Search results for "YEAST"

showing 10 items of 792 documents

RCS1, a gene involved in controlling cell size inSaccharomyces cerevisiae

1991

Cloning and sequencing of RCS1, Saccharomyces cerevisiae gene whose product seems to be involved in timing the budding event of the cell cycle, is described. A haploid strain in which the 3'-terminal region of the chromosomal copy of the gene has been disrupted produces cells that are, on average, twice the size of cells of the parental strain. The critical size for budding in the mutant is similarly increased, and the disruption mutation is dominant in a diploid heterozygous for the RCS1 gene. Spores from this diploid have a reduced ability to germinate, the effect being more pronounced in the spores carrying the disrupted copy of RCS1. However, disrupted cells recover from alpha-factor tr…

HeterozygoteMolecular Sequence DataSaccharomyces cerevisiaeMutantBioengineeringSaccharomyces cerevisiaemedicine.disease_causeApplied Microbiology and BiotechnologyBiochemistryGeneticsSpore germinationmedicineAmino Acid SequenceCloning MolecularDNA FungalGeneGene LibraryGeneticsBuddingMutationMembrane GlycoproteinsBase SequencebiologyCell CyclefungiSpores Fungalbiology.organism_classificationYeastMutationPloidyPlasmidsBiotechnologyYeast
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Can pressure-induced cell inactivation be related to cell volume compression? A case study for Saccharomyces cerevisiae

2013

In this paper, emphasis has been put on the relationship between volume compression and cell inactivation for the Saccharomyces cerevisiae strain CBS 1171 submitted to high hydrostatic pressure treatments. The influence of cell dehydration on pressure inactivation was first investigated. Inactivation was found to be strongly limited, or even completely prevented for cells with a water content of 60% w/w or below. Moreover, the volume compression undergone by a single yeast cell was assessed as a function of pressure and hydration conditions using a high-pressure setup for pressure-volume-temperature measurements. Direct measurements of volume compression were performed on cell pellets after…

High-pressure[SDV]Life Sciences [q-bio]Hydrostatic pressureSaccharomyces cerevisiaeCellHydrationYeast cellsCell inactivation03 medical and health sciences0404 agricultural biotechnologymedicine0303 health sciencesChromatography[ SDV ] Life Sciences [q-bio]biologyStrain (chemistry)030306 microbiologyChemistry04 agricultural and veterinary sciencesCompression (physics)biology.organism_classification040401 food scienceVolume compressionYeastMembranemedicine.anatomical_structureCytoplasmBiophysicsFood Science
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Thermoelectric Heat Exchange and Growth Regulation in a Continuous Yeast Culture

2018

We have designed a thermoelectric heat exchanger (TEHE) for microbial fermentations that is able to produce electric power from a microbial continuous culture using the intrinsic heat generated by microbial growth. While the TEHE was connected, the system proved able to stably self-maintain both the temperature and the optical density of the culture. This paves the way toward a more sustainable operation of microbial fermentations, in which energy could be saved by converting part of the metabolic heat into usable electric power.

Hot TemperatureMaterials scienceGrowth regulationBioelectric Energy SourcesBacterial growthOptical densityUSableMetabolic heatMicrobiologyHeat exchangeheat exchangeContinuous cultureElectricityYeastsPhase (matter)hemic and lymphatic diseasesThermoelectric effectHeat exchangerTemperature regulationPower productionProcess engineeringbusiness.industryOriginal ArticlesYeastChemical engineeringFermentationcontinuous cultureOriginal ArticlePeltier–Seebeck effectElectric powerbusinesspower productiontemperature regulation
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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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The Saccharomyces cerevisiae zinc finger proteins Msn2p and Msn4p are required for transcriptional induction through the stress response element (STR…

1996

The MSN2 and MSN4 genes encode homologous and functionally redundant Cys2His2 zinc finger proteins. A disruption of both MSN2 and MSN4 genes results in a higher sensitivity to different stresses, including carbon source starvation, heat shock and severe osmotic and oxidative stresses. We show that MSN2 and MSN4 are required for activation of several yeast genes such as CTT1, DDR2 and HSP12, whose induction is mediated through stress-response elements (STREs). Msn2p and Msn4p are important factors for the stress-induced activation of STRE dependent promoters and bind specifically to STRE-containing oligonucleotides. Our results suggest that MSN2 and MSN4 encode a DNA-binding component of the…

Hot TemperatureSaccharomyces cerevisiae ProteinsTranscription GeneticSaccharomyces cerevisiaeMolecular Sequence DataPlasma protein bindingSaccharomyces cerevisiaeGeneral Biochemistry Genetics and Molecular BiologyTranscription (biology)Osmotic PressureMolecular BiologyGeneTranscription factorZinc fingerGeneticsGeneral Immunology and MicrobiologybiologyBase SequenceGeneral NeurosciencePromoterZinc Fingersbiology.organism_classificationYeastCell biologyDNA-Binding ProteinsOxidative StressOligodeoxyribonucleotidesResearch ArticleProtein BindingTranscription Factors
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Lack of correlation between trehalose accumulation, cell viability and intracellular acidification as induced by various stresses in Saccharomyces ce…

1998

A pma1-1 mutant of Saccharomyces cerevisiae with reduced H+-ATPase activity and the isogenic wild-type strain accumulated high levels of trehalose in response to a temperature upshift to 40 éC and after addition of 10% ethanol, but only modest levels in response to a rapid drop in external pH and after addition of decanoic acid. There was, however, no correlation between the absolute levels of trehalose in the stressed cells and their viability. All these treatments induced a significant decrease in intracellular pH, and surprisingly, this decrease was very similar in both strains, indicating that intracellular acidification could not be the triggering mechanism for trehalose accumulation i…

Hot TemperatureTime FactorsATP synthaseEthanolIntracellular pHMutantSaccharomyces cerevisiaeTrehaloseSaccharomyces cerevisiaeBiologyHydrogen-Ion Concentrationbiology.organism_classificationMicrobiologyTrehaloseYeastArtificial Gene FusionFungal Proteinschemistry.chemical_compoundchemistryBiochemistryGlucosyltransferasesbiology.proteinViability assayAcidsIntracellularMicrobiology (Reading, England)
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Engineering of sugar transporters for improvement of xylose utilization during high-temperature alcoholic fermentation in Ogataea polymorpha yeast

2020

Abstract Background Xylose transport is one of the bottlenecks in the conversion of lignocellulosic biomass to ethanol. Xylose consumption by the wild-type strains of xylose-utilizing yeasts occurs once glucose is depleted resulting in a long fermentation process and overall slow and incomplete conversion of sugars liberated from lignocellulosic hydrolysates. Therefore, the engineering of endogenous transporters for the facilitation of glucose-xylose co-consumption is an important prerequisite for efficient ethanol production from lignocellulosic hydrolysates. Results In this study, several engineering approaches formerly used for the low-affinity glucose transporters in Saccharomyces cerev…

Hot TemperatureXylose transportersSaccharomyces cerevisiaelcsh:QR1-502Lignocellulosic biomassBioengineeringEthanol fermentationXyloseProtein EngineeringApplied Microbiology and BiotechnologyPichialcsh:MicrobiologyFungal Proteinschemistry.chemical_compoundHigh-temperature alcoholic fermentationOgataea (Hansenula) polymorphaEthanol fuelXylosebiologyChemistryResearchbiology.organism_classificationYeastBiochemistryAlcoholsFermentationFermentationOgataea polymorphaBiotechnology
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Characterization of cell wall proteins of yeast and hydrophobic mycelial cells of Candida albicans

1991

Cell surface hydrophobicity (CSH) of blastoconidia and blastoconidia bearing germ tubes of Candida albicans ATCC 26555 was monitored by assessing attachment of polystyrene microspheres to the cell surface, and we found that mature hyphae were significantly hydrophobic. Treatment of intact cells with low concentrations of beta-glucanase (Zymolyase 20T) or proteases abolished or significantly reduced attachment of latex beads to hyphae. This effect paralleled an obvious reduction in CSH of the entire cell population, as measured by an aqueous-hydrocarbon biphasic partitioning assay. Analysis of the cell wall material released by Zymolyase and adsorbed on polystyrene microspheres indicated tha…

HydrolasesImmunologyPopulationGerm tubeBiologyMicrobiologyBlastoconidiumFungal ProteinsCell wallCell WallCandida albicansCandida albicanseducationMercaptoethanolLatex beadsFungal proteineducation.field_of_studybiology.organism_classificationMicrospheresYeastMolecular WeightInfectious DiseasesSolubilityBiochemistryPolystyrenesParasitologyAdsorptionResearch ArticleInfection and Immunity
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Immobilisation of yeast cells on the surface of hydroxyapatite ceramics

2011

Hydroxyapatite (HAP) ceramics was tested for the first time for the possibility of being used as a new carrier for the immobilisation of yeast cells that are both model organisms for eukaryotic cell investigations and producers, which is important in classical and modern biotechnological processes. It was shown that under typical immobilisation conditions yeast (Saccharomyces cerevisiae) has no affinity to HAP ceramics. A novel method for yeast immobilisation was developed. This new method includes the joint incubation of a carrier with the cells, the sedimentation and adhesion of cells on the carrier and the dehydration of obtained preparations. It was shown that the sedimentation and adhe…

Hydroxyapatite ceramicsbiologyChemistrySaccharomyces cerevisiaeBioengineeringHeavy metalsAdhesionmedicine.diseasebiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistryYeastBiotechnological processstomatognathic systemBiochemistryChemical engineeringmedicineDehydrationEukaryotic cellProcess Biochemistry
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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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