Search results for "trehalose"

showing 10 items of 114 documents

Specific stress-induced storage of trehalose, glycerol and D-arabitol in response to oxidative and osmotic stress in Candida albicans.

2012

Candida albicans exponential yeast cells are able to face environmental challenges by mounting a rapid and efficient "general stress response". Here we show that one of the main components of this response consists of the intracellular protective accumulation of the non-reducing disaccharide trehalose and two polyols, glycerol and D-arabitol, an accumulation that occurs in a stress-specific dependent manner. Thus, oxidative exposures promoted a marked increase in both trehalose and D-arabitol in the wild type strain, RM-100, whereas the glycerol content remained virtually unaffected with respect to basal levels. In contrast, osmotic challenges induced the significant storage of glycerol acc…

GlycerolOsmotic shockBiophysicsOxidative phosphorylationBiologyBiochemistrychemistry.chemical_compoundSugar AlcoholsOsmotic PressureCandida albicansGlycerolCandida albicansMolecular BiologyTrehaloseCell Biologybiology.organism_classificationTrehaloseYeastOxidative StresschemistryBiochemistryMitogen-activated protein kinasebiology.proteinMitogen-Activated Protein KinasesOxidation-ReductionIntracellularBiochemical and biophysical research communications
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GFP-mut2 Proteins in Trehalose-Water Matrixes: Spatially Heterogeneous Protein-Water-Sugar Structures

2007

We report investigations on the properties of nanoenvironments around single-GFP-mut2 proteins in trehalose-water matrixes. Single-GFPmut2 molecules embedded in thin trehalose-water films were characterized in terms of their fluorescence brightness, bleaching dynamics, excited state lifetime, and fluorescence polarization. For each property, sets of approximately 100-150 single molecules have been investigated as a function of trehalose content and hydration. Three distinct and interconverting families of proteins have been found which differ widely in terms of bleaching dynamics, brightness, and fluorescence polarization, whose relative populations sizably depend on sample hydration. The r…

Green Fluorescent ProteinsBiophysicsAnalytical chemistryCarbohydratesMolecular ConformationPhase TransitionColloidchemistry.chemical_compoundMoleculeColloidsSupercoolingthrealosesingle molecule fluorescenceChemistryTrehaloseWaterSingle-molecule experimentFluorescenceTrehaloseSolutionsModels ChemicalChemical physicsCell BiophysicsGFPmut2Excited statelifetimesFluorescence anisotropy
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Role of Solvent on Protein-Matrix Coupling in MbCO Embedded in Water-Saccharide Systems: A Fourier Transform Infrared Spectroscopy Study

2006

AbstractEmbedding protein in sugar systems of low water content enables one to investigate the protein dynamic-structure function in matrixes whose rigidity is modulated by varying the content of residual water. Accordingly, studying the dynamics and structure thermal evolution of a protein in sugar systems of different hydration constitutes a tool for disentangling solvent rigidity from temperature effects. Furthermore, studies performed using different sugars may give information on how the detailed composition of the surrounding solvent affects the internal protein dynamics and structural evolution. In this work, we compare Fourier transform infrared spectroscopy measurements (300–20K) o…

Hot TemperatureProtein ConformationBiophysicsLactosechemistry.chemical_compoundProtein structureRaffinosePolysaccharidesSpectroscopy Fourier Transform InfraredCarbohydrate ConformationFourier transform infrared spectroscopySugarSpectroscopyMaltosechemistry.chemical_classificationMyoglobinBiomoleculeProtein dynamicsTrehaloseWaterProteinsTrehaloseSolventCrystallographyGlucosechemistryChemical physicsSolventsMuramidaseBiophysical Journal
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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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Thermal evolution of the CO stretching band in carboxy-myoglobin in the light of neutron scattering and molecular dynamics simulations

2008

Abstract As it is well known, the thermal behaviour of the CO stretching band in MbCO reflects the interconversion among protein’s taxonomic and lower tier substates. We compare here FTIR data on the thermal behaviour of the CO stretching band in MbCO embedded in non-liquid, water–trehalose matrixes, and neutron scattering data on dry and hydrated proteins and nucleic acids. The comparison, also in the light of simulative data, gives relevant information on the relationship between the mean square displacements of hydrogen atoms and the heme pocket thermal rearrangements in MbCO, as experienced by the bound CO, in the temperature region 100–200 K, and at higher temperature when large scale …

HydrogenChemistryProtein dynamicsAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementmyoglobin trehaloseNeutron scatteringtrehalose neutron simulationMolecular dynamicschemistry.chemical_compoundMyoglobinChemical physicsThermalPhysical and Theoretical ChemistryFourier transform infrared spectroscopyRelevant informationChemical Physics
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FTIR and SAXS study on MBCO-saccharide amorphous systems: protein-matrix reciprocal effects

2010

IRSAXScouplingsaccharidestrehaloseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Settore CHIM/02 - Chimica Fisica
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Effects of gamma-irradiation on trehalose–hydroxyethylcellulose microspheres loaded with vancomycin

2003

Ionizing radiation can be used as a drug sterilization technique, provided that the drug itself is not modified and that no toxic products are produced; moreover, if the irradiated product is a drug delivery system, the drug release characteristics must not be significantly altered by radiation. The aim of this work was to study the effects of sterilization by ionizing radiation on hydroxyethylcellulose/trehalose spherical micromatrices, containing the antibiotic vancomycin. Our experimental results showed that gamma-rays did not alter the chromophore groups of vancomycin (UV measurements), and did not modify the kinetic behavior of drug release from microspheres. Moreover, no significant c…

Ionizing radiationMicrosphereDrugmedia_common.quotation_subjectDrug delivery systemGamma-irradiationPharmaceutical Sciencelaw.inventionIonizing radiationchemistry.chemical_compoundVancomycinlawmedicineIrradiationCelluloseElectron paramagnetic resonanceESRmedia_commonRadiochemistryTrehaloseQuality controlGeneral MedicineSterilization (microbiology)Drug sterilizationTrehaloseMicrosphereschemistryGamma RaysDrug deliveryVancomycinBiotechnologymedicine.drugEuropean Journal of Pharmaceutics and Biopharmaceutics
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Trehalose interacts with phospholipid polar heads in Langmuir monolayers

2000

Surface pressure−area isotherms, surface potential-area isotherms and fluorescence microscopy were employed to study the behavior of phospholipid monolayers at the air/water interface when trehalose was added to the aqueous subphase. In the presence of this sugar, the critical area corresponding to the onset of surface potential increases, indicating that trehalose is participating in the network of hydrogen bonds between the phospholipid polar heads. In addition, it causes an expansion of the isotherm, hindering the formation of the liquid-condensed phase. The collapse area is significantly increased, indicating that trehalose takes part in the monolayer structure without being expelled ev…

LangmuirAqueous solutionHydrogen bondPhospholipidSurfaces and InterfacesCondensed Matter PhysicsTrehalosechemistry.chemical_compoundCrystallographychemistryPhase (matter)MonolayerElectrochemistryMoleculeGeneral Materials ScienceSpectroscopy
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Reply to Comment on “Trehalose Interacts with Phospholipid Polar Heads in Langmuir Monolayers”

2002

LangmuirChemistryPhospholipidSurfaces and InterfacesCondensed Matter PhysicsTrehalosechemistry.chemical_compoundBiochemistryMonolayerElectrochemistryBiophysicsPolarGeneral Materials ScienceSpectroscopyLangmuir
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Light-Induced Protein-Matrix Uncoupling and Protein Relaxation in Dry Samples of Trehalose-Coated MbCO at Room Temperature

2005

In humid samples of trehalose-coated carboxy-myoglobin (MbCO), thermally driven conformational relaxation takes place after photodissociation of the carbon monoxide (CO) molecule at room temperature. In such samples, because of the extreme viscosity of the external matrix, photodissociated CO cannot diffuse out of the protein and explores the whole (proximal and distal side) heme pocket, experiencing averaged protein heme pocket structures, as a result of the presence of Brownian motions. At variance, in very dry samples, a lower portion of the photodissociated CO diffuses from the distal to the proximal heme pocket side probing in nonaveraged structures. We revisit here the flash photolysi…

LightProtein ConformationBiophysicsBiochemistrychemistry.chemical_compoundProtein structureAnimalsHumansHemePhotolysisMyoglobinHydrogen bondLasersPhotodissociationRelaxation (NMR)TrehaloseHydrogen BondingCell BiologyGeneral MedicineProtein Structure TertiaryCrystallographychemistryMyoglobinFlash photolysisProtein BindingCarbon monoxideCell Biochemistry and Biophysics
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