Search results for "MOLECULAR SEQUENCE DATA"

showing 10 items of 1928 documents

Conjugative plasmid pIP501 undergoes specific deletions after transfer from Lactococcus lactis to Oenococcus oeni

2003

Conjugal transfer of plasmids pIP501 and its derivative pVA797 from Lactococcus lactis to Oenococcus oeni was assayed by filter mating. Plasmid pIP501 was transferred to a number of O. oeni strains whereas a single transconjugant of O. oeni M42 was recovered when pVA797 was used. Physical analysis of the transconjugant plasmids revealed that pIP501 and pVA797 underwent extensive deletions in O. oeni that affected the tra region (conjugal transfer) and SegB region (stability). All derivatives showed segregational instability in O. oeni, but were stably maintained in L. lactis. These differences correlated with the different plasmid copy numbers and the extent of deletions within the SegB reg…

DNA BacterialMolecular Sequence DataRestriction Mappingmedicine.disease_causeBiochemistryMicrobiologyPlasmidGene OrderGeneticsmedicineAmino Acid SequenceMolecular BiologySequence DeletionOenococcus oeniGeneticsMutationBase SequencebiologyStrain (chemistry)Lactococcus lactisConjugative plasmidGeneral Medicinebiology.organism_classificationStreptococcaceaeGram-Positive CocciLactococcus lactisGenes BacterialConjugation GeneticGene DeletionLeuconostocBacteriaPlasmidsArchives of Microbiology
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Nested PCR method for rapid and sensitive detection of Vibrio vulnificus in fish, sediments, and water

1995

A nested PCR for the detection of Vibrio vulnificus in fish farms was developed as an alternative to cultural methods by using universal primers flanking the V. vulnificus-specific sequences directed against 23S rRNA genes. This specific assay detected 10 fg of DNA or 12 to 120 cells in artificially inoculated samples without enrichment and within 24 h.

DNA BacterialMolecular Sequence DataVibrio vulnificusPolymerase Chain ReactionSensitivity and SpecificityApplied Microbiology and Biotechnologylaw.inventionMicrobiologylawVibrionaceae23S ribosomal RNAAnimalsRibosomal DNAPolymerase chain reactionDNA PrimersVibrioBase SequenceEcologybiologyFishesRibosomal RNAbiology.organism_classificationMolecular biologyVibrioRNA Ribosomal 23SEvaluation Studies as TopicGenes BacterialWater MicrobiologyNested polymerase chain reactionResearch ArticleFood ScienceBiotechnology
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Description of Enterovibrio nigricans sp. nov., reclassification of Vibrio calviensis as Enterovibrio calviensis comb. nov. and emended description o…

2009

Eleven strains of halophilic, facultative anaerobes isolated from healthy and diseased Dentex dentex and Sparus aurata (bony fishes) cultured in Spanish Mediterranean fisheries have been studied by a polyphasic approach that included a wide phenotypic characterization, DNA-DNA hybridization and phylogenetic analysis using 16S rRNA, recA and rpoD gene sequences. All strains were phylogenetically related to Enterovibrio species and Vibrio calviensis. On the basis of sequence analysis and DNA-DNA hybridization data, eight of the strains were identified as Enterovibrio coralii. The remaining three strains formed a tight, independent clade in all sequence analyses and showed less than 70 % DNA-D…

DNA BacterialMolecular Sequence DataVibrionaceaeSigma FactorDNA RibosomalMicrobiologyMicrobiologyVibrionaceaePhylogeneticsRNA Ribosomal 16SSequence Homology Nucleic AcidAnimalsCluster AnalysisPhylogenyEcology Evolution Behavior and SystematicsGeneticsbiologyPhylogenetic treeNucleic Acid HybridizationDentex dentexDNA-Directed RNA PolymerasesSequence Analysis DNAGeneral MedicineRibosomal RNAbiology.organism_classification16S ribosomal RNAVibrioBacterial Typing TechniquesPerciformesRec A RecombinasesSpainTaxonomy (biology)International Journal of Systematic and Evolutionary Microbiology
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Lactobacillus oeni sp. nov., from wine.

2009

Ten Lactobacillus strains, previously isolated from different Bobal grape wines from the Utiel-Requena Origin Denomination of Spain, were characterized phylogenetically, genotypically and phenotypically. The 16S rRNA genes were sequenced and phylogenetic analysis showed that they form a tight phylogenetic clade that is closely related to reference strains Lactobacillus satsumensis NRIC 0604T, ‘Lactobacillus uvarum’ 8 and Lactobacillus mali DSM 20444T. DNA–DNA hybridization results confirmed the separation of the strains from other Lactobacillus species. Genotypically, the strains could be differentiated from their closest neighbours by 16S amplified rDNA restriction analysis and random ampl…

DNA BacterialMolecular Sequence DataWineMicrobiologyDNA RibosomalMicrobiologyAesculinchemistry.chemical_compoundPhylogeneticsLactobacillusRNA Ribosomal 16SGenotypeCluster AnalysisAnaerobiosisEcology Evolution Behavior and SystematicsPhylogenyWinebiologyPhylogenetic treefood and beveragesNucleic Acid HybridizationGeneral MedicineSequence Analysis DNAbiology.organism_classification16S ribosomal RNACatalaseDNA FingerprintingBacterial Typing TechniquesRandom Amplified Polymorphic DNA TechniqueLactobacilluschemistrySpainBacteriaPolymorphism Restriction Fragment LengthInternational journal of systematic and evolutionary microbiology
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Cloning and sequencing of the dnaK region of Streptomyces coelicolor A3(2)

1993

Abstract The dnaK homologue of Streptomyces coelicolor A3(2) strain M145 has been cloned and sequenced. Nucleotide sequence analysis of a 2.5-kb region revealed an open reading frame (ORF) encoding a predicted DnaK protein of 618 amino acids (Mr = 66 274). The dnaK coding sequence displays extreme codon bias and shows a strong preference for CGY and GGY, for Arg and Gly codons, respectively. The predicted DnaK sequence has a high Lys:Arg ratio which is not typical of streptomycete proteins. The region immediately downstream from dnaK contains an ORF for a GrpE-like protein; the predicted start codon of grpE overlaps the last two codons of dnaK, indicating that the two genes are translationa…

DNA BacterialMolecular Sequence Datagenetic processesBacterial ProteinsStart codonGeneticsCoding regionHSP70 Heat-Shock ProteinsAmino Acid SequenceCloning MolecularCodonGeneHeat-Shock Proteinschemistry.chemical_classificationGeneticsBase SequencebiologyEscherichia coli ProteinsStreptomyces coelicolorNucleic acid sequenceStreptococcusGeneral Medicinebiology.organism_classificationAmino acidOpen reading framechemistryGenes BacterialProtein BiosynthesisCodon usage biasbiological sciencesbacteriaSequence AlignmentGene
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Sphingomonas fennica sp. nov. and Sphingomonas haloaromaticamans sp. nov., outliers of the genus Sphingomonas.

2007

Bacterial isolates obtained from polychlorophenol-contaminated sites in Finland (strain K101T) and from a Dutch drinking water well (strain A175T) were characterized taxonomically. 16S rRNA gene sequence analysis, determination of DNA G+C content, physiological characterization, estimation of the ubiquinone and polar lipid patterns and fatty acid content revealed that strains K101T and A175T were similar to Sphingomonas wittichii RW1T but also showed pronounced differences. The DNA G+C contents of the two novel strains were 63.6 and 66.1 mol%, respectively. On the basis of these results, two novel species of the genus Sphingomonas are described, for which the names Sphingomonas haloaromatic…

DNA BacterialMolecular Sequence Datamedicine.disease_causeMicrobiologyDNA RibosomalSphingomonasMicrobiologySphingomonas haloaromaticamansTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYRNA Ribosomal 16SBotanymedicineEcology Evolution Behavior and SystematicsPhylogenySphingomonas fennicaBase CompositionbiologyGeneral Medicinebiology.organism_classification16S ribosomal RNASphingomonasGenus SphingomonasSphingomonas wittichiiTaxonomy (biology)BacteriaChlorophenols
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Key roles for freshwater A ctinobacteria revealed by deep metagenomic sequencing

2014

Freshwater ecosystems are critical but fragile environments directly affecting society and its welfare. However, our understanding of genuinely freshwater microbial communities, constrained by our capacity to manipulate its prokaryotic participants in axenic cultures, remains very rudimentary. Even the most abundant components, freshwater Actinobacteria, remain largely unknown. Here, applying deep metagenomic sequencing to the microbial community of a freshwater reservoir, we were able to circumvent this traditional bottleneck and reconstruct de novo seven distinct streamlined actinobacterial genomes. These genomes represent three new groups of photoheterotrophic, planktonic Actinobacteria.…

DNA BacterialMolecular Sequence DatarhodopsinsFresh WaterCyanobacteria633 - Cultivos y producciones [CDU]GenomeFreshwater ecosystemActinobacteriaContig MappingPhylogeneticsRNA Ribosomal 16Slignin degradationGeneticsMicrococcineaePhylogenyEcology Evolution Behavior and SystematicsmetagenomicsbiologyEcologyHigh-Throughput Nucleotide SequencingSequence Analysis DNAbiology.organism_classificationfreshwater reservoirActinobacteriaSpainMetagenomicsMetagenomicsActinomycetalesWater MicrobiologyGenome BacterialGC-contentMolecular Ecology
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Mucilaginibacter frigoritolerans sp. nov., Mucilaginibacter lappiensis sp. nov. and Mucilaginibacter mallensis sp. nov., isolated from soil and liche…

2010

Five cold-adapted bacteria belonging to the genus Mucilaginibacter were isolated from lichen and soil samples collected from Finnish Lapland and investigated in detail by phenotypic and phylogenetic analyses. Based on 16S rRNA gene phylogeny, the novel strains represent three new branches within the genus Mucilaginibacter. The strains were aerobic, chemo-organotrophic, non-motile rods and formed pigmented, smooth, mucoid colonies on solid media. The strains grew between 0 and 33 °C (optimum growth at 25 °C) and at pH 4.5–8.0 (optimum growth at pH 6.0). The main cellular fatty acids were iso-C15 : 0, summed feature 3 (C16 : 1 ω7c/iso-C15 : 0 2-OH) and iso-C17 : 0 3-OH and the major respirato…

DNA BacterialMucilaginibacter frigoritoleransfood.ingredientLichensMolecular Sequence DataBiologymedicine.disease_causeMicrobiologyMicrobiologyfoodPhylogeneticsRNA Ribosomal 16SBotanymedicineLichenEcology Evolution Behavior and SystematicsFinlandPhylogenySoil MicrobiologyBase CompositionMucilaginibacter mallensisPhylogenetic treeBacteroidetesFatty AcidsMucilaginibacterVitamin K 2General MedicineSequence Analysis DNA16S ribosomal RNABacterial Typing TechniquesMucilaginibacter lappiensisInternational journal of systematic and evolutionary microbiology
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Identification of a third secondary carrier (DcuC) for anaerobic C4-dicarboxylate transport in Escherichia coli: roles of the three Dcu carriers in u…

1996

In Escherichia coli, two carriers (DcuA and DcuB) for the transport of C4 dicarboxylates in anaerobic growth were known. Here a novel gene dcuC was identified encoding a secondary carrier (DcuC) for C4 dicarboxylates which is functional in anaerobic growth. The dcuC gene is located at min 14.1 of the E. coli map in the counterclockwise orientation. The dcuC gene combines two open reading frames found in other strains of E. coli K-12. The gene product (DcuC) is responsible for the transport of C4 dicarboxylates in DcuA-DcuB-deficient cells. The triple mutant (dcuA dcuB dcuC) is completely devoid of C4-dicarboxylate transport (exchange and uptake) during anaerobic growth, and the bacteria are…

DNA BacterialMutantMolecular Sequence DataBiologymedicine.disease_causeMicrobiologyGene productBacterial ProteinsmedicineEscherichia coliDicarboxylic AcidsAmino Acid SequenceAnaerobiosisMolecular BiologyEscherichia coliPeptide sequenceGeneDicarboxylic Acid TransportersBase SequenceSequence Homology Amino AcidEscherichia coli ProteinsChromosome MappingBiological Transportbiology.organism_classificationIsoenzymesOpen reading frameMutagenesis InsertionalBiochemistryC4-dicarboxylate transportCarrier ProteinsBacteriaResearch ArticleJournal of bacteriology
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The long-term cytoskeletal rearrangement induced by rabbit enteropathogenic Escherichia coli is Esp dependent but intimin independent.

1999

Attaching and effacing rabbit enteropathogenic Escherichia coli (REPEC) of the O103 serogroup adhere diffusely on HeLa cells and trigger a slow progressive cytopathic effect (CPE) characterized by the recruitment of vinculin and the assembly of actin stress fibres. In contrast to REPEC O103, the reference human EPEC strain E2348/69 is unable to trigger the CPE. In this study, we have shown first that the fimbrial adhesin AF/R2, which mediates the diffuse adhesion of REPEC O103, was not sufficient to induce the CPE capability upon E2348/69. Non-polar mutants of REPEC O103 for espA, espB, espD and eae were then constructed. The four mutants were unable to induce attaching and effacing lesions…

DNA BacterialMutantMolecular Sequence DataMicrobiologyBacterial AdhesionMicrobiology03 medical and health sciencesBacterial ProteinsEscherichia coliAnimalsHumansEnteropathogenic Escherichia coliCytoskeletonAdhesins BacterialMolecular Biology[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyActinCytoskeleton030304 developmental biologyIntiminCytopathic effect0303 health sciencesAdhesins Escherichia colibiologyBase Sequence030306 microbiologyEscherichia coli ProteinsGenetic Complementation TestREARRANGEMENTbiochemical phenomena metabolism and nutritionVinculinBacterial adhesin[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyGenes Bacterialbiology.proteinRabbitsCarrier ProteinsBacterial Outer Membrane ProteinsHeLa CellsMolecular microbiology
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