Search results for "substrate"

showing 10 items of 1018 documents

ChemInform Abstract: Source of Selectivity in Oxidative Cross-Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3-Hexafluoropropan-2-ol.

2016

Abstract Solvents such as 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) with a high capacity for donating hydrogen bonds generate solvates that enter into selective cross-coupling reactions of aryls upon oxidation. When electric current is employed for oxidation, reagent effects can be excluded and a decoupling of nucleophilicity from oxidation potential can be achieved. The addition of water or methanol to the electrolyte allows a shift of oxidation potentials in a specific range, creating suitable systems for selective anodic cross-coupling reactions. The shift in the redox potentials depends on the substitution pattern of the substrate employed. The concept has been expanded from arene-phenol…

NucleophileChemistryReagentSubstrate (chemistry)Oxidative coupling of methaneGeneral MedicineElectrolyteSolvent effectsSelectivityPhotochemistryRedoxChemInform
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Influence of cyclopropene fatty acids (Baobab seed oil) feeding on the in vitro Δ9 desaturation of stearic acid in rat liver microsomes

1993

Abstract Δ9 desaturation of [1−14C] stearic acid to oleic acid was studied in liver microsomes of rats fed either fresh Baobab seed oil, containing cyclopropene fatty acids (malvalic acid and sterculic acids), or heated Baobab oil, containing only minor amounts of these acids. This was compared with rats fed a control oil mixture or a fat-free diet. Up to 50 nmol of substrate, Δ9 desaturation rate was the same in rats fed the three fat diets. From 50 to 150 nmol, the desaturation rates were practically constant in rats fed fresh Baobab seed oil. It increased in heated oil-fed rats at the same rate as in the control group, but more slowly than in the fat-free diet group. Fatty acid compositi…

Nutrition and DieteticsEndocrinology Diabetes and MetabolismLinoleic acidMalvalic acidClinical BiochemistrySubstrate (chemistry)MetabolismBiologyBiochemistrychemistry.chemical_compoundOleic acidBiochemistrychemistryMicrosomeArachidonic acidStearic acidFood scienceMolecular BiologyThe Journal of Nutritional Biochemistry
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Analytical, thermodynamical and kinetic characteristics of photoluminescence immunosensor for the determination of Ochratoxin A

2017

Ochratoxin A (OTA) is one of the most widespread and dangerous food contaminants. Therefore, rapid, label-free and precise detection of low OTA concentrations requires novel sensing elements with advanced bio-analytical properties. In the present paper we report photoluminescence (PL) based immunosensor for the detection of OTA. During the development of immunosensor photoluminescent ZnO nanorods (ZnO-NRs) were deposited on glass substrate. Then the ZnO-NRs were silanized and covalently modified by Protein-A (Glass/ZnO-NRs/Protein-A). The latest structure was modified by antibodies against OTA (Anti-OTA) in order to form OTA-selective layer (Glass/ZnO-NRs/Protein-A/Anti-OTA). In order to im…

Ochratoxin AOptical fiberMaterials sciencePhotoluminescenceBiomedical EngineeringBiophysicsAnalytical chemistryFood ContaminationBiosensing Techniques02 engineering and technology01 natural sciencesAntibodieslaw.inventionsymbols.namesakechemistry.chemical_compoundLimit of DetectionlawElectrochemistryHumansDetection limitNanotubesChromatography010401 analytical chemistrySubstrate (chemistry)General Medicine021001 nanoscience & nanotechnologyOchratoxins0104 chemical sciencesGibbs free energychemistrysymbolsNanorodGoldZinc Oxide0210 nano-technologySelectivityFood AnalysisBiotechnologyBiosensors and Bioelectronics
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NADPH-diaphorase activity of nitric oxide synthase in the olfactory bulb: co-factor specificity and characterization regarding the interrelation to N…

1994

The neuronal form of the enzyme nitric oxide synthase (nNOS) synthesizes the messenger molecule nitric oxide (NO). In addition to NO formation, nNOS exhibits a so-called NADPH-diaphorase (NADPH-d) activity. This study focused on the characterization of NADPH-d activity with regard to NO formation in the rat olfactory bulb. In this area of the brain pronounced staining is localized in discrete populations of neuronal somata and in olfactory glomeruli. Diaphorase staining combined with demonstration of nNOS by polyclonal antibodies revealed that NADPH-d activity of neuron somata is associated with nNOS immunoreactivity. It is concluded that neuron somata exhibit NADPH-d activity of nNOS. NAD…

Olfactory systemMaleHistologyMiconazoleCytochrome c GroupBiologyArginineNitric OxideNitric oxideSubstrate SpecificityRats Sprague-Dawleychemistry.chemical_compoundDiaphoraseAnimalsEgtazic AcidNADPH dehydrogenaseomega-N-MethylarginineStaining and LabelingCytochrome cNADPH DehydrogenaseMolecular biologyImmunohistochemistryOlfactory BulbTrifluoperazineOlfactory bulbRatsNitric oxide synthasenervous systemBiochemistrychemistrybiology.proteinOmega-N-Methylarginine26-DichloroindophenolAmino Acid OxidoreductasesAnatomyNitric Oxide SynthaseThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
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Neural Substrate to Associate Odorants and Pheromones: Convergence of Projections from the Main and Accessory Olfactory Bulbs in Mice

2012

In rodents olfactory stimuli are essential for socio-sexual behaviour. Volatile stimuli mainly activate the main olfactory system, whereas non-volatile ones, some of them considered as pheromones, activate the accessory olfactory system. Traditionally, it has been considered that the efferent projections of the main and the accessory olfactory bulbs innervate different telencephalic areas. Recent studies performed in rats and mice have challenged this view. In this work we explore in mice, through the use of anterograde tracer injections in the olfactory bulbs, the brain centres where olfactory and vomeronasal information might converge.

Olfactory systemStria terminalisVomeronasal organNeural substrateSex pheromoneEfferentBiologyAccessory Olfactory BulbNeuroscienceOlfactory bulb
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Regulation of tartrate metabolism by TtdR and relation to the DcuS–DcuR-regulated C4-dicarboxylate metabolism of Escherichia coli

2009

Escherichia coli catabolizes l-tartrate under anaerobic conditions to oxaloacetate by the use of l-tartrate/succinate antiporter TtdT and l-tartrate dehydratase TtdAB. Subsequently, l-malate is channelled into fumarate respiration and degraded to succinate by the use of fumarase FumB and fumarate reductase FrdABCD. The genes encoding the latter pathway (dcuB, fumB and frdABCD) are transcriptionally activated by the DcuS–DcuR two-component system. Expression of the l-tartrate-specific ttdABT operon encoding TtdAB and TtdT was stimulated by the LysR-type gene regulator TtdR in the presence of l- and meso-tartrate, and repressed by O2 and nitrate. Anaerobic expression required a functional fn…

OperonBiologymedicine.disease_causeMicrobiologyAntiportersSubstrate SpecificityOperonEscherichia colimedicinePromoter Regions GeneticTartratesEscherichia coliPsychological repressionHydro-LyasesRegulator geneNitratesEscherichia coli ProteinsPromoterGene Expression Regulation BacterialFumarate reductaseDNA-Binding ProteinsOxygenGlucoseBiochemistryDehydrataseFumaraseProtein KinasesTranscription FactorsMicrobiology
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Influence of Culture Medium on Multiplication of Lactic Bacteria Isolated From Organic Milk in Order to Obtain Biomass

2014

Abstract This paper aims to establish direct and predictive methods (statistical) the possibility of obtaining lactic bacteria Lactobacillus delbrueckii var. bulgaricus in higher amounts by using culture medium enriched with carbohydrates in different percentages, for using these in obtaining organic products. The results led to the selection of MRS culture medium enriched with 1% glucose, 2% lactose and 3% maltose as a substrate in order to use multiplication of lactic bacteria isolated from organic milk, collected from organic farms in the area of Sibiu, Romania.

Organic productbiologybusiness.industryfood and beveragesSubstrate (chemistry)BiomassMaltosebiology.organism_classificationBiotechnologychemistry.chemical_compoundchemistryLactobacillusOrganic farmingFood scienceLactoseOrganic milkbusinessManagement of Sustainable Development
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Improved scalable syntheses of mono- and bis-urethane derivatives of ornithine.

2001

In the search for a practical route to ornithine bisurethane derivatives useful for peptide synthesis, we elaborated the simple and efficient (86% yield) synthesis of N(epsilon)-tert-butoxycarbonyl-L-ornithine copper(II) complex (1). This served as substrate for obtaining N(epsilon)-tert-butoxycarbonyl-L-ornithine (2), N(alpha)-benzyloxycarbonyl-N(epsilon)-tert-butoxycarbonyl-L-ornithine (3) and N(alpha)-(9-fluorenyl)methoxycarbonyl-N(epsilon)-tert-butoxycarbonyl-L-ornithine (4). These were synthesized in 94-95% yields and with a purity above 99%.

OrnithineCalorimetry Differential ScanningChemistrychemistry.chemical_elementSubstrate (chemistry)General ChemistryGeneral MedicineOrnithineChemical synthesisCopperUrethanechemistry.chemical_compoundYield (chemistry)One pot reactionDrug DiscoveryPeptide synthesisOrganic chemistryIndicators and ReagentsProtecting groupChromatography High Pressure LiquidCopperChemicalpharmaceutical bulletin
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Oxidative Coupling Reactions of 1,3-Diarylpropene Derivatives to Dibenzo[a,c]cycloheptenes by PIFA

2011

The oxidative cyclization reactions of a variety of α-benzyl-cinnamates can be selectively performed with hypervalent iodine as an oxidant. The dibenzo[a,c]cycloheptenes were isolated in up to 55 % yield. When an oxo substrate is applied, the yield was significantly increased. With this synthetic approach, a central intermediate for the synthesis of metasequirin-B was obtained in three steps from very simple starting materials. For this transformation, both aryl moieties have to be activated.

Oxidative cyclizationArylOrganic ChemistryHypervalent moleculefood and beveragesSubstrate (chemistry)chemistry.chemical_elementIodineMedicinal chemistrychemistry.chemical_compoundChemical couplingchemistryYield (chemistry)Organic chemistryheterocyclic compoundsOxidative coupling of methanePhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Filter paper disk techniques for assay of nucleotidase

1977

A DE filter disk technique for assaying the activity of nucleotidase is described. This method is based on the observation that nucleotides bind to the filters at 5 mM Tris-HCl (pH 7.8) while nucleosides do not. As parameter for the nucleotidase activity the decrease of bound nucleotides is determined. In parallel experiments the amount of the product (nucleoside) formed can be measured by DEAE Sephadex column chromatography. The filter disk technique can be applied for the determination of vmax and Km of a nucleotidase by using different ribonucleosidase monophosphate substrates.

PaperNucleotidase activityThymus GlandSubstrate SpecificityNucleotidasesColumn chromatographyNucleotidasesNucleotidaseMethodsGeneticsAnimalsNucleotideMolecular Biologychemistry.chemical_classificationChromatographyFilter paperNucleotidesNucleosidesGeneral MedicineAdenosine MonophosphateKineticschemistryBiochemistryFilter (video)CattleNucleosideMolecular Biology Reports
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