Search results for "Microscopy"

showing 10 items of 3390 documents

Crystalline nanorods as possible templates for the synthesis of amorphous biosilica during spicule formation in Demospongiae.

2009

In tandem: High-resolution TEM shows that during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique (ADT) reveals that the nanorods have a layered structure that matches smectitic phyllosilicates. These intracellular nanorods have been considered as precursors of mature spicules. High-resolution microscopy shows that, during the initial stages of demosponge spicule formation, a primordial crystalline structure is formed within the axial filament. The recently developed electron diffraction tomography technique reveals that the nanorods have a layered stru…

SpiculeMaterials scienceElectronsCrystal structureBiochemistrybioinorganic chemistryDemospongeSponge spiculeMicroscopy Electron TransmissionX-Ray DiffractionnanostructuresAnimalsMolecular BiologyNanotubesbiologyElectron crystallographysilicateinOrganic Chemistrybioinorganic chemistry; electron crystallography; nanostructures; silicatein; spiculesbiology.organism_classificationSilicon DioxidespiculesAmorphous solidPoriferaCrystallographyelectron crystallographyElectron diffractionMicroscopy Electron ScanningMolecular MedicineNanorodChembiochem : a European journal of chemical biology
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Magnetic resonance imaging of the siliceous skeleton of the demosponge Lubomirskia baicalensis

2005

The skeletal elements (spicules) of the demosponge Lubomirskia baicalensis were analyzed; they are composed of amorphous, non-crystalline silica, and contain in a central axial canal the axial filament which consists of the enzyme silicatein. The axial filament, that orients the spicule in its longitudinal axis exists also in the center of the spines which decorate the spicule. During growth of the sponge, new serially arranged modules which are formed from longitudinally arranged spicule bundles are added at the tip of the branches. X-ray analysis revealed that these serial modules are separated from each other by septate zones (annuli). We describe that the longitudinal bundles of spicule…

SpiculebiologyAnatomyLubomirskia baicalensisbiology.organism_classificationSilicon DioxideSkeleton (computer programming)Magnetic Resonance ImagingModels BiologicalPoriferaRadiographySpongeDemospongeSponge spiculeNuclear magnetic resonanceApex (mollusc)Structural BiologyMicroscopy Electron ScanningAnimalsLongitudinal axisBody PatterningJournal of Structural Biology
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Axial growth of hexactinellid spicules: Formation of cone-like structural units in the giant basal spicules of the hexactinellid Monorhaphis

2008

The glass sponge Monorhaphis chuni (Porifera: Hexactinellida) forms the largest bio-silica structures on Earth; their giant basal spicules reach sizes of up to 3 m and diameters of 8.5 mm. Previously, it had been shown that the thickness growth proceeds by appositional layering of individual lamellae; however, the mechanism for the longitudinal growth remained unstudied. Now we show, that the surface of the spicules have towards the tip serrated relief structures that are consistent in size and form with the protrusions on the surface of the spicules. These protrusions fit into the collagen net that surrounds the spicules. The widths of the individual lamellae do not show a pronounced size …

SpiculebiologyHexactinellidSilicatesImmunogold labellingSilicon Dioxidebiology.organism_classificationPoriferalaw.inventionSuberites domunculaMicroscopy ElectronSpongeCrystallographySponge spiculeStructural BiologylawAnimalsElectrophoresis Polyacrylamide GelCollagenElectron microscopeElongationSuberitesJournal of Structural Biology
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Formation of spicules by sclerocytes from the freshwater spongeEphydatia muelleri in short-term cultures in vitro

1995

Cells from the freshwater sponge Ephydatia muelleri were isolated by dissociating hatching gemmules. During the first 24 h the cells reaggregated, but the aggregates progressively disintegrated again to single cells, among which the spicule-forming sclerocytes were recognized. Such cultures were used to study spicule (megascleres) formation in vitro. The isolated sclerocytes formed the organic central axial filament onto which they deposited inorganic silicon. The size of the spicules (200 to 350 microns in length) as well as the rate of spicule formation (1 to 10 microns/h) under in vitro conditions were similar to the values measured in vivo. Immediately after completion of spicule format…

SpiculebiologySilicatesFresh WaterCell BiologyGeneral Medicinebiology.organism_classificationIn vitroCulture MediaPoriferaCell biologyMicroscopy ElectronSpongeSponge spiculeCell cultureBotanyAnimalsEphydatia muelleriDevelopmental biologyCells CulturedDevelopmental BiologySclerocyteIn Vitro Cellular & Developmental Biology - Animal
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Supra-aggregates of fiber-forming anisotropic molecules.

2006

In this paper, the self-organization of fiber-forming anisotropic molecules is inspected both theoretically and experimentally. In the first part, a theoretical model which extends the de Gennes theory of thin films to assemblies of strongly anisotropic molecules is reported. The model predicts that solid supported thin films made up of fiber-forming discotic molecules can grow with both tangential and radial arrangement of the fibers, respectively leading to the formation of compact and holed supra- aggregates. These last systems form according to the following picture. The tangential growth minimizes the number of unfavorable free ends but introduces elastic strain especially in the centr…

Spin coatingCRYSTALChemistryIsotropyEvaporationFILMSMicroscopy Atomic ForceNANOSTRUCTURESSurfaces Coatings and FilmsCrystalCrystallographyModels ChemicalChemical physicsMaterials ChemistryAnisotropyThermodynamicsRhodamine 123Soft matterSelf-assemblyDewettingPhysical and Theoretical ChemistryAnisotropyMathematicsThe journal of physical chemistry. B
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3D Morphology, ultrastructure and development of Ceratomyxa puntazzi stages: first insights into the mechanisms of motility and budding in the Myxozo…

2012

Free, amoeboid movement of organisms within media as well as substrate-dependent cellular crawling processes of cells and organisms require an actin cytoskeleton. This system is also involved in the cytokinetic processes of all eukaryotic cells. Myxozoan parasites are known for the disease they cause in economical important fishes. Usually, their pathology is related to rapid proliferation in the host. However, the sequences of their development are still poorly understood, especially with regard to pre-sporogonic proliferation mechanisms. The present work employs light microscopy (LM), electron microscopy (SEM, TEM) and confocal laser scanning microscopy (CLSM) in combination with specific…

SporesIndolesPhalloidineParasitic Diseases AnimalBiophysicsMotilitylcsh:MedicineBiologyBiochemistryFish DiseasesMicroscopy Electron TransmissionCell MovementMolecular Cell BiologyOxazinesAnimalsBilePseudopodiaMyxozoaCytoskeletonlcsh:ScienceBiologyCell ProliferationAmoeboid movementBuddingLife Cycle StagesMultidisciplinaryMicroscopy ConfocalStaining and LabelingPhysicslcsh:RProteinsCell BiologyActin cytoskeletonCellular StructuresSea BreamCell biologyUltrastructureMicroscopy Electron Scanninglcsh:QFilopodiaZoologyCytokinesisCell DivisionResearch ArticleDevelopmental BiologyPLoS ONE
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Thickness measurement of soft thin films on periodically patterned magnetic substrates by phase difference magnetic force microscopy

2013

The need for accurate measurement of the thickness of soft thin films is continuously encouraging the development of techniques suitable for this purpose. We propose a method through which the thickness of the film is deduced from the quantitative measurement of the contrast in the phase images of the sample surface acquired by magnetic force microscopy, provided that the film is deposited on a periodically patterned magnetic substrate. The technique is demonstrated by means of magnetic substrates obtained from standard floppy disks. Colonies of Staphylococcus aureus adherent to such substrates were used to obtain soft layers with limited lateral (a levy microns) and vertical (hundreds of n…

Staphylococcus aureusCantileverMaterials scienceThickness measurementMagnetic domainSurface PropertiesMicroscopy Atomic ForceAtomic force microscopyOpticsPeriodic magnetic domainsHomogeneity (physics)Thin filmInstrumentationDetection limitPhase differenceBacteriabusiness.industryMagnetic PhenomenaThickness measurement Magnetic force microscopy Atomic force microscopy Periodic magnetic domains BacteriaAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsMagnetic force microscopyatomic force microscopy; bacteria; magnetic force microscopy; periodic magnetic domains; thickness measurementNanometreMagnetic force microscopebusiness
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ANTIMICROBIAL AND ANTISTAPHYLOCOCCAL BIOFILM ACTIVITY FROM THE SEA URCHIN PARACENTROTUS LIVIDUS

2009

Aims: Staphylococcal biofilm-associated infections are resistant to conventional antibiotics. Consequently, new agents are needed to treat them. With this aim, we focused on the effector cells (coelomocytes) of the sea urchin Paracentrotus lividus immune system. Methods and Results: We tested the activity of the 5-kDa peptide fraction of the cytosol from coelomocytes (5-CC) against a group of Gram-positive, Gram-negative bacteria and fungi. We determined minimal inhibitory concentrations (MICs) ranging from 253.7 to 15.8 mg ml(-1). We observed an inhibitory activity and antibiofilm properties of 5-CC against staphylococcal biofilms of reference strains Staphylococcus epidermidis DSM 3269 an…

Staphylococcus aureusMicrobial ViabilityMicroscopy ConfocalStaining and LabelingMicrobial Sensitivity TestsStaphylococcal InfectionsCell FractionationSettore BIO/19 - Microbiologia GeneraleThymosinCytosolAnti-Infective AgentsBiofilmsParacentrotusStaphylococcus epidermidisAnimalsPeptidesantimicrobial antimicrobial peptides biofilminnate immunity staphylococci
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Towards Laser-Textured Antibacterial Surfaces

2018

AbstractEscherichia coli and Staphylococcus aureus bacterial retention on mirror-polished and ultrashort pulse laser-textured surfaces is quantified with a new approach based on ISO standards for measurement of antibacterial performance. It is shown that both wettability and surface morphology influence antibacterial behavior, with neither superhydrophobicity nor low surface roughness alone sufficient for reducing initial retention of either tested cell type. Surface structures comprising spikes, laser-induced periodic surface structures (LIPSS) and nano-pillars are produced with 1030 nm wavelength 350 fs laser pulses of energy 19.1 μJ, 1.01 μJ and 1.46 μJ, respectively. SEM analysis, optic…

Staphylococcus aureusNanostructureMaterials scienceShear forcelcsh:Medicine02 engineering and technology010402 general chemistry01 natural sciencesArticleBacterial AdhesionContact angleMicroscopyEscherichia coliSurface roughnessLotus effectComposite materiallcsh:ScienceAsepsisMultidisciplinaryLaserslcsh:R021001 nanoscience & nanotechnology0104 chemical sciencesSteelWettabilitylcsh:QWetting0210 nano-technologyUltrashort pulseScientific Reports
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Lipid and phase specificity of α-toxin from S. aureus

2013

AbstractThe pore forming toxin Hla (α-toxin) from Staphylococcus aureus is an important pathogenic factor of the bacterium S. aureus and also a model system for the process of membrane-induced protein oligomerisation and pore formation. It has been shown that binding to lipid membranes at neutral or basic pH requires the presence of a phosphocholine-headgroup. Thus, sphingomyelin and phosphatidylcholine may serve as interaction partners in cellular membranes. Based on earlier studies it has been suggested that rafts of sphingomyelin are particularly efficient in toxin binding. In this study we compared the oligomerisation of Hla on liposomes of various lipid compositions in order to identif…

Staphylococcus aureusPore formationLiquid ordered phaseBacterial ToxinsLipid BilayersBiophysicsBiologyBiochemistryPhase Transitionchemistry.chemical_compoundHemolysin ProteinsMembrane LipidsMembrane MicrodomainsPhosphatidylcholineBinding siteLipid raftUnilamellar LiposomesPore-forming toxinLiposomeArtificial membranesBinding SitesCell MembraneOligomerisationCell BiologyS. aureusSphingomyelinsMembraneBiochemistrychemistryMicroscopy FluorescenceMutationPhosphatidylcholineslipids (amino acids peptides and proteins)Protein MultimerizationToxinSphingomyelinBiochimica et Biophysica Acta (BBA) - Biomembranes
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