Search results for " RNA"

showing 10 items of 1405 documents

Presence and coding properties of 2'-O-methyl-5-carbamoylmethyluridine (ncm5Um) in the wobble position of the anticodon of tRNA(Leu) (U*AA) from brew…

1992

AbstractThe unknown modified nucleoside U* has been isolated by enzymatic and HPLC protocols from tRNALeu(U*AA) recently discovered in brewer's yeast. The pure U* nucleoside has been characterized by electron impact mass spectroscopy, and comparison of its chromatographic and UV-absorption properties with those of appropriate synthetic compounds. The structure of U* was established as 2′-O-methyl-5-carbamoylmethyluridine (ncm5Um). The yeast tRNALeu (U*AA) is the only tRNA so far sequenced which has been shown to contain ncm5Um. The location of such a modified uridine at the first position of the anticodon restricts the decoding property to A of the leucine UUA codon.

IdentificationRNA Transfer LeuStereochemistryBiophysicsAminoacylationWobble base pairModified nucleosideSaccharomyces cerevisiaeBiochemistryMass SpectrometryFungal Proteinschemistry.chemical_compoundStructural BiologyGeneticsAnticodonMolecular BiologyUridineChromatography High Pressure Liquidchemistry.chemical_classificationMolecular StructureRNA FungalCell BiologyUridineYeastYeastEnzymechemistryBiochemistryTransfer RNAtRNALeu (U*AA)Spectrophotometry UltravioletLeucineNucleosideFEBS letters
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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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<i>Aeromonas hydrophila</i> subsp. <i>dhakensis</i> 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…

ImipenembiologySoil ScienceVirulencePlant ScienceGeneral Medicinebiochemical phenomena metabolism and nutritionRibosomal RNAbacterial infections and mycoses16S ribosomal RNAbiology.organism_classificationMicrobiologyAeromonasTicarcillinmedicinebacteriaCefoxitinEcology Evolution Behavior and SystematicsFecesmedicine.drugMicrobes and Environments
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Synthesis and expression of MHC class II molecules in the absence of attached invariant chains by recombinant-interferon-gamma-activated bone-marrow-…

1987

Pure populations of in vitro propagated bone marrow-derived macrophages are constitutively Ia negative. Co-culturing of these cells with recombinant interferon-gamma (rIFN-gamma) resulted in the appearance of high amounts of Ia antigens at the cell surface of essentially all cells. The continuous presence of the stimulus was a prerequisite for sustained Ia expression because removal of the stimulus resulted in rapid decline of surface Ia. Two-dimensional (2D) gel analysis (1D isoelectric focusing, 2D sodium dodecyl sulfate-polyacrylamide gel electrophoresis) of class II molecules synthesized by rIFN-gamma-stimulated bone marrow macrophages (BMM phi) revealed that, in contrast to class II co…

ImmunologyBone Marrow Cellslaw.inventionInterferon-gammaMicelawImmunology and AllergyAnimalsNorthern blotRNA MessengerGel electrophoresisMessenger RNAMHC class IIMice Inbred C3HPolymorphism GeneticbiologyIsoelectric focusingMacrophagesHistocompatibility Antigens Class IIDNAMacrophage ActivationMolecular biologyIn vitroRecombinant ProteinsGene Expression RegulationRecombinant DNAbiology.proteinIntracellularEuropean journal of immunology
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Isolation of Desulfovibrio intestinalis sp. nov. from the hindgut' of the lower termite Mastotermes darwiniensis.

1999

A Gram-negative, anaerobic sulfate-reducing bacterium was isolated from hindgut contents of the lower termite Mastotermes darwiniensis Froggatt (strain KMS2). Strain KMS2 is motile by a single polar flagellum. The isolate possesses desulfoviridin and catalase activity. The G+C content of its DNA is in the range of 54.5-55.5 mol% (strain KMS2). It respires hydrogen and different low molecular weight organic compounds in the presence of sulfate, thiosulfate, and sulfite, and also oxygen. The isolated strain ferments pyruvate. Fastest growth with a doubling time of 12.5 h was obtained at 37°C and not at 28°C, the temperature at which the termites were grown. The isolate showed a 16S rDNA seque…

ImmunologyMolecular Sequence DataIsopteraApplied Microbiology and BiotechnologyMicrobiologyMicrobiologychemistry.chemical_compoundSulfiteMastotermes darwiniensisGeneticsAnimalsMolecular BiologyRibosomal DNAPhylogenyThiosulfatebiologyBase SequenceHindgutGeneral Medicine16S ribosomal RNAbiology.organism_classificationIntestinesMicroscopy ElectronchemistryCatalasebiology.proteinDesulfovibrioBacteriaCanadian journal of microbiology
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Identification of modifications in microbial, native tRNA that suppress immunostimulatory activity

2012

2′-O-methylation of guanosine 18 is a naturally occurring tRNA modification that can suppress immune TLR7 responses.

ImmunologyMutantfungiBrief Definitive ReportRNAfood and beveragesvirus diseasesContext (language use)Biologybiochemical phenomena metabolism and nutritionmedicine.disease_causeTRNA MethyltransferasesTransplantationchemistry.chemical_compoundBiochemistrychemistryTransfer RNAmedicineImmunology and AllergyEscherichia coliDNAThe Journal of Experimental Medicine
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Biosynthesis of Lipopolysaccharide-Binding Protein in Rabbit Hepatocytes

1990

Studies reported here show that the recently discovered acute-phase protein, lipopolysaccharide-binding protein (LBP), is synthesized by hepatocytes. For these studies, explanted rabbit hepatocytes were grown in the presence of 35S-methionine. Biosynthetically labelled LBP in the cells and supernatant was identified using immunoprecipitation with rat anti-rabbit LBP antibody. This antibody immunoprecipitates both the LBP polypeptide and the glycosylated protein. With a cell-free translation system a comparison of RNA from normal rabbit liver with that isolated from acute-phase rabbit liver indicated that a translatable LBP message is only found in the RNA from acute-phase liver. Studies wit…

ImmunoprecipitationGene ExpressionPathology and Forensic Medicinechemistry.chemical_compoundhealth services administrationmedicineAnimalsRNA MessengerMolecular BiologyCells CulturedGlycoproteinsMessenger RNAMembrane GlycoproteinsbiologyTunicamycinBinding proteinRNApathological conditions signs and symptomsCell BiologyGeneral MedicineTunicamycinnervous system diseasesMolecular Weightbody regionsmedicine.anatomical_structureLiverchemistryBiochemistryHepatocytebiology.proteinpopulation characteristicsRabbitsAntibodyCarrier ProteinsLipopolysaccharide binding proteinAcute-Phase ProteinsPathobiology
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Evidence for a novel cytoplasmic processing event in ribosome maturation in the sea urchin Paracentrotus lividus

2010

In this work, we demonstrate the existence of a cytoplasmic processing step, never before described, involving both the pre-ribosomal subunits in the sea urchin Paracentrotus lividus. Northern-blot hybridization, primer extension, S1 mapping experiments and in situ hybridizations allowed us to demonstrate that cytoplasmic processed particles are successively re-imported into the nucleus, where maturation of their RNAs is completed prior to being exported to the cytoplasm. Our findings lead to the proposal of a new model of ribosome maturation and shuttling. Moreover, preliminary data from our laboratory suggest that the maturation pathway we propose in P. lividus may not be unique to the se…

In situCytoplasmSea urchinEmbryo NonmammalianRibosome maturation ; Processing ; Shuttling ; Sea urchin ; Pre-rRNAsSea Urchin ribosome maturation rRNA.ProcessingRibosomePrimer extensionParacentrotus lividusCellular and Molecular Neurosciencebiology.animalRNA PrecursorsmedicineAnimalsRNA Processing Post-TranscriptionalMolecular BiologySea urchinIn Situ HybridizationPharmacologybiologyPre-rRNAsCell BiologyRibosomal RNAbiology.organism_classificationMolecular biologyCell biologySettore BIO/18 - Geneticamedicine.anatomical_structureShuttlingCytoplasmOocytesParacentrotusMolecular MedicineFemaleRibosomesRibosome maturationNucleusCellular and Molecular Life Sciences
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Development of specific fluorescent oligonucleotide probes for in situ identification of wine lactic acid bacteria.

2003

A rapid method for the identification of lactic acid bacteria (LAB) from wine has been developed. This method is based on fluorescence in situ hybridisation (FISH), using fluorescent oligonucleotide probes, homologous to 16S rDNA of those species of LAB commonly found in wines. The protocol for the specific detection of these bacteria was established through the hybridisation of 36 reference strains. The specificity of the probes was evaluated by using pure cultures. Probes were used to identify species in different wines, making it evident that direct identification and quantification from natural samples without culturing is also possible. The results show that FISH is a promising techniq…

In situDNA BacterialMolecular Probe TechniquesWineBiologyMicrobiologyDNA Ribosomalchemistry.chemical_compoundGeneticsLactic AcidPediococcusMolecular BiologyIn Situ Hybridization FluorescenceFluorescent DyesWineBase SequenceOligonucleotidefood and beverages16S ribosomal RNAbiology.organism_classificationFluorescenceMolecular biologyLactic acidLactobacillusBiochemistrychemistryFermentationIdentification (biology)Oligonucleotide ProbesBacteriaLeuconostocFEMS microbiology letters
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Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020

2020

8 páginas, 3 figuras

Infecções Respiratórias0301 basic medicineMESH: Coronavirus InfectionsEpidemiology[SDV]Life Sciences [q-bio]Distribution (economics)WastewaterMESH: Base SequenceSevere Acute Respiratory SyndromeMESH: World Health OrganizationPandemicMESH: CoronavirusMESH: COVID-19SequencingViralCladeNomenclatureGenomebiologyNomenclatureCOVID-19; Europe; NGS; SARS-CoV-2; WGS; nomenclature; sequencing; Base Sequence; Betacoronavirus; COVID-19; Coronavirus; Coronavirus Infections; Europe; Genome Viral; Humans; Phylogeography; Pneumonia Viral; RNA Viral; RNA-Dependent RNA Polymerase; SARS-CoV-2; Severe Acute Respiratory Syndrome; Spatio-Temporal Analysis; World Health Organization; PandemicsC500sequencingEuropean region3. Good healthEuropePhylogeographyGeographyMESH: PhylogeographyMESH: RNA-Dependent RNA PolymeraseMESH: RNA ViralNGSMESH: BetacoronavirusRNA ViralSpatio-Temporal AnalysinomenclatureMESH: Genome ViralCoronavirus InfectionsCartographyHumanBioquímicaMESH: PandemicsSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)CoronaviruPneumonia Viral030106 microbiologyGenome ViralWorld Health OrganizationCOVID-19 ; Europe ; NGS ; SARS-CoV-2 ; WGS ; nomenclature ; sequencing03 medical and health sciencesBetacoronavirusMESH: Spatio-Temporal AnalysisSpatio-Temporal AnalysisMESH: Severe Acute Respiratory SyndromeVirologyHumansMESH: SARS-CoV-2PandemicsWhole genome sequencingMESH: HumansWhole Genome SequencingBetacoronaviruBase SequenceCoronavirus Infectionbusiness.industrySARS-CoV-2Public Health Environmental and Occupational HealthCOVID-19Pneumoniabiology.organism_classificationRNA-Dependent RNA PolymeraseB900Coronavirus030104 developmental biologyMESH: Pneumonia ViralRNASARS_CoV-23111 BiomedicineMESH: EuropeHuman medicinebusinessBetacoronavirusWGSEurosurveillance
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