Evidence map›Paper›PMID 12571023›Full record

ArticleApplied and environmental microbiology2003

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

Sandrine Delorme, Laurent Philippot, Veronique Edel-Hermann, Chrystel Deulvot, Christophe Mougel, Philippe Lemanceau

Abstract readComparative Study
In one paragraph

Article in Applied and environmental microbiology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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0cells of the map it votes in
10citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Roles of coreFrontiers in plant science · 2025
    Article
  2. Aquatic nitrous oxide reductase gene (Frontiers in microbiology · 2024
    Article
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sandrine DelormeUMR INRA/Université de Bourgogne, Microbiologie et Géochimie du Sol, INRA-CMSE, 21065 Dijon Cedex, France.
Laurent Philippot
Veronique Edel-Hermann
Chrystel Deulvot
Christophe Mougel
Philippe Lemanceau

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diversity of the membrane-bound nitrate reductase (narG) and nitrous oxide reductase (nosZ) genes in fluorescent pseudomonads isolated from soil and rhizosphere environments was characterized together with that of the 16S rRNA gene by a PCR-restriction fragment length polymorphism assay. Fragments of 1,008 bp and 1,433 bp were amplified via PCR with primers specific for the narG and nosZ genes, respectively. The presence of the narG and nosZ genes in the bacterial strains was confirmed by hybridization of the genomic DNA and the PCR products with the corresponding probes. The ability of the strains to either reduce nitrate or totally dissimilate nitrogen was assessed. Overall, there was a good correspondence between the reductase activities and the presence of the corresponding genes. Distribution in the different ribotypes of strains harboring both the narG and nosZ genes and of strains missing both genes suggests that these two groups of strains had different evolutionary histories. Both dissimilatory genes showed high polymorphism, with similarity indexes (Jaccard) of between 0.04 and 0.8, whereas those of the 16S rRNA gene only varied from 0.77 to 0.99. No correlation between the similarity indexes of 16S rRNA and dissimilatory genes was seen, suggesting that the evolution rates of ribosomal and functional genes differ. Pairwise comparison of similarity indexes of the narG and nosZ genes led to the delineation of two types of strains. Within the first type, the similarity indexes of both genes varied in the same range, suggesting that these two genes have followed a similar evolution. Within the second type of strain, the range of variations was higher for the nosZ than for the narG gene, suggesting that these genes have had a different evolutionary rate.

Indexed as

Genes, rRNAGenetic VariationDNA, RibosomalFluorescenceGenes, BacterialNitrate ReductaseNitrate ReductasesNitratesOxidoreductasesPlant RootsPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPseudomonasRNA, Ribosomal, 16SSoil MicrobiologyDNA, RibosomalNitrate ReductaseNitrate ReductasesNitratesnitrous oxide reductaseOxidoreductasesRNA, Ribosomal, 16S

Identifiers

PMID12571023
PMCPMC143668

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.