Search results for "circular"

showing 10 items of 856 documents

Protein aggregation/crystallization and minor structural changes: universal versus specific aspects.

2007

AbstractProtein association covers wide interests in biophysics, protein science, and biotechnologies, and it is often viewed as governed by conformation details. More recently, the existence of a universal physical principle governing aggregation/crystallization processes has been suggested by a series of experiments and shown to be linked to the universal scaling properties of concentration fluctuations occurring in the proximity of a phase transition (spinodal demixing in the specific case). Such properties have provided a quantitative basis for capturing kinetic association data on a universal master curve, ruled by the normalized distance of the state of the system from its instability…

SpinodalPhase transitionChemistryProtein ConformationCircular DichroismLasersBiophysicsNucleationSupramolecular AssembliesInstabilityUniversality (dynamical systems)law.inventionCrystallographyProtein structureModels ChemicallawChemical physicsAnimalsScattering RadiationMuramidaseCrystallizationCrystallizationScalingChickensBiophysical journal
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Innovation strategies geared toward the circular economy: A case study of the organic olive-oil industry

2018

Circular Economy (CE) focuses on the (re)design of processes and products aiming to minimize negative environmental impact, by reducing the use of non-renewable resources, increasing products durability, improving waste management and enhancing the market for secondary raw materials. In the management field very few contributions deal with the topic of CE as a model that firms can implement from a business model perspective. The aim of the present study is to describe, by using a case study in olive oil industry, how firms in practice adapt their business model towards CE paradigm and the influence of personal drivers and stakeholders in this adaptation. The findings reveal that circular ec…

Stakeholders theoryStrategy and ManagementTheory of planned behaviour010501 environmental sciencesDevelopmentBusiness modelManagement Monitoring Policy and Law01 natural sciencesPersonal attitude0502 economics and businessSettore AGR/01 - Economia Ed Estimo RuraleEnvironmental impact assessmentDevelopment3304 EducationAdaptation (computer science)Stakeholder theoryAgri-food industryIndustrial organization0105 earth and related environmental sciencesBusiness modelRenewable Energy Sustainability and the EnvironmentCircular economy05 social sciencesTheory of planned behaviorStrategy and Management1409 Tourism Leisure and Hospitality ManagementSustainabilitySustainabilityBusiness050203 business & managementOlive oil
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Synthesis and Characterization of Adducts Derived from the syn-Diastereomer of Benzo[a]pyrene 7,8-Dihydrodiol 9,10-Epoxide and the 5‘-d(CCTATAGATATCC…

1996

5'-d(CCTATAGATATCC) was reacted with each syn-enantiomer of trans-7,8-dihydroxy 9,10-epoxy 7,8,9,10-tetrahydrobenzo[a]pyrene (syn-BPDE). The (-)-enantiomer yielded one dominating adduct, whereas the (+)-enantiomer resulted in two major adducts. As indicated by optical spectroscopic methods, the major adduct derived from both (-)- and (+)-syn-BPDE involves cis addition of the C-10 position of the diol epoxide to the exocyclic amino group of deoxyguanosine [(-)-syn-BPDEc-N2-dG and (+)-syn-BPDEc-N2-dG, respectively], whereas the minor (+)-syn-BPDE adduct is identical to a trans adduct [(+)-syn-BPDEt-N2-dG]. The cis adducts as well as the (+)-syn-BPDEt-N2-dG adduct are chemically stable for sev…

Stereochemistry78-Dihydro-78-dihydroxybenzo(a)pyrene 910-oxideMolecular Sequence DataDiolOligonucleotidesEpoxideToxicologyAdductDNA Adductschemistry.chemical_compoundDrug StabilityDeoxyguanosineBase CompositionBase SequenceCircular DichroismTemperatureDiastereomerStereoisomerismGeneral MedicineFluorescenceSpectrometry Fluorescencenervous systemchemistryBenzo(a)pyreneNucleic Acid ConformationPyreneChemical Research in Toxicology
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Assignment of the Absolute Configuration and Total Synthesis of (+)-Caripyrin

2014

The antifungal secondary metabolite (+)-caripyrin was studied by vibrational circular dichroism spectroscopy. Analysis of the recorded data, with the Boltzmann weighted-average of the spectra calculated at the B3LYP/6-311G(d,p) level of theory for all relevant conformers, unequivocally proved the (R,R)-configuration for the dextrorotatory natural product. Based on this finding, a short enantioselective synthesis of (+)-caripyrin was developed.

StereochemistryChemistryOrganic ChemistryVibrational circular dichroismEnantioselective synthesisAbsolute configurationInfrared spectroscopyTotal synthesisPhysical chemistryPhysical and Theoretical ChemistrySpectroscopyConformational isomerismDextrorotatoryEuropean Journal of Organic Chemistry
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DNA interaction of CuII, NiII and ZnII functionalized salphen complexes: studies by linear dichroism, gel electrophoresis and PCR.

2013

The interaction of salphen-type NiII, CuII and ZnII complexes with native DNA was investigated by exploiting linear dichroism experiments. The NiII complex behaves as a typical intercalator, binding strongly and stiffening and unwinding the DNA. The strength of the DNA interaction is slightly weaker for the copper complex and much weaker for the zinc complex. Plasmid-DNA gel electrophoresis experiments indicated that while CuII and ZnII complexes do not induce the unwinding of supercoiled DNA, the NiII complex has a nuclease activity without the addition of external agents. On the other hand, as shown in the PCR assays, we demonstrate that, at the used concentrations, only the CuII complex …

StereochemistryIntercalation (chemistry)Molecular Conformationchemistry.chemical_elementZincPhenylenediaminesLinear dichroismCrystallography X-RayPolymerase Chain ReactionInorganic Chemistrychemistry.chemical_compoundBiomimetic MaterialsCoordination ComplexesNickelGel electrophoresisElectrophoresis Agar GelNucleaseDeoxyribonucleasesbiologyCircular DichroismDNASettore CHIM/08 - Chimica FarmaceuticaCopperCrystallographyZincAnticancerchemistrySettore CHIM/03 - Chimica Generale E Inorganicabiology.proteinDNA supercoilMetal complexeDNACopperDalton transactions (Cambridge, England : 2003)
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Flipping Motion To Bias the Organized Supramolecular Polymerization of N-Heterotriangulenes

2019

Synergistic experimental and theoretical studies have allowed the disentangling of the possible pathways for the supramolecular polymerization of a series of dicyanovinyl-bridged N-heterotriangulene (NHT) derivatives bearing benzamide units with achiral (1a) and chiral (1b,c) side chains. The synthesis of these bowl-shaped, self-assembling units yields a mixture of monomeric species with C3- and C1-symmetry. Both monomeric species are able to self-assemble into different supramolecular aggregates with sufficient stability to coexist in freshly prepared solutions. The dissimilar ratio of the aggregates initially generated results in different spectroscopic features and, more specifically, in…

Steric effectsCircular dichroismGeneral Chemical EngineeringSupramolecular chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSpectral line0104 chemical scienceschemistry.chemical_compoundCrystallographyMonomerchemistryPolymerizationMaterials ChemistrySide chain0210 nano-technologyBenzamideChemistry of Materials
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Structure elucidation of the adducts formed by fjord region Dibenzo[a,l]pyrene-11,12-dihydrodiol 13,14-epoxides with deoxyguanosine.

1999

Model adducts to be used in the identification of biologically formed adducts were synthesized by reaction of fjord-region dibenzo[a,l]pyrene 11,12-dihydrodiol 13,14-epoxides (DB[a,l]PDE) and deoxyadenosine (dA). The (+/-)-anti-DB[a,l]PDE was reacted with dA in dimethylformamide at 100 degrees C for 30 min to give four DB[a, l]PDE-14-N(6)dA adducts: (-)-anti-trans (26%), (+)-anti-trans (26%), (-)-anti-cis (17%), and (+)-anti-cis (17%). The (+/-)-syn-DB[a,l]PDE was reacted with dA under the same conditions to yield four DB[a, l]PDE-14-N(6)dA adducts and one N7Ade adduct: (+)-syn-cis (19%), (+)-syn-trans (13%), (-)-syn-cis (19%), (-)-syn-trans (13%), and (+/-)-syn-DB[a,l]PDE-14-N7Ade (22%). T…

Steric effectsCircular dichroismMagnetic Resonance SpectroscopyMolecular StructureStereochemistryDeoxyguanosineGeneral MedicineDNAFast atom bombardmentToxicologyMass SpectrometryAdductDihydroxydihydrobenzopyreneschemistry.chemical_compoundDNA AdductsStructure-Activity RelationshipSpectrometry FluorescenceDeoxyadenosinechemistryDimethylformamidePyreneStereoselectivityChromatography High Pressure LiquidChemical research in toxicology
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Bis- and Trisamides Derived From 1′-Aminoferrocene-1-carboxylic Acid and α-Amino Acids: Synthesis and Conformational Analysis

2009

Ferrocene derivatives with one or two achiral and chiral arms based on α-amino acids (Gly, l-Ala, l-Val) attached to the cyclopentadienyl rings were prepared by solution-phase peptide synthesis from N-acetyl- and N-Boc-protected 1′-aminoferrocene-1-carboxylic acids (Boc = tert-butoxycarbonyl). The conformational preference in the solid state of selected examples was elucidated by X-ray crystallography. The chiroptical properties of chiral bis- and trisamides were investigated by circular dichroism (CD) spectroscopy in solution. The conformational preference was studied by NMR and IR spectroscopy, as well as by molecular modeling (DFT). For the bisamides, a conformational library is observed…

Steric effectschemistry.chemical_classificationCircular dichroismMolecular modelChemistryStereochemistryOrganic ChemistryAmino acidInorganic Chemistrychemistry.chemical_compoundCyclopentadienyl complexIntramolecular forcePeptide synthesisPhysical and Theoretical ChemistryConformational isomerismOrganometallics
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(Strept)avidin as host for biotinylated coordination complexes: stability, chiral discrimination, and cooperativity

2005

Incorporation of a biotinylated ruthenium tris(bipyridine) [Ru(bpy)₂(Biot-bpy)]²⁺ (1) in either avidin or streptavidin-(strept)avidin-can be conveniently followed by circular dichroism spectroscopy. To determine the stepwise association constants, cooperativity, and chiral discrimination properties, diastereopure (Λ and δ)-1 species were synthesized and incorporated in tetrameric (strept)avidin to afford (δ-[Ru(bpy)₂(Biot-bpy)]²⁺)x⊂avidin, (Λ- [Ru(bpy)₂(Biot-bpy)]²⁺)x⊂avidin, (δ-[Ru(bpy)₂(Biot- bpy)]²⁺)x⊂streptavidin, and (Λ-[Ru(bpy)₂(Biot-bpy)]²⁺) x⊂streptavidin (x = 1-4) For these four systems, the overall stability constants are log β₄ = 28.6, 30.3, 36.2, and 36.4, respectively. Critical…

StreptavidinCircular dichroismProtein ConformationStereochemistryBiotinchemistry.chemical_elementCooperativity010402 general chemistry01 natural sciencesInorganic ChemistryStructure-Activity RelationshipBipyridinechemistry.chemical_compound22'-DipyridylBacterial ProteinsBiotinCoordination ComplexesBiotinylation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSMolecular Structurebiology010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryAvidinProtein Structure Tertiary0104 chemical sciencesRuthenium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographychemistryBiotinylation[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrybiology.proteinStreptavidinAvidin
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A Stereochemically Driven Supramolecular Polymerisation

2018

Anthracyclines self-assemble in water into dimers. In the presence of sufficiently high salt (NaCl) concentrations, solutions of the antibiotic doxorubicin, but not those of the closely related molecules daunomycin and epirubicin, turn into gels barely compatible with the presence of small oligomers. The use of spectroscopic, scattering, imaging and computational techniques, allowed light to be shed on the self-assembly process that triggered doxorubicin gelification. A complex picture emerged, with doxorubicin molecules assembled into long, highly chiral, supramolecular aggregates made of hundreds of units, showing redshifted fluorescence spectra, very short fluorescence lifetimes and smal…

Supramolecular chemistry02 engineering and technology010402 general chemistryPhotochemistrydoxorubicin01 natural sciencesCatalysisTurn (biochemistry)chemistry.chemical_compoundMolecular dynamicsanthracyclines; doxorubicin; fluorescence; circular dichroism; SAXS; molecular dynamicsMoleculeanthracyclinesScatteringOrganic ChemistrySAXSGeneral Chemistry021001 nanoscience & nanotechnologyFluorescencemolecular dynamicscircular dichroism0104 chemical sciencesMonomerchemistryPolymerizationfluorescence0210 nano-technologyChemistry - A European Journal
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