Search results for "terase"

showing 10 items of 446 documents

Presence of esterase inPinaceae pollen

1997

General esterases, like wall heterologous enzymes, may be implicated in allergenic mechanisms. We cytochemically examined the presence of these enzymes, bearing in mind thatPinus spp. is often considered a possible cause of allergies. Positive esterase results in fungus spores were found on the strip of a volumetric sampler. Data are reported here, together with the hypothesis of a possible esterase-allergenic link regarding fungus spores.

chemistry.chemical_classificationAllergyfungiImmunologyHeterologousPlant ScienceFungusBiologymedicine.disease_causemedicine.diseasebiology.organism_classificationEsteraseMicrobiologySporeEnzymeBiochemistrychemistryPollenmedicineImmunology and AllergyAerobiologia
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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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Isolation and characterization of a chlorogenic acid esterase from Aspergillus niger.

1980

Abstract The isolation and characterization of a specific chlorogenic acid esterase is described. The enzyme activity is measured by determination of the hydrolysis product caffeic acid. The enzyme had been concentrated by means of ultrafiltration and column-chromatography. The pH- and temperature optimum were 6.5 and 45 °C respectively. Divalent cations were not required for the enzyme activity. As other esterases, this enzyme is inhibited by di-isopropyl-phosphorofluoridate. The Km-value is 0.70 mᴍ chlorogenic acid, the molecular weight 240000. The described enzyme is specific for chlorogenic acid. On the other hand a typical unspecific esterase like the pig liver esterases does not split…

chemistry.chemical_classificationChromatographybiologyIsoelectric focusingSwineAspergillus nigerbiology.organism_classificationEsteraseGeneral Biochemistry Genetics and Molecular BiologyEnzyme assayIsoenzymesMolecular Weightchemistry.chemical_compoundHydrolysisKineticsEnzymeChlorogenic acidchemistryLiverCaffeic acidbiology.proteinAnimalsAspergillus nigerCarboxylic Ester HydrolasesZeitschrift fur Naturforschung. Section C, Biosciences
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Poly(silicate)-metabolizing silicatein in siliceous spicules and silicasomes of demosponges comprises dual enzymatic activities (silica polymerase an…

2007

Siliceous sponges can synthesize poly(silicate) for their spicules enzymatically using silicatein. We found that silicatein exists in silica-filled cell organelles (silicasomes) that transport the enzyme to the spicules. We show for the first time that recombinant silicatein acts as a silica polymerase and also as a silica esterase. The enzymatic polymerization/polycondensation of silicic acid follows a distinct course. In addition, we show that silicatein cleaves the ester-like bond in bis(p-aminophenoxy)-dimethylsilane. Enzymatic parameters for silica esterase activity are given. The reaction is completely blocked by sodium hexafluorosilicate and E-64. We consider that the dual function o…

chemistry.chemical_classificationCondensation polymerbiologyCell Biologyrespiratory systemBiochemistryEsteraseSilicatechemistry.chemical_compoundEnzymeSponge spiculechemistryPolymerizationBiochemistryPolymer chemistrybiology.proteinSilicic acidMolecular BiologyPolymeraseFEBS Journal
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Species-Specific Aggregation Factor In Sponges.

1978

In dissociated single cells from the sponge Geodia cydonium, DNA synthesis is initiated after incubation with a homologous, soluble aggregation factor. During the DNA-initiation phase the cyclic AMP- and cyclic GMP levels vary drastically; the cyclic AMP content drops from 2.2 pmol/10(6) cells to 0.3 pmol/10(6) cells while the cyclic GMP content increases from 0.6 pmol to 3.7 pmol/10(6) cells. The activity of neither the adenylate cyclase nor of the guanylate cyclase isolated from cells which have been incubated for different periods of time with the aggregation factor, is changed. The soluble as well as the particulate enzyme activities were checked in vitro. The cyclic nucleotide receptor…

chemistry.chemical_classificationDNA synthesisAdenylate kinasePhosphodiesteraseCell BiologyGeneral MedicineBiologyCyclaseCell aggregationDissociation constantCyclic nucleotidechemistry.chemical_compoundchemistryBiochemistryNucleotideCell Proliferation
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Chemical conjugation of dexamethasone to a polyaspartamide and in vitro evaluation studies

2004

Two macromolecular conjugates of dexamethasone containing different drug amounts were synthesized using PHEA as the polymeric carrier and a succinic group as spacer. The content of linked drug was equal to 25.3% w/w (conjugate A) and 12.7% w/w (conjugate B). Both polymeric conjugates, unlike the free drug, were water-soluble and the amount of unlinked drug was evaluated to be approximately about 0.01% w/w. Both conjugates were relatively stable in vitro at pH 7.4 whereas in the presence of esterase only the conjugate B was able to release drug under the used experimental conditions. This dissimilar behavior has been attributed to the distinct macromolecular conformations assumed in aqueous …

chemistry.chemical_classificationDrugStereochemistrymedia_common.quotation_subjectPharmaceutical ScienceProdrugEsteraseCombinatorial chemistryDexamethasoneIn vitroPolyaspartamideHydrolysisEnzymechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug-polymer conjugatesMacromoleculemedia_commonConjugateJournal of Drug Delivery Science and Technology
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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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Potential active-site residues in polyneuridine aldehyde esterase, a central enzyme of indole alkaloid biosynthesis, by modelling and site-directed m…

2002

In the biosynthesis of the antiarrhythmic alkaloid ajmaline, polyneuridine aldehyde esterase (PNAE) catalyses a central reaction by transforming polyneuridine aldehyde into epi-vellosimine, which is the immediate precursor for the synthesis of the ajmalane skeleton. The PNAE cDNA was previously heterologously expressed in E. coli. Sequence alignments indicated that PNAE has a 43% identity to a hydroxynitrile lyase from Hevea brasiliensis, which is a member of the α/β hydrolase superfamily. The catalytic triad, which is typical for this family, is conserved. By site-directed mutagenesis, the members of the catalytic triad were identified. For further detection of the active residues, a model…

chemistry.chemical_classificationHydroxynitrile lyasebiologyStereochemistryMutagenesisActive siteBiochemistryPolyneuridine-aldehyde esteraseEnzymechemistryBiochemistryHydrolaseCatalytic triadbiology.proteinSite-directed mutagenesisEuropean Journal of Biochemistry
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Sildenafil protects human mammary epithelial cells against ROS production induced by estradiol

2010

Several studies suggest that xanthine dehydrogenase (XDH) and its oxidase form (XO) play an important role in various types of ischemic and vascular injuries. Recently, we have demonstrated that estradiol (E2) induces a significant decrease of the expression and activity of XDH and of its conversion to XO in human mammary epithelial cells. E2 is known to induce upregulation of eNOS gene expression in aortic endothelial cells. Because the XO-derived O2·- combines with ·NO to yield ONOO-, and considering that ONOO- converts XDH to XO, the resulting increase of XO activity and reactive oxygen species production would eventually lead to a further increase of ONOO- production, thus creating a vi…

chemistry.chemical_classificationOxidase testmedicine.medical_specialtyReactive oxygen speciesNADPH oxidasebiologyEndocrinology Diabetes and MetabolismPhosphodiesteraseGeneral Medicinemedicine.disease_causeMolecular biologyEndocrinologyEnzymeEndocrinologyDownregulation and upregulationchemistryXanthine dehydrogenaseSettore BIO/10 - BiochimicaInternal medicinemedicinebiology.proteinMolecular BiologyOxidative stressestradiol (E2) human mammaty epithelial cells (HMECs) oxidative stress inhibition reactive oxygen species (ROS) production sildenafil xanthine dehydrogenase (XDH) xanthine oxidase (XO).Hormone Molecular Biology and Clinical Investigation
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Use of two-dimensional thin-layer chromatography for the components study of poly(adenosine diphosphate ribose)

1990

Two-dimensional thin-layer chromatography on cellulose plates has been used for separating and quantifying the three adenosine derivatives: AMP, phosphoribosyl AMP (PRAMP), and (PR)2AMP obtained by venom phosphodiesterase digestion of poly(ADP-ribose). In vitro synthesized polymer, up to 300 derivatives in length were studied. Some parameters of the complexity of poly(ADP-ribose) could be deduced from our results: (i) The first branching point appears in fragments of approximately 21 derivatives in length. (ii) The branching points are located at regular distances of approximately 41 derivatives from each other.

chemistry.chemical_classificationPoly Adenosine Diphosphate RiboseChromatographyPolymersChemistryBiophysicsPoly Adenosine Diphosphate RiboseCell BiologyBranching pointsPolymerBiochemistryAdenosineAdenosine MonophosphateIn vitroThin-layer chromatographyVenom phosphodiesterasechemistry.chemical_compoundmedicineElectrophoresis Polyacrylamide GelChromatography Thin LayerCelluloseMolecular Biologymedicine.drugAnalytical Biochemistry
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