Search results for " FTIR spectroscopy"

showing 10 items of 14 documents

Chromophore-Protein Interplay During the Phytochrome Photocycle Revealed by Step-Scan FTIR Spectroscopy

2018

Phytochrome proteins regulate many photoresponses of plants and microorganisms. Light absorption causes isomerization of the biliverdin chromophore, which triggers a series of structural changes to activate the signaling domains of the protein. However, the structural changes are elusive, and therefore the molecular mechanism of signal transduction remains poorly understood. Here, we apply two-color step-scan infrared spectroscopy to the bacteriophytochrome from Deinococcus radiodurans. We show by recordings in H2O and D2O that the hydrogen bonds to the biliverdin D-ring carbonyl become disordered in the first intermediate (Lumi-R) forming a dynamic microenvironment, then completely detach …

0301 basic medicineInfrared spectroscopyMolecular Dynamics SimulationBiochemistryCatalysis03 medical and health scienceschemistry.chemical_compoundchromophore-protein interplayColloid and Surface ChemistryBacterial ProteinsSpectroscopy Fourier Transform InfraredPeptide bondta116BiliverdinbiologyPhytochromeHydrogen bondBiliverdineta1182WaterHydrogen BondingDeinococcus radioduransGeneral ChemistryChromophorePhotochemical Processesbiology.organism_classification030104 developmental biologychemistryBiophysicsProtein Conformation beta-StrandDeinococcusPhytochromevalokemiaproteiinitSignal transductionstep-scan FTIR spectroscopyAdenylyl CyclasesJournal of the American Chemical Society
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Effect of Hydration Procedure of Fumed Silica Precursor on the Formation of Luminescent Carbon Centers in SiO 2 :C Nanocomposites

2019

The effect of hydration procedure of fumed silica precursor on photoluminescent properties of carbonized silica (SiO2:C) nanocomposite after chemo/thermal treatments is studied. Main structural effect is the formation of chemical bonding of phenyl groups to silica surface via multiple CSiO bonding bridges. Synthesized samples demonstrate very broad photoluminescence (PL) bands in near ultraviolet and visible ranges with maximum intensity dependent on temperature of thermal annealing. Two main trends in luminescence properties are: 1) hydration-induced blue shift of PL in comparison with PL of unhydrated series; 2) red shift of PL bands with increasing synthesis temperature regardless hydr…

Materials scienceNanocompositechemistry.chemical_elementSiO2 nanoparticles carbon cluster phenyltrimethoxysilane photoluminescence FTIR spectroscopySurfaces and InterfacesCondensed Matter PhysicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringchemistryMaterials ChemistryElectrical and Electronic EngineeringLuminescenceCarbonFumed silicaphysica status solidi (a)
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Crypthecodinium cohnii Growth and Omega Fatty Acid Production in Mediums Supplemented with Extract from Recycled Biomass

2022

Crypthecodinium cohnii is a marine heterotrophic dinoflagellate that can accumulate high amounts of omega-3 polyunsaturated fatty acids (PUFAs), and thus has the potential to replace conventional PUFAs production with eco-friendlier technology. So far, C. cohnii cultivation has been mainly carried out with the use of yeast extract (YE) as a nitrogen source. In the present study, alternative carbon and nitrogen sources were studied: the extraction ethanol (EE), remaining after lipid extraction, as a carbon source, and dinoflagellate extract (DE) from recycled algae biomass C. cohnii as a source of carbon, nitrogen, and vitamins. In mediums with glucose and DE, the highest specific biomass gr…

QH301-705.5omega-3 fatty acidPharmaceutical Sciencefood and beveragesCrypthecodinium cohnii<i>Crypthecodinium cohnii</i>Article<i>Crypthecodinium cohnii</i>; omega-3 fatty acid; biomass recycling; dinoflagellate extract; FTIR spectroscopybiomass recyclingFTIR spectroscopyDrug Discoverydinoflagellate extractBiology (General)Pharmacology Toxicology and Pharmaceutics (miscellaneous)Marine Drugs
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Metallic Ions Effects on the Heat-aggregation Process of b-Lactoglobulin

2007

Settore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Aggregation metallic ions FTIR spectroscopy
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Infrared Spectroscopy In Urolithiasis In Children

2014

Settore MED/14 - NefrologiaSettore CHIM/01 - Chimica Analiticaurolithiasis FTIR spectroscopy urinary stones children
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FDA dimension reduction techniques and components separation in Fourier-transform infrared spectroscopy

2020

FTIR spectroscopy is a measurement technique used to obtain an infrared spectrum of absorption of a solid (or a liquid or a gas), for the characterization of specific chemical components of materials. When repeated measures are taken on samples of materials, the result is a collection of spectra representing a set of samples from continous functions (signals) defined in the domain of the frequencies. An unifying approach to the study of a collection of FTIR spectra is proposed to deal with the presence of random shifts in the peaks, the identification of representative spectra and finally the characterization of the observed differences: in the functional data framework, the performance of …

Settore SECS-S/01 - StatisticaShape analysis functional data reduction of dimensionality FTIR spectroscopy
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Investigation of phthalocyanine crystals exposed to NO2 ambient gas

2002

Crystals of free base phthalocyanine (H2pc) and its unsubstituted metal derivatives Mpc (where M=Ni, Cu, Zn, Pb, and pc=C32H16N8 2−=phthalocyanine ligand) were examined after being exposed to NO2 ambient gas. Scanning electron microscopy (SEM) supported by X-ray microprobe analysis (EDAX), UV–Vis and FTIR spectroscopy as well as X-ray powder diffractometry (XRD) were applied to study the crystals chemistry and surface morphology. The NO2 molecules were found to penetrate the crystal unit which led to the breakdown of the phthalocyanine macrocycle. The surface of the doped crystals has been scaled and covered by a layer composed predominantly of phthalimide. Despite vacuum desorption, it has…

X-ray powder diffractometryMicroprobeScanning electron microscopePhthalocyaninesAnalytical chemistryInorganic ChemistryMetalCrystalchemistry.chemical_compoundAdsorptionchemistryvisual_artDesorptionMaterials Chemistryvisual_art.visual_art_mediumPhthalocyanineUV–Vis and FTIR spectroscopyPhysical and Theoretical ChemistryFourier transform infrared spectroscopyScanning electron microscopyX-ray microprobeNitrogen dioxidePolyhedron
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Infrared Spectroscopy of Ruthenium Tetroxide and High-resolution analysis of the v3 band

2015

International audience

[PHYS.NUCL] Physics [physics]/Nuclear Theory [nucl-th][PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th][PHYS.NEXP] Physics [physics]/Nuclear Experiment [nucl-ex]Isotopic shiftRuthenium TetroxideHigh resolution FTIR spectroscopy[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]ComputingMilieux_MISCELLANEOUSSimulation
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On-line measurements of RuO$_4$ during a PWR severe accident

2015

International audience; After the Fukushima accident, it became essential to have a way to monitor in real time the evolution of a nuclear reactor during a severe accident, in order to react efficiently and minimize the industrial, ecological and health consequences of the accident. Among gaseous fission products, the tetroxide of ruthenium RuO$_4$ is of prime importance since it has a significant radiological impact. Ruthenium is a low volatile fission product but in case of the rupture of the lower head by the molten corium, the air entering into the vessel oxidizes Ru into gaseous RuO$_4$, which is not trapped by the Filtered Containment Venting Systems. To monitor the presence of RuO$_4…

[PHYS.NUCL] Physics [physics]/Nuclear Theory [nucl-th][PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th][PHYS.NEXP] Physics [physics]/Nuclear Experiment [nucl-ex]TetroxideHigh resolution FTIR spectroscopyFission product[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]Severe accidentRuthenium
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Role of residual water hydrogen bonding in sugar/water/biomolecule systems: a possible explanation fortrehalose peculiarity

2007

We report on the set of experimental and simulative evidences which enabled us to suggest how biological structures embedded in a non-liquid water–saccharide solvent are anchored to the surrounding matrix via a hydrogen bond network. Such a network, whose rigidity increases by decreasing the sample water content, couples the degrees of freedom of the biostructure to those of the matrix and gives place to protein–saccharide–water structures (protein–solvent conformational substates). In particular, the whole set of data evidences that, while the protein–sugar interaction is well described in terms of a water entrapment hypothesis, the water replacement hypothesis better describes the sugar–m…

chemistry.chemical_classificationChemistryHydrogen bondStereochemistryBiomoleculeCondensed Matter PhysicsTrehaloseSolventchemistry.chemical_compoundtrehalose water FTIR spectroscopyRigidity (electromagnetism)MembraneChemical physicsMoleculeGeneral Materials ScienceSupercoolingJournal of Physics: Condensed Matter
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