Search results for "hydrolysis"

showing 10 items of 632 documents

Influence of the Liquefied Starch Composition and pH on the Saccharification at the Obtaining of Maltose Syrup

1970

In this paper the influence of the composition of the liquefied starch and of pH on the quality of saccharification at the obtaining of maltose syrup is investigated. A large number of experiments (68) in various liquefaction conditions show that Dextrose Equivalent (DE) and the composition in hydrolysis products with Degree of Polymerisation higher as four (DP ≥4) in the liquefied starch have a strong influence on the saccharification products, mainly on the maltose content in the maltose syrups. The liquefied starch with DE lower as 25 has smaller amounts of DP ≥4 (40 to 60%), whereas the liquefied starch with DE between 25 and 27 has high amounts of DP ≥4 (60 to 80%). For the production …

ChromatographybiologyChemistryStarchDextrose equivalentGeography Planning and DevelopmentMaltoseManagement Monitoring Policy and Lawchemistry.chemical_compoundHydrolysisYield (chemistry)biology.proteinComposition (visual arts)AmylaseChemical compositionBulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Agriculture
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Modelling of Starch Gelatinisation and Liquefaction with the Enzyme Liquozyme

2011

In this paper the influence of the enzyme Liquozyme Supra concentration (0.4-1.2 kg/t dry substance DS) and gelatinisation time (3-11 min.) on the liquefied starch quality is investigated. The composition in sugars with different Degrees of Polymerisation (DP) as DP1 (glucose), DP2 (maltose), DP3 (maltotriose), DP4 (maltotetrose) and oligosaccharides with DP≥5 is analysed by using HPLC with RI detector. The products obtained have different DP, the main components being oligosaccharides with DP≥5, followed by small amount of DP3+DP4 and much smaller concentrations of DP1; no DP2 is produced by this enzyme. Two quality criteria: the percent of oligosaccharides with DP≥5 and the percent of DP1…

ChromatographybiologyChemistryStarchGeography Planning and DevelopmentLiquefactionMaltoseManagement Monitoring Policy and LawMaize starchchemistry.chemical_compoundHydrolysisbiology.proteinMaltotrioseComposition (visual arts)Alpha-amylaseBulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca. Agriculture
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Characterization of an ethanol-tolerant 1,4-β-xylosidase produced byPichia membranifaciens

2012

Aims:  The purification and biochemical properties of the 1,4-β-xylosidase of an oenological yeast were investigated. Methods and Results:  An ethanol-tolerant 1,4-β-xylosidase was purified from cultures of a strain of Pichia membranifaciens grown on xylan at 28°C. The enzyme was purified by sequential chromatography on DEAE cellulose and Sephadex G-100. The relative molecular mass of the enzyme was determined to be 50 kDa by SDS-PAGE. The activity of 1,4-β-xylosidase was optimum at pH 6·0 and at 35°C. The activity had a Km of 0·48 ± 0·06 mmol l−1 and a Vmax of 7·4 ± 0·1 μmol min−1 mg−1 protein for p-nitrophenyl-β-d-xylopyranoside. Conclusions:  The enzyme characteristics (pH and thermal st…

ChromatographybiologyPichia membranifaciensXylosebiology.organism_classificationApplied Microbiology and BiotechnologyXylanYeastEnzyme assayHydrolysischemistry.chemical_compoundchemistryBiochemistrybiology.proteinHemicelluloseEthanol fuelLetters in Applied Microbiology
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Simultaneous Kinetic Determination of Carbamate Pesticides after Derivatization withp-Aminophenol by Using Partial Least Squares

1996

Abstract A method has been developed for the fast spectrophotometric determination of propoxur, carbaryl, and ethiofencarb in water samples using injection analysis in the stopped-flow mode. The method is based on the reaction between p -aminophenol and the phenolic compounds obtained from the pesticides, after a previous hydrolysis with 0.05 M NaOH at room temperature for 15 min. The partial least-squares treatment of the spectrophotometry kinetic data provides a simultaneous determination of the three carbamate pesticides assayed with a relative accuracy error lower than 5% in complex mixtures also containing formetanate, which is only partially hydrolyzed under the experimental condition…

Chromatographymedicine.diagnostic_testPropoxurAnalytical Chemistrychemistry.chemical_compoundHydrolysischemistryFormetanateEthiofencarbSpectrophotometryCarbarylPartial least squares regressionmedicineDerivatizationSpectroscopyMicrochemical Journal
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Comparison of spectrophotometric and HPLC methods for determining sialic acid in infant formulas

2011

Abstract Two methods for determining sialic acid in infant formulas – spectrophotometry and HPLC with fluorescence detection – have been optimised and validated, the first one allows to determine total sialic acid while the second allows to differentiate the two main forms of sialic acid (N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc)). A common sample preparation procedure (hydrolysis and purification) for both methods has been proposed. The linearity (from 6 to 150 μg of total sialic acid in the assay for spectrophotometry, and from 12.5 to 250 ng and 1 to 5 ng of Neu5Ac and Neu5Gc, respectively, for HPLC) is adequate. The detection and quantification limits (0.29…

Chromatographymedicine.diagnostic_testRelative standard deviationGeneral MedicineHigh-performance liquid chromatographyFluorescenceAnalytical ChemistrySialic acidHydrolysischemistry.chemical_compoundInfant formulachemistrySpectrophotometrymedicineSample preparationFood ScienceFood Chemistry
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Ferricytochrome c encapsulated in silica nanoparticles: structural stability and functional properties.

2004

Using a modified sol-gel technique, we have succeeded in encapsulating ferric cytochrome c in silica nanoparticles obtained from hydrolysis and polycondensation of tetramethylorthosilicate. Particles dimensions have been determined with dynamic light scattering; this technique yields an hydrodynamic radius of about 100 nm, each nanoparticle containing about 10(2)-10(3) proteins. If stored in the cold at low ionic strength, nanoparticles are stable for more than one week, even if a slow radius increase with time is observed. CD measurements show that encapsulated proteins exhibit substantially increased stability against guanidinium hydrochloride induced denaturation. Reduction kinetics of e…

Circular dichroismSiliconHydrodynamic radiusTime FactorsLightProtein ConformationBiophysicsNanoparticleBiosensing TechniquesDithioniteLigandsBiochemistryBiomaterialsSodium dithionitechemistry.chemical_compoundDynamic light scatteringmedicineAnimalsScattering RadiationDenaturation (biochemistry)HorsesGuanidineIonsCarbon MonoxideChromatographyDose-Response Relationship DrugMyoglobinCircular DichroismHydrolysisSilicatesOrganic ChemistryCytochromes cWaterGeneral MedicineKineticschemistryChemical engineeringSol-gel process Sol-gels scanning electronFerricmedicine.drugBiopolymers
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Cloning, purification, and nucleotide-binding traits of the catalytic subunit A of the V1VO ATPase from Aedes albopictus.

2007

The Asian tiger mosquito, Aedes albopictus, is commonly infected by the gregarine parasite Ascogregarina taiwanensis, which develops extracellularly in the midgut of infected larvae. The intracellular trophozoites are usually confined within a parasitophorous vacuole, whose acidification is generated and controlled by the V(1)V(O) ATPase. This proton pump is driven by ATP hydrolysis, catalyzed inside the major subunit A. The subunit A encoding gene of the Aedes albopictus V(1)V(O) ATPase was cloned in pET9d1-His(3) and the recombinant protein, expressed in the Escherichia coli Rosetta 2 (DE3) strain, purified by immobilized metal affinity- and ion-exchange chromatography. The purified prote…

Circular dichroismVacuolar Proton-Translocating ATPasesATPaseProtein subunitGene ExpressionGenes InsectBiologyIn Vitro Techniquesmedicine.disease_causelaw.inventionAdenosine TriphosphateATP hydrolysislawAedesCatalytic DomainmedicineAnimalsNucleotideCloning MolecularEscherichia coliDNA Primerschemistry.chemical_classificationPhotoaffinity labelingBase SequenceMolecular biologyProtein SubunitsSpectrometry FluorescenceBiochemistrychemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationbiology.proteinRecombinant DNAInsect ProteinsBiotechnologyProtein expression and purification
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Aerobic granular sludge treating high strength citrus wastewater: Analysis of pH and organic loading rate effect on kinetics, performance and stabili…

2017

Abstract In the present paper, the feasibility of citrus wastewater treatment with aerobic granular sludge sequencing batch reactors (AGSBR) was investigated. Two AGSBRs (named R1 and R2, respectively) were operated for 90 days under different organic loading rates (OLR) and pH in two experimental periods. The OLR ranged approximately between 3.0 kg TCOD m−3d−1 and 7 kg TCOD m−3d−1 during Period I, whereas between 7 kg TCOD m−3d−1 and 15 kg TCOD m−3d−1 during Period II. pH was maintained at 7.0 and 5.5 in R1 and R2, respectively. The results revealed that under high OLR and unbalanced feast/famine regime (Period I), the development of fast-growing microorganisms (fungi and filamentous bacte…

CitrusEnvironmental EngineeringMicroorganismSegmented filamentous bacteria0208 environmental biotechnologyOLR02 engineering and technology010501 environmental sciencesManagement Monitoring Policy and LawWastewater01 natural sciencesWaste Disposal FluidHydrolysisBioreactorsEffluentWaste Management and Disposal0105 earth and related environmental sciencesCitrus wastewaterTotal organic carbonSettore ICAR/03 - Ingegneria Sanitaria-AmbientaleSewageChemistrypHChemical oxygen demandGeneral MedicineHydrogen-Ion ConcentrationPulp and paper industryAerobiosis020801 environmental engineeringKineticsWastewaterAerobic granular sludgeSewage treatmentBiokineticJournal of environmental management
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Enzymatic cleaning of inorganic ultrafiltration membranes used for whey protein fractionation

2003

Abstract The aim of this work was to study the cleaning of inorganic membranes fouled by whey protein solutions using proteolytic enzymes. Tami ® 150+4T membranes (Tami Industries, S.A., 26110 Nyons, France) of 400 kg/mol molecular weight cut-off (MWCO) and a ZrO 2 filtering layer were selected to carry out the tests and Maxatase ® XL (Genencor International, 2333 CN Leiden, The Netherlands) and P3-Ultrasil ® 62 (Henkel Iberica, S.A., 08025 Barcelona, Spain) were investigated as cleaning agents. Cleaning efficiency was observed to be a function of the operating conditions. The operating conditions studied were the pH of the cleaning solution, the enzymatic agent concentration and cleaning t…

Cleaning agentWhey proteinChromatographyChemistryUltrafiltrationProteolytic enzymesFiltration and SeparationFractionationPermeationBiochemistryHydrolysisMembraneGeneral Materials SciencePhysical and Theoretical ChemistryJournal of Membrane Science
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Substrate determinants for cleavage in cis and in trans by the hepatitis C virus NS3 proteinase

1995

Processing of the hepatitis C virus polyprotein is accomplished by a series of cotranslational and posttranslational cleavages mediated by host cell signalases and two virally encoded proteinases. Of these the NS3 proteinase is essential for processing at the NS3/4A, NS4A/4B, NS4B/5A, and NS5A/5B junctions. Processing between NS3 and NS4A occurs in cis, implying an intramolecular reaction mechanism, whereas cleavage at the other sites can also be mediated in trans. Sequence analysis of the amino termini of mature cleavage products and comparisons of amino acid residues around the scissile bonds of various hepatitis C virus isolates identified amino acid residues which might contribute to su…

Cleavage factorvirusesMolecular Sequence DataImmunologyHepacivirusCleavage and polyadenylation specificity factorViral Nonstructural ProteinsBiologyCleavage (embryo)MicrobiologySubstrate SpecificityScissile bondVirologyHumansAmino Acid SequenceAmino AcidsPeptide sequencechemistry.chemical_classificationNS3Cleavage stimulation factorHydrolysisSerine Endopeptidasesbiochemical phenomena metabolism and nutritionAmino acidchemistryBiochemistryMutagenesisInsect ScienceProtein Processing Post-TranslationalRNA HelicasesHeLa CellsResearch ArticleJournal of Virology
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