ArticleApplied and environmental microbiology2003
Comparative genetic diversity of the narG, nosZ, and 16S rRNA genes in fluorescent pseudomonads.
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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Who cites it
10 citing papers in PubMed.
- Roles of coreFrontiers in plant science · 2025Article
- Aquatic nitrous oxide reductase gene (Frontiers in microbiology · 2024Article
- Distribution of Denitrification among Haloarchaea: A Comprehensive Study.Microorganisms · 2021Article
- Aerobic Denitrification and Heterotrophic Sulfur Oxidation in the GenusFrontiers in microbiology · 2021Article
- Distinct Expression of the Two NO-Forming Nitrite Reductases in Thermus antranikianii DSM 12462Microbial ecology · 2020Article
- Community structures and comparison of nosZ and 16S rRNA genes from culturable denitrifying bacteria.Folia microbiologica · 2020Article
- Identification of traits shared by rhizosphere-competent strains of fluorescent pseudomonads.Microbial ecology · 2012Article
- Assessment of genetic and functional relationship of antagonistic fluorescent pseudomonads of rice rhizosphere by repetitive sequence, protein coding sequence and functional gene analyses.Journal of microbiology (Seoul, Korea) · 2010Article
- Genome-derived criteria for assigning environmental narG and nosZ sequences to operational taxonomic units of nitrate reducers.Applied and environmental microbiology · 2009Article
- Frequency and diversity of nitrate reductase genes among nitrate-dissimilating Pseudomonas in the rhizosphere of perennial grasses grown in field conditions.Microbial ecology · 2005Article
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6 authors.
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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.
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