Search results for "Hydroxyacetone"

showing 10 items of 10 documents

Organosulfates in atmospheric aerosol: synthesis and quantitative analysis of pm<sub>2.5</sub> from xi'an, northwestern c…

2018

Abstract. The sources, formation mechanism and amount of organosulfates (OS) in atmospheric aerosol are not yet well understood, partly due to the lack of authentic standards for quantification. In this study, we report an improved robust procedure for the synthesis of organosulfates with different functional groups. Nine authentic organosulfate standards were synthesized and four standards (benzyl sulfate, phenyl sulfate, glycolic acid sulfate, and hydroxyacetone sulfate) were used to quantify their ambient concentrations. The authentic standards and ambient aerosol samples were analyzed using an optimized ultra performance liquid chromatography–electrospray ionization-tandem mass spectrom…

Atmospheric Scienceparticulate organosulfates010504 meteorology & atmospheric sciences010501 environmental sciences01 natural scienceschemistry.chemical_compoundambient aerosolhaze eventsSulfateGlycolic acid0105 earth and related environmental sciencesDetection limitTotal organic carbondicarboxylic-acidsHydroxyacetonemass-spectrometryAerosolaromatic organosulfateschemistryEnvironmental chemistrychemical-compositionarctic aerosolsisopreneQuantitative analysis (chemistry)secondary organic aerosolOrganosulfate
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On the Mechanistic Origins of the pH-Dependency in Au-Catalyzed Glycerol Electro-Oxidation: Insight from First Principles Calculations

2021

Electrocatalytic oxidation of glycerol (EOG) is an attractive approach to convert surplus glycerol to value-added products. Experiments have shown that EOG activity and selectivity depend on the electrocatalyst, but also on the electrode potential, the pH, and the electrolyte. For broadly employed gold (Au) electrocatalysts, experiments have demonstrated high EOG activity under alkaline conditions with glyceric acid as a primary product, whereas under acidic and neutral conditions Au is rather inactive producing only small amounts of dihydroxyacetone. In the present computational work, we have performed an extensive mechanistic study to understand the pH- and potential-dependency of Au-cata…

Glyceric acidchemistry.chemical_compoundReaction mechanismchemistryInorganic chemistryHydroxideDihydroxyacetoneSelectivityElectrocatalystRedoxElectrode potential
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Enzymes for the NADPH-dependent reduction of dihydroxyacetone and D-glyceraldehyde and L-glyceraldehyde in the mould Hypocrea jecorina

2006

The mould Hypocrea jecorina (Trichoderma reesei) has two genes coding for enzymes with high similarity to the NADP-dependent glycerol dehydrogenase. These genes, called gld1 and gld2, were cloned and expressed in a heterologous host. The encoded proteins were purified and their kinetic properties characterized. GLD1 catalyses the conversion of d-glyceraldehyde and l-glyceraldehyde to glycerol, whereas GLD2 catalyses the conversion of dihydroxyacetone to glycerol. Both enzymes are specific for NADPH as a cofactor. The properties of GLD2 are similar to those of the previously described NADP-dependent glycerol-2- dehydrogenases (EC 1.1.1.156) purified from different mould species. It is a reve…

HypocreaDihydroxyacetoneGlyceraldehydeBiochemistrychemistry.chemical_compoundHypocreaGlyceraldehydeGlycerolCloning MolecularMolecular BiologyTrichoderma reeseichemistry.chemical_classificationbiologyGlycerol dehydrogenaseGlyceraldehyde-3-Phosphate DehydrogenasesHypocrea jecorinaCell Biologybiology.organism_classificationRecombinant ProteinsL-glyceraldehydeEnzymeGlycerol-3-phosphate dehydrogenasechemistryBiochemistryDihydroxyacetoneGlycerol dehydrogenaseNADP-specific glycerol dehydrogenaseNADPSugar Alcohol DehydrogenasesFEBS Journal
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A Combined Theoretical and Experimental Approach for Platinum Catalyzed 1,2-Propanediol Aqueous Phase Reforming

2017

Decomposition pathways of 1,2-propanediol (1,2-PDO) on platinum were investigated by means of experiments and quantum-mechanical calculations. Different reaction paths on a Pt(111) model surface were computationally screened. Gas and liquid phase products distribution for aqueous phase reforming of 1,2-PDO solutions was experimentally analyzed. A mechanistic approach was used to trace the preferred paths according to calculated activation barriers of the elementary steps; in this way, the presence or absence of some hypothesized intermediates in the experiments was computationally rationalized. Hydroxyacetone was demonstrated to be among the most favored decomposition products. The competit…

Inorganic chemistrySurfaces Coatings and Filmchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisPropanediolchemistry.chemical_compoundComputational chemistryPhysical and Theoretical ChemistryCarbon chainElectronic Optical and Magnetic MaterialHydroxyacetoneDecarbonylationAqueous two-phase system021001 nanoscience & nanotechnologyDecomposition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnergy (all)General Energychemistry0210 nano-technologyPlatinumThe Journal of Physical Chemistry C
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Copurification of dihydroxyacetone-phosphate acyl-transferase and other peroxisomal proteins from liver of fenofibrate-treated rats.

1997

Dihydroxyacetone-phosphate acyl-transferase (DHAP-AT), a peroxisomal membrane-bound enzyme that catalyzes the first step of ether-glycerolipid synthesis, was purified from liver of rats treated with fenofibrate, a peroxisome proliferator. The protocol first included isolation of peroxisomes, their purification through a discontinuous gradient and solubilization of membranes in CHAPS. DHAP-AT was further purified by four chromatographic steps, namely low-pressure size-exclusion, cation-exchange, hydroxylapatite and chromatofocusing. The chromatofocusing step led to a 4000-fold increase in the specific activity of DHAP-AT with respect to the liver homogenate with a yield of about 0.2%. Trypsi…

MaleMolecular Sequence DataBiochemistryMicrobodiesCopurificationchemistry.chemical_compoundFenofibrateProtein purificationAnimalsAmino Acid SequenceRats WistarPeptide sequenceDihydroxyacetone phosphatechemistry.chemical_classificationOxidase testChromatofocusingMembrane ProteinsGeneral MedicinePeroxisomeMolecular biologyRatsEnzymechemistryBiochemistryLiverSolubilitySequence AnalysisAcyltransferasesBiochimie
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In situ hybridization of dihydroxyacetone phosphate acyltransferase, the regulating enzyme involved in plasmalogen biosynthesis

2005

International audience; In situ hybridization can be carried out using different methods. The experimenter has to choose various parameters: the type of tissue fixation, the time of incubation, and the duration of the exposure time. All these parameters are determinant for the sensitivity and the resolution of this technique. This publication of technical aspects described different experiments performed for in situ hybridization on liver tissue. We may conclude on the parameters to optimize each step of the hybridization procedure. Moreover, this technique could be transposed to the brain and applied to little structures with a light expression of DHAP-AT.

MaleTime FactorsTissue FixationLIVERPlasmalogenIn situ hybridizationIn Vitro TechniquesBiologySensitivity and Specificity03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compound0302 clinical medicineBiosynthesisLiver tissueAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyRNA MessengerRats WistarBRAINMolecular Biology030304 developmental biologyDihydroxyacetone phosphateIN SITU HYBRIDIZATIONchemistry.chemical_classification0303 health sciencesBase SequenceReverse Transcriptase Polymerase Chain ReactionRatsMolecular hybridizationEnzymechemistryBiochemistryDIHYDROXYACETONE PHOSPHATE ACYLTRANSFERASEAcyltransferaseAcyltransferases030217 neurology & neurosurgeryPLASMALOGENSubcellular Fractions
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Die α-Glycerophosphat-Oxydation des Heuschreckenbrustmuskels (Locusta migratoria)

1956

The conditions were studied for the glycerophosphate oxidation by homogenate from locust flight muscle, and the O2-consumption was measured. Maximal oxidation rates were found with 0.087m glycerophosphate, 8 × 10−6m cytochromec, 7 × 10−6m DPN and pH 7.5. The production of dihydroxyacetone phosphate is followed by further oxidation steps, as could be shown by estimation of the different fractions of acid-soluble phosphate. Comparative studies were made on different insects and vertebrates. The rate of succinate oxidation by insect muscle was found to be ten times higher than that of vertebrate muscle. The relation of glycerophosphate oxidation to succinate oxidation is quite different in ins…

PharmacologyMuscle metabolismAlpha-glycerophosphatebiologymedia_common.quotation_subjectPectoral muscleCell BiologyInsectCarbohydratebiology.organism_classificationPhosphateCellular and Molecular Neurosciencechemistry.chemical_compoundBiochemistrychemistryMolecular MedicineMolecular BiologyLocustDihydroxyacetone phosphatemedia_commonExperientia
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Production of ethyl lactate by activated carbon-supported Sn and Zn oxide catalysts utilizing lignocellulosic side streams

2021

Abstract In this study, activated carbon-supported Sn and Zn oxide catalysts were prepared from hydrolysis lignin and used for the conversion of model solutions of trioses, hexoses, and lignocellulosic biomass hydrolysates to ethyl lactate. Both catalysts, SnO2@AC and ZnO@AC, were able to produce ethyl lactate in high yields. SnO2@AC was a more active and selective catalyst in triose (dihydroxyacetone) conversion, providing 99% yield to ethyl lactate. ZnO@AC, by contrast, was more selective in glucose and hydrolysate conversion, with a yield of 60% and 85%, respectively. The ethyl lactate yields were significantly higher than those from the optimized model solution experiments when using Zn…

Process Chemistry and TechnologyDihydroxyacetoneLignocellulosic biomassCatalysisHydrolysateCatalysischemistry.chemical_compoundHydrolysischemistryYield (chemistry)medicineOrganic chemistryEthyl lactateActivated carbonmedicine.drugApplied Catalysis A: General
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In situ ATR-IR studies in aqueous phase reforming of hydroxyacetone on Pt/ZrO2 and Pt/AlO(OH) catalysts: The role of aldol condensation

2018

Abstract In situ Attenuated Total Reflection Infrared (ATR-IR) spectroscopy was used to study Aqueous Phase Reforming of hydroxyacetone on Pt/AlO(OH) and Pt/ZrO2 catalysts at 230 °C/ 30 bar. Formation of strongly adsorbed aldol condensation products was observed on the surface of Pt/ZrO2 and ZrO2 in contrast to Pt/AlO(OH) and AlO(OH). Peak assignments were supported by DFT calculations of the IR spectra of the condensation products in vacuum and in the presence of water. Aldol condensation of hydroxyacetone leading to compounds with high molecular weight with unsaturated bonds was suggested as a first step in coke formation. Carbonaceous deposits on the surface of the ZrO2 support are oxyge…

UT-Hybrid-DInfrared spectroscopyAqueous phase reforming02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesCatalysisCatalysiIn situLiquid phaseCatalysischemistry.chemical_compoundAdsorptionGeneral Environmental ScienceATR-IR spectroscopy2300Process Chemistry and TechnologyHydroxyacetoneCondensationAqueous two-phase system021001 nanoscience & nanotechnology0104 chemical sciencesAldol condensationchemistryAttenuated total reflectionAldol condensation0210 nano-technologyApplied Catalysis B: Environmental
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Imidazol-4-carbinole aus Iminoestern und Dihydroxyaceton. 2. Mitt. über Imidazolsynthesen mit flüssigem Ammoniak

1974

Imidazol-4-carbinole 3 mit funktionellen Gruppen am C-Atom 2 lassen sich aus Iminoestern 1 und Dihydroxyaceton (2) in flussigem Ammoniak unter Druck darstellen. Imidazole-4-carbinols from Iminoesters and Dihydroxyacetone Imidazole-4-carbinols 3 with functional groups at C-atom 2 are obtained from iminoesters 1 and dihydroxyacetone (2) in liquid ammonia under pressure.

chemistry.chemical_compoundChemistryDrug DiscoveryLiquid ammoniaPharmaceutical ScienceDihydroxyacetoneMedicinal chemistryArchiv der Pharmazie
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