Search results for "yeast"

showing 10 items of 792 documents

Oxidative stress responses and lipid peroxidation damage are induced during dehydration in the production of dry active wine yeasts.

2009

The tolerance of the yeast Saccharomyces cerevisiae to desiccation is important for the use of this microorganism in the wine industry, since active dry wine yeast is routinely used as starter for must fermentations. Many studies have shown the complexity of the cellular effects caused by water loss, including oxidative injuries on macromolecular components. However the technological interest of yeast drying was not addressed in those studies, and the dehydration conditions were far from the industrial practice. In the present study a molecular approach was used to characterize the relevant injuring conditions during pilot plant dehydrations under two different drying temperatures (i.e., 35…

Time FactorsWineSaccharomyces cerevisiaeBiologymedicine.disease_causeMicrobiologyLipid peroxidationchemistry.chemical_compoundIndustrial MicrobiologyGlutaredoxinGene Expression Regulation FungalmedicineBiomassDesiccationWinemakingWinefood and beveragesGeneral MedicineGlutathioneYeastYeast in winemakingOxidative StressBiochemistrychemistryFermentationLipid PeroxidationOxidation-ReductionOxidative stressFood ScienceInternational journal of food microbiology
researchProduct

Interaction of an odorant lactone with model phospholipid bilayers and its strong fluidizing action in yeast membrane

2003

International audience; Some odorant lactones are naturally present in fruits or in fermented products; they can also be used as food additives and can be produced by microorganisms at the industrial scale by biotechnological processes. Gamma-decalactone was previously shown to have antimicrobial properties. We determined by infrared spectroscopy measurements that this compound rapidly diffused into model phospholipid bilayers (within 2 min), modifying the general physical state of a dimyristoyl-L-alpha-phosphatidylcholine (DMPC) film. In vivo, the lactone strongly increased membrane fluidity in the model yeast Yarrowia lipolytica, as evaluated by fluorescence anisotropy measurements. This …

Time Factors[SDV.BIO]Life Sciences [q-bio]/BiotechnologyLipid BilayersYarrowiaMESH : Models BiologicalLactonesMESH : Spectroscopy Fourier Transform InfraredMESH: Dimyristoylphosphatidylcholinechemistry.chemical_compoundMESH : DimyristoylphosphatidylcholineSpectroscopy Fourier Transform InfraredMembrane fluidityOrganic chemistryMESH : Anti-Bacterial Agents[INFO.INFO-BT]Computer Science [cs]/BiotechnologyAntibacterial agentMESH : Spectrometry FluorescencebiologyMESH: Lipid BilayersMESH: Indicators and Reagentsfood and beveragesGeneral MedicineAnti-Bacterial AgentsMESH : LactonesMembraneBenzyl alcoholDimyristoylphosphatidylcholine[ INFO.INFO-BT ] Computer Science [cs]/BiotechnologyMESH: LactonesMESH: Spectrometry FluorescenceMESH : Time FactorsMESH : YarrowiaPhospholipid[SDV.BC]Life Sciences [q-bio]/Cellular BiologyModels BiologicalMicrobiologyMESH: Spectroscopy Fourier Transform InfraredMESH : Indicators and ReagentsMESH: Anti-Bacterial Agents[ SDV.BC ] Life Sciences [q-bio]/Cellular BiologyMESH: Time FactorsMESH: Models Biological[ SDV.BIO ] Life Sciences [q-bio]/BiotechnologyYarrowiaBiological membranebiology.organism_classificationYeastSpectrometry FluorescencechemistryIndicators and ReagentsMESH: YarrowiaMESH : Lipid BilayersFood ScienceInternational Journal of Food Microbiology
researchProduct

Killer toxins in new isolates of the yeasts Hanseniaspora uvarum and Pichia kluyveri

1985

From various habitats (plant material, fruits, soil), yeasts belonging to the species of Pichia kluyveri and Hanseniaspora uvarum were isolated that showed killer activity. According to the activity spectrum against other yeasts these strains belonged to 11 different groups that were distinguishable from the killer strains K1-K10. The isoelectric points of the killer proteins were in the range of pH 3.5–3.9, the activity optimum was observed at pH 4.2–4.6. Above pH 5 and above a temperature of 25–35°C the killer proteins were inactivated.

ToxinPichia kluyveriBiological activityBiologymedicine.disease_causebiology.organism_classificationHanseniasporaMicrobiologyYeastMicrobiologyIsoelectric pointHanseniaspora uvarumGeneticsmedicineMolecular BiologyPichiaFEMS Microbiology Letters
researchProduct

A complete set of nascent transcription rates for yeast genes

2010

The amount of mRNA in a cell is the result of two opposite reactions: transcription and mRNA degradation. These reactions are governed by kinetics laws, and the most regulated step for many genes is the transcription rate. The transcription rate, which is assumed to be exercised mainly at the RNA polymerase recruitment level, can be calculated using the RNA polymerase densities determined either by run-on or immunoprecipitation using specific antibodies. The yeast Saccharomyces cerevisiae is the ideal model organism to generate a complete set of nascent transcription rates that will prove useful for many gene regulation studies. By combining genomic data from both the GRO (Genomic Run-on) a…

Transcription factoriesSaccharomyces cerevisiae ProteinsTranscription GeneticRNA StabilityGenes FungalDNA transcriptionlcsh:MedicineYeast and Fungal ModelsRNA polymerase IISaccharomyces cerevisiaeBiologyBiochemistryGenètica molecularchemistry.chemical_compoundSaccharomycesModel OrganismsMolecular cell biologyTranscripció genèticaGene Expression Regulation FungalRNA polymeraseGeneticsRNA MessengerRNA synthesislcsh:ScienceBiologyRNA polymerase II holoenzymeGeneticsMultidisciplinaryGeneral transcription factorGene Expression Profilinglcsh:RPromoterGenomicsChromatinFunctional GenomicsNucleic acidsGenòmicaRNA processingchemistrybiology.proteinRNAlcsh:QRNA Polymerase IIGene expressionTranscription factor II DTranscription factor II BResearch Article
researchProduct

Expression levels of a filament-specific transcriptional regulator are sufficient to determine Candida albicans morphology and virulence

2009

Candida albicans , the major human fungal pathogen, undergoes a reversible morphological transition from single yeast cells to pseudohyphal and hyphal filaments (elongated cells attached end-to-end). Because typical C. albicans infections contain a mixture of these morphologies it has, for many years, been difficult to assess the relative contribution of each form to virulence. In addition, the regulatory mechanisms that determine growth in pseudohyphal and hyphal morphologies are largely unknown. To address these questions we have generated a C. albicans strain that can be genetically manipulated to grow completely in the hyphal form under non-filament-inducing conditions in vitro. This w…

Transcription GeneticPopulationHyphaeVirulenceMicrobiologyMiceCandida albicansGene expressionTranscriptional regulationmedicineAnimalsCandida albicanseducationeducation.field_of_studyMultidisciplinaryVirulencebiologyCandidiasismedicine.diseasebiology.organism_classificationYeastCorpus albicansDisease Models AnimalCommentarySystemic candidiasisTranscription FactorsProceedings of the National Academy of Sciences
researchProduct

ADR1 and SNF1 Mediate Different Mechanisms in Transcriptional Regulation of Yeast POT1 Gene

1994

We studied the consequences of adr1 and snf1 mutations on POT1 gene expression in different growth conditions. The results obtained reveal that ADR1 and SNF1 genes affect POT1 transcription in different ways: ADR1 has a minor role in derepression in low concentration of glucose but is essential for activation in stationary phase whereas SNF1 is essential for derepression and activation, although it does not seem to be directly involved in the molecular mechanism of activation in stationary phase.

Transcription GeneticRecombinant Fusion ProteinsGenes FungalBiophysicsSaccharomyces cerevisiaeBiologyMicrobodiesBiochemistryTranscription (biology)Gene Expression Regulation FungalGene expressionTranscriptional regulationAcetyl-CoA C-AcetyltransferaseLuciferasesMolecular BiologyGeneDerepressionRegulation of gene expressionGeneticsfungiGene Transfer TechniquesCell BiologyYeastCulture MediaCell biologycarbohydrates (lipids)GlucoseStationary phaseMutationProtein KinasesBiochemical and Biophysical Research Communications
researchProduct

External conditions inversely change the RNA polymerase II elongation rate and density in yeast.

2013

Elongation speed is a key parameter in RNA polymerase II (RNA pol II) activity. It affects the transcription rate, while it is conditioned by the physicochemical environment it works in at the same time. For instance, it is well-known that temperature affects the biochemical reactions rates. Therefore in free-living organisms that are able to grow at various environmental temperatures, such as the yeast Saccharomyces cerevisiae, evolution should have not only shaped the structural and functional properties of this key enzyme, but should have also provided mechanisms and pathways to adapt its activity to the optimal performance required. We studied the changes in RNA pol II elongation speed …

Transcription GeneticSaccharomyces cerevisiaeBlotting WesternBiophysicsRNA polymerase IISaccharomyces cerevisiaeBiochemistryPolymerase Chain Reactionchemistry.chemical_compoundStructural BiologyRNA polymeraseGeneticsNucleotideMolecular BiologyDNA Primerschemistry.chemical_classificationbiologyBase SequenceTemperaturebiology.organism_classificationYeastReal-time polymerase chain reactionEnzymechemistryBiochemistryBiophysicsbiology.proteinRNA Polymerase IIElongationBiochimica et biophysica acta
researchProduct

The Kelch protein NS1-BP interacts with alpha-enolase/MBP-1 and is involved in c-Myc gene transcriptional control

2007

Alpha-enolase is a key glycolytic enzyme that plays a functional role in several physiological processes depending on the cellular localization. The enzyme is mainly localized in the cytoplasm whereas an alternative translated form, named MBP-1, is predominantly nuclear. The MBP-1 protein has been characterized as a c-Myc promoter binding protein that negatively controls transcription. In the present study, we identified the kelch protein NS1-BP as one of the alpha-enolase/MBP-1 partners by using a yeast two-hybrid screening. Although NS1-BP has been originally described as a protein mainly localized in the nucleus, we provide evidence that NS1-BP also interacts with actin in human cells, a…

Transcription GeneticTranscription FactorGlycolysiAlpha-enolaseKelch proteinsRNA-Binding ProteinHeLa CellChlorocebus aethiopsTranscriptional regulationPromoter Regions GeneticCellular localizationNuclear ProteinbiologyNuclear ProteinsRNA-Binding ProteinsCell biologyDNA-Binding ProteinsProtein TransportCOS CellsYeast two-hybrid assayGlycolysisHumanProtein BindingSubcellular FractionsImmunoprecipitationDNA-Binding ProteinTwo-hybrid screeningEnolaseChlorocebus aethiopProto-Oncogene Proteins c-mycCOS CellBiomarkers TumorAnimalsHumansKelch proteinMolecular BiologyActinTumor Suppressor ProteinAnimalTumor Suppressor ProteinsBinding proteinc-Myc transcriptionCell BiologyMolecular biologyActinsKelch proteinSubcellular FractionSettore BIO/18 - GeneticaGene Expression RegulationCytoplasmPhosphopyruvate Hydratasebiology.proteinHeLa CellsTranscription FactorsBiochimica et Biophysica Acta (BBA) - Molecular Cell Research
researchProduct

DNA chips for yeast biotechnology. The case of wine yeasts.

2002

The yeast Saccharomyces cerevisiae is one of the most popular model organisms. It was the first eukaryote whose genome was sequenced. Since then many functional analysis projects have tried to find the function of many genes and to understand its metabolism in a holistic way. Apart from basic science this microorganism is of great interest in several biotechnology processes, such as winemaking. Only global studies of the cell as a whole can help us to understand many of the technical problems facing winemaking. DNA chip technology is one of the most promising tools for the analysis of cell physiology. Yeast has been the model organism for the development of this technique. Many of the studi…

Transcription Geneticved/biology.organism_classification_rank.speciesSaccharomyces cerevisiaeGene ExpressionBioengineeringWineSaccharomyces cerevisiaeBiologyApplied Microbiology and BiotechnologyGenomeModel organismWinemakingOligonucleotide Array Sequence AnalysisWineEthanolved/biologybusiness.industryfood and beveragesGeneral MedicineSequence Analysis DNAbiology.organism_classificationBiological EvolutionYeastBiotechnologyYeast in winemakingGene Expression RegulationFermentationCarbohydrate MetabolismDNA microarrayGenome FungalbusinessBiotechnologyJournal of biotechnology
researchProduct

A genomic view of mRNA turnover in yeast

2011

The steady-state mRNA level is the result of two opposing processes: transcription and degradation; both of which can provide important points to regulate gene expression. In the model organism yeast Saccharomyces cerevisiae, it is now possible to determine, at the genomic level, the transcription and degradation rates, as well as the mRNA amount, using DNA chip or parallel sequencing technologies. In this way, the contribution of both rates to individual and global gene expressions can be analysed. Here we review the techniques used for the genomic evaluation of the transcription and degradation rates developed for this yeast, and we discuss the integration of the data obtained to fully an…

Transcription Geneticved/biology.organism_classification_rank.speciesSaccharomyces cerevisiaeSaccharomyces cerevisiaeComputational biologyGeneral Biochemistry Genetics and Molecular BiologyTranscripció genèticaStress PhysiologicalTranscription (biology)YeastsGene expressionRNA MessengerModel organismGeneGeneticsMassive parallel sequencingGeneral Immunology and Microbiologybiologyved/biologyRNA FungalGenomicsGeneral Medicinebiology.organism_classificationYeastGenòmicaRNAGenome FungalDNA microarrayTranscriptomeGeneral Agricultural and Biological SciencesComptes Rendus Biologies
researchProduct