Search results for "23S"

showing 10 items of 24 documents

DNA extraction from soils: old bias for new microbial diversity analysis methods.

2001

ABSTRACT The impact of three different soil DNA extraction methods on bacterial diversity was evaluated using PCR-based 16S ribosomal DNA analysis. DNA extracted directly from three soils showing contrasting physicochemical properties was subjected to amplified ribosomal DNA restriction analysis and ribosomal intergenic spacer analysis (RISA). The obtained RISA patterns revealed clearly that both the phylotype abundance and the composition of the indigenous bacterial community are dependent on the DNA recovery method used. In addition, this effect was also shown in the context of an experimental study aiming to estimate the impact on soil biodiversity of the application of farmyard manure o…

DNA BacterialRibosomal Intergenic Spacer analysisContext (language use)BiologyApplied Microbiology and BiotechnologyDNA RibosomalPolymerase Chain Reactionlaw.inventionSoillawRNA Ribosomal 16SBotanyMethodsRibosomal DNAPolymerase chain reactionSoil Microbiology[SDV.EE]Life Sciences [q-bio]/Ecology environmentErrataEcologyBacteriabusiness.industryRibosomal RNADNA extractionAmplified Ribosomal DNA Restriction AnalysisBiotechnology[SDV.EE] Life Sciences [q-bio]/Ecology environmentRNA Ribosomal 23SbusinessSoil microbiologyFood ScienceBiotechnologyApplied and environmental microbiology
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Use of a species-specific multiplex PCR for the identification of pediococci.

2008

In this study, the 23S rRNA genes of nine different Pediococcus type strains were sequenced. By using a multiple sequence alignment with 23S rDNA sequences of related lactic acid bacteria two primer pairs were constructed, one for the general identification of the genus Pediococcus and one for the identification of the atypical species, P. dextrinicus. Furthermore, a primer set for a rapid multiplex PCR identification of the eight typical Pediococcus species was developed. With this technique, the species P. damnosus, P. parvulus, P. inopinatus, P. cellicola, P. pentosaceus, P. acidilactici, P. claussenii, and P. stilesii could be discriminated simultaneously in a single PCR. Experiments wi…

DNA BacterialSequence analysisFood ContaminationWineMicrobiologyPolymerase Chain ReactionSensitivity and Specificitylaw.inventionMicrobiologySpecies Specificity23S ribosomal RNAlawMultiplex polymerase chain reactionPediococcusPolymerase chain reactionWinebiologyBase Sequencefood and beveragesGeneral MedicineSequence Analysis DNARibosomal RNAbiology.organism_classificationRNA Ribosomal 23SPediococcusPrimer (molecular biology)Sequence AlignmentFood ScienceInternational journal of food microbiology
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A TaqMan-based real-time PCR assay for the specific detection and quantification ofLeuconostoc mesenteroidesin meat products

2007

A new real-time PCR procedure was developed for the specific detection and quantification of Leuconostoc mesenteroides in meat products. It is a TaqMan assay based on 23S rRNA gene targeted primers and probe. Specificity was evaluated using purified DNA from 132 strains: 102 lactic acid bacteria (LAB), including 57 reference strains and 46 food isolates, belonging to genus Leuconostoc and related genera, and 30 non-LAB strains. Quantification was linear over at least 5 log units using both serial dilutions of purified DNA and calibrated cell suspensions from Leuconostoc mesenteroides ssp. dextranicum CECT 912T. This assay was able to detect at least five genomic equivalents, using purified …

DNA BacterialSerial dilutionMolecular Sequence DataSensitivity and SpecificityMicrobiologychemistry.chemical_compound23S ribosomal RNAGeneticsTaqManAnimalsMolecular BiologyDNA PrimersChromatographybiologyReverse Transcriptase Polymerase Chain Reactionfood and beveragesSequence Analysis DNARibosomal RNAbiology.organism_classificationMolecular biologyLactic acidMeat ProductsRNA Ribosomal 23SReal-time polymerase chain reactionchemistryLactobacillaceaeLeuconostoc mesenteroidesBacteriaFEMS Microbiology Letters
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Low incidence of Vibrio vulnificus among Vibrio isolates from sea water and shellfish of the western Mediterranean coast.

1999

A specific search for Vibrio vulnificus in natural marine samples from the Spanish Mediterranean Sea was carried out by nested PCR and cultural approaches using thiosulphate-citrate-bile salts-sucrose agar (TCBS) and cellobiose-polymixin B-colistin agar (CPC), incubated at 40 degrees C, as selective media. Presumptive colonies were identified by PCR using specific primers against 23S rRNA sequences. This species was isolated from sea water and edible bivalves, mainly after preenrichment in alkaline peptone water (APW) at 40 degrees C followed by CPC agar. None of the V. vulnificus isolates identified corresponded to serovar E. Dominant Vibrio species on directly inoculated TCBS plates incub…

Donax trunculusSerotypeVeterinary medicinefood.ingredientColony Count MicrobialVibrio vulnificusApplied Microbiology and BiotechnologyDNA RibosomalPolymerase Chain ReactionMediterranean seafoodSpecies SpecificityVibrionaceaeMediterranean SeaAgarAnimalsSeawaterSerotypingShellfishShellfishVibriobiologyEcologyGeneral Medicinebiology.organism_classificationVibrioCulture MediaRNA Ribosomal 23SMolluscaWater MicrobiologyBiotechnologyJournal of applied microbiology
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Phylogenetic relationships within the family Halomonadaceae based on comparative 23S and 16S rRNA gene sequence analysis.

2010

A phylogenetic study of the family Halomonadaceae was carried out based on complete 16S rRNA and 23S rRNA gene sequences. Several 16S rRNA genes of type strains were resequenced, and 28 new sequences of the 23S rRNA gene were obtained. Currently, the family includes nine genera (Carnimonas, Chromohalobacter, Cobetia, Halomonas, Halotalea, Kushneria, Modicisalibacter, Salinicola and Zymobacter). These genera are phylogenetically coherent except Halomonas, which is polyphyletic. This genus comprises two clearly distinguished clusters: group 1 includes Halomonas elongata (the type species) and the species Halomonas eurihalina, H. caseinilytica, H. halmophila, H. sabkhae, H. almeriensis, H. hal…

GeneticsHalomonasPhylogenetic treebiologyMolecular Sequence DataGenes rRNAGeneral MedicineSequence Analysis DNARibosomal RNAbiology.organism_classificationMicrobiologyDNA RibosomalBacterial Typing TechniquesHalomonadaceaeType speciesHalomonadaceaeRNA Ribosomal 23SSpecies Specificity23S ribosomal RNARNA Ribosomal 16SRibosomal DNAHalomonas salariaEcology Evolution Behavior and SystematicsPhylogenyInternational journal of systematic and evolutionary microbiology
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Evolution of fermenting microbiota in tarhana produced under controlled technological conditions

2011

PubMedID: 21839387 The purpose of this study was to evaluate the evolution of lactic acid bacteria (LAB) and yeasts during the fermentation of tarhana produced with some pasteurised ingredients and carried out at 30 and 40 °C. The chemical parameters were those typical for tarhana production. Coliform bacteria were not detected during fermentation, while LAB and yeasts were in the range 10 7-10 8 colony forming units (CFU) g -1. Plate counts showed an optimal development of both fermenting microbial groups and the differences in cell concentrations were not significant (P > 0.05). LAB were isolated during fermentation and grouped on the basis of phenotypic and polymorphic characteristics…

IdentificationTurkeyMicrobiologyMicrobiologyEvolution Molecularchemistry.chemical_compoundTarhana23S ribosomal RNAYeastsLactic acid bacteriabiologyLactobacillus brevisTemperaturePediococcus acidilacticifood and beveragesTechnological parametersHydrogen-Ion Concentrationbiology.organism_classificationLactic acidColiform bacteriaLactobacilluschemistryFermentationFermentationEdible GrainFermentation Identification Lactic acid bacteria Tarhana Technological parameters YeastsLactobacillus plantarumBacteriaFood Science
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Identification of Three Clinically Relevant Borrelia burgdorferi Sensu Lato Genospecies by PCR-Restriction Fragment Length Polymorphism Analysis of 1…

2004

ABSTRACT We report the results of a study of the prevalences of three clinically relevant Borrelia burgdorferi sensu lato genospecies ( Borrelia burgdorferi sensu stricto, Borrelia afzelii , and Borrelia garinii ) in 1,040 questing Ixodes ticks from all regions of Latvia, where Lyme borreliosis is endemic. The prevalences of Borrelia in Ixodes ricinus and Ixodes persulcatus were 22.6 and 27.9%, respectively. Molecular typing of B. burgdorferi from infected ticks was performed by restriction fragment length polymorphism (RFLP) analysis of PCR-amplified fragments of the 16S-23S ( rrs-rrlA ) rRNA intergenic spacer by using species-specific primers and subsequent sequencing. The dominant Borrel…

Microbiology (medical)Ixodes ricinusGenotypeMolecular Sequence DataIxodes persulcatusBorrelia afzeliimedicine.disease_causePolymerase Chain ReactionBorrelia burgdorferi GroupRNA Ribosomal 16SBorreliaparasitic diseasesDNA Ribosomal SpacermedicineAnimalsBorrelia burgdorferiLyme DiseaseIxodesbiologyBacteriologySequence Analysis DNAbacterial infections and mycosesbiology.organism_classificationLatviaVirologyRNA Ribosomal 23SLyme disease microbiologyIxodesBorrelia gariniiPolymorphism Restriction Fragment LengthJournal of Clinical Microbiology
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New potent antibacterials against Gram-positive multiresistant pathogens: effects of side chain modification and chirality in linezolid-like 1,2,4-ox…

2014

The effects of side chain modification and chirality in linezolid-like 1,2,4-oxadiazoles have been studied to design new potent antibacterials against Gram-positive multidrug-resistant pathogens. The adopted strategy involved a molecular modelling approach, the synthesis and biological evaluation of new designed compounds, enantiomers separation and absolute configuration assignment. Experimental determination of the antibacterial activity of the designed (S)-1-((3-(4-(3-methyl-1,2,4-oxadiazol-5- yl)phenyl)-oxazolidin-2-one-5-yl)methyl)-3-methylthiourea and (S)-1-((3-(3-fluoro-4-(3-methyl-1,2,4- oxadiazol-5-yl)phenyl)-oxazolidin-2-one-5-yl)methyl)-3-methylthiourea against multidrug resistan…

Multidrug-resistant bacteriaClinical BiochemistryAntibioticsDrug ResistanceMolecular ConformationPharmaceutical ScienceBiochemistrychemistry.chemical_compoundAntibioticsDrug Resistance Multiple BacterialDrug DiscoveryAcetamidesSide chainOxadiazolesAbsolute configurationBacterialStereoisomerismHep G2 CellsBIO/10 - BIOCHIMICA23SAnti-Bacterial AgentsMolecular Docking SimulationRNA Ribosomal 23SDrug design Linezolid Antibiotics Multidrug-resistant bacteria EnantiomersMolecular MedicineAntibacterial activityMultipleMethicillin-Resistant Staphylococcus aureusStaphylococcus aureusmedicine.drug_classStereochemistryCell SurvivalMicrobial Sensitivity TestsGram-Positive BacteriaDrug designmedicineHumansMolecular BiologyOxazolidinonesRibosomalBinding SitesOrganic ChemistryAntibioticLinezolidSettore CHIM/06 - Chimica OrganicaSettore CHIM/08 - Chimica FarmaceuticaMultiple drug resistancechemistryEnantiomersMED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICALinezolidRNANucleic Acid ConformationEnantiomerChirality (chemistry)Bioorganicmedicinal chemistry
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Partial Methylation at Am100 in 18S rRNA of Baker's Yeast Reveals Ribosome Heterogeneity on the Level of Eukaryotic rRNA Modification

2014

Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we could specifically demonstrate that a significant amount of S. cerevisiae ribosomes are not methylated at 2'-O-ribose of A100 residue in the 18S rRNA. Furthermore, using LC-UV-MS/MS of a respective 18S rRNA fragment, we could not only corroborate the partial methylation at A100, but could also quantify the methylated versus non-methylated A100 residue. Here, we exhibit that only 68% of A100 in t…

Science5.8S ribosomal RNAYeast and Fungal ModelsSaccharomyces cerevisiaeMycologyBiologyMethylationBiochemistryMicrobiologyMolecular GeneticsModel OrganismsMolecular cell biologyRRNA modification23S ribosomal RNANucleic Acidsddc:570GeneticsEukaryotic Small Ribosomal SubunitBiologyNucleic Acid ComponentsGeneticsMultidisciplinaryQRTranslation (biology)DNAMethylationRibosomal RNAYeastRNA processingBiochemistryRNA RibosomalRibosome SubunitsMedicineRNARibosomesResearch ArticlePLoS ONE
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Characterization of Streptomyces venezuelae ATCC 10595 rRNA gene clusters and cloning of rrnA

1996

Streptomyces venezuelae ATCC 10595 harbors seven rRNA gene clusters which can be distinguished by BglII digestion. The three rRNA genes present in each set are closely linked with the general structure 16S-23S-5S. We cloned rrnA and sequenced the 16S-23S spacer region and the region downstream of the 5S rRNA gene. No tRNA gene was found in these regions.

Streptomyces venezuelaeMolecular Sequence Data5.8S ribosomal RNADNA RibosomalMicrobiology18S ribosomal RNA5S ribosomal RNASpecies SpecificityRibosomal protein23S ribosomal RNARNA Ribosomal 16SCloning MolecularInternal transcribed spacerMolecular BiologyGeneticsbiologyRNA Ribosomal 5SNucleic Acid HybridizationRNA ProbesRibosomal RNAbiology.organism_classificationMolecular biologyStreptomycesRNA Ribosomal 23SGenes BacterialRNA RibosomalMultigene FamilyResearch ArticleJournal of Bacteriology
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