6533b837fe1ef96bd12a2934

RESEARCH PRODUCT

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

Véronique Edel-hermannChristophe MougelLaurent PhilippotChrystel DeulvotSandrine DelormePhilippe Lemanceau

subject

BiologyNitrate reductaseDNA RibosomalNitrate ReductasePlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyFluorescencelaw.invention03 medical and health sciencesPlant MicrobiologyNitrate ReductaseslawPseudomonasRNA Ribosomal 16SGenetic variationGeneSoil MicrobiologyPolymerase chain reactionComputingMilieux_MISCELLANEOUS030304 developmental biology2. Zero hungerGenetics[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesNitratesEcology030306 microbiologyPseudomonasGenetic VariationGenes rRNARibosomal RNA16S ribosomal RNAbiology.organism_classificationMolecular biologygenomic DNA[SDV.EE] Life Sciences [q-bio]/Ecology environmentGenes BacterialOxidoreductasesPolymorphism Restriction Fragment LengthFood ScienceBiotechnology

description

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.

https://hal.inrae.fr/hal-02674671