Search results for "Ethanolamine"

showing 10 items of 122 documents

One‐Pot Synthesis of Superparamagnetic CoO‐MCM‐41 Nanocomposites with Uniform and Highly Dispersed Magnetic Nanoclusters

2004

Superparamagnetic CoO-MCM-41 mesoporous nanocomposites, with variable cobalt amounts, in the form of well-dispersed CoO-like clusters, were prepared in a large compositional range by a one-step reproducible procedure employing co-hydrolysis and co-condensation of the inorganic precursors in a water/triethanolamine medium. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

NanocompositeNanoparticlechemistry.chemical_elementNanoclustersInorganic ChemistryMCM-41Chemical engineeringchemistryTriethanolaminePolymer chemistrymedicineMesoporous materialCobaltSuperparamagnetismmedicine.drugEuropean Journal of Inorganic Chemistry
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�ber adrenolytische Wirkungen von d,l,1-(4-oxy-phenyl)-1-oxy-2-n-butylamino-aethan

1950

PharmacologyChemistryPharmacology toxicologyEthanolaminesGeneral MedicineMedicinal chemistryNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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Hydrolytic action of phospholipase A2 in monolayers in the phase transition region: direct observation of enzyme domain formation using fluorescence …

1990

Phospholipase A2, a ubiquitous lipolytic enzyme highly active in the hydrolysis of organized phospholipid substrates, has been characterized optically in its action against a variety of phospholipid monolayers using fluorescence microscopy. By labeling the enzyme with a fluorescent marker and introducing it into the subphase of a Langmuir film balance, the hydrolysis of lipid monolayers in their liquid-solid phase transition region could be directly observed with the assistance of an epifluorescence microscope. Visual observation of hydrolysis of different phospholipid monolayers in the phase transition region in real-time could differentiate various mechanisms of hydrolytic action against …

Phase transition12-DipalmitoylphosphatidylcholineStereochemistryBiophysicsPhospholipidBiochemistryPhospholipases Achemistry.chemical_compoundPhospholipase A2Phase (matter)MonolayerEnzyme StabilityFluorescence microscopeLipid bilayer phase behaviorParticle SizePhospholipidsFluorescent DyesElapid VenomsPhospholipase ABinding SitesbiologyHydrolysisPhosphatidylethanolaminesCell BiologyImage EnhancementPhospholipases A2chemistryMicroscopy FluorescencePhospholipasesBiophysicsbiology.proteinlipids (amino acids peptides and proteins)DimyristoylphosphatidylcholineBiochimica et biophysica acta
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Lipid Composition Analysis Reveals Mechanisms of Ethanol Tolerance in the Model YeastSaccharomyces cerevisiae

2021

Saccharomyces cerevisiae is an important unicellular yeast species within the biotechnological and the food and beverage industries. A significant application of this species is the production of ethanol, where concentrations are limited by cellular toxicity, often at the level of the cell membrane. Here, we characterize 61 S. cerevisiae strains for ethanol tolerance and further analyze five representatives with various ethanol tolerances. The most tolerant strain, AJ4, was dominant in coculture at 0 and 10% ethanol. Unexpectedly, although it does not have the highest noninhibitory concentration or MIC, MY29 was the dominant strain in coculture at 6% ethanol, which may be linked to differen…

Phosphatidylethanolamine0303 health sciencesEthanolEcologybiology030306 microbiologyChemistrySaccharomyces cerevisiaeLipidomebiology.organism_classificationApplied Microbiology and BiotechnologySaccharomycesYeastCell membrane03 medical and health scienceschemistry.chemical_compoundmedicine.anatomical_structureMembranemedicineFood science030304 developmental biologyFood ScienceBiotechnologyApplied and Environmental Microbiology
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Validation of liposomal lipid composition by thin-layer chromatography.

2012

Liposomes of different sizes are frequently used model systems for cellular membranes. To mimic the cellular environment, these liposomes are often prepared from a mixture of different lipids in organic solution. The preparation involves, at some point, the transfer into aqueous solution. Thus, both the total amount of lipid and the relative amount of each lipid species might deviate from the original composition in the organic solvent. We used thin-layer chromatography combined with a lipid extraction step to check whether the liposomes in the final aqueous solution have the intended composition. This allows determination of the lipid composition not only for large unilamellar vesicles, bu…

PhosphatidylethanolamineLiposomeAqueous solutionChromatographyChemistryVesiclePharmaceutical ScienceLipidsThin-layer chromatographychemistry.chemical_compoundMembranePhosphatidylcholineLiposomeslipids (amino acids peptides and proteins)Chromatography Thin LayerSphingomyelinJournal of liposome research
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The Pandinus imperator haemolymph lipoprotein, an unusual phosphatidylserine carrying lipoprotein.

2009

The haemolymph lipoprotein of the scorpion, Pandinus imperator was isolated and characterised. Contrary to the lipoproteins of insects and the discoidal HDL-lipoproteins of a crayfish and polychaete, the Pandinus lipoprotein consists of three instead of two apoproteins (apoPiLp I = 230 kDa, apoPiLp II = 130 kDa and apoPiLp III = 120 kDa). The apolipoproteins are arranged in varying stoichiometries as judged by cross-linking experiments. In lipoprotein samples from individual animals, the two smaller subunits occurred in a 1:1 stoichiometry, while the relative amount of the 230 kDa peptide varied. The lipoprotein is a slightly heart-shaped HDL with a diameter of approximately 15 nm. It is pr…

PhosphatidylethanolamineMolecular massLipoproteinsBiological TransportPhosphatidylserinePhosphatidylserinesBiologybiology.organism_classificationBiochemistryMolecular WeightScorpionsPandinuschemistry.chemical_compoundHigh-density lipoproteinBiochemistrychemistryInsect SciencePhosphatidylcholineHemolymphHemolymphAnimalsInsect Proteinslipids (amino acids peptides and proteins)Molecular BiologyLipoproteinInsect biochemistry and molecular biology
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n-3 PUFAs modulate T-cell activation via protein kinase C-α and -ε and the NF-κB signaling pathway

2005

We elucidated the mechanisms of action of two n-3 PUFAs, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), in Jurkat T-cells. Both DHA and EPA were principally incorporated into phospholipids in the following order: phosphatidylcholine < phosphatidylethanolamine < phosphatidylinositol/phosphatidylserine. Furthermore, two isoforms of phospholipase A(2) (i.e., calcium-dependent and calcium-independent) were implicated in the release of DHA and EPA, respectively, during activation of these cells. The two fatty acids inhibited the phorbol 12-myristate 13-acetate (PMA)-induced plasma membrane translocation of protein kinase C (PKC)-alpha and -epsilon. The two n-3 PUFAs also inhibited t…

PhosphatidylethanolaminePhospholipase Amitogen-activated protein kinaseProtein Kinase C-epsilonQD415-436Cell BiologyPhosphatidylserineBiologyfatty acidsBiochemistryJurkat cellsCell biologychemistry.chemical_compoundEndocrinologychemistryBiochemistryDocosahexaenoic acidlipids (amino acids peptides and proteins)Phosphatidylinositolnuclear factor κBProtein kinase Cpolyunsaturated fatty acidsJournal of Lipid Research
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Epoxidation of benzo[a]pyrene-7,8-dihydrodiol by human CYP1A1 in reconstituted membranes. Effects of charge and nonbilayer phase propensity of the me…

2002

Human cytochrome P4501A1 (CYP1A1) is one of the key enzymes in the bioactivation of environmental pollutants such as benzo[a]pyrene (B[a]P) and other polycyclic aromatic hydrocarbons. To evaluate the effect of membrane properties and distinct phospholipids on the activity of human CYP1A1 purified insect cell-expressed human CYP1A1 and of human NADPH-P450 reductase were reconstituted into phospholipid vesicle membranes. Conversion rates of up to 36 pmol x min(-1) x pmol(-1) CYP1A1 of the enantiomeric promutagens (-)- and (+)-trans-7,8-dihydroxy-7,8-dihydro-B[a]P (7,8-diol) to the genotoxic diolepoxides were achieved. The highest rates were obtained when negatively charged lipids such as phos…

PhosphatidylethanolamineStereochemistryVesiclePhospholipidMembranes ArtificialPhosphatidylserineBiochemistryRecombinant ProteinsDihydroxydihydrobenzopyreneschemistry.chemical_compoundMembraneBiochemistrychemistryBenzo(a)pyrenepolycyclic compoundsCytochrome P-450 CYP1A1PyreneAnimalsEpoxy CompoundsHumansheterocyclic compoundsPhosphatidylinositolPhospholipidsEuropean journal of biochemistry
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Effect of Gibberellin on Mature Euonymus europaeus L. Seeds

1992

The release from dormancy of Euonymus europaeus L. embryos by a brief treatment with GA 3 has been studied. During 48 h incubation of dormant embryos in GA-free medium, phospholipid levels increased at first, then declined sharply over the last 6 h. When the embryos were placed in GA, medium during this 6 h period levels of total phospholipids as well as of phosphatidylethanolamine increased whilst phosphatidylinositol and phosphatidylcholine declined slightly

Phosphatidylethanolamineanimal structuresPhospholipidPlant ScienceBiologybiology.organism_classificationchemistry.chemical_compoundHorticulturechemistryGerminationPhosphatidylcholineembryonic structuresBotanyDormancyEuonymus europaeusGibberellinIncubationAnnals of Botany
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Synthesis of fluorinated first generation starburst molecules containing a triethanolamine core and 1,2,4-oxadiazoles

2006

Abstract 5-Pentafluorophenyl-1,2,4-oxadiazoles, differently substituted at C(3), have been synthesized and used to functionalize the aliphatic primary hydroxyl functionalities of triethanolamine, under mild conditions. UV–visible absorption and emission spectra are reported, for both tri- and difunctionalised molecules, showing their potential applications as light-emitters in optoelectronic devices.

Primary (chemistry)PL spectraChemistryPl spectraOrganic Chemistry124-oxadiazolestarburst moleculeBiochemistryFirst generationfluoroarylationInorganic ChemistryTriethanolaminePolymer chemistrymedicineEnvironmental ChemistryMoleculeEmission spectrumPhysical and Theoretical ChemistryAbsorption (chemistry)medicine.drug
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