Search results for "Chela"

showing 10 items of 415 documents

Iron-binding compounds and related outer membrane proteins in Vibrio cholerae non-O1 strains from aquatic environments

1990

A total of 156 strains of Vibrio cholerae non-O1 from aquatic origins were examined for the presence of iron uptake mechanisms and compared with O1 strains and other Vibrio species. All non-O1 strains were able to grow in iron-limiting conditions, with MICs of ethylenediaminedi (O-hydroxyphenylacetic acid) ranging from 20 microM to 2 mM. The production of siderophores was demonstrated by growth in chrome azurol S agar and cross-feeding assays. All strains produced phenolate-type compounds, as assessed by the chemical tests and by bioassays with Salmonella typhimurium enb-7. Some of the strains also promoted the growth of S. typhimurium enb-1 (which can use only enterobactin as a siderophore…

SiderophoreVibrio anguillarumChromatography PaperIronBiological Transport ActiveSiderophoresBiologymedicine.disease_causeIron Chelating AgentsApplied Microbiology and BiotechnologyMicrobiologychemistry.chemical_compoundEnterobactinVibrio cholerae non-O1VibrionaceaemedicineSerotypingEscherichia coliVibrio choleraeEcologybiology.organism_classificationchemistryBiochemistryVibrio choleraeSpectrophotometryVibriobactinWater MicrobiologyFood ScienceBiotechnologyBacterial Outer Membrane ProteinsResearch Article
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Solution structure of R2Sn(IV)-β-N-Acetyl-Neuraminate (R=Me, Bu) complexes in D2O and DMSO-d6: experimental NMR and DFT computational study.

2007

Two diorganotin(IV)-NANA complexes (NANA (1) = beta-N-acetyl-Neuraminic Acid = 5-amino-3,5-dideoxy-D-glycero-beta-D-galactononulosic acid) with formula Me(2)Sn(iv)NANA (2) and Bu(2)Sn(IV)NANA (3) were synthesized and characterized by (1)H, (13)C and (119)Sn NMR spectroscopy, both in D(2)O and DMSO-d(6) solutions. The experimental data in DMSO suggested the monosaccharide bidentate chelation via O1 carboxylate and vicinal O2 alkoxide atoms, which, in D(2)O, can be dynamically extended to a third binding site (O8 atom) of the pendant chain. Coordination at the tin atom is discussed on the basis of experimental NMR data and DFT calculation.

Magnetic Resonance SpectroscopyDenticityMolecular StructureStereochemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyMedicinal chemistrySolutionsInorganic Chemistrychemistry.chemical_compoundchemistryAlkoxideOrganotin CompoundsSialic AcidsSide chainDimethyl SulfoxideNeuraminic AcidsChelationCarboxylateNMR structural characterization; Alkyltin(IV); N-acetilneuraminic acid; DFT theroretical calculationsDeuterium OxideTinMathematical ComputingVicinalNMR DFT sialic acid
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Formation of layered titania and zirconia catalysed by surface-bound silicatein

2005

Silicatein immobilised on self-assembled polymer layers using a histidine-tag chelating anchor group retains its hydrolytical activity for the formation of biosilica, and catalyses the formation of layered arrangements of biotitania and biozirconia.

Nitrilotriacetic AcidSiliconeducationMineralogyLigandsCatalysisCatalysisSpectroscopy Fourier Transform InfraredMaterials ChemistryCubic zirconiaChelationSurface plasmon resonanceTitaniumchemistry.chemical_classificationMetals and AlloysGeneral ChemistryPolymerSurface Plasmon ResonanceEnzymes ImmobilizedCathepsinsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChemical engineeringMicroscopy Electron ScanningCeramics and CompositesZirconiumChemical Communications
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Specific Protein Docking to Chelator Lipid Monolayers Monitored by FT-IR Spectroscopy at the Air–Water Interface

1996

Specific proteinAir water interfaceChemistryAnalytical chemistryInfrared spectroscopyGeneral MedicineGeneral ChemistryCatalysisMolecular recognitionDocking (molecular)MonolayerFt ir spectroscopyPhysical chemistryChelationAngewandte Chemie International Edition in English
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Activation of C−H Bonds in Five-Membered Heterocycles by a Half-Sandwich Yttrium Alkyl Complex

2001

Inorganic Chemistrychemistry.chemical_classificationChemistrychemistry.chemical_elementOrganic chemistryChelationLewis acids and basesYttriumMedicinal chemistryAlkylEuropean Journal of Inorganic Chemistry
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Antioxidant activity of TunisianGeranium robertianumL. (Geraniaceae)

2013

The present investigation focuses on the methanolic extract obtained from Geranium robertianum L. (Geraniaceae) (Herb Robert), a herbal plant used in traditional medicine for the treatment of human and animal diseases. The antioxidant capacities of the extract were evaluated using 1,1-diphenyl-2- picrylhydrazyl radical, β-carotene/linoleic acid and reducing power and metal chelating activity assays. The amount of total phenolic content, flavonoids and condensed tannins was very high, and the correlation between the antioxidant activity potential and total phenolic level of the extract was pointed out.

PolyphenolMetal chelating activityAntioxidantDPPHGeraniumLinoleic acidmedicine.medical_treatmentMetal chelating activityPlant ScienceBiochemistryAntioxidantsAnalytical Chemistrychemistry.chemical_compoundβ-carotene/linoleic acidAntioxidant activityBotanyGeranium robertianummedicinePlants MedicinalTraditional medicinebiologyPlant ExtractsOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationGeranium robertianum LchemistryProanthocyanidinPolyphenolReducing powerGeraniaceaeDPPHNatural Product Research
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Organometallic complexes with biological molecules: XII. Solid-state and solution studies on dialkyltin(IV)- and trialkyltin(IV)-thiaminepyrophosphat…

1999

Dialkyltin(IV) and trialkyltin(IV) derivatives of the coenzyme thiaminepyrophosphate (H2TPP) have been synthesized with general formula R2Sn(HTPP)2·nH2O (Alk = Me, n = 2; Alk = Bu, n = 4) and R3SnHTPP·nH2O (R=Me, n = 2; R = Bu, n = 1), respectively. The solid-state structure of the complexes has been investigated through infrared and Mossbauer spectroscopy. The infrared data suggest the involvement of only phosphate oxygen atoms in the coordination of both dialkyl- and trialkyl-tin(IV) moieties, with phosphate anions behaving as monoanionic bidentate bridging or chelating groups, with the tin(IV) involved in six- and five-fold coordination geometries, respectively, in R2Sn(HTPP)2·nH2O (R = …

Inorganic ChemistryDenticityOctahedronChemistryStereochemistryBase pairMössbauer spectroscopyInfrared spectroscopyChelationGeneral ChemistryCarbon-13 NMRHydrateMedicinal chemistryApplied Organometallic Chemistry
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(Ni2), (Ni3), and (Ni2 + Ni3): A Unique Example of Isolated and Cocrystallized Ni2 and Ni3 Complexes

2009

Structural and magnetic characterization of compound {[Ni(2)(L)(2)(OAc)(2)][Ni(3)(L)(2)(OAc)(4)]}.2CH(3)CN (3) (HL = the tridentate Schiff base ligand, 2-[(3-methylamino-propylimino)-methyl]-phenol) shows that it is a rare example of a crystal incorporating a dinuclear Ni(II) compound, [Ni(2)(L)(2)(OAc)(2)], and a trinuclear one, [Ni(3)(L)(2)(OAc)(4)]. Even more unusual is the fact that both Ni(II) complexes, [Ni(2)(L)(2)(OAc)(2)] (1) and [Ni(3)(L)(2)(OAc)(4)(H(2)O)(2)].CH(2)Cl(2).2CH(3)OH (2), have also been isolated and structurally and magnetically characterized. The structural analysis reveals that the dimeric complexes [Ni(2)(L)(2)(OAc)(2)] in cocrystal 3 and in compound 1 are almost i…

Inorganic Chemistrychemistry.chemical_compoundCrystallographySchiff baseMolecular geometryTridentate ligandchemistryOctahedral molecular geometryChelationPhysical and Theoretical ChemistryAcetate ionCocrystalInorganic Chemistry
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Open-chain polyamine ligands bearing an anthracene unit - Chemosensors for logic operations at the molecular level

2001

In this work the absorption and the fluorescence emission properties as well as the protonation sequence of three open chain polyamine ligands of different dimensions bearing an anthracene unit were studied. The protonation and stability constants with Ni2+, Cu2+, Zn2+, and Cd2+ have been determined in 0.15 mol·dm−3 NaCl at 298.1 ± 0.1 K. The values of both protonation and stability constants follow the expected trends according to the number of nitrogen donors, sequence of chelate rings and hydrophilic−hydrophobic balance. Chelation enhancement of the fluorescence emission (CHEF) was observed for some complexes of these ligands with Zn2+ and Cd2+. In contrast the analog complexes containin…

inorganic chemicalsAnthraceneQuenching (fluorescence)Inorganic chemistrychemistry.chemical_elementProtonationFluorescenceCopperInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artvisual_art.visual_art_mediumChelationAbsorption (chemistry)
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Peptide-metal complexes: obtention and role in increasing bioavailability and decreasing the pro-oxidant effect of minerals.

2020

Bioactive peptides derived from food protein sources have been widely studied in the last years, and scientific researchers have been proving their role in human health, beyond their nutritional value. Several bioactivities have been attributed to these peptides, such as immunomodulatory, antimicrobial, antioxidant, antihypertensive, and opioid. Among them, metal-binding capacity has gained prominence. Mineral chelating peptides have shown potential to be applied in food products so as to decrease mineral deficiencies since peptide-metal complexes could enhance their bioavailability. Furthermore, many studies have been investigating their potential to decrease the Fe pro-oxidant effect by f…

chemistry.chemical_classificationGastrointestinal tractMineralsAntioxidantmedicine.medical_treatmentMineral deficiencyBiological AvailabilityPeptideGeneral MedicinePro-oxidantmedicine.diseaseIndustrial and Manufacturing EngineeringHydrolysateBioavailabilitychemistryBiochemistryCoordination ComplexesmedicineHumansChelationPeptidesReactive Oxygen SpeciesFood ScienceCritical reviews in food science and nutrition
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