Search results for "PORP"

showing 10 items of 567 documents

Porphyra (Bangiophyceae) Transcriptomes Provide Insights Into Red Algal Development And Metabolism.

2012

The red seaweed Porphyra (Bangiophyceae) and related Bangiales have global economic importance. Here, we report the analysis of a comprehensive transcriptome comprising ca. 4.7 million expressed sequence tag (EST) reads from P. umbilicalis (L.) J. Agardh and P. purpurea (Roth) C. Agardh (ca. 980 Mbp of data generated using 454 FLX pyrosequencing). These ESTs were isolated from the haploid gametophyte (blades from both species) and diploid conchocelis stage (from P. purpurea). In a bioinformatic analysis, only 20% of the contigs were found to encode proteins of known biological function. Comparative analysis of predicted protein functions in mesophilic (including Porphyra) and extremophilic …

GametophyteGeneticsExpressed sequence tagbiologyBangiophyceaePlant ScienceRed algaeAquatic Sciencebiology.organism_classificationPorphyraTranscriptomeRibosomal proteinBotanyGeneJournal of phycology
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Electroactive polymeric material with condensed structure on the basis of magnesium(II) polyporphine

2011

International audience; Previous publication of the authors presented evidences that electroch emical oxidation of Mg(II) porphine (fully unsubstituted porphyrin, MgP) in acetonitrile (AN) at a very low potential leads to deposition of films at electrode surface corresponding to typical electroactive polymers, with their reversible transition betwee n the electronconducting and insulating states depending on the electrode potential/oxidation level ("film of type I"). It is demonstrated in the actual publication that these films in contact with a monomer-free solution are subject to an irreversible transformation to quite a different material ("film of type II") under the influence of a high…

General Chemical EngineeringAnalytical chemistryInfrared spectroscopy02 engineering and technology010402 general chemistryElectrochemistry01 natural scienceschemistry.chemical_compoundTransition metalX-ray photoelectron spectroscopy[CHIM.ANAL]Chemical Sciences/Analytical chemistryelectroactive materialsElectrochemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryconducting polymermagnesium porphineConductive polymer[CHIM.ORGA]Chemical Sciences/Organic chemistryelectropolymerization[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMonomerchemistryPhysical chemistryC-C coupling0210 nano-technologyunsubstituted porphyrinElectrode potentialElectrochimica Acta
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Separation and identification of petroporphyrins extracted from the oil shales of Tarfaya: geochemical study

2002

Abstract Vanadyl and nickel porphyrins were isolated from the oil shales of Tarfaya (Morocco) by extraction followed by column chromatography. The ratios and characteristics of these porphyrin complexes were essentially obtained on the basis of UV–visible and mass spectrometry data. Geochemical information could be drawn from these data. The nature and the contents of the metals coordinated and non-coordinated to porphyrin systems were also determined in this study.

General Chemical EngineeringOrganic ChemistryExtraction (chemistry)Analytical chemistryEnergy Engineering and Power Technologychemistry.chemical_elementMass spectrometryPorphyrinchemistry.chemical_compoundNickelFuel TechnologyColumn chromatographychemistrypolycyclic compoundsSolvent extractionOil shaleFuel
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Evolution of the Mayo Kebbi region as revealed by zircon dating: An early (ca. 740Ma) Pan-African magmatic arc in southwestern Chad

2006

Abstract The Mayo Kebbi region in SW Chad is part of the NNE-SSW trending Neoproterozoic Central African Fold Belt (CAFB) and is made up of three calc-alkaline granitoid suites emplaced into a metavolcanic–metasedimentary sequence. The first suite is represented by mafic to intermediate rocks (gabbro-diorite and metadiorite) emplaced between 737 and 723 Ma during early Pan-African convergence. The second consists of the Mayo Kebbi batholith and includes tonalites, trondhjemites and granodiorites, emplaced during several magmatic pulses between 665 and 640 Ma. The third suite includes porphyritic granodiorite and hypersthene monzodiorite dated at ca. 570 Ma. The Mayo Kebbi domain extends sou…

GeochemistryHyperstheneGeologyFold (geology)Diachronousengineering.materialPorphyriticBatholithBack-arc basinengineeringMaficGeologyEarth-Surface ProcessesZirconJournal of African Earth Sciences
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Porphyrin-bile acid conjugates: from saccharide recognition in the solution to the selective cancer cell fluorescence detection.

2008

This paper describes the preparation and use of conjugates of porphyrins and bile acids as ligands to bind to tumor expressed saccharides. Bile acid-porphyrin conjugates were tested for recognition of saccharides that are typically present on malignant tumor cells. Fluorescence microscopy, in vitro PDT cell killing, and PDT of subcutaneous 4T1 mouse tumors is reported. High selectivity for saccharide cancer markers and cancer cells was observed. This in vivo and in vitro study demonstrated high potential use for these compounds in targeted photodynamic therapy.

GlycosylationPorphyrinsmedicine.drug_classmedicine.medical_treatmentCarbohydratesPhotodynamic therapyApoptosisDNA FragmentationLigandsBiochemistrySensitivity and SpecificityCell LineBile Acids and Saltschemistry.chemical_compoundMiceStructure-Activity RelationshipIn vivoNeoplasmsmedicineFluorescence microscopeBiomarkers TumorAnimalsHumansPhysical and Theoretical ChemistryCell Line TransformedCell ProliferationMice Inbred BALB CBinding SitesBile acidDose-Response Relationship DrugMolecular StructureChemistryOrganic ChemistryCancer3T3 Cellsmedicine.diseasePorphyrinSolutionsCell killingBiochemistryMicroscopy FluorescencePhotochemotherapyCancer cellDrug Screening Assays AntitumorHeLa CellsOrganicbiomolecular chemistry
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Study of the Mode and Efficiency of DNA Binding in the Damage Induced by Photoactivated Water Soluble Porphyrins

2013

We have investigated the DNA binding interactions and in vitro photoactivated DNA damage induced by a neutral water soluble porphyrin derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrin (TTHPP) and its zinc derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrinato zinc(II) (Zn-TTHPP) upon visible light irradiation through various spectroscopic techniques and employing repair endonucleases. These porphyrin derivatives exhibited high affinity toward DNA through groove binding interactions as evidenced through the UV-vis absorption, emission, circular dichroism spectral and viscosity changes. Interestingly, the free base porphyrin derivative, TTHPP generated efficient sing…

HematoporphyrinCircular dichroismPorphyrinsSinglet oxygenDNA damageCircular DichroismSpectrum AnalysisWaterDNAGeneral MedicinePhotochemical ProcessesPhotochemistryBiochemistryPorphyrinchemistry.chemical_compoundchemistryDNA glycosylasePhotosensitizerPhysical and Theoretical ChemistryDNADNA DamagePhotochemistry and Photobiology
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Nature of O2, CO, and CN binding to hemoprotein models

2004

Parametrization of a molecular-mechanics program to include terms specific for five- and six-coordinate transition metal complexes results in computer-simulated structures of hemo complexes. The principal new feature peculiar to five- and six-coordination is a term that measures the effect of electron-pair repulsion modified by the ligand electronegativity and takes into account the different structural possibilities. The work consists in the modification of program molecular mechanics for penta and hexacoordination. The model system takes into account the structural differences of the fixing center in the hemoglobin subunits. The customary proximal histidine is added. The macrocycle hemo I…

HemeproteinBent molecular geometryHemoglobin SubunitsCondensed Matter PhysicsLigand (biochemistry)PorphyrinAtomic and Molecular Physics and OpticsElectronegativitychemistry.chemical_compoundchemistryMyoglobinComputational chemistryPhysical and Theoretical ChemistryHistidineInternational Journal of Quantum Chemistry
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Nature of FeIII–O2, FeII–CO and FeIII–CN complexes of hemoprotein models

2003

Abstract Parametrization of a molecular-mechanics program to include terms specific for 5- and 6-coordinate transition metal complexes results in computer-simulated structures of hemo complexes. The principal new feature peculiar to 5- and 6-coordination is a term that measures the effect of electron-pair repulsion modified by the ligand electronegativity and takes into account the different structural possibilities. The work consists in the modification of program molecular mechanics for 5- and 6-coordination. The model system takes into account the structural differences of the fixing centre in the haemoglobin (Hb) subunits. The customary proximal histidine is added. The macrocycle hemo I…

HemeproteinLigandBent molecular geometryPorphyrinInorganic ChemistryElectronegativitychemistry.chemical_compoundTransition metalMyoglobinchemistryComputational chemistryMaterials ChemistryPhysical and Theoretical ChemistryHistidinePolyhedron
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Hole burning and pressure phenomena in chromoproteins

1993

Abstract We investigated the behavior of spectral holes under pressure at various frequencies within the inhomogeneous band for two proteins, namely myoglobin and horseradish peroxidase. In order to achieve narrow bandwidth hole burning, the heme chromophore was replaced by protoporphyrin IX and mesoporphyrin IX, respectively. In myoglobin, we found that the pressure induced shift of the holes varied in a strongly non-linear fashion, when the burn-frequency was tuned across the absorption band. In horseradish peroxidase the pressure shift was linear with burn-frequency but changed in a dramatic fashion upon complex formation with a substrate molecule. These observations are interpreted with…

HemeproteinbiologyProtoporphyrin IXChemistryBiophysicsGeneral ChemistryChromophoreCondensed Matter PhysicsPhotochemistryBiochemistryHorseradish peroxidaseMolecular physicsAtomic and Molecular Physics and Opticschemistry.chemical_compoundMyoglobinAbsorption bandbiology.proteinHemePeroxidaseJournal of Luminescence
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Iron Porphyrins as Models of Cytochromec Oxidase

2001

A series of iron porphyrins has been synthesized as models of cytochrome c oxidase; their activity as 4 e− catalysts in the reduction of dioxygen has been studied at pH 7. These compounds have been obtained by grafting very different residues onto the same iron complex, namely tripodal tetraamines, pickets, and straps, in order to change the environment of the metal center. In the case of porphyrins bearing a tripodal cap, the secondary amines have been alkylated with different substituents so as to modify the electronic environment of the distal pocket. Surprisingly, when the iron porphyrin is functionalized with four identical acrylamido pickets, the resulting complex exhibits biomimetic …

HemeproteinbiologyStereochemistryChemistryCytochrome cOrganic Chemistrychemistry.chemical_elementO2 reductionGeneral ChemistryZincMedicinal chemistryPorphyrinCatalysisMetalchemistry.chemical_compoundvisual_artbiology.proteinvisual_art.visual_art_mediumCytochrome c oxidaseEfficient catalystChemistry - A European Journal
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