Search results for "CRYSTAL-STRUCTURE"

showing 10 items of 61 documents

Comparative analysis of two paradigm bacteriophytochromes reveals opposite functionalities in two-component signaling

2021

Bacterial phytochrome photoreceptors usually belong to two-component signaling systems which transmit environmental stimuli to a response regulator through a histidine kinase domain. Phytochromes switch between red light-absorbing and far-red light-absorbing states. Despite exhibiting extensive structural responses during this transition, the model bacteriophytochrome from Deinococcus radiodurans (DrBphP) lacks detectable kinase activity. Here, we resolve this long-standing conundrum by comparatively analyzing the interactions and output activities of DrBphP and a bacteriophytochrome from Agrobacterium fabrum (Agp1). Whereas Agp1 acts as a conventional histidine kinase, we identify DrBphP a…

Histidine KinaseLightPROTEINSScienceAgrobacteriumHISTIDINE KINASESKinasesMolecular Dynamics SimulationPhotoreceptors MicrobialTRANSDUCTIONArticleCYANOBACTERIAL PHYTOCHROME CPH1ACTIVATIONBacterial ProteinsProtein DomainsCRYSTAL-STRUCTUREPHOSPHORYLATIONX-ray crystallographyBacterial structural biologyQREARRANGEMENTSphotoreceptorsAGROBACTERIUM-TUMEFACIENSPhosphoric Monoester HydrolasesINSIGHTSbacterial phytochromesEnzyme mechanismsbacteriaDeinococcus3111 BiomedicineSignal Transduction
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Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu 2 IM](HC 2 O 4 ) as CO 2 shuttle

2017

International audience; This manuscript describes the using of biosourced L-valine, oxalic acid and glyoxal to produce a biobased imidazolium hydrogen oxalate [iBu(2)IM](HC2O4) which is converted to its related hydrogen carbonate salt by a simple electrolysis without using strong base. The addition of weak protic acids to the latter compound leads to a rapid and quantitative CO2 release with formation of the starting hydrogen oxalate salt or a new halide free bio-based ionic liquid [iBu(2)IM](AcO) which is able to adsorb reversibly the CO2 at room temperature. The protonation reactions, combined with electrolysis, could then be a promising alternative solution for storage and transport of C…

HydrogenOxalic acidInorganic chemistryHalideSalt (chemistry)chemistry.chemical_elementProtonation010402 general chemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesOxalatelaw.inventionefficientionic liquidschemistry.chemical_compoundlawstabilized phosphenium adductsEnvironmental Chemistry[CHIM]Chemical Scienceselectrochemical reductioncaptureacidsmethanolchemistry.chemical_classificationElectrolysis010405 organic chemistrycrystal-structurePollution0104 chemical scienceschemistrydimethyl-sulfoxideIonic liquid
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Vibrational Properties of CuO and Cu4O3 from First-Principles Calculations, and Raman and Infrared Spectroscopy

2012

International audience; A combined experimental and theoretical study is reported on the vibrational properties of tenorite CuO and paramelaconite Cu4O3. The optically active modes have been measured by Raman scattering and infrared absorption spectroscopy. First-principles calculations have been carried out with the LDA+U approach to account for strong electron correlation in the copper oxides. The vibrational properties have been computed ab initio using the so-called direct method. Excellent agreement is found between the measured Raman and infrared peak positions and the calculated phonon frequencies at the Brillouin zone center, which allows the assignment of all prominent peaks of the…

INITIO MOLECULAR-DYNAMICSPhononInfraredAnalytical chemistryAb initioCOPPERInfrared spectroscopyPARAMELACONITE02 engineering and technologyCUPRIC OXIDEengineering.material010402 general chemistryAUGMENTED-WAVE METHOD01 natural sciencesMolecular physicssymbols.namesakeTHIN-FILMSCRYSTAL-STRUCTUREPhysical and Theoretical ChemistryCARBON-MONOXIDESpectroscopyChemistryCU2O[CHIM.MATE]Chemical Sciences/Material chemistryParamelaconite021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsREDUCTIONGeneral Energy[ CHIM.MATE ] Chemical Sciences/Material chemistryengineeringsymbols0210 nano-technologyRaman spectroscopyRaman scatteringThe Journal of Physical Chemistry C
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Prussian Blue Analogues of Reduced Dimensionality

2012

Abstract: Mixed-valence polycyanides (Prussian Blue analogues) possess a rich palette of properties spanning from room-temperature ferromagnetism to zero thermal expansion, which can be tuned by chemical modifications or the application of external stimuli (temperature, pressure, light irradiation). While molecule-based materials can combine physical and chemical properties associated with molecular-scale building blocks, their successful integration into real devices depends primarily on higher-order properties such as crystal size, shape, morphology, and organization. Herein a study of a new reduced-dimensionality system based on Prussian Blue analogues (PBAs) is presented. The system is …

LANGMUIR-BLODGETT-FILMSMaterials scienceSpin glassORDERING TEMPERATUREsingle-chain magnetsNanotechnologyiron(ii) complex02 engineering and technologyCrystal structure010402 general chemistrySINGLE-CHAIN MAGNETSlangmuir-blodgett-films01 natural sciencesThermal expansionBiomaterialsCrystalchemistry.chemical_compoundPHOTOINDUCED MAGNETIZATIONTHIN-FILMSDEGREES-Cphotoinduced magnetizationMoleculeGeneral Materials ScienceCRYSTAL-STRUCTURESThin filmPrussian bluePhysicsGeneral Chemistry021001 nanoscience & nanotechnologyIRON(II) COMPLEX0104 chemical sciencesHYBRID FILMSordering temperaturesquare grid networkChemistrychemistryFerromagnetismSQUARE GRID NETWORKthin-filmshybrid filmsdegrees-c0210 nano-technologyEngineering sciences. Technologycrystal-structuresBiotechnologySmall
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Characterization of Flux-Grown SmxNd1–xVO4 Compounds and High-Pressure Behavior for x = 0.5

2019

The crystal structure and the vibrational and optical characteristics of flux-grown mixed lanthanide vanadate compounds SmxNd1–xVO4 (x = 0, 0.1, 0.25, 0.5, 0.75 and 1) are reported. A linear, monot...

LanthanideMaterials scienceAnalytical chemistryPHONON02 engineering and technologyCrystal structure010402 general chemistryPRVO401 natural sciencesRAMANX-RAY-DIFFRACTIONLATTICE-DYNAMICSCONTRACTIONSPECTRAVanadateEFFECTIVE IONIC-RADIICRYSTAL-STRUCTURESPhysical and Theoretical Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)X-RAY-DIFFRACTION; EFFECTIVE IONIC-RADII; CRYSTAL-STRUCTURES; LATTICE-DYNAMICS; ENERGY-TRANSFER; RAMAN; PHONON; CONTRACTION; SPECTRA; PRVO4General EnergyHigh pressure0210 nano-technologyENERGY-TRANSFERFlux (metabolism)
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An unprecedented hetero-bimetallic three-dimensional spin crossover coordination polymer based on the tetrahedral [Hg(SeCN)4]2− building block

2019

[EN] Self-assembly of octahedral FeII ions, trans-1,2-bis(4-pyridyl) ethane (bpe) bridging ligands and [Hg(XCN)(4)](2-) (X = S (1), Se (2)) tetrahedral building blocks has afforded a new type of hetero-bimetallic Hg-II-Fe-II spin-crossover (SCO) 3D 6,4-connected coordination polymer (CP) formulated {Fe(bpe)[Hg(XCN)(4)]}(n). For X = S (1), the ligand field is close to the crossing point but 1 remains paramagnetic over all temperatures. In contrast, for X = Se (2) the complex undergoes complete thermal induced SCO behaviour centred at T-1/2 = 107.8 K and complete photoconversion of the low spin state into a metastable high-spin state (LIESST effect) with T-LIESST = 66.7 K. The current results…

Ligand field theoryMaterials scienceSpin statesCoordination polymerCrystal structureMagnetic-Properties010402 general chemistry01 natural sciencesCatalysisLIESSTParamagnetismchemistry.chemical_compoundSpin crossoverPressureMaterials ChemistrySpectroscopic investigationsPolynuclear complexesCrystal-StructureBehavior010405 organic chemistryMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyOctahedronchemistryFISICA APLICADATransitionX-RayCeramics and CompositesHg(Scn)(4)(2-) UnitStateChemical Communications
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The three-dimensional structure of Drosophila melanogaster (6–4) photolyase at room temperature

2021

A crystal structure of a photolyase at room temperature confirms the structural information obtained from cryogenic crystallography and paves the way for time-resolved studies of the photolyase at an X-ray free-electron laser.

MECHANISMMaterials scienceAbsorption spectroscopyDNA repairfotobiologia02 engineering and technologyCrystal structureREPAIR ACTIVITY03 medical and health sciencesCOLI DNA PHOTOLYASEX-RAY-DIFFRACTIONCryptochromeStructural BiologyAnimalsserial crystallographyCRYSTAL-STRUCTURECRYPTOCHROMEPhotolyaseSERIAL FEMTOSECOND CRYSTALLOGRAPHY030304 developmental biology0303 health sciencesCrystallographyflavoproteinsFADResolution (electron density)TemperaturebanaanikärpänenDNAkidetiede(6-4) photolyase021001 nanoscience & nanotechnologyResearch PapersRADICAL TRANSFER(6–4) photolyaseroom-temperature structureCrystallographyphotolyasesDrosophila melanogasterRECONSTITUTIONX-ray crystallography1182 Biochemistry cell and molecular biologylämpötilaproteiinit0210 nano-technologyDeoxyribodipyrimidine Photo-LyasePHOTOACTIVATIONVisible spectrumActa Crystallographica Section D Structural Biology
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New Magnetic Thin Film Hybrid Materials Built by the Incorporation of Octanickel(II)-oxamato Clusters Between Clay Mineral Platelets

2011

We report on a new method based on the combination of Langmuir-Schaefer deposition with self-assembly to insert highly anisotropic Ni(8) molecules in a hybrid organic-inorganic nanostructure. Spectroscopic, crystallographic, and magnetic data prove the successful insertion of the guest cationic molecule between templating clay platelets. These results open a new route toward the highly controlled fabrication of tailored functional organic-inorganic nanomaterials.

MULTIPLET STRUCTURENanostructureFabricationNICKELCationic polymerizationchemistry.chemical_elementNanotechnologyCrystal structureDINICKEL(II) COMPLEXESNanomaterialsMOLECULESNickelchemistryMoleculeCRYSTAL-STRUCTURECOREGeneral Materials ScienceVACANCY LEVELSPhysical and Theoretical ChemistryHybrid materialSPIN-EXCHANGEThe Journal of Physical Chemistry Letters
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Aminopropyltransferases involved in polyamine biosynthesis localize preferentially in the nucleus of plant cells

2012

Plant aminopropyltransferases consist of a group of enzymes that transfer aminopropyl groups derived from decarboxylated S-adenosyl-methionine (dcAdoMet or dcSAM) to propylamine acceptors to produce polyamines, ubiquitous metabolites with positive charge at physiological pH. Spermidine synthase (SPDS) uses putrescine as amino acceptor to form spermidine, whereas spermine synthase (SPMS) and thermospermine synthase (TSPMS) use spermidine as acceptor to synthesize the isomers spermine and thermospermine respectively. In previous work it was shown that both SPDS1 and SPDS2 can physically interact with SPMS although no data concerning the subcellular localization was reported. Here we study the…

Macromolecular AssembliesProteomicsS-AdenosylmethioninePlant anatomyImmunohistoquímicaArabidopsislcsh:MedicineSecondary MetabolismSpermineExpressionPlant ScienceSpermidine synthaseBiochemistrychemistry.chemical_compoundBimolecular fluorescence complementationCytosolMolecular Cell BiologyPolyaminesPlant Genomicslcsh:SciencePlant Growth and DevelopmentMultidisciplinarybiologyPlant BiochemistryArabidopsis-ThalianaGenomicsImmunohistochemistryMetabolismeFunctional GenomicsBiochemistrySpermine synthasePlant proteinPlant PhysiologyMechanismResearch ArticleHistologyAcyltransferasePlant Cell BiologyActive Transport Cell NucleusSpermidine SynthaseBimolecular fluorescence complementationProtein InteractionsBiologyCell NucleusCrystal-Structurelcsh:RHistologiaBotanyProtein interactionsSubcellular localizationAnatomia vegetalExpressió gènicaMolecular WeightSpermidineMetabolismchemistryDecarboxylasebiology.proteinPutrescineBotànicalcsh:QGene expressionSpermidine synthase
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Thermal stability and enhanced thermoelectric properties of the tetragonal tungsten bronzes Nb8-xW9+xO47 (0 <x <5)

2017

Thermoelectric materials are believed to play a fundamental role in the energy field over the next years thanks to their ability of directly converting heat into usable electric energy. To increase their integration in the commercial markets, improvements of the efficiencies are needed. At the same time, cheap and non-toxic materials are required along with easily upscalable production cycles. Compounds of the tetragonal tungsten bronze (TTB) series Nb8-xW9+xO47 fulfill all these requirements and are promising materials. Their adaptive structure ensures glass-like values of the thermal conductivity, and the substitution on the cation side allows a controlled manipulation of the electronic p…

Materials scienceEQUILIBRIATITANIUM-OXYGEN SYSTEMCRYSTALLOGRAPHIC SHEARchemistry.chemical_elementNanotechnology02 engineering and technologyTemperature cyclingThermal treatmentTungsten010402 general chemistry01 natural sciencesTHERMOPOWERPHYSICSTetragonal crystal systemThermal conductivityThermoelectric effectMETAL-OXIDESGeneral Materials ScienceThermal stabilityCRYSTAL-STRUCTURESRenewable Energy Sustainability and the EnvironmentMOLYBDENUMGeneral ChemistryPERFORMANCE021001 nanoscience & nanotechnologyThermoelectric materials0104 chemical sciencesChemical engineeringchemistry0210 nano-technologyPB
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