6533b873fe1ef96bd12d4d98

RESEARCH PRODUCT

16S rDNA analysis for characterization of denitrifying bacteria isolated from three agricultural soils

D. ChènebyAlain HartmannLaurent PhilippotCatherine HénaultJ. C. Germon

subject

2. Zero hunger0303 health sciencesEcologybiology030306 microbiology16S RDNAbiology.organism_classificationSoil type16S ribosomal RNAApplied Microbiology and BiotechnologyMicrobiologyAmplified Ribosomal DNA Restriction Analysis03 medical and health sciencesDenitrifying bacteriaPhylogenetic diversity[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyMicrobial population biologyBotanyRibosomal DNA[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyBacteriaComputingMilieux_MISCELLANEOUS030304 developmental biology

description

Bacteria capable of denitrification are spread among phylogenetically diverse groups. In the present investigation, molecular methods (amplified ribosomal DNA restriction analysis (ARDRA) and partial 16S rDNA gene sequencing) were used to determine the genetic diversity of culturable denitrifying soil bacteria. The purpose of this work was to study the microbial density and diversity of denitrifying communities isolated from two luvisols and a rendosol. The denitrifying bacterial density was significantly higher in the two luvisols (3x10(6) and 4x10(6) bacteria g(-1) dry soil) than in the rendosol (4x10(5) bacteria g(-1) dry soil). Denitrifying isolates from soils were grouped according to the similarity of their restriction patterns into 26 ARDRA types. Interestingly ARDRA analysis suggests that some denitrifying isolates are specific to a soil type while others seem to be geographically widespread. The number of individual isolates found in each ARDRA type appeared to be highly variable between the two sampling dates but some denitrifying types were capable of persisting in soil. The tree obtained from the partial sequences revealed five major branches exhibiting highest identity to the following genera: (i) Burkholderia-Ralstonia, (ii) Pseudomonas, (iii) Xanthomonas-Frateuria, (iv) Bacillus and (v) Streptomyces. Our 16S rDNA-based analysis clearly reveals broad diversity exceeding that previously described in the literature.

https://hal.inrae.fr/hal-02685030