Search results for "acids"

showing 10 items of 3520 documents

Primary Structure of Selected Archaeal Mesophilic and Extremely Thermophilic Outer Surface Layer Proteins

2002

The archaea are recognized as a separate third domain of life together with the bacteria and eucarya. The archaea include the methanogens, extreme halophiles, thermoplasmas, Sulfate reducers and Sulfur metabolizing thermophiles, which thrive in different habitats such as anaerobic niches, salt lakes, and marine hydrothermals systems and continental solfataras. Many of these habitats represent extreme environments in respect to temperature, osmotic pressure and pH-values and remind on the conditions of the early earth. The cell envelope structures were one of the first biochemical characteristics of archaea studied in detail. The most common archaeal cell envelope is composed of a single cry…

Hot TemperaturebiologyArchaeal ProteinsThermophileThermoplasmaMembrane ProteinsProtein Sorting Signalsbiology.organism_classificationArchaeaApplied Microbiology and BiotechnologyMicrobiologyProtein Structure SecondaryHalophileBiochemistryExtreme environmentAmino Acid SequenceAmino AcidsCell envelopeProtein stabilizationSequence AlignmentS-layerEcosystemEcology Evolution Behavior and SystematicsArchaeaSystematic and Applied Microbiology
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Characterization of Gibberella fujikuroi complex isolates by fumonisin B-1 and B-2 analysis and by RAPD and restriction analysis of PCR-amplified int…

2000

Summary Twenty nine isolates of Fusarium spp. (twenty four of them belonging to the Gibberella fujikuroi complex) isolated from banana and corn from different geographical regions were analyzed for their ability to produce fumonisins B 1 and B 2 and for genetic relatedness using random amplified polymorphic DNA (RAPD) and restriction analysis of PCR amplification products of the 5.8s ribosomal DNA-intervening internal transcribed spacer regions (ITS I-5.8S-ITS II). For RAPD analysis, six of twenty oligonucleotide primers were selected after testing with five Fusarium spp. isolates and used to characterize 24 additional isolates. DNA fragments from the 29 isolates of Fusarium spp., which wer…

HpaIIGibberellaCarboxylic AcidsZingiberalesBiologyApplied Microbiology and BiotechnologyMicrobiologyDNA RibosomalFumonisinsPolymerase Chain ReactionZea maysHaeIIIFusariummedicineInternal transcribed spacerDNA FungalEcology Evolution Behavior and SystematicsChromatography High Pressure LiquidPhylogenyDNA PrimersGeneticsfood and beveragesGenetic VariationSpacer DNAbiology.organism_classificationGibberellinsRAPDRandom Amplified Polymorphic DNA TechniqueRestriction enzymeGibberella fujikuroiRestriction fragment length polymorphismPolymorphism Restriction Fragment Lengthmedicine.drug
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Inhibition of CD1 antigen presentation by human cytomegalovirus.

2008

ABSTRACTThe betaherpesvirus human cytomegalovirus (HCMV) encodes several molecules that block antigen presentation by the major histocompatibility complex (MHC) proteins. Humans also possess one other family of antigen-presenting molecules, the CD1 family; however, the effect of HCMV on CD1 expression is unknown. The majority of CD1 molecules are classified on the basis of homology as group 1 CD1 and are present almost exclusively on professional antigen-presenting cells such as dendritic cells, which are a major target for HCMV infection and latency. We have determined that HCMV encodes multiple blocking strategies targeting group 1 CD1 molecules. CD1 transcription is strongly inhibited by…

Human cytomegalovirusTranscription GeneticvirusesImmunologyAntigen presentationCD1Cytomegaloviruschemical and pharmacologic phenomenaMajor histocompatibility complexmedicine.disease_causeMicrobiologycomplex mixturesCell LineAntigens CD1Immune systemAntigenVirologyMHC class ImedicineHumansCells CulturedAntigen PresentationbiologyImmunityhemic and immune systemsmedicine.diseaseVirologyProtein TransportHerpes simplex virusGene Expression RegulationInsect Sciencebiology.proteinPathogenesis and Immunitylipids (amino acids peptides and proteins)Journal of virology
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Reproductive effects in German cockroaches by ecdysteroid agonist RH-0345, juvenile hormone analogue methoprene and carbamate benfuracarb

2004

1379-1176 (Print) Journal Article Research Support, Non-U.S. Gov't; Blatta germanica is the more prevalent cockroach species in Algeria. In the present study, we tested the effect on reproduction in B. germanica of two insect growth regulators, RH-0345, a benzoylhydrazine analogue that mimics the action of 20-hydroxyecdysone, and methoprene, one of the most commercially important juvenile hormone analogues, and a novel carbamate insecticide, benfuracarb. The compounds were applied topically (10 and 20 microg/insect for RH-0345, and 1 and 10 microg/insect for methoprene) or orally administrated (at 2% for benfuracarb) on newly emerged females and evaluated on reproductive events during the a…

Hydrazines/*toxicitybeta-Alanine/*analogs & derivatives/*toxicityBenzofurans/*toxicityBenzoic Acids/*toxicityOvary/drug effectsJuvenile HormonesOocytes/cytology/drug effectsTopicalInsecticides/*toxicityAdministrationAnimalsFemaleBlattellidae/drug effects/*growth & developmentMethoprene/*toxicityReproduction/drug effects
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Identification of biological markers of liver X receptor (LXR) activation at the cell surface of human monocytes.

2012

Background Liver X receptor (LXR) α and LXR β (NR1H3 and NR1H2) are oxysterol-activated nuclear receptors involved in the control of major metabolic pathways such as cholesterol homeostasis, lipogenesis, inflammation and innate immunity. Synthetic LXR agonists are currently under development and could find applications in various fields such as cardiovascular diseases, cancer, diabetes and neurodegenerative diseases. The clinical development of LXR agonists requires the identification of biological markers for pharmacodynamic studies. In this context, monocytes represent an attractive target to monitor LXR activation. They are easily accessible cells present in peripheral blood; they expres…

Hydrocarbons FluorinatedCD226Celllcsh:MedicineBiochemistryMonocytesDrug DiscoveryMolecular Cell Biologypolycyclic compoundsSignaling in Cellular Processeslcsh:ScienceLiver X ReceptorsSulfonamidesMultidisciplinarymedicine.diagnostic_testfood and beveragesCell DifferentiationOrphan Nuclear ReceptorsFlow CytometryNuclear SignalingCholesterolmedicine.anatomical_structureGene Knockdown Techniqueslipids (amino acids peptides and proteins)Research ArticleSignal TransductionAgonistmedicine.drug_classImmune CellsImmunologyContext (language use)Biologydigestive systemFlow cytometryAntigens CDDNA-binding proteinsmedicineHumansRNA MessengerLiver X receptorBiologyCluster of differentiationMacrophagesCell Membranelcsh:RProteinsLipid MetabolismMetabolismGene Expression RegulationNuclear receptorImmunologyCancer researchlcsh:QBiomarkersCytometryFoam CellsDevelopmental BiologyPLoS ONE
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A Stereocontrolled Protocol to Highly Functionalized Fluorinated Scaffolds through a Fluoride Opening of Oxiranes

2016

A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesis of various fluorine-containing, highly functionalized cycloalkane derivatives. The method involves the stereoselective epoxidation of some unsaturated cyclic beta-amino acid derivatives as model compounds, followed by a regioselective fluoride opening of oxiranes under various conditions with Deoxofluor and XtalFluor-E reagents, thereby offering an insight into this new epoxide opening methodology with fluoride.

Hydrocarbons FluorinatedPharmaceutical ScienceEpoxideAlkenesstereoselectivity010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Fluorideschemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistryamino acidsSulfur Compoundsoxirane; fluorination; amino acids; stereoselectivity; regioselectivity010405 organic chemistryOrganic ChemistryRegioselectivityStereoisomerismfluorination0104 chemical sciencesCycloalkanechemistryChemistry (miscellaneous)oxiraneregioselectivityReagentEpoxy CompoundsMolecular MedicineStereoselectivityFluorideMolecules
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From Defined Reactive Diblock Copolymers to Functional HPMA-Based Self-Assembled Nanoaggregates

2008

This paper describes the synthesis of functional amphiphilic poly( N-(2-hydroxypropyl) methacrylamide)-block-poly(lauryl methacrylate) copolymers by RAFT polymerization via the intermediate step of activated ester block copolymers (pentafluoro-phenyl methacrylate). Block copolymers with molecular weights from 12000-28000 g/mol and PDIs of about 1.2 have been obtained. The amphiphilic diblock copolymers form stable super structures (nanoaggregates) by self-organization in aqueous solution. The diameters of these particles are between 100 and 200 nm and depend directly on the molecular weight of the block copolymer. Furthermore, we investigated the impact of these nanoaggregates on cell viabi…

Hydrodynamic radiusPolymers and PlasticsCell SurvivalPolymersRadical polymerizationBiocompatible MaterialsBioengineeringMethacrylateCell LineBiomaterialschemistry.chemical_compoundDogsCell MovementMaterials TestingPolymer chemistryAmphiphileMaterials ChemistryCopolymerAnimalsMethacrylamideReversible addition−fragmentation chain-transfer polymerizationCell ShapeLauric AcidsChain transferMolecular WeightchemistryMethacrylatesNanoparticlesBiomacromolecules
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Synthesis and Characterization of Stimuli-Responsive Star-Like Polypept(o)ides: Introducing Biodegradable PeptoStars

2017

tar-like polymers are one of the smallest systems in the class of core crosslinked polymeric nanoparticles. This article reports on a versatile, straightforward synthesis of three-arm star-like polypept(o)ide (polysarcosine-block-polylysine) polymers, which are designed to be either stable or degradable at elevated levels of glutathione. Polypept(o)ides are a recently introduced class of polymers combining the stealth-like properties of the polypeptoid polysarcosine with the functionality of polypeptides, thus enabling the synthesis of materials completely based on endogenous amino acids. The star-like homo and block copolymers are synthesized by living nucleophilic ring opening polymerizat…

Hydrodynamic radiusPolymers and PlasticsPolymersBioengineeringBiodegradable Plastics02 engineering and technologyDegree of polymerization010402 general chemistry01 natural sciencesRing-opening polymerizationBiomaterialsDrug Delivery SystemsDynamic light scatteringNucleophilePolymer chemistryMaterials ChemistryCopolymerHumansAmino Acidschemistry.chemical_classificationPolymer021001 nanoscience & nanotechnologyGlutathione0104 chemical sciencesAmino acidHEK293 CellschemistryNanoparticlesPeptides0210 nano-technologyHeLa CellsBiotechnologyMacromolecular Bioscience
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Lewis acid-catalyzed Beckmann rearrangement of ketoximes in ionic liquids

2009

Abstract The Beckmann rearrangement of five ketoximes was done in 17 different ionic liquids by using four Lewis acids. The effect of the type of cation and the type of anion in the ionic liquid on the rate of the rearrangement reaction and product composition is compared and discussed. The effects of the hydrophobicity and the hydrogen bonding ability of ionic liquids on the rearrangement of ketoximes were investigated, as well as the catalytical activity of the Lewis acids.

Hydrogen bondProcess Chemistry and TechnologyGeneral ChemistrySigmatropic reactionCatalysisIonCatalysischemistry.chemical_compoundchemistryBeckmann rearrangementIonic liquidPolymer chemistryOrganic chemistryRearrangement reactionLewis acids and basesCatalysis Communications
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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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