Search results for " gel"

showing 10 items of 1051 documents

Role of two operators in regulating the plasmid-borne raf operon of Escherichia coli

1994

The plasmid-borne raf operon encodes functions required for the inducible uptake and utilization of raffinose in Escherichia coli K12. The expression of three structural genes for alpha-galactosidase (rafA), Raf permease (rafB) and sucrose hydrolase (rafD) is negatively controlled by the binding of RafR repressor (rafR) to two operator sites, O1 and O2, that flank the -35 sequence of the raf promoter, PA. In vitro, O1 and O2 are occupied on increasing the concentration of RafR, without detectable preference for one site or the other or any indication of cooperative binding. Nucleotide substitutions at positions 3, 4 or 5 in an operator half-site prevented repressor binding, supporting a mod…

DNA BacterialOperator Regions GeneticOperonBase pairMolecular Sequence DataRepressorBiologyBinding CompetitiveRaffinoseTranscription (biology)OperonEscherichia coliGeneticsBinding siteSite-directed mutagenesisMolecular BiologyBase SequenceHelix-Loop-Helix MotifsStructural geneCooperative bindingGene Expression Regulation BacterialDNA-Binding ProteinsRepressor ProteinsBiochemistryGenes Bacterialalpha-GalactosidaseMutagenesis Site-DirectedAutoradiographyElectrophoresis Polyacrylamide GelPlasmidsMolecular and General Genetics MGG
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A chromosome map of the Flavescence dorée phytoplasma

2008

International audience; The Flavescence dorée phytoplasma (FD-P), a non-cultivable, plant-pathogenic bacterium of the class Mollicutes, is the causal agent of a quarantine disease affecting vineyards of southern Europe, mainly in southern France and northern Italy. To investigate FD-P diversity and phytoplasma genetic determinants governing the FD-P life cycle, a genome project has been initiated. A physical map of the chromosome of FD-P strain FD92, purified from infected broad beans, was constructed by performing restriction digests of the chromosome and resolving the fragments by PFGE. Single and double digestions of the chromosome with the enzymes SalI, BssHII, MluI and EagI were perfor…

DNA BacterialPhytoplasmaBACTERIOLOGIEMolecular Sequence DataCARTOGRAPHIE GENETIQUEMicrobiologyRestriction fragmentFLAVESCENCE DOREEMALADIE DES PLANTES03 medical and health sciencesBacterial ProteinsMOLLICUTEDeoxyribonucleases Type II Site-Specific030304 developmental biologySouthern blotGenetics0303 health sciencesbiology030306 microbiologyChromosomeFabaceaeGenes rRNASequence Analysis DNAGenome projectGENETIQUEPhysical Chromosome Mappingbiology.organism_classificationElectrophoresis Gel Pulsed-FieldBlotting SouthernRestriction site[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyItalyPHYTOPLASME DE LA FLAVESCENCE DOREEPhytoplasmabiology.proteinMollicutesCARTE CHROMOSOMIQUEFranceRRNA Operon
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R plasmids in environmental Vibrio cholerae non-O1 strains.

1988

The occurrence of drug resistance and its plasmid-mediated transferability was investigated in 140 environmental strains of Vibrio cholerae non-O1 and 6 strains of Vibrio cholerae, both O1 and non-O1, of clinical origin. Of the 146 strains tested, 93% were resistant to at least one drug and 74% were resistant to two or more antibiotics. The O1 strains were susceptible to all antibiotics used. A total of 26 of 28 selected resistant wild strains carried R plasmids that were transferable by intraspecific and intergeneric matings. The most common transmissible R factor determined resistance to ampicillin, amoxicillin, and sulfanilamide (30%), followed by resistance to ampicillin and amoxicillin…

DNA BacterialR FactorsFresh WaterDrug resistancemedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyPlasmidVibrio cholerae non-O1VibrionaceaeAmpicillinmedicineSeawaterVibrio choleraeElectrophoresis Agar GelEcologybiologyVirulenceGenetic transferDrug Resistance MicrobialSulfanilamidebiology.organism_classificationAnti-Bacterial AgentsVibrio choleraeConjugation GeneticWater MicrobiologyFood ScienceBiotechnologymedicine.drugResearch Article
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Response ofBacillus subtilis spores to dehydration and UV irradiation at extremely low temperatures

1996

Spores of Bacillus subtilis have been exposed to the conditions of extreme dehydration (argon/silica gel; simulated space vacuum) for up to 12 weeks at 298 K and 80 K in the dark. The inactivation has been correlated with the production of DNA-double strand-breaks. The temperature-dependence of the rate constants for inactivation or production of DNA-double strand-breaks is surprisingly low. Controls kept in the frozen state at 250 K for the same period of time showed no sign of deterioration. In another series of experiments the spores have been UV irradiated (253.7 nm) at 298 K, 200 K and 80 K after exposure to dehydrating conditions for 3 days. Fluence-effect relationships for inactivati…

DNA BacterialVacuumUltraviolet Rayschemistry.chemical_elementBacillus subtilisPhotochemistrychemistry.chemical_compoundReaction rate constantmedicineDehydrationIrradiationEcology Evolution Behavior and SystematicsSpores BacterialBacteriological TechniquesArgonbiologyChemistrySilica gelGeneral Medicinemedicine.diseasebiology.organism_classificationSporeCold TemperatureBiochemistrySpace and Planetary ScienceBacillus subtilisDNA DamageOrigins of Life and Evolution of the Biosphere
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Assessment of Salmonella spp. in feces, cloacal swabs, and eggs (eggshell and content separately) from a laying hen farm.

2011

Microbial pathogens of the genus Salmonella are among the leading causes of foodborne illness in the world. The present study was done on a laying hen farm with a Salmonella enterica serovar Enteritidis-positive result according to the testing specified by European regulation 2160/2003. The aim of this study was to compare the Salmonella contamination on a laying hen farm with the Salmonella presence in the hen eggs. The strains were isolated by ISO method 6579:2002 (standard method for the detection of Salmonella spp. in the European regulation for food and animal feeding stuffs, animal feces, and environmental samples from the primary production stage, including poultry farms) and were co…

DNA BacterialVeterinary medicineSalmonellaSalmonella enteritidisEggsmedicine.disease_causeEgg ShellFecesAnimal scienceCloacamedicinemedia_common.cataloged_instanceFood microbiologyAnimalsEuropean UnionEuropean unionEggshellDeoxyribonucleases Type II Site-SpecificFecesPoultry Diseasesmedia_commonSalmonella Infections AnimalChi-Square Distributionbiologybusiness.industryGeneral MedicinePoultry farmingbiology.organism_classificationElectrophoresis Gel Pulsed-FieldSalmonella enteritidisSalmonella entericaFood MicrobiologyAnimal Science and ZoologyFemalebusinessChickensPoultry science
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Blattabacteria, the endosymbionts of cockroaches, have small genome sizes and high genome copy numbers.

2008

Summary Blattabacteria are intracellular endosymbionts of cockroaches and primitive termites that belong to the class Flavobacteria and live only in specialized cells in the abdominal fat body of their hosts. In the present study we determined genome sizes as well as genome copy numbers for the endosymbionts of three cockroach species, Blattella germanica, Periplaneta americana and Blatta orientalis. The sole presence of blattabacteria in the fat body was demonstrated by rRNA-targeting techniques. The genome sizes of the three blattabacteria were determined by pulsed field gel electrophoresis. The resulting total genome sizes for the three symbionts were all approximately 650 15 kb. Compari…

DNA Bacterialanimal structuresmedia_common.quotation_subjectFat BodyCockroachesInsectBiologyMicrobiologyGenomechemistry.chemical_compoundbiology.animalAnimalsPeriplanetaEcology Evolution Behavior and SystematicsIn Situ Hybridizationmedia_commonGeneticsCockroachBacteroidetesIntracellular parasitefungiBlattaBacteroidetesBlattellidaebiology.organism_classificationElectrophoresis Gel Pulsed-FieldchemistryDNAGenome BacterialPeriplanetaEnvironmental microbiology
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Microbiological quality of carbonated drinking water produced with in-home carbonation systems.

2005

The microbiological quality of carbonated water produced with tap water in commercial in-home carbonation systems was determined, the results being discussed in the context of the microbiological quality of the tap water used, the properties of the drink makers, and the procedures of preparation and washing of various parts of the appliance. The last-mentioned data were received from each participant of the study by questionnaire. Escherichia coli, coliforms, fecal streptococci and spore-forming sulphite-reducing anaerobes were used as indicators for the hygienic quality of the water. Tap-water samples were collected according to the usual procedure when filling the carbonating bottle, i.e.…

DNA Bacterialbusiness.product_categoryBacteriaChemistryCarbonationPublic Health Environmental and Occupational HealthContext (language use)Carbonated BeveragesMicrobiological qualityContaminationPulp and paper industryMicrobiologyElectrophoresis Gel Pulsed-FieldTap waterWater SupplyBottleEquipment ContaminationWater qualityMineral WatersbusinessWater pollutionHousehold ArticlesWater MicrobiologyEnvironmental MonitoringInternational journal of hygiene and environmental health
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Characterisation of a Cryptosporidium parvum-specific cDNA clone and detection of parasite DNA in mucosal scrapings of infected mice.

1998

A cDNA library was constructed using total RNA extracted from oocysts and sporozoites of the protozoan parasite Cryptosporidium parvum. The expression library was screened with an anti-C. parvum antiserum and a clone, Cp3.4, with a 2043 bp insert, was extracted. Southern blot analysis demonstrated a single copy gene that was located on a 1.6 Mb chromosome. The gene was found to be C. parvum specific as Cp3.4 did not cross-hybridise with chromosomal DNA from three other apicomplexan parasites. The cDNA encodes a polypeptide with a predicted membrane helix at its C-terminal end which is flanked by stretches of acidic amino acids. Overall, the polypeptide has a low isoelectric point (pI) of 3.…

DNA ComplementaryGenes ProtozoanMolecular Sequence DataProtozoan ProteinsCryptosporidiosisBiologyMolecular cloninglaw.inventionMicelawIleumComplementary DNAparasitic diseasesParasite hostingAnimalsAmino Acid SequenceRNA MessengerCloning MolecularIntestinal MucosaMolecular BiologyGenePolymerase chain reactionSouthern blotRepetitive Sequences Nucleic AcidCryptosporidium parvumcDNA libraryReverse Transcriptase Polymerase Chain ReactionChromosome MappingSequence Analysis DNADNA Protozoanbiology.organism_classificationMolecular biologyElectrophoresis Gel Pulsed-FieldBlotting SouthernCryptosporidium parvumParasitologyRNA ProtozoanMolecular and biochemical parasitology
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Plant progesterone 5β-reductase is not homologous to the animal enzyme. Molecular evolutionary characterization of P5βR from Digitalis purpurea

2007

Plants of the genus Digitalis produce cardiac glycosides, i.e. digoxin, which are widely used for congestive heart failure. Progesterone 5beta-reductase (P5betaR) is a key enzyme in the biosynthesis of these natural products. Here, we have carried out the purification and partial amino acid sequencing of the native P5betaR from foxglove (Digitalis purpurea), and isolated a cDNA encoding this enzyme. Similarly to other steroid 5beta-reductases, the recombinant P5betaR catalyzes the stereospecific reduction of the Delta(4)-double bond of several steroids with a 3-oxo,Delta(4,5) structure. The gene encoding P5betaR is expressed in all plant organs, and maximally transcribed in leaves and matur…

DNA ComplementarySubfamilyRecombinant Fusion ProteinsMolecular Sequence DataPlant ScienceHorticultureReductaseBiochemistryGas Chromatography-Mass SpectrometryEvolution Molecularchemistry.chemical_compoundPhylogeneticsComplementary DNACardenolideAnimalsAmino Acid SequenceMolecular BiologyGenePhylogenyProgesteronePlant Proteinschemistry.chemical_classificationGeneticsDigitalisBase SequenceMolecular StructureSequence Homology Amino AcidbiologyProgesterone ReductaseReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingDigitalis purpureaGeneral Medicinebiology.organism_classificationEnzymeModels ChemicalBiochemistrychemistryElectrophoresis Polyacrylamide GelPhytochemistry
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Characterization of a cDNA encoding RP43, a CUB-domain-containing protein from the tube of Riftia pachyptila (Vestimentifera), and distribution of it…

2000

A major 43kDa protein from the protective tube of Riftiapachyptila (Vestimentifera), named RP43, was partly microsequenced after isolation by SDS/PAGE from the protein fraction of tubes collected around the hydrothermal vents at the East Pacific Rise. On the basis of the partial peptide sequences obtained, experiments using reverse-transcriptase-mediated PCR and rapid amplification of cDNA ends led to the complete cDNA sequence. Analysis of deduced amino acid sequence of RP43 showed the presence of CUB domains (100–110-residue-spanning domains first reported in the complement subcomponents C1r/C1s, epidermal-growth-factor-related sea urchin protein and bone morphogenetic protein 1) that se…

DNA ComplementaryTranscription GeneticAnnelidaMolecular Sequence DataChitinPeptideBioinformaticsBiochemistryEpitheliumBone morphogenetic protein 1Rapid amplification of cDNA endsSequence Analysis ProteinComplementary DNAbiology.animalAnimalsAmino Acid SequenceRNA MessengerCloning MolecularMolecular BiologyPeptide sequenceSea urchinChromatography High Pressure LiquidIn Situ Hybridizationchemistry.chemical_classificationMessenger RNABase SequenceSequence Homology Amino AcidbiologyReverse Transcriptase Polymerase Chain ReactionHelminth ProteinsSequence Analysis DNACell BiologyBlotting NorthernCUB domainProtein Structure TertiaryCell biologychemistryElectrophoresis Polyacrylamide GelEpidermisProtein BindingResearch ArticleBiochemical Journal
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