Search results for "Malates"

showing 10 items of 30 documents

Electrochemical Characterization of Polyelectrolyte/Gold Nanoparticle Multilayers Self-Assembled on Gold Electrodes

2006

Polyelectrolyte/gold nanoparticle multilayers composed of poly(l-lysine) (pLys) and mercaptosuccinic acid (MSA) stabilized gold nanoparticles (Au NPs) were built up using the electrostatic layer-by-layer self-assembly technique upon a gold electrode modified with a first layer of MSA. The assemblies were characterized using UV-vis absorption spectroscopy, cyclic and square-wave voltammetry, electrochemical impedance spectroscopy, and atomic force microscopy. Charge transport through the multilayer was studied experimentally as well as theoretically by using two different redox pairs [Fe(CN)(6)](3-/4-) and [Ru(NH(3))(6)](3+/2+). This paper reports a large sensitivity to the charge of the out…

Materials sciencePolymersSurface PropertiesStatic ElectricityAnalytical chemistryMetal NanoparticlesNanoparticleElectrochemistryRedoxIonElectrolytesElectron transferElectrochemistryMaterials ChemistryPolylysineParticle SizePhysical and Theoretical ChemistryElectrodesThiomalatesMolecular StructurePolyelectrolyteSurfaces Coatings and FilmsChemical sciencesElectrodeGoldElectric currentThe Journal of Physical Chemistry B
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Technological properties of Oenococcus oeni strains isolated from typical southern Italian wines.

2010

Aims:  To isolate indigenous Oenococcus oeni strains suitable as starters for malolactic fermentation (MLF), using a reliable polyphasic approach. Methods and Results: Oenococcus oeni strains were isolated from Nero di Troia wines undergoing spontaneous MLF. Samples were taken at the end of alcoholic fermentation and during MLF. Wine samples were diluted in a sterile physiological solution and plated on MRS and on modified FT80. Identification of O. oeni strains was performed by a polymerase chain reaction (PCR) experiment using strain-specific primers. Strains were further grouped using a multiplex RAPD-PCR analysis. Then, six strains were inoculated in two wine-like media with two differe…

OrganolepticMalatesmalic acidregional winesWineBiologyEthanol fermentationApplied Microbiology and BiotechnologyPolymerase Chain ReactionMicrobiologychemistry.chemical_compoundStarterStress PhysiologicalMalolactic fermentationSulfitesFood scienceLactic Acidmalolactic starterOenococcusOenococcus oeniWineEthanolLo18food and beveragesHydrogen-Ion Concentrationbiology.organism_classificationRandom Amplified Polymorphic DNA TechniquechemistryFermentationFermentationMalic acidOenococcus oeniLetters in applied microbiology
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Multispectral fluorescence sensitivity to acidic and polyphenolic changes in Chardonnay wines – The case study of malolactic fermentation

2022

International audience; In this study, stationary and time-resolvedfluorescence signatures, were statistically and chemometrically analyzed among three typologies of Chardonnay wines (A, B and C) with the objectives to evaluate their sensitivity to acidic and polyphenolic changes. For that purpose, a dataset was built using Excitation Emission Matrices of fluorescence (N = 103) decomposed by a Parallel Factor Analysis (PARAFAC), andfluorescence decays (N = 22), mathematically fitted, using the conventional exponential modeling and the phasor plot representation. Wine PARAFAC component C4 coupledwith its phasor plot g and s values enable the description of malolactic fermentation (MLF) occur…

PARAFAC componentsMultispectral imageMalatesWine010402 general chemistry01 natural sciencesFluorescenceAnalytical Chemistrychemistry.chemical_compoundFluorescence lifetimeOrganic acidsMalolactic fermentationPhenol[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyWineExcitation emission matrixQuenching (fluorescence)ChromatographyChemistryMalolactic fermentation010401 analytical chemistryPhasor plotTraceabilityGeneral MedicineFluorescence0104 chemical sciencesPolyphenolFermentation[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood ScienceFood Chemistry
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Influence of carboxylic acids on the stereospecific nicotinamide adenine dinucleotide-dependent and nicotinamide adenine dinucleotide-independent lac…

1971

Leuconostoc mesenteroides increased its lactic acid production from glucose threefold when malic acid was added to the culture. This increase resulted also in a reduction of the ratio of d -lactic acid to l -lactic acid (31.5 to 1.23). Addition of malic acid increased 6.5-fold the specific activity of nicotinamide adenine dinucleotide (NAD)-linked l -lactate dehydrogenase and increased 3.2-fold that of NAD-linked d -lactate dehydrogenase. The Michaelis constant ( K m ) for NAD of the NAD-linked l -lactate dehydrogenase increased with the addition of malate, but no change was observed in the K m values for the respective d -enzyme. The effect of carboxylic acids on the NAD-linked l -lactate…

Physiology and MetabolismCarboxylic AcidsMalatesDehydrogenaseNicotinamide adenine dinucleotideBiologyMicrobiologyMalate dehydrogenasechemistry.chemical_compoundMolecular BiologyCell-Free SystemL-Lactate DehydrogenaseStereoisomerismElectrophoresis DiscNADMolecular biologyStimulation ChemicalLactic acidCulture MediaCitric acid cycleGlucosechemistryBiochemistryLactatesNAD+ kinaseBranched-chain alpha-keto acid dehydrogenase complexOxoglutarate dehydrogenase complexAcidsLeuconostocJournal of bacteriology
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Regulation of aerobic and anaerobic D-malate metabolism of Escherichia coli by the LysR-type regulator DmlR (YeaT).

2010

ABSTRACT Escherichia coli K-12 is able to grow under aerobic conditions on d -malate using DctA for d -malate uptake and the d -malate dehydrogenase DmlA (formerly YeaU) for converting d -malate to pyruvate. Induction of dmlA encoding DmlA required an intact dmlR (formerly yeaT ) gene, which encodes DmlR, a LysR-type transcriptional regulator. Induction of dmlA by DmlR required the presence of d -malate or l - or meso -tartrate, but only d -malate supported aerobic growth. The regulator of general C 4 -dicarboxylate metabolism (DcuS-DcuR two-component system) had some effect on dmlA expression. The anaerobic l -tartrate regulator TtdR or the oxygen sensors ArcB-ArcA and FNR did not have a m…

Physiology and MetabolismRegulatorMalatesDehydrogenasemedicine.disease_causeMicrobiologyMalate dehydrogenaseMicrobiologyMalate DehydrogenasemedicineAnaerobiosisMolecular BiologyEscherichia coliTartratesChromatography High Pressure LiquidbiologyEscherichia coli K12Escherichia coli ProteinsMetabolismGene Expression Regulation Bacterialbiology.organism_classificationbeta-GalactosidaseAerobiosisBiochemistryMutationFermentationAnaerobic exerciseBacteriaJournal of bacteriology
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Effects of yeast proteolytic activity on Oenococcus oeni and malolactic fermentation

2006

International audience; Alcoholic fermentation of synthetic must was performed using either Saccharomyces cerevisiae or a mutant Delta pep4, which is deleted for the proteinase A gene. Fermentation with the mutant Delta pep4 resulted in 61% lower levels of free amino acids, and in 62% lower peptide concentrations at the end of alcoholic fermentation than in the control. Qualitative differences in amino acid composition were observed. Changes observed in amino acids in peptides were mainly quantitative. After alcoholic fermentation each medium was inoculated with Oenococcus oeni. Malolactic fermentation in the medium with the Delta pep4 strain took 10 days longer than the control. This diffe…

Saccharomyces cerevisiae ProteinsNitrogenMalatesWineSaccharomyces cerevisiaeEthanol fermentationMicrobiology03 medical and health sciencesMalate DehydrogenaseProteinase APEP4EndopeptidasesGeneticsMalolactic fermentationLactic acid bacteriaNitrogen metabolismAmino AcidsMolecular Biology030304 developmental biologyOenococcus oenichemistry.chemical_classification0303 health sciencesbiology030306 microbiologyProteolytic enzymesfood and beveragesFree amino nitrogenbiology.organism_classificationYeastYeastAmino acidGram-Positive Cocci[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryBiochemistryFermentationPeptideFermentation
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Effectiveness of salivary stimulation using xylitol-malic acid tablets as coadjuvant treatment in patients with gastro-oesophageal reflux disease : e…

2020

[Background] Besides dental erosion syndrome, other oral syndromes could benefit from the stimulation of sali-vary secretion, in patients with gastro-oesophageal reflux disease (GORD). Our aims is evaluate the improvement of oral extra-oesophageal manifestations in patients with GORD using xylitol–malic acid tablets to stimulate salivary secretion.

Salivamedicine.medical_specialtyErythemaMalatesGastroenterology03 medical and health sciences0302 clinical medicineGastro-Internal medicinemedicineotorhinolaryngologic diseasesHumansSalivaGeneral DentistryXylitolOral Medicine and Pathologybusiness.industryResearchdigestive oral and skin physiologyRefluxHeartburnTooth wearfood and beverages030206 dentistryDry mouth:CIENCIAS MÉDICAS [UNESCO]digestive system diseasesClinical trialstomatognathic diseasesOtorhinolaryngologyGastroesophageal refluxErosionRegurgitation (digestion)UNESCO::CIENCIAS MÉDICASGastroesophageal RefluxQuality of LifeSurgerymedicine.symptombusinessTablets
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Genetic organization of the mle locus and identification of a mleR-like gene from Leuconostoc oenos

1996

Characterization of the mle locus harboring the malolactic enzyme gene mleA and malate permease gene mleP from Leuconostoc oenos was completed in this study by mRNA analysis. Northern (RNA) blot experiments revealed a 2.6-kb transcript, suggesting an operon structure harboring mleA and mleP genes. Primer extension analysis showed that the mle operon has a single transcription start site located 17 nucleotides upstream of the ATG translation start site for the mleA gene. We found sequences, TTGACT and TATGAT (which are separated by 18 bp), that are closely related to the gram-positive and Escherichia coli consensus promoter sequences. Upstream of the mleA gene, an 894-bp open reading frame t…

Sequence analysisOperonMolecular Sequence DataLeuconostoc oenosMalatesLocus (genetics)BiologyApplied Microbiology and BiotechnologyOpen Reading FramesOperon[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyAmino Acid SequenceLactic AcidGenemalolactic enzymeGeneticsRegulation of gene expressionmalateBase SequenceEcologyLactococcus lactisNucleic acid sequenceChromosome MappingregulationBlotting Northernbiology.organism_classificationMolecular biologyOpen reading frameGenes BacterialLeuconostocResearch ArticleFood ScienceBiotechnologyApplied and Environmental Microbiology
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Absence of malolactic activity is a characteristic of H+-ATPase-deficient mutants of the lactic acid bacterium Oenococcus oeni.

2003

ABSTRACT The lack of malolactic activity in H + -ATPase-deficient mutants of Oenococcus oeni selected previously was analyzed at the molecular level. Western blot experiments revealed a spot at 60 kDa corresponding to the malolactic enzyme only in the parental strain. Moreover, the mleA transcript encoding the malolactic enzyme was not detected by reverse transcription (RT)-PCR analysis of mutants. These results suggest that the malolactic operon was not transcribed in ATPase-deficient mutants. The mleR gene encoding a LysR-type regulatory protein which should be involved in expression of the malolactic genes was described previously for O. oeni . Results obtained in this study show that th…

Transcription GeneticOperonMutantImmunoblottingMalatesApplied Microbiology and Biotechnologychemistry.chemical_compoundMalate DehydrogenaseMalolactic fermentationLactic AcidGeneOenococcus oeniEcologybiologyReverse Transcriptase Polymerase Chain ReactionLactococcus lactisGene Expression Regulation Bacterialbiology.organism_classificationPhysiology and BiotechnologyMolecular biologyLactic acidGram-Positive CocciLactococcus lactisProton-Translocating ATPaseschemistryBiochemistryLeuconostoc mesenteroidesMutationGene DeletionLeuconostocFood ScienceBiotechnologyApplied and environmental microbiology
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Saccharomyces cerevisiae-Oenococcus oeni interactions in wine: current knowledge and perspectives.

2003

Winemaking can be summarized as the biotransformation of must into wine, which is performed principally by Saccharomyces cerevisiae strains during the primary or alcoholic fermentation. A secondary fermentation, the so-called malolactic fermentation (MLF) is a biodeacidification that is often encouraged, since it improves wine stability and quality. Malolactic fermentation usually occurs either spontaneously or after inoculation with selected bacteria after alcoholic fermentation. The main organism responsible for MLF, the lactic acid bacterium Oenococcus oeni, develops in physicochemically harsh conditions, which may lead to MLF failure. Furthermore, yeast that ferment must before or toget…

WinebiologySaccharomyces cerevisiaePopulation DynamicsMalatesfood and beveragesWineGeneral MedicineSaccharomyces cerevisiaeEthanol fermentationbiology.organism_classificationMicrobiologyYeastGram-Positive CocciBiochemistryFermentationMalolactic fermentationFood MicrobiologyFermentationLactic AcidLeuconostocFood ScienceWinemakingOenococcus oeniInternational journal of food microbiology
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