6533b7d0fe1ef96bd125a4f2

RESEARCH PRODUCT

Quantification of denitrifying bacteria in soils by nirK gene targeted real-time PCR.

Sonia HenryLaurent PhilippotJuan C. López-gutiérrezEzékiel BaudoinFabrice Martin-laurentAlain Brauman

subject

Microbiology (medical)Fastidious organismDNA BacterialDenitrificationNitrite ReductasesMicroorganismMolecular Sequence DataRhodobacter sphaeroidesBiologyMicrobiologyAchromobacter cycloclastesPolymerase Chain ReactionSensitivity and SpecificityMicrobiologychemistry.chemical_compoundDenitrifying bacteriaNitrateGram-Negative BacteriaEscherichia coliBradyrhizobiumMolecular BiologyPhylogenySoil MicrobiologyAlcaligenes faecalisBase SequenceSequence Analysis DNANitrite reductasebiology.organism_classificationchemistryBiochemistryNitrogen fixationBacteriaSinorhizobium meliloti

description

Abstract Denitrification, the reduction of nitrate to nitrous oxide or dinitrogen, is the major biological mechanism by which fixed nitrogen returns to the atmosphere from soil and water. Microorganisms capable of denitrification are widely distributed in the environment but little is known about their abundance since quantification is performed using fastidious and time-consuming MPN-based approaches. We used real-time PCR to quantify the denitrifying nitrite reductase gene (nirK), a key enzyme of the denitrifying pathway catalyzing the reduction of soluble nitrogen oxide to gaseous form. The real-time PCR assay was linear over 7 orders of magnitude and sensitive down to 102 copies by assay. Real-time PCR analysis of different soil samples showed nirK densities of 9.7×104 to 3.9×106 copies per gram of soil. Soil real-time PCR products were cloned and sequenced. Analysis of 56 clone sequences revealed that all cloned real-time PCR products exhibited high similarities to previously described nirK. However, phylogenetic analysis showed that most of environmental sequences are not related to nirK from cultivated denitrifiers.

10.1016/j.mimet.2004.07.002https://pubmed.ncbi.nlm.nih.gov/15488276