Search results for "substrate"

showing 10 items of 1018 documents

Wastewater COD characterization: analysis of respirometric and physical-chemical methods for determining biodegradable organic matter fractions

2010

BACKGROUND: In this work, a comprehensive study of the respirometric and physical–chemical methods has been performed to evaluate the information provided by these two methodologies in order to assess the biodegradable organic matter fractions of wastewater. RESULTS: First, an analysis was performed of the influence of the initial substrate on biomass ratio (F0/X0) in the assessment of readily biodegradable organic matter, SS, through respirometric experiments. In order to achieve an adequate assessment of the SS component, similar conditions (given by the initial F0/X0 ratio) must be employed in experiments that are carried to determine SS and YH (heterotrophic yield). Second, a comparativ…

chemistry.chemical_classificationRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical EngineeringOrganic ChemistryChemical oxygen demandBiomassSubstrate (chemistry)BiodegradationPollutionInorganic ChemistryRespirometryFuel TechnologyWastewaterEnvironmental chemistryOrganic matterSewage treatmentWaste Management and DisposalBiotechnologyJournal of Chemical Technology & Biotechnology
researchProduct

Nucleoside phosphotransferase of chick embryo

1979

This paper describes a purification procedure and some properties of a nonspecific nucleoside phosphotransferase of chick embryo, an activity which catalyzes the transfer of chick embryo, an activity which catalyzes the transfer of the phosphate ester from a deoxyribonucleotide or a pyrimidine ribonucleotide to a deoxyribonucleoside acceptor. The enzyme is very unstable to heat, dilution and dialysis and it is almost entirely inactivated by DEAE-cellulose chromatography or gel filtration. A marked enhancement in its stability is caused by numerous nucleotides. In these experiments at least 920-fold purification was obtained by using dTTP (50 microM) as nucleotide protector. The enzyme, puri…

chemistry.chemical_classificationRibonucleotideClinical BiochemistrySize-exclusion chromatographyChick EmbryoCell BiologyGeneral MedicineHydrogen-Ion ConcentrationThymidine KinaseSubstrate SpecificityMolecular WeightDeoxyribonucleosidechemistry.chemical_compoundDeoxyribonucleotideEnzymeIsoelectric pointchemistryBiochemistryNucleoside phosphotransferaseChromatography GelAnimalsNucleotideMolecular BiologyMolecular and Cellular Biochemistry
researchProduct

Aqueous selective photocatalytic oxidation of salicyl alcohol by TiO2 catalysts: Influence of some physico-chemical features

2021

Abstract Partial photocatalytic oxidation of salicyl alcohol (2-hydroxybenzyl alcohol) to salicylaldehyde in water was investigated under environmental friendly conditions in the presence of home-prepared and commercial TiO2 (Merck and Aeroxide P25) samples under UVA irradiation. The photocatalysts were characterized by using BET, XRD, SEM and/or TEM techniques. The effects of crystallinity degree, pH (3–11) and presence of a hole trap (ethanol) on the photocatalytic activity and product selectivity were investigated. 4-Hydroxybenzyl alcohol was also used to study the influence of the position of the substituent group in the aromatic ring. High alcohols conversion and product selectivity va…

chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionEthanolSubstituentSubstrate (chemistry)AlcoholGeneral ChemistryAldehydeCatalysischemistry.chemical_compoundchemistryEnvironmental friendly conditions Photocatalysis Salicyl alcohol Salicylaldehyde Salicylic acid Selective oxidationTiO2PhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelectivityNuclear chemistry
researchProduct

ChemInform Abstract: Epoxidation of Olefins with a Silica-Supported Peracid.

2012

Anhydrous [2-percarboxyethyl] functionalized silica (2a) is an advantageous oxidant for performing the epoxidation of olefins 1. Epoxides 3 do not undergo the ring-opening reactions catalyzed by the acidic silica surface, except for particularly activated cases such as styrene oxide. The hydrophilic and acidic character of the silica surface does not interfere with the directing effects exerted by allylic H-bond acceptor substituents. The alkenes 1 carrying hydroxyl groups react with silica-supported peracid 2a faster than unsubstituted alkenes, thus reversing the trend known for reactions with soluble peracids. These results are attributed to the H-bond interactions of substrate 1 with the…

chemistry.chemical_classificationSilanolchemistry.chemical_compoundAllylic rearrangementchemistryCarboxylic acidStyrene oxidePolymer chemistryAnhydrousSubstrate (chemistry)General MedicineAcceptorCatalysisChemInform
researchProduct

Lateral versus perpendicular segregation in mixed polymer brushes.

2002

Grafting of incompatible polymers on a substrate prevents macrophase separation and the chains self-assemble laterally. Mixed brushes are exposed to different solvents and the morphology is observed via atomic force and x-ray photoemission microscopy. In a nonselective solvent the different species segregate into parallel cylinders ("ripple structure"). Upon exposure to a selective solvent, we encounter a transition to a "dimple" structure, in which the unfavored component forms clusters. Simultaneously, we observe an enhanced perpendicular segregation. The experimental observations are compared to self-consistent field calculations, where qualitative agreement is found.

chemistry.chemical_classificationSolventMaterials scienceMorphology (linguistics)chemistryField (physics)Chemical physicsDimpleRipplePerpendicularGeneral Physics and AstronomyPolymerSubstrate (electronics)Physical review letters
researchProduct

Consecutive Selective Adsorption of Pentamidine and Phosphate Biomolecules on a Self-Assembled Layer:  Reversible Formation of a Chemically Selective…

1996

In situ ellipsometric film thickness measurements, FT-IR external reflectance spectroscopy, and potentiometric measurements indicated that the amphiphile pentamidine (PAM), a bisbenzamidine, associated by self-assembly with a preformed self-assembled monolayer of a mercaptoalkanoic acid on gold. The structural properties of PAM and the nature of the substrate were ideal for the formation of a densely packed monolayer. This process was fully reversible, as demonstrated by changing the pH of the surrounding medium. Thus, disassembly−reassembly occurred when the pH was cycled between 8.7 and 3. The bilayer structure, featuring a positively charged amidinium surface, was subsequently used for s…

chemistry.chemical_classificationStereochemistryBilayerBiomoleculeSubstrate (chemistry)PhosphatePhotochemistryAnalytical Chemistrychemistry.chemical_compoundchemistrySelective adsorptionMonolayerAmphiphileSurface chargeAnalytical Chemistry
researchProduct

Molecular self-assembly on an insulating surface: interplay between substrate templating and intermolecular interactions

2012

We report on molecular self-assembly of biphenyl-4,4'-dicarboxylic acid (BPDCA) on CaCO3(10 (1) over bar4) under ultra-high vacuum conditions. Two-dimensional, ordered islands are obtained upon deposition at room temperature, coexisting with a streaky structure that is ascribed to individual, mobile molecules forming a two-dimensional gas-like phase. High-resolution non-contact atomic force microscopy (NC-AFM) images of the molecular islands reveal an ordered inner structure that is dominated by rows of molecules aligned side by side running along the [(42) over bar 61] crystallographic direction. A detailed analysis of these rows exhibits inter-row distances that are multiples of the calci…

chemistry.chemical_classificationStructure formationHydrogen bondIntermolecular forceSubstrate (electronics)Condensed Matter Physics530CrystallographyDicarboxylic acidchemistryPhase (matter)MoleculeMolecular self-assemblyGeneral Materials ScienceJournal of Physics: Condensed Matter
researchProduct

Synthesis of .beta.-ionone in an aldehyde/xanthine oxidase/.beta.-carotene system involving free radical formation

1994

The enzymic cooxidation of β-carotene (BC) by xanthine oxidase (XO) in aqueous solutions leads to β-ionone (BI) and derivatives: epoxy-β-ionone (EPBI), dihydroactinidiolide, β-cyclocitral, pseudoionone, etc. We demonstrate, in this article, that this is due to free radical (R . ) formation during the first hour of stirring and the use of aldehydes as substrate. The bleaching of BC does not occur when the common substrate of XO, xanthine, is used; this proves that the superoxide anion O 2 .- alone is not active on BC. BI formation in this case is not observed

chemistry.chemical_classificationSuperoxideStereochemistryDihydroactinidiolideSubstrate (chemistry)XanthineIononeMedicinal chemistryAldehydechemistry.chemical_compoundchemistryXanthine oxidaseFree Radical FormationBiotechnologyBiotechnology Progress
researchProduct

Precise structural investigation of symmetric diblock copolymer thin films with resonant soft X-ray reflectivity

2013

Symmetric diblock copolymers are known to form lamellar structures in the bulk of an organic thin film. Polymer/polymer and polymer/substrate interfaces play a critical role in this application. Here, we report the investigation of multiple buried interfaces by using a novel technique resonant soft X-ray reflectivity which benefits from enhanced contrast between different polymers near the carbon K-edge. This allows us to obtain a precise interface structure. We also present an alternative method to determine optical constants of polymers by fitting X-ray reflectivity of polymers with known structural parameters at specific soft X-ray energies. This approach is compared with the way of obta…

chemistry.chemical_classification[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]Materials sciencechemistry.chemical_elementGeneral ChemistrySubstrate (electronics)PolymerCondensed Matter PhysicsMolecular physicsXANESCrystallographychemistryCopolymerLamellar structure[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Thin filmRefractive indexCarbon[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
researchProduct

Chapter 17: The cholinesterases: a discussion of some unanswered questions

1993

Publisher Summary During the past three decades, a vast body of specificity and kinetic data relating to the cholinesterases has accumulated, which must now be explained by the extremely interesting new sequence and X-ray crystallographic results presented by MassouliC et al. As this chapter shows, the cholinesterases are remarkable among enzymes in having a broad specificity embracing both charged and uncharged substrates but with a clearly expressed preference, at any rate in the aliphatic series, for the acylcholine configuration: a classical example of the principle of complementariness between substrate and active site as the basis for enzyme action. It is well known that AChE exists i…

chemistry.chemical_classificationbiologyActive siteSubstrate (chemistry)AcetylcholinesteraseIsozymeSynapsechemistry.chemical_compoundmedicine.anatomical_structureEnzymeBiochemistrychemistrybiology.proteinmedicineBasal laminaButyrylcholinesterase
researchProduct