Search results for "Dihydroxyacetone"

showing 7 items of 7 documents

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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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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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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