Search results for "Gradation"

showing 10 items of 1275 documents

Bioactivity Performance of Pure Mg after Plasma Electrolytic Oxidation in Silicate-Based Solutions

2021

The biodegradable metals, including magnesium (Mg), are a convenient alternative to permanent metals but fast uncontrolled corrosion limited wide clinical application. Formation of a barrier coating on Mg alloys could be a successful strategy for the production of a stable external layer that prevents fast corrosion. Our research was aimed to develop an Mg stable oxide coating using plasma electrolytic oxidation (PEO) in silicate-based solutions. 99.9% pure Mg alloy was anodized in electrolytes contained mixtures of sodium silicate and sodium fluoride, calcium hydroxide and sodium hydroxide. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), contact angle (CA), …

LuminescencePlasma GasesPharmaceutical ScienceSodium silicate02 engineering and technologymagnesium01 natural sciencesdegradation rateAnalytical Chemistrychemistry.chemical_compoundCoated Materials BiocompatibleCoatingDrug DiscoveryMagnesiumPhosphorusPlasma electrolytic oxidation021001 nanoscience & nanotechnologyAnti-Bacterial AgentsBody FluidsSolutionsChemistry (miscellaneous)Sodium hydroxideMolecular Medicine0210 nano-technologyOxidation-ReductionStaphylococcus aureusMaterials scienceplasma electrolytic oxidationCell SurvivalOxidechemistry.chemical_elementMicrobial Sensitivity Testsengineering.material010402 general chemistryElectrolysisArticleCorrosionlcsh:QD241-441biocompatibilitylcsh:Organic chemistryCell Line TumorHumansPhysical and Theoretical Chemistryantibacterial propertiesElectrodesAnodizingSilicatesOrganic ChemistrySpectrometry X-Ray Emission0104 chemical sciencessilicate bathchemistryengineeringCalciumNuclear chemistryMolecules
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Degradation of Carotenoids in Apricot (Prunus armeniaca L.) During Drying Process

2013

"Carotenoids are natural compounds whose nutritional importance comes from the provitamin A activity of some of them and their protection against several serious human disorders. The degradation of carotenoids was investigated during apricot drying by microwave and convective hot-air at 60 and 70 A degrees C. Seven carotenoids were identified: antheraxanthin, lutein, zeaxanthin, beta-cryptoxanthin, 13-cis-beta-carotene, all-trans-beta-carotene and 9-cis-beta-carotene; among these, all-trans-beta-carotene was found to be about 50 % of total carotenoids. First-order kinetic models were found to better describe all-trans-beta-carotene reduction during drying, with a degradation rate constant (…

LuteinHot TemperatureFood HandlingDry basisXanthophyllschemistry.chemical_compoundDrug StabilityIsomerismZeaxanthinsBotanyFood scienceDesiccationCarotenoidCryptoxanthinschemistry.chemical_classificationbiologyAntheraxanthinLuteinPlant physiologybiology.organism_classificationbeta CarotenePrunus armeniacaCarotenoidsZeaxanthinKineticschemistryChemistry (miscellaneous)FruitDegradation (geology)PrunusNutritive ValueBiomarkersFood Science
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Kinetics of carotenoids degradation and furosine formation in dried apricots (Prunus armeniaca L.)

2017

Abstract The kinetics of carotenoid and color degradation, as well as furosine formation, were investigated in apricot fruits during convective heating at 50, 60 and 70 °C. Degradation of carotenoids and color, expressed as total color difference (TCD), followed a first and zero order kinetic, respectively. The activation energy (Ea) for carotenoids degradation ranged from 73.7 kJ/mol for 13- cis -β-carotene to 120.7 kJ/mol for lutein, being about 91 kJ/mol for all- trans -β-carotene. Violaxanthin and anteraxanthin were the most susceptible to thermal treatment. The furosine evolution was fitted at zero order kinetic model. The Ea for furosine formation was found to be 83.3 kJ/mol and the Q…

LuteinHot TemperatureFood HandlingPrunus armeniacaApricotKineticsColorThermal treatmentActivation energyXanthophylls01 natural scienceschemistry.chemical_compound0404 agricultural biotechnologyApricot; Carotenoids; Color; Drying; Furosine; Kinetics; Food ScienceFurosineDesiccationCarotenoidDryingchemistry.chemical_classificationCarotenoidKineticChromatographybiologyChemistryLysine010401 analytical chemistry04 agricultural and veterinary sciencesSettore AGR/15 - Scienze E Tecnologie Alimentaribiology.organism_classification040401 food sciencePrunus armeniacaCarotenoids0104 chemical sciencesKineticsBiochemistryModels ChemicalFruitDegradation (geology)Nutritive ValueViolaxanthinFood Science
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Biochemical and Immunological implications of Lutein and Zeaxanthin

2021

Throughout history, nature has been acknowledged for being a primordial source of various bioactive molecules in which human macular carotenoids are gaining significant attention. Among 750 natural carotenoids, lutein, zeaxanthin and their oxidative metabolites are selectively accumulated in the macular region of living beings. Due to their vast applications in food, feed, pharmaceutical and nutraceuticals industries, the global market of lutein and zeaxanthin is continuously expanding but chemical synthesis, extraction and purification of these compounds from their natural repertoire e.g., plants, is somewhat costly and technically challenging. In this regard microbial as well as microalga…

LuteinOxidative degradationQH301-705.5Drug CompoundingBioactive moleculesReviewBiologyCatalysisInorganic ChemistryBiological Factorschemistry.chemical_compoundNutraceuticalDrug StabilityZeaxanthinsHumansMacula LuteaFood scienceBiology (General)Physical and Theoretical Chemistrymacular carotenoidsCRISPR/Cas9QD1-999Molecular BiologyCarotenoidSpectroscopyGene Editingchemistry.chemical_classificationgenetic engineeringEsterificationLuteinOrganic Chemistryfood and beveragesGeneral MedicineResearch needseye diseasesComputer Science ApplicationsZeaxanthinChemistryantioxidantschemistryXanthophyllbioavailabilitylutein binding proteinInternational Journal of Molecular Sciences
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Optimized RNA extraction and northern hybridization in streptomycetes.

2010

Abstract Northern blot hybridization is a useful tool for analyzing transcript patterns. To get a picture of what really occurs in vivo, it is necessary to use a protocol allowing full protection of the RNA integrity and recovery and unbiased transfer of the entire transcripts population. Many protocols suffer from severe limitations including only partial protection of the RNA integrity and/or loss of small sized molecules. Moreover, some of them do not allow an efficient and even transfer in the entire sizes range. These difficulties become more prominent in streptomycetes, where an initial quick lysis step is difficult to obtain. We present here an optimized northern hybridization protoc…

LysisPopulationtotal RNA purificationComputational biologyBiologynorthern hybridizationSettore BIO/19 - Microbiologia GeneraleStreptomycesGeneral Biochemistry Genetics and Molecular BiologyRNA degradationNorthern bloteducationlcsh:QH301-705.5GeneticsRNA glyoxylationeducation.field_of_studylcsh:R5-920streptomyceteBiochemistry Genetics and Molecular Biology(all)alkaline blottingMethodologyRNAbiology.organism_classificationBlotNorthern hybridizationSettore BIO/18 - Geneticalcsh:Biology (General)RNA processingstreptomycetesRNA extractionlcsh:Medicine (General)Biological procedures online
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Western blotting as a method for studying cell-biomaterial interactions: The role of protein collection

2000

Research of cell-biomaterial interactions is building on knowledge and methods available in cell and molecular biology. Western blotting is one of the options to characterize protein expression in cell populations. Method transfer to biomaterial model systems is not trivial because of the structure that exists in many biomaterials, preventing the collection of cell lysate by mechanical means. In this technical report, we describe the influence of different protein collection methods in a model system for cell-biomaterial interactions, consisting of endothelial cells exposed to different stimuli. In particular, the influence of trypsinization before lysis, and handling complexity were determ…

Lysismedicine.diagnostic_testCellBiomedical EngineeringTyrosine phosphorylationProtein tyrosine phosphataseProtein degradationBiologyTrypsinizationBiomaterialsBlotchemistry.chemical_compoundmedicine.anatomical_structureBiochemistrychemistryWestern blotmedicineJournal of Biomedical Materials Research
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Drawing the Materials Balance for an MBT cycle from Routine Process Measures in a Plant located in Venice

2007

An observation term was carried on in an MBT plant owned and run by a public Company to treat MSW left by separate collection. All observations and measurements were made without interfering with the ordinary operation rules, in order to assess the efficiency of one process cycle for a given batch of waste. Analytical data came from both a) process instruments and b) physical analysis of a batch of waste entering / exiting from a selected bio-cell. From the process mass losses (about 37% – including moisture evaporation – in that single process cycle) the theoretical amounts of water and carbon dioxide produced by biodegradation were calculated. A verification of the results was tried throu…

MBTprocess mass balanceaerobic degradationorganic waste
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Dynamics and identification of soil microbial populations actively assimilating carbon from 13C-labelled wheat residue as estimated by DNA- and RNA-S…

2007

International audience; This work is the first report on the use of DNA-, RNA-SIP approaches to elucidate the dynamics and the diversity of bacterial populations actively assimilating C derived from plant residues labelled at more than 90% (13)C. Wheat-residues, were incorporated and incubated into soil microcosms for 28 days. At the end of the incubation time, no more than 55% of the total CO(2) released was (13)C-labelled, suggesting the occurrence of an important priming effect process. After 7 days, more than 30% of the whole DNA extracted were labelled, allowing an efficient separation of labelled from unlabelled DNA using density gradient centrifugation. The genetic structure of bacte…

MESH: Sequence Analysis DNAMESH: Biodegradation EnvironmentalMESH : Carbon Radioisotopes[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryMESH : EcosystemRNA Ribosomal 16SMESH : DNA BacterialMESH: EcosystemCarbon RadioisotopesMESH: Carbon RadioisotopesTriticumSoil Microbiology2. Zero hunger0303 health sciencesCarbon IsotopesbiologyPlanctomycetesBacterial04 agricultural and veterinary sciencesMESH: RNA Ribosomal 16S[ SDE.MCG ] Environmental Sciences/Global ChangesRNA BacterialBiodegradation EnvironmentalBiodegradationMESH : Carbon IsotopesProteobacteriaMESH: RNA BacterialSoil microbiologySequence AnalysisDNA Bacterial16SRibosomal Intergenic Spacer analysis[SDE.MCG]Environmental Sciences/Global ChangesMESH : Biodegradation EnvironmentalMESH : Soil Microbiology[ SDV.SA.SDS ] Life Sciences [q-bio]/Agricultural sciences/Soil studyMESH: Triticum[SDV.SA.SDS]Life Sciences [q-bio]/Agricultural sciences/Soil studyMicrobiologyActinobacteriaEnvironmental03 medical and health sciencesMESH : Triticum[SDV.EE.ECO]Life Sciences [q-bio]/Ecology environment/EcosystemsBotanyMESH : BacteriaGemmatimonadetesEcology Evolution Behavior and SystematicsEcosystemRibosomal[SDV.GEN]Life Sciences [q-bio]/GeneticsBacteria030306 microbiologySoil organic matterMESH: Carbon IsotopesSequence Analysis DNADNAMESH : RNA BacterialRibosomal RNA[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/Geochemistrybiology.organism_classificationMESH: DNA Bacterial[ SDV.EE.ECO ] Life Sciences [q-bio]/Ecology environment/EcosystemsMESH : RNA Ribosomal 16SMESH: BacteriaMESH: Soil Microbiology040103 agronomy & agriculture0401 agriculture forestry and fisheriesRNA[ SDV.GEN ] Life Sciences [q-bio]/GeneticsMESH : Sequence Analysis DNA
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Oxidation Enhances Human Serum Albumin Thermal Stability and Changes the Routes of Amyloid Fibril Formation

2014

Oxidative damages are linked to several aging-related diseases and are among the chemical pathways determining protein degradation. Specifically, interplay of oxidative stress and protein aggregation is recognized to have a link to the loss of cellular function in pathologies like Alzheimer's and Parkinson's diseases. Interaction between protein and reactive oxygen species may indeed induce small changes in protein structure and lead to the inhibition/modification of protein aggregation process, potentially determining the formation of species with different inherent toxicity. Understanding the temperate relationship between these events can be of utmost importance in unraveling the molecul…

Macromolecular AssembliesProtein Foldinglcsh:MedicineProtein aggregationBiochemistryPhysical Chemistry01 natural sciencesProtein Structure SecondaryProtein structurePathologylcsh:Sciencechemistry.chemical_classification0303 health sciencesMultidisciplinarybiologyProtein StabilityChemistryPhysicsNeurodegenerationTemperatureNeurodegenerative DiseasesHuman serum albuminChemistryNeurologyBiochemistryMedicineOxidation-ReductionMolecular PathologyResearch Articlemedicine.drugAmyloidBiophysicsSerum albuminProtein degradation010402 general chemistry03 medical and health sciencesDiagnostic MedicinemedicineHumansProtein InteractionsBiologySerum Albumin030304 developmental biologyAmyloid Fluorescence Oxidation Protein aggregation Spectoscopy Light Scattering Serum AlbuminReactive oxygen specieslcsh:RProteinsHydrogen Peroxidemedicine.diseaseProtein tertiary structure0104 chemical sciencesKineticsbiology.proteinlcsh:QProtein MultimerizationGeneral Pathology
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Phosphonate degradation by Spirulina strains: cyanobacterial biofilters for the removal of anticorrosive polyphosphonates from wastewater

2011

The ability of Spirulina spp. to metabolize the recalcitrant xenobiotic Dequest 2054(®) [hexamethylenediamine-N,N,N',N'-tetrakis(methylphosphonic acid)], a CaSO(4) inhibitor used for boiler treatment and reverse osmosis desalination, was investigated. The compound served as sole source of phosphorus, but not of nitrogen, for cyanobacterial growth. In vivo utilization was followed by (31)P NMR analysis. The disappearance of the polyphosphonate proceeded only with actively dividing cells, and no release of inorganic phosphate was evident. However, no difference was found between P-starved and P-fed cultures. Maximal utilization reached 1.0 ± 0.2 mmoll(-1), corresponding to 0.56 ± 0.11 mmol g(…

Magnetic Resonance SpectroscopyOrganophosphonatesBioengineeringBiologyCyanobacteriaApplied Microbiology and BiotechnologyBiochemistryWaste Disposal FluidXenobioticschemistry.chemical_compoundBioremediationOrganophosphorus CompoundsbioremediationSpirulina31P NMR31 P NMRpolyphosphonateSpirulina spp.Methylphosphonic acidChromatographySpirulina sppBiodegradationwastewater treatmentBiodegradation Environmentalxenobiotic biodegradationchemistryBiochemistryWastewaterBiofilterpolyphosphonate; xenobiotic biodegradation; 31P NMR; Spirulina spp.; wastewater treatment; bioremediationSewage treatmentXenobioticFiltrationBiotechnologyWaste disposal
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