Search results for "Saccharomyce"

showing 10 items of 875 documents

Partial vinylphenol reductase purification and characterization from Brettanomyces bruxellensis

2008

International audience; Brettanomyces is the major microbial cause for wine spoilage worldwide and causes significant economic losses. The reasons are the production of ethylphenols that lead to an unpleasant taint described as 'phenolic odour'. Despite its economic importance, Brettanomyces has remained poorly studied at the metabolic level. The origin of the ethylphenol results from the conversion of vinylphenols in ethylphenol by Brettanomyces hydroxycinnamate decarboxylase. However, no information is available on the vinylphenol reductase responsible for the conversion of vinylphenols in ethylphenols. In this study, a vinylphenol reductase was partially purified from Brettanomyces bruxe…

Chromatography GasBrettanomycesMolecular Sequence DataVINYLPHENOL REDUCTASEBrettanomyces bruxellensisWineReductaseMicrobiology[ CHIM ] Chemical SciencesFungal Proteins03 medical and health sciencesHydrolysisOpen Reading FramesPhenolsOxidoreductaseGenetics[CHIM]Chemical SciencesAmino Acid SequenceMolecular Biology030304 developmental biologychemistry.chemical_classificationWineVOLATILE PHENOL0303 health sciencesbiology030306 microbiologyChemistryGuaiacolTemperatureBRETTANOMYCESHydrogen-Ion Concentrationbiology.organism_classificationNADAmino acidMolecular WeightKineticsEnzymeBiochemistryDETERIORATION MICROBIENNESaccharomycetalesBRUTTANOMYCES BRUXELLENSISFood MicrobiologyElectrophoresis Polyacrylamide GelOxidoreductases
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Volatile components from flower-heads of Centaurea nicaeensis All., C. parlatoris Helder and C. solstitialis L. ssp. schouwii (DC.) Dostál growing wi…

2008

The volatile constituents of the flowerheads of Centaurea nicaeensis All., C. parlatoris Helder and C. solstitialis L. ssp. schouwii (DC.) Dostal were extracted by hydrodistillation and analysed by GC and GC-MS. Altogether 113 components were identified. Fatty acids and hydrocarbons were the most abundant components in the oils. Caryophyllene and caryophyllene oxide were the main compounds of the sesquiterpene fraction. The study on the biological activity of the oils shows no significant activity.

Chromatography GasNonacosanePalmitic AcidCentaureaPlant ScienceFlowersMicrobial Sensitivity TestsSaccharomyces cerevisiaeSesquiterpeneBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundFusariumlawBotanyCandida albicansOils VolatilePlant OilsEssential oilPolycyclic SesquiterpenesbiologyPlant ExtractsTerpenesCaryophylleneOrganic ChemistryBiological activityAsteraceaebiology.organism_classificationchemistryCaryophyllene oxideItalyCentaureaPseudomonas aeruginosaSesquiterpenesBacillus subtilisNatural product research
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Complete decontamination and regeneration of DNA purification silica colum

2008

Silica columns are among the most used DNA purification systems, allowing a good yield of high-quality nucleic acids without organic extractions. Silica column regeneration protocols reported up to now to remove DNA traces are time-consuming, and their effectiveness on genomic DNA has not been demonstrated. Here we report a very rapid regeneration procedure that ensures no DNA carryover, independent of its size, without impairing column efficiency. The method takes advantage of the improved DNA removal by low concentrations of Triton X-100.

ChromatographyOctoxynolBiophysicsFungal geneticsSilica decontaminationGenomic DNACell BiologyHuman decontaminationSaccharomyces cerevisiaeDNA separation by silica adsorptionSilicon DioxideBiochemistryDNA extractionPolymerase Chain Reactionchemistry.chemical_compoundgenomic DNAchemistrySpin column-based nucleic acid purificationNucleic acidGenome FungalParticle SizeDNA FungalMolecular BiologyDNAChromatography High Pressure Liquid
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Staining mitochondria in Saccharomyces cerevisiae.

1969

After testing various procedures (amidoblack 10B, acid fuchsin-methyl blue, Luxol fast blue MBS-phloxine, toluidine blue O, Jams green B and pinacyanol), three stains can be recommended for staining both types of mitochondria (globose and threadlike) in the cells of Saccharomyces cerevisiae: (1) 0.1% solution of amidoblack 10B in citrate buffer (pH 3.0) for 10 min; (2) 0.01% solution of toluidine blue O in phosphate buffer (pH 6.0) for 30 min; (3) 0.01% solution of Janus green B in distilled water (pH 5.6) for 30 min. The latter stain is most specific because its staining reaction depends upon the action of the mitochondrial enzyme cytochrome c oxidase. Yet, low concentrations and short inc…

ChromatographyTime FactorsStaining and LabelingJanus Green BSaccharomyces cerevisiaeBiologyBuffersHydrogen-Ion Concentrationbiology.organism_classificationStainLuxol fast blue stainStainingMitochondriaElectron Transport Complex IVchemistry.chemical_compoundSaccharomyceschemistryBiochemistryDistilled waterbiology.proteinMethodsCytochrome c oxidaseAnatomyColoring AgentsIncubationStain technology
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A rapid spectrofluorimetric method for the determination of the degree of synchronism inSaccharomyces cerevisiae

1985

A fluorescence technique that allows direct measurement of DNA and synchrony levels inSaccharomyces cerevisiae cell cultures is reported. The spectrofluorimetric estimation of DNA with 4,6-diamidino-2-phenylindole (AT-dye) does not require prior extraction, is highly stable, and requires small quantities of cells.

ChromatographybiologySaccharomyces cerevisiaeFluorescence spectrometryGeneral Medicinebiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyFluorescencechemistry.chemical_compoundBiochemistrychemistrySynchronismDNACurrent Microbiology
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Fractionation of glycoside aroma precursors in neutral grapes. Hydrolysis and conversion by Saccharomyces cerevisiae

2004

Abstract Glycoconjugated aroma precursors from neutral grape varieties were fractionated on 5 g C18 RP cartridge. Each of the seven fractions collected was divided in three parts: first part was hydrolysed with Pectinol in order to determine total aromatic heterosides, while the second part was treated with an active strain of the yeast Saccharomyces cerevisiae UCLM 325 and the third part with acetonic powder of the same yeast strain. The studied strain proved effective in the hydrolysis of the heterosides of nerol and geraniol, cis-8-hydroxy-linalool, 8-hydroxy-dihydro-linalool, some benzenoids and some norisoprenoids derivatives such as vomifoliol and 3-oxo-α-ionol. Only whole cells are a…

Citronellolchemistry.chemical_classificationChromatographybiologyGlycosideGrapeSaccharomyces cerevisiaebiology.organism_classificationNorisoprenoidsSaccharomycesYeastGlycosidechemistry.chemical_compoundchemistryAroma precursorNerolGeraniolAromaFood ScienceLWT - Food Science and Technology
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Saccharomyces cerevisiae signature genes for predicting nitrogen deficiency during alcoholic fermentation

2007

Genome-wide analysis of the wine yeast strain Saccharomyces cerevisiae PYCC4072 identified 36 genes highly expressed under conditions of low or absent nitrogen in comparison with a nitrogen-replete condition. Reverse transcription-PCR analysis for four of these transcripts with this strain and its validation with another wine yeast strain underlines the usefulness of these signature genes for predicting nitrogen deficiency and therefore the diagnosis of wine stuck/sluggish fermentations.

Ciências Agrárias::Biotecnologia Agrária e Alimentar:Biotecnologia Agrária e Alimentar [Ciências Agrárias]Saccharomyces cerevisiae ProteinsNitrogenSaccharomyces cerevisiaeGenes FungalSaccharomyces cerevisiaeEthanol fermentationBiologyApplied Microbiology and BiotechnologySaccharomycesGenètica molecular03 medical and health sciencesSaccharomycesGene Expression Regulation Fungal030304 developmental biologyOligonucleotide Array Sequence AnalysisWineGenetics0303 health sciencesScience & TechnologyEcologyModels Genetic030306 microbiologyNitrogen deficiencyReverse Transcriptase Polymerase Chain Reactionfood and beveragesbiology.organism_classificationPhysiology and BiotechnologyYeastYeast in winemakingBiochemistryAlcoholsFermentationFermentationFood ScienceBiotechnology
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Strategies for improving production and purification of a recombinant protein: rP30 of Toxoplasma gondii expressed in the yeast Schizosaccharomyces p…

2007

Abstract Many problems concerned with the production and the purification of recombinant proteins must be addressed prior to launching an industrial production process. Among these problems, attention is focused on low-level expression that complicates the purification step and can jeopardise the process. The expression of a membrane protein, rP30, of Toxoplasma gondii in the yeast Schizosaccharomyces pombe led to a secretion of only 0.5 μg ml−1. In order to obtain a sufficient quantity for biochemical characterization and evaluation in vitro diagnostic test development, strategies for both production and purification had to be optimized. First, the influence of four nitrogen sources (three…

Clinical BiochemistryIon chromatographyProtozoan ProteinsAntigens ProtozoanRaw materialBiochemistryChromatography AffinityAnalytical Chemistrylaw.inventionAffinity chromatographylawSchizosaccharomycesYeast extractAnimalsBiomassChromatographybiologyChemistryCell BiologyGeneral Medicinebiology.organism_classificationYeastRecombinant ProteinsBiochemistrySchizosaccharomyces pombeFermentationRecombinant DNAFermentationToxoplasmaJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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The molecular characterization of new types of Saccharomyces cerevisiae × S. kudriavzevii hybrid yeasts unveils a high genetic diversity.

2012

11 pages, 2 tables, 4 figures. --Article first published online: 6 JAN 2012. --This is the pre-peer reviewed version of the following article: Peris, D., Belloch, C., Lopandić, K., Álvarez-Pérez, J. M., Querol, A. and Barrio, E. (2012), The molecular characterization of new types of Saccharomyces cerevisiae × S. kudriavzevii hybrid yeasts unveils a high genetic diversity. Yeast, 29: 81–91. which has been published in final form at http://dx.doi.org/10.1002/yea.2891

Clinical yeastsDietaryWineSaccharomyces cerevisiaeSaccharomyces kudriavzeviiGenètica molecularSaccharomyces hybrids
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Ecology of yeasts associated with kernels of several durum wheat genotypes and their role in co-culture with Saccharomyces cerevisiae during dough le…

2021

International audience; This work was performed to investigate on the yeast ecology of durum wheat to evaluate the interaction between kernel yeasts and the commercial baker's yeast Saccharomyces cerevisiae during dough leavening. Yeast populations were studied in 39 genotypes of durum wheat cultivated in Sicily. The highest level of kernel yeasts was 2.9 Log CFU/g. A total of 413 isolates was collected and subjected to phenotypic and genotypic characterization. Twenty-three yeast species belonging to 11 genera have been identified. Filobasidium oeirense, Sporobolomyces roseus and Aureobasidium pullulans were the species most commonly found in durum wheat kernels. Doughs were co-inoculated …

Co-fermentationFood Handling[SDV]Life Sciences [q-bio]Saccharomyces cerevisiaeFlourNon-saccharomycesDough leaveningTriticum turgidum subsp. durumSaccharomyces cerevisiaeCandida parapsilosisMicrobiology03 medical and health sciencesStarterWheat kernelYeastsHumansTriticum030304 developmental biologyLeavening agent2. Zero hunger0303 health sciencesWheat kernelsbiology030306 microbiologyEcologyfood and beveragesBreadbiology.organism_classificationYeastCoculture TechniquesAureobasidium pullulansCo-fermentationTasteFermentationSeedsFermentationNon-saccharomyceFood Science
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