Search results for "purification"

showing 10 items of 271 documents

Anaerobic removal of 1-methoxy-2-propanol under ambient temperature in an EGSB reactor

2015

Two laboratory-scale expanded granular sludge bed (EGSB) reactors were operated at 18 and 25 °C, respectively, for the treatment of synthetic wastewater composed of ethanol and 1-methoxy-2-propanol (M2P) in a mass ratio of 4:1. Reactors were operated first with continuous wastewater supply and after with discontinuous substrate supply (5 days a week, 16 h a day) to simulate shift working conditions. Under continuous wastewater supply chemical oxygen demand (COD), removal efficiency higher than 95 % was achieved at the end of the trial applying organic loading rates (OLR) of 29 and 43 kg COD m(-3) day(-1) at 18 and 25 °C; thus, corresponding to M2P OLR of 6.4 and 9.3 kg COD m(-3) day(-1), re…

ChemistryChemical oxygen demandEnvironmental engineeringSubstrate (chemistry)BioengineeringPortable water purificationGeneral MedicineQuímicaWastewaterPulp and paper industryMethaneWater PurificationPropanolchemistry.chemical_compoundBioreactorsWastewaterPropylene GlycolsBioreactorSewage treatmentAnaerobiosisBiotechnology
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Purification of a fetal bovine serum factor that inhibits DNA synthesis in chick embryo retinas

1992

Chick embryo retina DNA synthesis Fetal bovine serum Growth-inhibitory factor In vitro effect Purification procedure
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Assessing and modeling nitrite inhibition in microalgae-bacteria consortia for wastewater treatment by means of photo-respirometric and chlorophyll f…

2022

Abstract Total nitrite (TNO2 = HNO2 + NO−2) accumulation due to the activity of ammonia-oxidizing bacteria (AOB) was monitored in microalgae-bacteria consortia, and the inhibitory effect of nitrite/free nitrous acid (NO2-N/FNA) on microalgae photosynthesis and inhibition mechanism was studied. A culture of Scenedesmus was used to run two sets of batch reactors at different pH and TNO2 concentrations to evaluate the toxic potential of NO2-N and FNA. Photo-respirometric tests showed that NO2-N accumulation has a negative impact on net oxygen production rate (OPRNET). Chlorophyll a fluorescence analysis was used to examine the biochemical effects of NO2-N stress and the mechanism of NO2-N inhi…

ChlorophyllPhotosynthetic reaction centrechemistry.chemical_classificationNitrous acidChlorophyll aEnvironmental EngineeringBacteriabiologyChemistryChlorophyll AElectron acceptorbiology.organism_classificationPollutionFluorescenceWater Purificationchemistry.chemical_compoundMicroalgaeEnvironmental ChemistryNitriteWaste Management and DisposalChlorophyll fluorescenceNitritesScenedesmusPhotosystemNuclear chemistryScience of The Total Environment
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Insect immunity. Constitutive expression of a cysteine-rich antifungal and a linear antibacterial peptide in a termite insect

2001

0021-9258 (Print) Journal Article Research Support, Non-U.S. Gov't; Two novel antimicrobial peptides, which we propose to name termicin and spinigerin, have been isolated from the fungus-growing termite Pseudacanthotermes spiniger (heterometabole insect, Isoptera). Termicin is a 36-amino acid residue antifungal peptide, with six cysteines arranged in a disulfide array similar to that of insect defensins. In contrast to most insect defensins, termicin is C-terminally amidated. Spinigerin consists of 25 amino acids and is devoid of cysteines. It is active against bacteria and fungi. Termicin and spinigerin show no obvious sequence similarities with other peptides. Termicin is constitutively p…

ChromatographyCysteine/*chemistryIsoptera/*immunologyBase SequenceProtein ConformationfungiAntifungal Agents/*chemistry/isolation & purification/pharmacologyMolecular Sequence DataSequence HomologyImmunohistochemistryAmino AcidAnti-Bacterial Agents/*chemistry/isolation & purification/pharmacologyRecombinant Proteins/chemistry/isolation & purification/pharmacologyHigh Pressure LiquidAnimalsAmino Acid SequencePeptidesDNA Primers
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Purification and molecular weight determination of the membrane protein cytochrome o-complex from Rhodospirillum rubrum by high-performance liquid ch…

1988

ChromatographyCytochromebiologyChemistryClinical BiochemistryRhodospirillum rubrumGeneral Medicinebiology.organism_classificationHigh-performance liquid chromatographyAnalytical ChemistryMembrane proteinProtein purificationbiology.proteinGeneral Materials ScienceFresenius' Zeitschrift für analytische Chemie
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Study on a photocatalytic membrane reactor for water purification

2000

Abstract Some results obtained in a photocatalytic membrane reactor, to be used for degradation of toxic organic species dissolved in water, are reported. The catalyst, TiO 2 P25 Degussa, was immobilised by means of a flat sheet polymeric membrane and 4-Nitrophenol (4-NP) was used as a model molecule to evaluate the reactor performance. A preliminary investigation of the stability, under UV irradiation, of some eligible polymeric membranes was carried out by using scanning electron microscopy (SEM), optical microscopy (OM), determinations of water permeation flux (WPF) and total organic carbon (TOC). These tests showed that commercial membranes made of fluoride + PP (FS 50 PP-Dow), polysulp…

ChromatographyMaterials scienceMembrane reactorScanning electron microscopePolyacrylonitrilePortable water purificationGeneral ChemistryPermeationCatalysischemistry.chemical_compoundMembraneChemical engineeringchemistryPhotocatalysisWater treatment
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Complete decontamination and regeneration of DNA purification silica colum

2008

Silica columns are among the most used DNA purification systems, allowing a good yield of high-quality nucleic acids without organic extractions. Silica column regeneration protocols reported up to now to remove DNA traces are time-consuming, and their effectiveness on genomic DNA has not been demonstrated. Here we report a very rapid regeneration procedure that ensures no DNA carryover, independent of its size, without impairing column efficiency. The method takes advantage of the improved DNA removal by low concentrations of Triton X-100.

ChromatographyOctoxynolBiophysicsFungal geneticsSilica decontaminationGenomic DNACell BiologyHuman decontaminationSaccharomyces cerevisiaeDNA separation by silica adsorptionSilicon DioxideBiochemistryDNA extractionPolymerase Chain Reactionchemistry.chemical_compoundgenomic DNAchemistrySpin column-based nucleic acid purificationNucleic acidGenome FungalParticle SizeDNA FungalMolecular BiologyDNAChromatography High Pressure Liquid
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Packings and stationary phases for biopolymer separations by HPLC

1987

Packings and stationary phases applied to high resolution separations of proteins, enzymes, and nucleic acids must satisfy a series of distinct criteria that are different from those usually required by HPLC of low molecular weight non-biologically active analytes. These requirements have been met through substantial improvements in classical gel media together with novel developments in silica supports, and have led to a family of products with tailor-made and reproducible properties. Supports consisting of cross-linked organic gels, and inorganic materials (mostly silicas) are now available with graduated particle sizes, pore sizes, porosities and surface areas as well as non-porous beads…

ChromatographyResolution (mass spectrometry)ChemistryOrganic ChemistryClinical BiochemistrySize-exclusion chromatographyFractionationengineering.materialBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectPhase (matter)Protein purificationengineeringBiopolymerChromatographia
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Rapid detergent exchange in solutions of the membrane protein bacteriorhodopsin by preparative high-performance liquid chromatography (HPLC)

1984

ChromatographybiologyChemistryHydrophilic interaction chromatographyClinical BiochemistryFast protein liquid chromatographyBacteriorhodopsinGeneral MedicineHigh-performance liquid chromatographyAnalytical ChemistryMembrane proteinProtein purificationbiology.proteinGeneral Materials ScienceThermoresponsive polymers in chromatographyFresenius' Zeitschrift für analytische Chemie
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Use of an enzyme-assisted method to improve protein extraction from olive leaves.

2013

The improvement of protein extraction from olive leaves using an enzyme-assisted protocol has been investigated. Using a cellulase enzyme (Celluclast® 1.5L), different parameters that affect the extraction process, such as the influence and amount of organic solvent, enzyme amount, pH and extraction temperature and time, were optimised. The influence of these factors was examined using the standard Bradford assay and the extracted proteins were characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The optimum extraction parameters were: 30% acetonitrile, 5% (v/v) Celluclast® 1.5L at pH 5.0 and 55°C for 15min. Under these conditions, several protein extracts…

ChromatographybiologyChemistryPlant ExtractsSodiumExtraction (chemistry)Temperaturechemistry.chemical_elementGeneral MedicineCellulaseChemical FractionationAnalytical ChemistrySolventPlant LeavesElectrophoresisCellulaseOleaProtein purificationbiology.proteinElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisBradford protein assayFood SciencePlant ProteinsFood chemistry
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