Search results for "TRIAC"

showing 10 items of 203 documents

Effects of organic matter complexation on partitioning of transition metals into calcite: Cave-analogue crystal growth experiments

2022

We highlight the potential for first row transition metals to carry paleohydrological signals in speleothems, and argue that these metals constitute valuable proxies for climate reconstructions. Metal availability to speleothems is hypothesised to be restricted by organic complexation, which strongly limits the free ion activity of transition metals (Co2+, Ni2+ and Cu2+) in dripwater, thereby creating a kinetic overprint on metal concentrations and isotope ratios in speleothem calcite. This study presents the results of the first cave-analogue experiments of transition metal partitioning into calcite in the absence and presence of organic ligands. The Geological Microclimate (GeoMic) system…

chemistry.chemical_classificationCalcitegeographyAqueous solutiongeography.geographical_feature_categoryInorganic chemistryNitrilotriacetic acidSpeleothemF800Metalchemistry.chemical_compoundchemistryTransition metalGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumOrganic matterChelation
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Improving lipase activity in solvent-free media by interfacial activation-based molecular bioimprinting

1997

Abstract Nine lipases of mammalian, fungal and bacterial origin and two different model reactions, direct esterification and transesterification (alcoholysis), have been used to probe the potential in solvent-free media of the recently reported strategy of interfacial activation-based molecular (bio)imprinting (IAMI) [Mingarro et al., Proc. Natl. Acad. Sci. USA , 92 (1995) 3308]. The results demonstrate that the imprinting treatment permits nonaqueous rate accelerations which are lipase-dependent and span in some cases up to higher than two orders of magnitude. For several lipases, the method allows conversion yields after short reaction times (in either of the model reactions assayed) whic…

chemistry.chemical_classificationCarboxylic Ester HydrolasesSolvent freebiologyChemistryProcess Chemistry and TechnologyTriacylglycerol lipaseBioengineeringTransesterificationBiochemistryCatalysisInorganic saltsEnzymebiology.proteinOrganic chemistryLipaseJournal of Molecular Catalysis B: Enzymatic
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Isolierung und Charakterisierung einer Acetylester-Hydrolase aus Aspergillus rtiger / Isolation and Characterization of an Acetylester-Hydrolase from…

1980

Abstract The characteristic features of an acetic acid esters hydrolyzing enzyme (acetylesterase, EC 3.1.1.16) are described. The pH- and temperature optimum were 7.0 and 40 °C respectively. The stability of the enzyme regarding different pH- and temperature conditions was investigated. The molecular weight of the acetylesterase could be determined to 160000. A small acetic ester hydrolyzing activity was found too with a molecular weight of about 25000. The activity was not inhibited by addition of di-isopropylphosphorofluoridate (DFP) or physostigmine. The KM-value for glyceryl triacetate was about 90 mM. Concentration of the enzyme was done by ultrafiltration and column-chromatography. Th…

chemistry.chemical_classificationChromatographybiologyChemistryAspergillus nigerUltrafiltrationSubstrate (chemistry)Acetylesterasebiology.organism_classificationGeneral Biochemistry Genetics and Molecular BiologyEnzymeHydrolaseAcetic Acid EstersGlyceryl triacetateZeitschrift für Naturforschung C
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Growth of fibrous aggregates of silica nanoparticles: Fibre growth by mimicking the biogenic silica patterning processes

2009

We describe the self-assembly of discrete SiO2 nanofibers via grafting of silicatein side chains to a polymer backbone. The covalent binding of silicatein to the backbone of the polymer is based on the affinity of the nitrilotriacetic acid (NTA) side chain, which serves as a ligand for the immobilization of His-tagged silicatein. The surface charge and the bulkiness of the protein moieties prevent the entropically favoured coil formation of the polymer and force it to adopt an open chain structure after hydrolysis of the silica precursors. The probes were characterized by scanning force microscopy (SFM) and optical light microscopy. Surface complexation of the resulting silica nanoparticles…

chemistry.chemical_classificationLigandNitrilotriacetic acidGeneral ChemistryPolymerCondensed Matter Physicschemistry.chemical_compoundchemistryChemical engineeringNanofiberPolymer chemistryMicroscopySide chainSurface chargeHigh-resolution transmission electron microscopySoft Matter
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Enzyme-Mediated Deposition of a TiO2Coating onto Biofunctionalized WS2 Chalcogenide Nanotubes

2009

A chemically specific and facile method for the biofunctionalization of WS2 nanotubes (NT-WS2) is reported. The covalent modification strategy is based on the affinity of the nitrilotriacetic acid (NTA) side chain, which serves as a ligand for the surface binding to NT-WS2 and simultaneously as an anchor group for the binding of His-tagged proteins to the polymer backbone. The polymer functionalized WS2 nanotubes can be solubilized either in water or organic solvents; they are stable for at least one week. The probes were characterized by FT-IR and UV-vis spectroscopy. The immobilization of silicatein, a hydrolytic protein encountered in marine sponges, was visualized by scanning force micr…

chemistry.chemical_classificationMaterials scienceChalcogenideScanning electron microscopeNitrilotriacetic acidNanotechnologyPolymerengineering.materialCondensed Matter PhysicsLigand (biochemistry)Electronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundChemical engineeringchemistryCoatingTransmission electron microscopyElectrochemistryengineeringSide chainAdvanced Functional Materials
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Fabrication of a Silica Coating on Magnetic γ-Fe2O3 Nanoparticles by an Immobilized Enzyme

2008

Silicatein, a hydrolytic protein encountered in marine sponges, was immobilized on maghemite (γ-Fe2O3) nanoparticles that were surface functionalized with a reactive mulfunctional polymer. This polymer carries an anchor group based on dopamine which is capable of binding to the γ-Fe2O3 surface and a reactive functional group which allows binding of various biomolecules onto inorganic nanoparticles. This functional nitrilotriacetic acid (NTA) group allows immobilization of His-tagged silicatein on the surface of the γ-Fe2O3 nanoparticles. The surface-bound protein retains its native hydrolytic activity to catalyze formation of silica through copolymerization of alkoxysilanes Si(OR)4. Functio…

chemistry.chemical_classificationMaterials scienceImmobilized enzymeGeneral Chemical EngineeringBiomoleculeInorganic chemistryNitrilotriacetic acidMaghemiteNanoparticleGeneral Chemistryengineering.materialchemistry.chemical_compoundchemistryChemical engineeringMaterials ChemistryengineeringCopolymerMagnetic nanoparticlesSurface modificationChemistry of Materials
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Evidence for the involvement of acylglycerides on chitin synthetase activity inCandida albicans

1991

The effect of a lipase activity (EC 3.1.1.3) on the chitin synthetase from Candida albicans has been studied, both on the active and the trypsin activated enzyme. Removal of fatty acids from acylglycerides by lipase has an inhibitory effect on the activity as well as on the ‘in vitro’ activation process by trypsin in the membrane-bound enzyme and in the chitosomes. This would indicate that an adequate lipid environment is required for both the activation process and proper function of the synthetase activity.

chemistry.chemical_classificationTriacylglycerol lipaseChitin synthaseBiologyTrypsinbiology.organism_classificationMicrobiologyYeastMicrobiologychemistry.chemical_compoundEnzymechemistryBiochemistryChitinGeneticsmedicinebiology.proteinLipaseCandida albicansMolecular Biologymedicine.drugFEMS Microbiology Letters
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Enzyme-mediated enantioselective acylation of secondary amines in organic solvents

1991

Abstract Porcine pancreatic lipase (PPL) and lipase Amano P catalyze the enantioselective acylation of cyclic 1,2- and 1,3-amino alcohol derivatives in organic solvents. The enatiomeric excesses (ee′s) were shown to depend on the enzyme, reaction time, temperature and type of substrate.

chemistry.chemical_classificationbiologyOrganic ChemistryEnantioselective synthesisTriacylglycerol lipaseSubstrate (chemistry)AlcoholBiochemistryCatalysisAcylationchemistry.chemical_compoundEnzymechemistryDrug Discoverybiology.proteinOrganic chemistryLipaseTetrahedron Letters
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Study of a lipase from Candida rugosa Diddens and Lodder

1993

Lipasic system of Candida rugosa (CBS 613) strain was studied. The enzyme was purified in one step by hydrophobic chromatography. The properties of this lipase were determined. It is an oligomeric enzyme composed of five identical monomers of 46 kg · mol−1. Its optimum reaction conditions are pH = 7 and temperature = 40°C. This enzyme presents a rapid thermal denaturation and then a more stable form. It is a cell-bound lipase which is induced by triacyl glycerols. This enzyme presents a high specificity for external positions on glycerol. Unterschung einer Lipase aus Candida rugosa Diddens und Lodder Die Reinigung einer Lipase aus Candida rugosa (CBS 613) wurde in einer einzigen Stufe durch…

chemistry.chemical_classificationbiologyStereochemistry[SDV]Life Sciences [q-bio]Triacylglycerol lipaseFungi imperfectibiology.organism_classificationYeastCandida rugosa[SDV] Life Sciences [q-bio]EnzymechemistryBiochemistrybiology.proteinSubstrate specificityLipase
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Lipase-enhanced activity in flavour ester reactions by trapping enzyme conformers in the presence of interfaces

1998

In order to improve the lipase-catalyzed synthesis of flavour esters, we have used the reported strategy of interfacial activation-based molecular (bio)imprinting [Mingarro et al. 1995. Proc. Natl. Acad. Sci. U.S.A. 92: 3308], later called trapping in the presence of amphiphile interfaces (TPI) [Mingarro et al. 1996. Biochemistry 35: 9935]. Five lipases of fungal and mammalian origin typically used for esterification process have been explored to improve production by TPI treatment. A marked enhancement of enzymatic activity has been observed in all TPI-treated lipases assayed and the activation factor obtained was up to 90-fold. The dependence on chain length of acyl donors in the esterifi…

chemistry.chemical_classificationbiologyTrapping enzymeStereochemistryFlavourTriacylglycerol lipaseBioengineeringAlcoholApplied Microbiology and Biotechnologychemistry.chemical_compoundEnzymechemistryAmphiphilebiology.proteinOrganic chemistryLipaseConformational isomerismBiotechnologyBiotechnology and Bioengineering
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