Search results for "substrate"

showing 10 items of 1018 documents

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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Enzymatic and Chemo-Enzymatic Approaches Towards Natural and Non-Natural Alkaloids: Indoles, Isoquinolines, and Others

2010

Abstract The multi-step enzyme catalysed biosyntheses of monoterpenoid indole and isoquinoline alkaloids are described. Special emphasis is placed on those pathways leading to alkaloids of pharmacological and medicinal significance which have been fully elucidated at the enzyme level. The successful identification and cloning of cDNAs of single enzymes and their application provides great opportunities to develop novel strategies for both in vitro and in vivo alkaloid production in whole plants or tissue cultures, as well as in microbial systems such as Escherichia coli and yeast. Enzyme crystallisation, 3D analyses and site-directed mutation allowed rational engineering of enzyme substrate…

chemistry.chemical_classificationCloningIndole testendocrine systemorganic chemicalsAlkaloidSubstrate (chemistry)medicine.disease_causecomplex mixturesYeastchemistry.chemical_compoundEnzymechemistryBiochemistrymedicineheterocyclic compoundsIsoquinolineEscherichia coli
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Surface anchoring on liquid crystalline polymer brushes

2002

We present a Monte Carlo study of the surface anchoring of a nematic fluid on swollen layers of grafted liquid crystalline chain molecules. The liquid crystalline particles are modeled by soft repulsive ellipsoids, and the chains are made of the same particles. An appropriately modified version of the configurational bias Monte Carlo algorithm is introduced, which removes and redistributes chain bonds rather than whole monomers. With this algorithm, a wide range of grafting densities could be studied. The substrate is chosen such that it favors a planar orientation (parallel to the surface). Depending on the grafting density, we find three anchoring regimes: planar, tilted, and perpendicula…

chemistry.chemical_classificationCondensed Matter - Materials ScienceQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyAnchoringPolymerSubstrate (electronics)Condensed Matter - Soft Condensed MatterCondensed Matter::Soft Condensed MatterPlanarchemistryHardware and ArchitectureLiquid crystalChemical physicsPerpendicularSoft Condensed Matter (cond-mat.soft)Monte Carlo algorithmComputer Physics Communications
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The binary pyrene/heptakis-(6-amino-6-deoxy)-β-cyclodextrin complex: A suitable chiral discriminator. Spectrofluorimetric study of the effect of some…

2002

The effect of some α-amino acids and their esters on the stability of the binary pyrene/heptakis-(6-amino-6-deoxy)-β-cyclodextrin (py/am-β-CD) complex has been studied by means of fluorescence spectroscopy at two pH values (8.0 and 9.0). The binary complex was generally stabilized by adding the ternary agent at pH 8.0. A more varied substrate effect is observed at pH 9.0 where am-β-CD is present in the uncharged form. The conditional constant (β2) values determined by L/D α-amino acids show that the binary complex is a suitable receptor for chiral recognition. The enantiomer selectivity values obtained, ranging from 1.2 up to 7.4, are generally higher than those reported for α-amino acids a…

chemistry.chemical_classificationCyclodextrinStereochemistryOrganic Chemistrycyclodextrins amino acidsSubstrate (chemistry)Settore CHIM/06 - Chimica OrganicaMedicinal chemistryCatalysisFluorescence spectroscopyAmino acidInorganic Chemistrychemistry.chemical_compoundchemistryPyrenePhysical and Theoretical ChemistryEnantiomerTernary operationSelectivity
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Role of hexagonal structure-forming lipids in diadinoxanthin and violaxanthin solubilization and de-epoxidation

2005

In this study, we have examined the influence of different lipids on the solubility of the xanthophyll cycle pigments diadinoxanthin (Ddx) and violaxanthin (Vx) and on the efficiency of Ddx and Vx de-epoxidation by the enzymes Vx de-epoxidase (VDE) from wheat and Ddx de-epoxidase (DDE) from the diatom Cyclotella meneghiniana, respectively. Our results show that the lipids MGDG and PE are able to solubilize both xanthophyll cycle pigments in an aqueous medium. Substrate solubilization is essential for de-epoxidase activity, because in the absence of MGDG or PE Ddx and Vx are present in an aggregated form, with limited accessibility for DDE and VDE. Our results also show that the hexagonal st…

chemistry.chemical_classificationDiatomsBilayerGalactolipidsPhosphatidylethanolaminesLipid BilayersHexagonal phaseDiadinoxanthinSubstrate (chemistry)BiologyXanthophyllsbeta CaroteneBiochemistrySubstrate Specificitychemistry.chemical_compoundEnzymeBiochemistrychemistrySolubilityXanthophyllThylakoidPhosphatidylcholinesOxidoreductasesViolaxanthin
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On the behaviour of the (Z)-Phenylhydrazones of some 5-alkyl-3-benzoyl-1,2,4-oxadiazoles in solution and in the gas phase: kinetic and spectrometric …

2008

Abstract Rate constants, k A,R , for the rearrangement of the ( Z )-phenylhydrazones ( 1a – e ) of a series of 5-alkyl-3-benzoyl-1,2,4-oxadiazoles substituted at C(5) with linear alkyl chains of different length (from C 4 up to C 12 ) into the relevant 4-acylamino-2,5-diphenyl-1,2,3-triazoles ( 2a – e ) have been measured in dioxan/water in the base-catalyzed region (pS + 10.5–12.6). For each substrate log  k A,R are linearly related to pS + . The significant decrease of the slopes of these straight lines (from 0.96 down to 0.78) upon increasing the length of the linear alkyl chain at C(5) and that of the reactivity (down to 14–26%) upon increasing the substrate concentration suggest a decr…

chemistry.chemical_classificationDirect evidenceStereochemistryOrganic ChemistrySubstrate (chemistry)124-oxadiazoleKinetic energyBiochemistryCrystallographyReaction rate constantchemistryDrug DiscoveryProton NMRReactivity (chemistry)Self-assemblymononuclear rearrangementAlkyl
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Enzymatic activity of circular sortase A under denaturing conditions: An advanced tool for protein ligation

2014

Abstract Staphylococcus aureus sortase A is a transpeptidase that is extensively used in various protein research applications. Sortase A is highly selective and does not require any cofactors for the catalysis of protein ligation and, importantly, can be produced in high yields. However, the primary disadvantage of this transpeptidase is its inability to access the recognition site within the highly structured regions of folded substrates. To overcome this problem, we developed an Escherichia coli expression system that produces milligram quantities of circularly closed sortase A; efficient enzyme cyclization was achieved by Synechocystis sp. PCC6803 intein-mediated post-translational spli…

chemistry.chemical_classificationEnvironmental EngineeringBiomedical EngineeringSubstrate (chemistry)BioengineeringProtein engineeringBiologymedicine.disease_causeCofactorchemistry.chemical_compoundEnzymechemistryBiochemistrySortaseSortase Amedicinebiology.proteinEDANSEscherichia coliBiotechnologyBiochemical Engineering Journal
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Protochlorophyllide Reduction: Mechanisms and Evolution¶

2007

Protochlorophyllide (Pchlide) reductases are key enzymes in the process of chlorophyll biosynthesis. In this review, current knowledge on the molecular organization, substrate specificity and assembly of the light-dependent reduced nicotinamide adenine dinucleotide phosphate:Pchlide oxidoreductases are discussed. Characteristics of light-independent enzymes are also described briefly, and the possible reasons for the selection of light-dependent enzymes during the course of evolution are discussed.

chemistry.chemical_classificationEnzymeReduced nicotinamide-adenine dinucleotideProtochlorophyllideBiochemistrychemistrySubstrate specificityGeneral MedicinePhysical and Theoretical ChemistryChlorophyll biosynthesisBiologyBiochemistryPhotochemistry and Photobiology
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Simulation of Metabolism for The Calculation of Enzyme Activities in Stress Metabolism

1988

Abstract Using data of indirect calorimetry, total energy turnover as well as the rate of combustion of carbohydrates, fat and amino acids can be calculated. For the evaluation, simple standard procedures (4) are used. These procedures presume, that several assumptions are satisfied, e.g. a complete degradation of the energy delivering substrates and undisturbed enzyme activities. To be able to interprete also measurements, which are performed in the post-traumatic state as well as for estimation of the extent and consequences of reduced enzyme activities, a new method for the simulation of metabolism was developed. Hie underlying model considers a reduced activity of key enzymes and a swit…

chemistry.chemical_classificationEnzymechemistryBiochemistryGluconeogenesisDegradation (geology)Substrate (chemistry)MetabolismCalorimetryPyruvate dehydrogenase complexAmino acidIFAC Proceedings Volumes
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The Catalytic Mechanism of Carboxylesterases: A Computational Study

2014

The catalytic mechanism of carboxylesterases (CEs, EC 3.1.1.1) is explored by computational means. CEs hydrolyze ester, amide, and carbamate bonds found in xenobiotics and endobiotics. They can also perform transesterification, a reaction important, for instance, in cholesterol homeostasis. The catalytic mechanisms with three different substrates (ester, thioester, and amide) have been established at the M06-2X/6-311++G**//B3LYP/6-31G* level of theory. It was found that the reactions proceed through a mechanism involving four steps instead of two as is generally proposed: (i) nucleophilic attack of serine to the substrate, forming the first tetrahedral intermediate, (ii) formation of the ac…

chemistry.chemical_classificationEsterificationStereochemistrycomputational studiesHydrolysisSubstrate (chemistry)AlcoholTransesterificationcatalytic mechanismCrystallography X-RayThioesterBiochemistryCatalysischemistry.chemical_compoundcarboxylesterasesNucleophilechemistryhydrolysisTetrahedral carbonyl addition compoundAmideBiocatalysisCarboxylic Ester Hydrolases
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