Search results for "Sequence analysis"

showing 10 items of 1349 documents

In situ activity of a bacteriocin-producing Lactococcus lactis strain. Influence on the interactions between lactic acid bacteria during sourdough fe…

2005

Aims:  To biochemically characterize the bacteriocin produced by Lactococcus lactis ssp. lactis M30 and demonstrate its effect on lactic acid bacteria (LAB) during sourdough propagation. Methods and Results:  A two-peptide bacteriocin produced by L. lactis ssp. lactis M30 was purified by ion exchange, hydrophobic interaction and reversed phase chromatography. Mass spectrometry of the two peptides and sequence analysis of the ltnA2 gene showed that the bacteriocin was almost identical to lacticin 3147. During a 20-day period of sourdough propagation the stability of L. lactis M30 was demonstrated, with concomitant inhibition of the indicator strain Lactobacillus plantarum 20, as well as the …

DNA BacterialColony Count MicrobialLactobacillus sanfranciscensisPolymerase Chain ReactionApplied Microbiology and Biotechnologychemistry.chemical_compoundBacteriocinsBacteriocinbiologyLactococcus lactisfood and beveragesBreadSequence Analysis DNAGeneral MedicineLactobacillaceaebiology.organism_classificationbatteriocine impasti acidi batteri latticiAnti-Bacterial AgentsCulture MediaLactic acidLactococcus lactisLactobacilluschemistryBiochemistryGenes BacterialFermentationFood MicrobiologyFermentationLactobacillus plantarumBacteriaLactobacillus plantarumBiotechnologySettore AGR/16 - Microbiologia Agraria
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Impact of analytic provenance in genome analysis

2014

Background Many computational methods are available for assembly and annotation of newly sequenced microbial genomes. However, when new genomes are reported in the literature, there is frequently very little critical analysis of choices made during the sequence assembly and gene annotation stages. These choices have a direct impact on the biologically relevant products of a genomic analysis - for instance identification of common and differentiating regions among genomes in a comparison, or identification of enriched gene functional categories in a specific strain. Here, we examine the outcomes of different assembly and analysis steps in typical workflows in a comparison among strains of Vi…

DNA BacterialComparative genomicsGeneticsComputational BiologySequence assemblyMicrobiologiaMolecular Sequence AnnotationSequence Analysis DNAComputational biologyGene AnnotationBiologyGenomeAnnotationProceedingsWorkflowGenes BacterialBacteris patògensGeneticsIdentification (biology)DNA microarrayVibrio vulnificusGenome BacterialBiotechnologyBMC Genomics
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A single primer pair gives a specific ortholog amplicon in a wide range of Cyanobacteria and plastid-bearing organisms: applicability in inventory of…

2010

The scarcity of universally applied molecular markers for algae has resulted in the development of multiple, independent and not easily comparable systems. The goal of this work is to increase the number of available molecular markers and to generate easily comparable systems. Thereby, we have designed a primer pair capable of amplifying a broad range of organisms: Cyanobacteria, Chlorophyta, Chlorarachniophyta, Cryptophyta, Euglenida, Glaucophyta, Rhodophyta, Stramenopiles and Streptophyta including plants. This primer pair can amplify a portion of the 23S rRNA gene with sufficient variability to identify reference material form collections across a broad range of taxa and perform phylogen…

DNA BacterialDNA PlantGlaucophytaCyanobacteriaPhylogeneticsChlorophytaGeneticsCryptophytaGlaucophytaPlastidsPlastidMolecular BiologyEcology Evolution Behavior and SystematicsPhylogenyDNA PrimersGeneticsPhylogenetic treebiologyStreptophytaSequence Analysis DNARibosomal RNAAmpliconbiology.organism_classificationRNA Ribosomal 23SEvolutionary biologyRhodophytaStreptophytaStramenopilesMolecular phylogenetics and evolution
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Sequencing orphan species initiative (SOS): Filling the gaps in the 16S rRNA gene sequence database for all species with validly published names

2013

Yarza, Pablo et al.

DNA BacterialDatabaseBacteriaSequence analysisSequence Analysis DNABiologyRibosomal RNAcomputer.software_genreClassificationApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalType (biology)23S ribosomal RNAPhylogeneticsRNA Ribosomal 16SInternational Code of Nomenclature of BacteriacomputerGeneEcology Evolution Behavior and SystematicsPhylogenySequence (medicine)
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A taxonomic survey of lactic acid bacteria isolated from wheat (Triticum durum) kernels and non-conventional flours

2007

In order to explore the correspondence between raw material- and mature sourdough-lactic acid bacterial (LAB) communities, 59 Italian wheat (Triticum durum) grain samples, one bran and six non-conventional flour samples were analyzed through a culture-dependent approach. The highest cell count by an agar medium specific for LAB was 2.16 log CFU/g. From about 2300 presumptive LAB (Gram-positive and catalase-negative) colonies collected, a total of 356 isolates were subjected to identification by a genetic polyphasic strategy consisting of RAPD-PCR analysis, partial 16S rRNA gene sequencing, species-specific and multiplex PCRs. The isolates were recognized as 137 strains belonging to Aerococc…

DNA BacterialDietary FiberLactococcusEnterococcus mundtiiFlourMolecular Sequence Dataculture-dependent niethods genetic polyphasic approach lactic acid bacteria non-conventional flours sourdough Triticum durumColony Count MicrobialGram-Positive BacteriaApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalMicrobiologyLactobacillusRNA Ribosomal 16SSequence Homology Nucleic Acidmetodi coltura-dipendenti approccio polifasico genetico impasti acidiFood scienceLactic AcidEcology Evolution Behavior and SystematicsPhylogenyTriticumgenetic polyphasic approachsourdoughbiologyfood and beveragesGenes rRNASequence Analysis DNAbiology.organism_classification16S ribosomal RNACatalaseDNA FingerprintingRandom Amplified Polymorphic DNA Techniquelactic acid bacteriaRNA BacterialEnterococcusItalyTriticum durumAerococcusPediococcusEdible Grainnon-conventional floursculture-dependent niethodsEnterococcus faecium
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Genotyping of Legionella pneumophila serogroup 1 strains isolated in Northern Sicily, Italy.

2008

During a three-year period, from April 2002 to May 2005, one hundred-forty-seven samples, taken from technical systems of water distribution at point of use, were repeatedly collected at six different sites in Northern Sicily and assayed for the presence of Legionella pneumophila serogroup 1 and serogroups 2 to 14. At the first samplings, the water distribution systems of all the sites were heavily contaminated, and disinfection treatments by the superheat and flush method were therefore performed. Treatments were always successful against L. pneumophila sg.1, but only in a few cases against all other serogroups. Eighty-six strains of L. pneumophila sg. 1, isolated from 26 of these samples,…

DNA BacterialDisinfectionMolecular EpidemiologySettore MED/07 - Microbiologia E Microbiologia ClinicaGenotypeCluster AnalysisFresh WaterSequence Analysis DNAAmplified Fragment Length Polymorphism AnalysisLegionella pneumophila Surveillance Water distribution system Molecular typing Amplified fragment length polymorphismSicilyBacterial Typing TechniquesLegionella pneumophila
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Enterococcus asini sp. nov. isolated from the caecum of donkeys (Equus asinus)

1998

Several Gram-positive, non-spore-forming and non-motile bacteria consisting of pairs or chains of cocci were isolated during an investigation of the bacterial flora of the caecum of donkeys. Physiological and metabolic data indicated that the strains belong to the genus Enterococcus; phenotypic traits of these organisms were not consistent with any of the currently known Enterococcus species. 16S rRNA gene sequence analysis placed these strains in the genus Enterococcus. Their closest relatives are Enterococcus avium, Enterococcus faecium and Enterococcus pseudoavium with a sequence similarity of 97.4%. This group of strains can be differentiated from the other Enterococcus spp. by their ph…

DNA BacterialEnterococcus avium[SDE] Environmental SciencesARN RIBOSOMAL[SDV]Life Sciences [q-bio]Molecular Sequence DataImmunologyved/biology.organism_classification_rank.speciesMicrobiologyMicrobiologyCaecumEnterococcus pseudoaviumRNA Ribosomal 16SAnimalsCecumGram-Positive Bacterial InfectionsPhylogenyComputingMilieux_MISCELLANEOUSBase CompositionBase SequencebiologySequence Analysis RNAved/biologyEquidaebiochemical phenomena metabolism and nutritionRibosomal RNAANE16S ribosomal RNAbiology.organism_classification[SDV] Life Sciences [q-bio]RNA BacterialEnterococcus[SDE]Environmental SciencesEnterococcusBacteriaEnterococcus faecium
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Aeromonas hydrophila subsp. dhakensis isolated from feces, water and fish in Mediterranean Spain.

2012

Eight Aeromonas hydrophila-like arabinose-negative isolates from diverse sources (i.e., river freshwater, cooling-system water pond, diseased wild European eels, and human stools) sampled in Valencia (Spain) during 2004-2005, were characterized by 16S rRNA gene sequencing and extensive biochemical testing along with reference strains of most Aeromonas species. These isolates and all reference strains of A. hydrophila subsp. dhakensis and A. aquariorum showed a 16S rRNA sequence similarity of 99.8-100%, and they all shared an identical phenotype. This matched exactly with that of A. hydrophila subsp. dhakensis since all strains displayed positive responses to the Voges-Prokauer test and to t…

DNA BacterialFresh WaterMicrobial Sensitivity TestsAmoxicillin-Potassium Clavulanate CombinationCefoxitinFecesDrug Resistance Multiple BacterialRNA Ribosomal 16SAnimalsHumansTicarcillinemerging pathogen16S rRNA gene sequencingBase SequenceSequence Analysis RNAA. hydrophila subsp. dhakensisFishesArticlesbiochemical phenomena metabolism and nutritionbacterial infections and mycosesAeromonas hydrophilaImipenemPhenotypeSpainphenotypic profilebacteriaMicrobes and environments
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Detection and organization of atrazine-degrading genetic potential of seventeen bacterial isolates belonging to divergent taxa indicate a recent comm…

2007

A collection of 17 atrazine-degrading bacteria isolated from soils was studied to determine the composition of the atrazine-degrading genetic potential (i.e. trzN, trzD and atz) and the presence of IS1071. The characterization of seven new atrazine-degrading bacteria revealed for the first time the trzN-atzBC gene composition in Gram-negative bacteria such as Sinorhizobium sp. or Polaromonas sp. Three main atrazine-degrading gene combinations (i) trzN– atzBC, (ii) atzABC– trzD and (iii) atzABCDEF were observed. The atz and trz genes were often located on plasmids, suggesting that plasmid conjugation could play an important role in their dispersion. In addition, the observation of these gene…

DNA BacterialGene Transfer HorizontalATRAZINEMolecular Sequence DataBIODEGRADATIONatrazine; insertion sequences; biodegradation; atz genes; trz genesBiologyMicrobiologyMicrobiologyEvolution MolecularTransposition (music)03 medical and health scienceschemistry.chemical_compoundPlasmidGram-Negative BacteriaATZ GENESGeneticsInsertion sequenceMolecular BiologyGeneSoil MicrobiologySEQUENCE D'INSERTION030304 developmental biologyRecombination GeneticGenetics0303 health sciencesINSERTION SEQUENCES030306 microbiologyCatabolismChromosomeSequence Analysis DNATRZ GENESbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryGenes BacterialDNA Transposable ElementsMetabolic Networks and PathwaysDNABacteriaPlasmids
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Domain organization and evolution of multifunctional autoprocessing repeats-in-toxin (MARTX) toxin in Vibrio vulnificus.

2011

ABSTRACT The objective of this study was to analyze multifunctional autoprocessing repeats-in-toxin (MARTX) toxin domain organization within the aquatic species Vibrio vulnificus as well as to study the evolution of the rtxA1 gene. The species is subdivided into three biotypes that differ in host range and geographical distribution. We have found three different types (I, II, and III) of V. vulnificus MARTX (MARTX Vv ) toxins with common domains (an autocatalytic cysteine protease domain [CPD], an α / β-hydrolase domain, and a domain resembling that of the LifA protein of Escherichia coli O127:H6 E2348/69 [Efa/LifA]) and specific domains (a Rho-GTPase inactivation domain [RID], a domain of …

DNA BacterialGene Transfer HorizontalBacterial ToxinsMolecular Sequence DataVibrio vulnificusmedicine.disease_causeApplied Microbiology and BiotechnologyBacterisMicrobiologyEvolution MolecularVibrionaceaemedicineEvolutionary and Genomic MicrobiologyVibrio vulnificusGeneEscherichia coliGenètica bacterianaGeographyEcologybiologyToxinSequence Analysis DNAbiology.organism_classificationCysteine proteaseBacterial Typing TechniquesProtein Structure TertiaryHorizontal gene transferBacteris patògensBacteriaFood ScienceBiotechnology
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