ugo Marchesi; Maria Pia Rossi; Paola Di Prospero
Journal:  Appl Environ Microbiol       Date:  2002-02       Impact factor: 4.792

5.  Differentiation of Burkholderia species by PCR-restriction fragment length polymorphism analysis of the 16S rRNA gene and application to cystic fibrosis isolates.

Authors:  C Segonds; T Heulin; N Marty; G Chabanon
Journal:  J Clin Microbiol       Date:  1999-07       Impact factor: 5.948

6.  Characterization by 16S rRNA sequence analysis of pseudomonads causing blotch disease of cultivated Agaricus bisporus.

Authors:  S A Godfrey; S A Harrow; J W Marshall; J D Klena
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

7.  Effect of Two Plant Species, Flax (Linum usitatissinum L.) and Tomato (Lycopersicon esculentum Mill.), on the Diversity of Soilborne Populations of Fluorescent Pseudomonads.

Authors:  P Lemanceau; T Corberand; L Gardan; X Latour; G Laguerre; J Boeufgras; C Alabouvette
Journal:  Appl Environ Microbiol       Date:  1995-03       Impact factor: 4.792

8.  Metabolic and Genotypic Fingerprinting of Fluorescent Pseudomonads Associated with the Douglas Fir-Laccaria bicolor Mycorrhizosphere.

Authors:  P Frey; P Frey-Klett; J Garbaye; O Berge; T Heulin
Journal:  Appl Environ Microbiol       Date:  1997-05       Impact factor: 4.792

9.  A highly selective PCR protocol for detecting 16S rRNA genes of the genus Pseudomonas (sensu stricto) in environmental samples.

Authors:  F Widmer; R J Seidler; P M Gillevet; L S Watrud; G D Di Giovanni
Journal:  Appl Environ Microbiol       Date:  1998-07       Impact factor: 4.792

10.  Colonization of wheat roots by an exopolysaccharide-producing pantoea agglomerans strain and its effect on rhizosphere soil aggregation

Authors: 
Journal:  Appl Environ Microbiol       Date:  1998-10       Impact factor: 4.792

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