Search results for "saccharomyces"

showing 10 items of 861 documents

Yeast interaction on Chardonnay wine composition: Impact of strain and inoculation time.

2022

Abstract It is of great importance to understand the molecular characteristics and substantial chemical transformations due to yeast-yeast interaction. Non-targeted metabolomics was used to unravel must in fermentation composition, inoculated with non-Saccharomyces (NS) yeasts and Saccharomyces cerevisiae (S) for sequential fermentation. ultrahigh-resolution mass spectrometry was able to distinguish thousands of metabolites and provides deep insights into grape must composition allowing better understanding of the yeast-yeast interactome. The dominance of S, characterized by a metabolic richness not found with NS, is dependent on inoculation time and on the yeast species present. Co-inocula…

chemistry.chemical_classificationWineChardonnay Wine ; Inoculation Time ; Metabolomics ; Sequential Fermentation ; Yeast-yeast InteractionbiologyChemistrySaccharomyces cerevisiaeWineSaccharomyces cerevisiaeGeneral MedicinePentose phosphate pathwaybiology.organism_classificationInteractomeYeastAnalytical ChemistryMetabolomicsYeast DriedBiochemistryFermentationVitisFermentationAmino acid synthesisFood Science
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Relationship between Metabolic Fluxes and Sequence-Derived Properties of Enzymes

2014

Metabolic fluxes are key parameters of metabolic pathways being closely related to the kinetic properties of enzymes, thereby could be dependent on. This study examines possible relationships between the metabolic fluxes and the physical-chemical/structural features of enzymes from the yeast Saccharomyces cerevisiae glycolysis pathway. Metabolic fluxes were quantified by the COPASI tool using the kinetic models of Hynne and Teusink at varied concentrations of external glucose. The enzyme sequences were taken from the UniProtKB and the average amino acid (AA) properties were computed using the set of Georgiev’s uncorrelated scales that satisfy the VARIMAX criterion and specific AA indices th…

chemistry.chemical_classificationbiologyArticle SubjectSaccharomyces cerevisiaebiology.organism_classificationYeastUncorrelatedAmino acidMetabolic pathwayEnzymechemistryBiochemistryLinear regressionGlycolysisResearch ArticleInternational Scholarly Research Notices
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Untersuchungen �ber die L-�pfels�ure-abbauenden Enzyme von Schizosaccharomyces acidodevoratus

1970

Der Abbau von L-Apfelsaure wird bei Schizosaccharomyces acidodevoratus von einer Malat-Dehydrogenase (EC 1.1.1.37) und einer Oxalacetat-Decarboxylase (EC 4.1.1.3) katalysiert. Stoffwechselprodukt ist Brenztraubensaure. Eine Pyruvat-Decarboxylase (EC 4.1.1.1) und Alkohol-Dehydrogenase (EC 1.1.1.1) wandeln die Brenztraubensaure in Alkohol und CO2 um. In einer Nebenreaktion entsteht Acetoin. Lactat-Dehydrogenase (EC 1.1.1.27) ist nicht nachweisbar.

chemistry.chemical_classificationbiologyGeneral Medicinebiology.organism_classificationBiochemistryMicrobiologychemistry.chemical_compoundEnzymechemistryBiochemistryMicrobial ecologyGeneticsMalic acidMolecular BiologySchizosaccharomycesArchiv f�r Mikrobiologie
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Purification and characterization of an exopolyphosphatase from Saccharomyces cerevisiae.

1994

An exopolyphosphatase (polyphosphate phosphohydrolase; EC 3.6.1.11) activity that cleaves inorganic polyphosphates to orthophosphate has been purified to apparent homogeneity (> 95% pure) from Saccharomyces cerevisiae. The exopolyphosphatase is a monomeric protein with a polypeptide molecular mass of 28 kDa. The enzyme, which can be stabilized in the presence of Triton X-100, has a pH optimum of 7.5 and requires, for maximal activity, Co2+ or Mg2+ ions. In the absence of these ions, the exopolyphosphatase binds to polyphosphate but does not degrade it, allowing affinity purification of the enzyme on a polyphosphate-modified zirconia support. o-Vanadate, Cu2+, and Ca2+ are effective inhibito…

chemistry.chemical_classificationbiologyMolecular massChemistryPolyphosphateSaccharomyces cerevisiaeCell Biologybiology.organism_classificationBiochemistryPyrophosphateDivalentchemistry.chemical_compoundEnzymeAffinity chromatographyBiochemistryMolecular BiologyExopolyphosphataseJournal of Biological Chemistry
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Influence of fatty acids on the growth of wine microorganisms Saccharomyces cerevisiae and Oenococcus oeni

1998

The effects of fatty acids, extracted during prefermentation grape skin-contact on Saccharomyces cerevisiae and Oenococcus oeni, were studied. The influence of skin-contact on total fatty acid content was evaluated both in Chardonnay must and in synthetic medium. Prior to alcoholic fermentation, the skin-contact contributes to a large enrichment of long-chain fatty acids (C 16 to C 18:3 ). These results induced a positive effect on yeast growth and particularly on cell viability. In the skin-contact fermented media, levels of C 12 and especially C 10 are lower and macromolecules content higher than in controls. This production of extracellular mannoproteins and the reduction of medium-chain…

chemistry.chemical_classificationbiologySaccharomyces cerevisiaeFatty acidBioengineeringEthanol fermentationbiology.organism_classificationApplied Microbiology and BiotechnologyYeastYeast in winemakingchemistryBiochemistryMalolactic fermentationFermentationBiotechnologyOenococcus oeniJournal of Industrial Microbiology and Biotechnology
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Determination of the stability of protein pools from the cell wall of fungi.

2002

Stability of the protein populations present in the cell wall of three ascomycetous fungi Candida albicans, Saccharomyces cerevisiae and Yarrowia lipolytica was investigated. Cell wall proteins were either labeled with biotin or radiolabeled with amino acids, and chased for a period of time representing several generations. Proteins linked by non-covalent or covalent bonds were separated and their turnover was analyzed. No significant turnover took place during the chase period, and in fact radioactive proteins were accumulated in the wall during the period possibly by transfer through the secretory pathway. This transfer did not involve de novo protein synthesis; it was inhibited by azide,…

chemistry.chemical_classificationbiologySaccharomyces cerevisiaeMutantBiotinYarrowiaGeneral Medicinebiology.organism_classificationMicrobiologyAmino acidCell wallFungal Proteinschemistry.chemical_compoundBiotinchemistryBiochemistryAscomycotaCell WallProtein biosynthesisMolecular BiologySecretory pathwayResearch in microbiology
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Killer Toxins of Yeasts: Inhibitors of Fermentation and Their Adsorption.

2019

The killer toxin (KT 28), a glycoprotein of Saccharomyces cerevisiae strain 28, was almost completely adsorbed by bentonite, when applied at a concentration of 1 g per liter. No significant differences were found between several types of bentonite. Killer toxin KT 28 is similarly adsorbed by intact yeast cells or by a commercial preparation of yeast cell walls that has been recommended to prevent stuck fermentations. An investigation of the cell wall fractions revealed that the toxin KT 28 was mainly adsorbed by mannan, that removed the toxin completely. The alkali-soluble and the alkali-insoluble β-1,3- and β-1,6-D-glucans lowered the toxin concentration to one tenth of the original amount…

chemistry.chemical_classificationbiologyStrain (chemistry)ToxinSaccharomyces cerevisiaemedicine.disease_causebiology.organism_classificationMicrobiologyYeastMicrobiologyCell wallchemistryBiochemistrymedicineFermentationGlycoproteinFood ScienceMannanJournal of food protection
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Influence of Nitrogen Content on Grape Non-Saccharomyces Glycosidic Activities

2019

This study investigated the influence of nitrogen content on both β-glucosidase and β-xylosidase activities from non-Saccharomyces yeasts. Enzymatic activities were induced by the presence of xylan polysaccharides in the medium. Results show that optimizing β-glucosidase and β-xylosidase enzymatic activities can be determined not only by sugar or ethanol content or pH, but also by the concentration of N in the medium. This is the first work studying the influence of N content on glycolytic enzymes produced by non-Saccharomyces yeasts.

chemistry.chemical_classificationbiologychemistry.chemical_elementGlycosidic bond04 agricultural and veterinary sciencesHorticulturePolysaccharidebiology.organism_classificationXylanSaccharomycesNitrogen040501 horticultureEnzymechemistryEthanol contentFood science0405 other agricultural sciencesSugarFood ScienceAmerican Journal of Enology and Viticulture
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Über den Abbau von L-Äpfelsäure durch Hefen verschiedener Gattungen mit Malatenzym

1974

Summary (1) The aerobic assimilation of malic acid is not a character of certain yeast genera or species as was shown by testing more than 300 different strains. Single strains of the following-species were found to grow on malic acid as the only carbon source: Candida pulcherrima, C. utilis, C. mycoderma, Torulopsis famata, Pichia membranaefaciens, P. wickerhamii, Hansenula capsulata, Trigonopsis variabilis , and Zygosaccharomyces chevalieri . (2) During fermentation C. pulcherrima and T. famata decompose up to 40% and C. utilis up to 80% of the L-malic acid that is present in the medium. (3) L-Malic acid is decomposed to CO 2 and the corresponding amounts of ethanol or pyruvate by cell fr…

chemistry.chemical_classificationbiologyfungiMalic enzymefood and beveragesGeneral MedicineZygosaccharomycesbiology.organism_classificationMalate dehydrogenaseYeastchemistry.chemical_compoundchemistryBiochemistryOxidoreductaseFermentationMalic acidPichiaZentralblatt für Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite Naturwissenschaftliche Abteilung: Allgemeine, Landwirtschaftliche und Technische Mikrobiologie
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Impact of Starmerella bacillaris and Zygosaccharomyces bailii on ethanol reduction and Saccharomyces cerevisiae metabolism during mixed wine fermenta…

2021

AbstractThe bulk of grape juice fermentation is carried out by the yeast Saccharomyces cerevisiae, but non-Saccharomyces yeasts can modulate many sensorial aspects of the final products in ways not well understood. In this study, some of such non-conventional yeasts were screened as mixed starter cultures in a fermentation defined medium in both simultaneous and sequential inoculations. One strain of Starmerella bacillaris and another of Zygosaccharomyces bailii were chosen by their distinct phenotypic footprint and their ability to reduce ethanol levels at the end of fermentation, particularly during simultaneous vinification. S. bacillaris losses viability strongly at the end of mixed fer…

chemistry.chemical_compoundBiochemistrychemistrybiologyZygosaccharomyces bailiiSaccharomyces cerevisiaeCatabolite repressionGlycolysisFermentationMetabolismbiology.organism_classificationTrehaloseYeast
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