Search results for "Culture media"

showing 10 items of 272 documents

Molecular events associated with glucose repression of invertase in Saccharomyces cerevisiae.

1986

When S. cerevisiae growing in the presence of glucose (repressive condition) was shifted to higher temperatures, invertase was secreted. This secretion required protein synthesis, but was independent of RNA formation (Mormeneo & Sentandreu 1982). In addition accumulation of invertasespecific messenger RNA occurred in the absence of protein synthesis but was expressed only after synthesis of protein. Invertase mRNA was continuously synthesized under repressive conditions and the levels of this mRNA were regulated by the presence of glucose. The hexose regulated the concentration of this mRNA at the level of transcription and/or by sensitization of this messenger RNA. The expression of the in…

Glycoside HydrolasesTranscription GeneticSaccharomyces cerevisiaeSaccharomyces cerevisiaeCycloheximideBiologyMicrobiologyEnzyme Repressionchemistry.chemical_compoundTranscription (biology)Protein biosynthesisRNA MessengerCycloheximideMaltoseMolecular BiologyMessenger RNAbeta-FructofuranosidaseTemperatureRNA FungalGeneral MedicineMaltosebiology.organism_classificationCulture MediaInvertaseGlucoseBiochemistrychemistryEnzyme RepressionAntonie van Leeuwenhoek
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Differential specificity of substrate-attached lectins stimulating spreading of GH3-cells under serum-free, hormone-supplemented culture conditions

1982

Most mammalian cells are capable of growth in culture only when they are supplied with an appropriate substrate to which they can adhere and spread. To prepare suitable substrates different lectins were attached onto polystyrene tissue-culture dishes after coating with polylysine. GH3-cells (a pituitary-tumor-cell line) were seeded into the culture dishes containing serum-free, hormone-supplemented medium. When succinylated Concanavalin A (s-Con A), which binds specifically to mannose residues, is attached to the surface an extraordinary spreading of GH3-cells is induced within 15 to 20 min after seeding. Other lectins with a different sugar-binding specificity are less effective in inducin…

HistologyCellMannosePituitary neoplasmBiologyCell LinePathology and Forensic MedicineStructure-Activity Relationshipchemistry.chemical_compoundCell MovementLectinsCell AdhesionConcanavalin AmedicineAnimalsPituitary NeoplasmsCell adhesionSubstrate (chemistry)Cell BiologyHormonesCulture MediaKineticsmedicine.anatomical_structurechemistryBiochemistryCell cultureConcanavalin APolylysinebiology.proteinMannoseCell and Tissue Research
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Different effectors of dimorphism in Yarrowia lipolytica

2002

Yarrowia lipolytica is an ascomycete with biotechnological potential. In common media, the fungus grows as a mixture of yeast-like and short mycelial cells. The environmental factors that affect dimorphism in the wild-type strain, W29, and its auxotrophic derivative, PO1a, were analyzed. In both strains, pH was the most important factor regulating the dimorphic transition. Mycelium formation was maximal at pH near neutrality and decreased as pH was lowered to become almost null at pH 3. Carbon and nitrogen sources, namely glucose and ammonium, were also important for mycelium formation; and their effect was antagonized by some alternative carbon and nitrogen sources. Citrate was an importan…

Hot TemperatureNitrogenAuxotrophyYarrowiaFungusBiochemistryMicrobiologyCitric Acidchemistry.chemical_compoundBotanyCyclic AMPMorphogenesisGeneticsAmmoniumMolecular BiologyMyceliumSex CharacteristicsbiologyEffectorfungiYarrowiaGeneral MedicineHydrogen-Ion Concentrationbiology.organism_classificationCarbonYeastCulture MediaBiochemistrychemistryStarvationDimorphic fungusArchives of Microbiology
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Biosorption of copper by wine-relevant lactobacilli

2011

Must and wine may be contaminated with elevated copper concentrations by the use of fungicides or in course of the vinification process. Hitherto only a few practicable and harmless procedures exist to reduce an excess of copper from must and wine. For this reason we investigated the biosorption of copper by eight wine-relevant Lactobacillus species. Both, living and heat-inactivated cells revealed a significant degree of Cu adsorption. It was shown that Cu binding correlated positively with an increasing pH value of the environment. The highest binding capacity of the tested lactic acid bacteria was found for L. buchneri DSM 20057 with a maximum of 46.17 μg Cu bound per mg cell in deionize…

Hot Temperaturechemistry.chemical_elementWineMicrobiologychemistry.chemical_compoundAdsorptionLactobacillusFood microbiologyOrganic chemistryVitisFood scienceWinebiologyBiosorptionfood and beveragesGeneral MedicineHydrogen-Ion ConcentrationWine faultbiology.organism_classificationCopperCulture MediaLactic acidLactobacilluschemistryFood MicrobiologyAdsorptionCopperFood ScienceInternational Journal of Food Microbiology
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Growth and macromolecular content of the dimorphic fungus Aureobasidium pullulans and the effect of hydroxyurea and other inhibitors

1988

The growth kinetics and the macromolecular content of the yeast and ethanol-induced hyphal forms of Aureobasidium pullulans were studied. During the morphological transition from yeasts to hyphae, both the protein and RNA content decreased significantly, the mycelial form containing only 76% of the amount of protein in the yeasts, and 38% of the RNA. The DNA was the only component tested whose level increased during the transition. Among several compounds inhibiting macromolecular synthesis, only hydroxyurea showed a remarkable effect on the morphology of A. pullulans, inducing the mycelial morphology. The macromolecular composition of hydroxyurea-treated cultures changed with time in a way…

HyphaPolysorbatesBiologyMicrobiologyMicrobiologyFungal Proteinschemistry.chemical_compoundHydroxyureaDNA FungalMolecular BiologyMyceliumEthanolRNARNA FungalGeneral MedicineFungi imperfectibiology.organism_classificationYeastCulture MediaQuaternary Ammonium CompoundsAureobasidium pullulansKineticsGlucoseBiochemistrychemistryMitosporic FungiDimorphic fungusDNAAntonie van Leeuwenhoek
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Water resource recovery by means of microalgae cultivation in outdoor photobioreactors using the effluent from an anaerobic membrane bioreactor fed w…

2016

[EN] With the aim of assessing the potential of microalgae cultivation for water resource recovery (WRR), the performance of three 0.55 m3 flat-plate photobioreactors (PBRs) was evaluated in terms of nutrient removal rate (NRR) and biomass production. The PBRs were operated outdoor (at ambient temperature and light intensity) using as growth media the nutrient-rich effluent from an AnMBR fed with pre-treated sewage. Solar irradiance was the most determining factor affecting NRR. Biomass productivity was significantly affected by temperatures below 20 °C. The maximum biomass productivity (52.3 mg VSS·L−1·d−1) and NRR (5.84 mg NH4-N·L−1·d−1 and 0.85 mg PO4-P·L−1·…

INGENIERIA HIDRAULICAEnvironmental EngineeringLight020209 energyFlat-plate photobioreactorsBiomassSewagePhotobioreactorBioengineering02 engineering and technology010501 environmental sciencesWastewater01 natural sciencesPhotobioreactorsNutrientBioreactorsNutrient removal0202 electrical engineering electronic engineering information engineeringMicroalgaeBiomassWaste Management and DisposalEffluentTECNOLOGIA DEL MEDIO AMBIENTE0105 earth and related environmental sciencesResource recoverySewageRenewable Energy Sustainability and the Environmentbusiness.industryEnvironmental engineeringTemperatureMembranes ArtificialGeneral MedicineOutdoor cultivationCulture MediaLight intensityWastewaterWater ResourcesEnvironmental sciencebusinessWater MicrobiologyBiotechnologyScenedesmusBioresource technology
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Yeast ecology of vineyards within Marsala wine area (western Sicily) in two consecutive vintages and selection of autochthonous Saccharomyces cerevis…

2012

In this work, the yeast ecology associated with the spontaneous fermentation of Grillo cultivar grapes from 10 vineyards was analyzed from grape harvest till complete consumption of must sugars. The microbiological investigation started with the plate count onto two culture media to distinguish total yeasts (TY) and presumptive Saccharomyces (PS). Yeasts were randomly isolated and identified by a combined genotypic approach consisting of restriction fragment length polymorphism (RFLP) of 5.8S rRNA gene and 26S rRNA and sequencing of D1/D2 domain of the 26S rRNA gene, which resulted in the recognition of 14 species belonging to 10 genera. The distribution of the yeasts within the vineyards s…

IdentificationGenotypeSaccharomyces cerevisiaeAcetic Acid; Culture Media; DNA Fungal; Ethanol; Fermentation; Genotype; Hydrogen Sulfide; Microsatellite Repeats; Polymerase Chain Reaction; Polymorphism Restriction Fragment Length; RNA Ribosomal; Saccharomyces cerevisiae; Sicily; Sulfites; Temperature; Vitis; WineBioengineeringWineSaccharomyces cerevisiaeBiologyApplied Microbiology and BiotechnologySaccharomycesPolymerase Chain ReactionEnological aptitudeYeastsGenotypeSulfitesVitisHydrogen SulfidePolymorphismDNA FungalSicilyAcetic AcidRibosomalWineEthanolEcologyIdentification; Enological aptitudes; Saccharomyces cerevisiae; Spontaneous wine fermentation; YeastsTemperatureDNARibosomal RNASpontaneous wine fermentationbiology.organism_classificationYeastCulture MediaFungalRestriction Fragment LengthRNA RibosomalFermentationRNAFermentationRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthBiotechnologySettore AGR/16 - Microbiologia AgrariaMicrosatellite RepeatsJournal of bioscience and bioengineering
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Listeria monocytogenes EGD-e biofilms: no mushrooms but a network of knitted chains.

2008

ABSTRACT Listeria monocytogenes is a food pathogen that can attach on most of the surfaces encountered in the food industry. Biofilms are three-dimensional microbial structures that facilitate the persistence of pathogens on surfaces, their resistance toward antimicrobials, and the final contamination of processed goods. So far, little is known about the structural dynamics of L. monocytogenes biofilm formation and its regulation. The aims of this study were, by combining genetics and time-lapse laser-scanning confocal microscopy (LSCM), (i) to characterize the structural dynamics of L. monocytogenes EGD-e sessile growth in two nutritional environments (with or without a nutrient flow), and…

Image ProcessingMESH : Analysis of Variance[ SDV.MP.BAC ] Life Sciences [q-bio]/Microbiology and Parasitology/BacteriologyMESH : Green Fluorescent Proteinsmedicine.disease_causeMESH: Listeria monocytogenesApplied Microbiology and BiotechnologyBacterial Adhesionlaw.inventionGreen fluorescent proteinPlasmidComputer-AssistedlawGenes ReporterImage Processing Computer-AssistedMESH : Bacterial ProteinsMESH: Microscopy ConfocalPathogenMESH: Bacterial Proteins2. Zero hunger0303 health sciencesMicroscopyMicroscopy ConfocalPhotobleachingEcologybiologyMESH: KineticsMESH : Genes ReporterMESH: Image Processing Computer-AssistedMESH : BiofilmsConfocalMESH : KineticsMESH: PhotobleachingMESH : Image Processing Computer-AssistedBiotechnologyPlasmidsMESH : Bacterial AdhesionConfocalGreen Fluorescent ProteinsMESH: BiofilmsMESH : PhotobleachingMicrobiology03 medical and health sciencesMESH: Gene Expression ProfilingMESH: Green Fluorescent ProteinsListeria monocytogenesBacterial ProteinsConfocal microscopyMESH: PlasmidsMESH: Analysis of VariancemedicineMESH: Bacterial AdhesionMESH : Microscopy ConfocalReporter030304 developmental biologyAnalysis of Variance030306 microbiologyMESH : Gene Expression ProfilingGene Expression ProfilingMESH: Genes ReporterBiofilmbiochemical phenomena metabolism and nutritionbiology.organism_classification[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/BacteriologyListeria monocytogenesCulture MediaKineticsGenesMESH : PlasmidsBiofilmsMESH: Culture MediaFood MicrobiologyMESH : Culture MediaMESH : Listeria monocytogenesBacteriaFood ScienceApplied and environmental microbiology
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The glyceraldehyde-3-phosphate dehydrogenase polypeptides encoded by the Saccharomyces cerevisiae TDH1, TDH2 and TDH3 genes are also cell wall protei…

2001

The authors show that the glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) of Saccharomyces cerevisiae, previously thought to be restricted to the cell interior, is also present in the cell wall. GAPDH activity, proportional to cell number and time of incubation, was detected in intact wild-type yeast cells. Intact cells of yeast strains containing insertion mutations in each of the three structural TDH genes (tdh1, tdh2 and tdh3) and double mutants (tdh1 tdh2 and tdh1 tdh3) also displayed a cell-wall-associated GAPDH activity, in the range of parental wild-type cells, although with significant differences among strains. A cell wall location of GAPDH was further confirmed …

Immunoelectron microscopySaccharomyces cerevisiaeCellBlotting WesternGenes FungalSaccharomyces cerevisiaeBiologyMicrobiologyCell wallstomatognathic systemBacterial ProteinsCell WallmedicineFluorescent Antibody Technique IndirectMicroscopy ImmunoelectronGlyceraldehyde 3-phosphate dehydrogenaseGlyceraldehyde-3-Phosphate Dehydrogenasesbiology.organism_classificationFlow CytometryMolecular biologyYeastCulture MediaCytosolmedicine.anatomical_structureBiochemistryCytoplasmMutationbiology.proteinMicrobiology (Reading, England)
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Persistent and Transient Replication of Full-Length Hepatitis C Virus Genomes in Cell Culture

2002

ABSTRACT The recently developed subgenomic hepatitis C virus (HCV) replicons were limited by the fact that the sequence encoding the structural proteins was missing. Therefore, important information about a possible influence of these proteins on replication and pathogenesis and about the mechanism of virus formation could not be obtained. Taking advantage of three cell culture-adaptive mutations that enhance RNA replication synergistically, we generated selectable full-length HCV genomes that amplify to high levels in the human hepatoma cell line Huh-7 and can be stably propagated for more than 6 months. The structural proteins are efficiently expressed, with the viral glycoproteins E1 and…

ImmunologyReplicationGenome ViralHepacivirusBiologyVirus ReplicationMicrobiologyVirusViral ProteinsGene FrequencyVirologyTumor Cells CulturedHumansSubgenomic mRNAchemistry.chemical_classificationEndoplasmic reticulumRNAHepatitis CMolecular biologyNS2-3 proteasechemistryViral replicationCell cultureCulture Media ConditionedInsect ScienceRNA ViralGlycoproteinSubcellular FractionsJournal of Virology
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