Search results for "rase"

showing 10 items of 4343 documents

Top consumer abundance influences lake methane efflux

2015

Lakes are important habitats for biogeochemical cycling of carbon. The organization and structure of aquatic communities influences the biogeochemical interactions between lakes and the atmosphere. Understanding how trophic structure regulates ecosystem functions and influences greenhouse gas efflux from lakes is critical to understanding global carbon cycling and climate change. With a whole-lake experiment in which a previously fishless lake was divided into two treatment basins where fish abundance was manipulated, we show how a trophic cascade from fish to microbes affects methane efflux to the atmosphere. Here, fish exert high grazing pressure and remove nearly all zooplankton. This re…

DNA Bacterial0106 biological sciencesBiogeochemical cycleFood Chain010504 meteorology & atmospheric sciencesta1172General Physics and AstronomyjärvetPolymerase Chain Reaction01 natural sciencesZooplanktonArticleZooplanktonGeneral Biochemistry Genetics and Molecular BiologyCarbon CycleCarbon cycleFood chainRNA Ribosomal 16SlakesAnimalsEcosystemBiomass14. Life underwaterTrophic cascadeEcosystemFinland0105 earth and related environmental sciencesTrophic levelBiomass (ecology)MultidisciplinaryBacteriaEcology010604 marine biology & hydrobiologyFishesGeneral Chemistry15. Life on land6. Clean waterekosysteemit (ekologia)DaphniaPerches13. Climate actionta1181Environmental scienceecosystemsMethaneNature Communications
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Comprehensive DNA methylation analysis of the Aedes aegypti genome

2016

AbstractAedes aegypti mosquitoes are important vectors of viral diseases. Mosquito host factors play key roles in virus control and it has been suggested that dengue virus replication is regulated by Dnmt2-mediated DNA methylation. However, recent studies have shown that Dnmt2 is a tRNA methyltransferase and that Dnmt2-dependent methylomes lack defined DNA methylation patterns, thus necessitating a systematic re-evaluation of the mosquito genome methylation status. We have now searched the Ae. aegypti genome for candidate DNA modification enzymes. This failed to reveal any known (cytosine-5) DNA methyltransferases, but identified homologues for the Dnmt2 tRNA methyltransferase, the Mettl4 (…

DNA Bacterial0301 basic medicineBisulfite sequencingDNA methyltransferaseArticleMass Spectrometry03 medical and health sciences0302 clinical medicineRNA TransferAedesAnimalsAmino Acid SequenceDNA (Cytosine-5-)-MethyltransferasesEpigeneticsGeneticsGenomeMultidisciplinaryTRNA methylationSequence Homology Amino AcidWhole Genome SequencingbiologyTRNA MethyltransferaseSequence Analysis DNAMethylationDNA Methylation030104 developmental biology030220 oncology & carcinogenesisDNA methylationbiology.proteinInsect ProteinsDemethylaseSequence AlignmentScientific Reports
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Two new Salmonella genomic islands 1 from Proteus mirabilis and description of blaCTX-M-15 on a variant (SGI1-K7)

2018

Objectives To characterize the structure of Salmonella genomic islands 1 (SGI1s) from two clinical Proteus mirabilis isolates: one producing an ESBL and the other a penicillinase. Methods WGS completed by PCR and Sanger sequencing was performed to determine sequences of SGI1s from Pm2CHAMA and Pm37THOMI strains. Results Two new variants of SGI1 named SGI1-Pm2CHAMA (53.6 kb) and SGI1-K7 (55.1 kb) were identified. The backbone of SGI1-Pm2CHAMA shared 99.9% identity with that of SGI1. Its MDR region (26.3 kb) harboured two class 1 integrons (an In2-type integron and an In4-type integron) containing in particular a qacH cassette (encoding a quaternary ammonium compound efflux pump). These two i…

DNA Bacterial0301 basic medicineMicrobiology (medical)Transposable elementSalmonellaGenomic Islands030106 microbiologyBiologyIntegronmedicine.disease_causePolymerase Chain Reactionbeta-LactamasesIntegronsTransposition (music)03 medical and health sciencessymbols.namesakePlasmidSalmonellaDrug Resistance Multiple BacterialmedicineHumansPharmacology (medical)Proteus mirabilisPharmacologySanger sequencingGeneticsWhole Genome SequencingGenetic Variationbiology.organism_classificationProteus mirabilisEnterobacteriaceaeAnti-Bacterial AgentsHospitalizationInfectious DiseasesGenes Bacterialsymbolsbiology.proteinFranceProteus InfectionsPlasmidsJournal of Antimicrobial Chemotherapy
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An MLSA approach for the taxonomic update of the Splendidus clade, a lineage containing several fish and shellfish pathogenic Vibrio spp.

2016

A multilocus sequence analysis was undertaken in order to redefine the Splendidus clade of the genus Vibrio, a large group of species containing several pathogenic members that affect fish and shellfish, and are difficult to identify through both phenotypic and genotypic approaches. The study included analysis of partial sequences of recA, gyrB, mreB, rpoD and pyrH genes, as well as the 16S rRNA gene. Seventeen type strain species were included that were complemented with other reference strains and a collection of isolates tentatively identified as members of this clade, as well as a set of other Vibrio species. The clade was well defined and stable in all analyses, and was confirmed to co…

DNA Bacterial0301 basic medicineVibrio cyclitrophicusSequence analysisLineage (evolution)030106 microbiologyZoologySigma FactorApplied Microbiology and BiotechnologyMicrobiologyMicrobiologyFish Diseases03 medical and health sciencesTransferasesRNA Ribosomal 16SAnimalsCladePhylogenyEcology Evolution Behavior and SystematicsShellfishShellfishVibrioBase SequencebiologyStrain (biology)FishesSubcladeDNA-Directed RNA PolymerasesSequence Analysis DNAbiology.organism_classification16S ribosomal RNAOstreidaeBacterial Typing TechniquesRec A RecombinasesDNA GyraseSeasonsMultilocus Sequence TypingSystematic and Applied Microbiology
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Purification of Leuconostoc mesenteroides citrate lyase and cloning and characterization of the citCDEFG gene cluster

1998

ABSTRACT A citrate lyase (EC 4.1.3.6 ) was purified 25-fold from Leuconostoc mesenteroides and was shown to contain three subunits. The first 42 amino acids of the β subunit were identified, as well as an internal peptide sequence spanning some 20 amino acids into the α subunit. Using degenerated primers from these sequences, we amplified a 1.2-kb DNA fragment by PCR from Leuconostoc mesenteroides subsp. cremoris . This fragment was used as a probe for screening a Leuconostoc genomic bank to identify the structural genes. The 2.7-kb gene cluster encoding citrate lyase of L. mesenteroides is organized in three open reading frames, citD , citE , and citF , encoding, respectively, the three ci…

DNA BacterialATP citrate lyaseMolecular Sequence DataGene ExpressionBiologymedicine.disease_causeMicrobiologyBacterial ProteinsCarbon-Sulfur LigasesMultienzyme ComplexesGene clusterAcyl Carrier ProteinEscherichia colimedicineLeuconostocAmino Acid SequenceCloning MolecularMolecular BiologyEscherichia coliBase SequenceSequence Homology Amino AcidStructural geneOxo-Acid-LyasesSequence Analysis DNALyasebiology.organism_classificationEnzymes and ProteinsMolecular biologyOxaloacetate decarboxylaseBiochemistryGenes BacterialLeuconostoc mesenteroidesMultigene FamilyCoenzyme A-TransferasesLeuconostoc
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Taxonomic and functional diversity of atrazine‐degrading bacterial communities enriched from agrochemical factory soil

2010

Aims: To characterize atrazine-degrading potential of bacterial communities enriched from agrochemical factory soil by analysing diversity and organization of catabolic genes. Methods and Results: The bacterial communities enriched from three different sites of varying atrazine contamination mineralized 65–80% of 14C ring-labelled atrazine. The presence of trzN-atzBC-trzD, trzN-atzABC-trzD and trzN-atzABCDEF-trzD gene combinations was determined by PCR. In all enriched communities, trzN-atzBC genes were located on a 165-kb plasmid, while atzBC or atzC genes were located on separated plasmids. Quantitative PCR revealed that catabolic genes were present in up to 4% of the community. Restricti…

DNA BacterialATRAZINEDIVERSITYBACTERIAL COMMUNITYBIODEGRADATIONPolymerase Chain ReactionApplied Microbiology and BiotechnologyActinobacteriaMicrobiologySoil03 medical and health sciencesPlasmidATZ GENESSoil PollutantsRibosomal DNAGenePhylogenySoil MicrobiologyGene Library030304 developmental biology2. Zero hunger0303 health sciencesBacteriabiologyHerbicides030306 microbiologyBacteroidetesSequence Analysis DNAGeneral MedicineAtrazine ; Biodegradation ; Bacterial community ; Diversity ; atz genes ; trz genesTRZ GENESbiology.organism_classification16S ribosomal RNA[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyGenes Bacterial13. Climate actionProteobacteriaBacteriaPlasmidsBiotechnologyJournal of Applied Microbiology
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Putrescine as a signal to modulate the indispensable ABA increase under cold stress.

2009

2 páginas -- PAGS nros. 219-220

DNA BacterialAcclimatizationMutantArabidopsisCold acclimationPlant ScienceBiologyGenes Plantchemistry.chemical_compoundGene Expression Regulation PlantpolyamineFreezingCold acclimationputrescineMode of actionAnalysis of VarianceArabidopsis ProteinsReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingfungiWild typefood and beveragesfreezing toleranceArticle AddendumComplementationCold TemperatureMutagenesis InsertionalArginine decarboxylasechemistryBiochemistryABARNA PlantMutationPutrescinegene expressionPolyamineArginine decarboxylaseAbscisic AcidResearch ArticlePlant signalingbehavior
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A Sensitive Method for Identification of DNA Dependent DNA Polymerases in Acrylamide Gels after Seperation by Micro Disc Electrophoresis

1973

Abstract DNA polymerase, disc electrophoresis, template affinity Two sensitive methods are described for detection of DNA dependent DNA polymerase activities in polyacrylamide gels after their fractionation by micro-disc electrophoresis. One technique is based on the increase in fluorescence of the ethidium bromide complex with template polydeoxyribonucleotides brought about by the action of the polymerases. The sensitivity of the previously described technique has been enhanced. Another method, 14 fold as sensitive, uses radioactive precursors in the enzyme assay after electrophoretic separation; washing, slicing and counting allows to evaluate incorporation into acid insoluble polymer, re…

DNA BacterialAcrylamidesbiologyDNA polymeraseElectrophoresis DiscTritiummedicine.disease_causeFluorescenceGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundBiochemistrychemistryDisc electrophoresisEthidiumAcrylamideDNA NucleotidyltransferasesEscherichia coliMethodsbiology.proteinmedicineGelsEscherichia coliDNA-directed DNA polymeraseDensitometryDNA NucleotidyltransferasesZeitschrift für Naturforschung C
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Direct conjugal transfers of Ti plasmid to soil microflora

2002

The bacterial species in soil that can receive a Ti plasmid by conjugation from Agrobacterium spp. were investigated. In order to have direct access to the potential reservoir of Ti plasmid amongst soil microflora, the conjugal system consisting of a multiply auxotrophic derivative of C58 (ST-96-4) and a derivative of pTiC58Delta(acc)R (pSTiEGK) containing a triple antibiotic-resistance cassette in traM was used to transfer the Ti plasmid in a complex soil microflora used as the recipient. Numerous transconjugants were obtained by this method but none was identified as Agrobacterium. This could be explained by the low density of Agrobacterium in the tested soil. As indicated by analysis of …

DNA BacterialAgrobacteriumSequence analysisAuxotrophy[SDV]Life Sciences [q-bio]Molecular Sequence DataMicrobial Sensitivity TestsPolymerase Chain ReactionMicrobiology03 medical and health sciencesTi plasmidRNA Ribosomal 16SGenetics[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyEcology Evolution Behavior and SystematicsPhylogenySoil MicrobiologyComputingMilieux_MISCELLANEOUS030304 developmental biologyDNA Primers0303 health sciencesbiologyBase Sequence030306 microbiologyDrug Resistance MicrobialSequence Analysis DNARibosomal RNAbiology.organism_classificationSinorhizobiumConjugation GeneticMicrobial geneticsSoil microbiologyPolymorphism Restriction Fragment LengthPlasmidsRhizobium
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Freezing Induces Biased Results in the Molecular Detection of Flavobacterium columnare

2006

ABSTRACT Specific PCR detection and electron microscopy of Flavobacterium columnare revealed the risk of false-negative results in molecular detection of this fish pathogen. Freezing and thawing destroyed the cells so that DNA was for the most part undetectable by PCR. The detection of bacteria was also weakened after prolonged enrichment cultivation of samples from infected fish.

DNA BacterialApplied Microbiology and BiotechnologyFlavobacteriumPolymerase Chain ReactionBacterial geneticsMicrobiologylaw.inventionchemistry.chemical_compoundlawFreezingMethodsPathogenFalse Negative ReactionsPolymerase chain reactionEcologybiologybiology.organism_classificationFlavobacteriaceaeMicroscopy ElectronchemistryFlavobacterium columnareBacteriaDNAFlavobacteriumFood ScienceBiotechnology
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