Search results for "Bacteria"

showing 10 items of 4919 documents

Molecular topology: a useful tool for the search of new antibacterials.

2000

Molecular topology has been applied to find new lead antibacterial compounds. Among the selected compounds, hesperidin, neohesperidin and Mordant Brown 24 stand out, with minimum inhibitory concentrations 90, MIC90<0.3 mg / mL.

chemistry.chemical_classificationNeohesperidinMolecular modelBacteriamedicine.drug_classStereochemistryOrganic ChemistryClinical BiochemistryAntibioticsFlavonoidPharmaceutical ScienceMordantBiochemistryCombinatorial chemistryAnti-Bacterial AgentsHesperidinchemistry.chemical_compoundchemistryDrug DiscoverymedicineMolecular MedicineMolecular BiologyTopology (chemistry)Antibacterial agentBioorganicmedicinal chemistry letters
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Photoaffinity labeling of the coupling factor 1 from the thermophilic bacterum PS3 by 8-azido ATP

1984

AbstractTo localize the nucleotide binding sites of the F1ATPase (TF1) from the thermophilic bacterium PS3 we have used 14C-labeled 8-azido ATP (8-N3ATP) as photoaffmity label. 8-N3ATP is hydrolyzed by the F,ATPase in the absence of ultraviolet light. Irradiation by ultraviolet light of the enzyme in the presence of 8-N3ATP results in reduction of ATPase activity and in preferential nucleotide specific labeling of the α subunits (0.8–0.9 mol 8-N3ATP/TF1,α:β = 4:1). Inactivation and labeling do not depend on the presence of Mg2+. Both effects decrease upon addition of various nucleotide di- or triphosphates.

chemistry.chemical_classificationPhotoaffinity labelingStereochemistryNoncatalytic nucleotide binding siteThermophileBiophysicsCell BiologyBiochemistryCoupling (electronics)HydrolysisEnzymechemistryStructural BiologyPhotoaffinity labelingMoleBacterial F1ATPaseGeneticsUltraviolet lightCatalytic nucleotide binding siteNucleotideThermophilic bacterium PS3Molecular BiologyFEBS Letters
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1998

Reaction centers (RC) from the species Erythrobacter (Eb.) litoralis, Erythromonas (Em.) ursincola and Sandaracinobacter (S.) sibiricus have been purified by LDAO treatment of light-harvesting-reaction center complexes and DEAE chromatography. The content and overall organisation of the RCs' chromophores, determined by linear dichroism (LD) and absorption spectroscopy, are similar to those isolated from anaerobic photosynthetic bacteria. The redox properties of the primary electron donor are pH-independent and very similar to those determined for anaerobic photosynthetic bacteria with midpoint potential values equal to 445 (± 10), 475 and 510 mV for Eb. litoralis, S. sibiricus and Em. ursin…

chemistry.chemical_classificationPhotosynthetic reaction centreErythrobacter litoralisCytochromebiologyAerobic bacteriaStereochemistryCell BiologyPlant ScienceGeneral MedicineElectron acceptorbiology.organism_classificationPhotosynthesisBiochemistryMicrobiologychemistrybiology.proteinPhotosynthetic bacteriaBacteriaPhotosynthesis Research
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Characterization of HLA-DR- and TCR-binding residues of an immunodominant and genetically permissive peptide of the 16-kDa protein of Mycobacterium t…

2004

The 16-kDa protein of Mycobacterium tuberculosis represents an important antigenic target during bacillary latency and, consequently, should be considered as candidate subunit vaccine component. In this study, we have used CD4 T cell clones that recognize the peptide p91-110, an immunodominant and genetically permissive epitope, in the context of five different HLA-DR molecules and truncated and substituted variants of this peptide, to identify the minimal binding sequence (HLA-DR-binding core) and the minimal stimulatory sequence (TCR-binding core), as well as the residues that contact HLA-DR molecules and the TCR. We have found a common 9-mer sequence, spanning amino acids 93-101, as the …

chemistry.chemical_classificationProtein subunitT-LymphocytesImmunologyT-cell receptorReceptors Antigen T-CellContext (language use)PeptideHuman leukocyte antigenHLA-DR AntigensMycobacterium tuberculosisBiologyMolecular biologyEpitopeAmino acidchemistryPepscanBacterial ProteinsImmunology and AllergyHumansPeptidesEuropean journal of immunology
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Coupling of the guanosine glycosidic bond conformation and the ribonucleotide cleavage reaction: implications for barnase catalysis.

2007

To examine the possible relationship of guanine-dependent GpA conformations with ribonucleotide cleavage, two potential of mean force (PMF) calculations were performed in aqueous solution. In the first calculation, the guanosine glycosidic (Gχ) angle was used as the reaction coordinate, and computations were performed on two GpA ionic species: protonated (neutral) or deprotonated (negatively charged) guanosine ribose O2 ′. Similar energetic profiles featuring two minima corresponding to the anti and syn Gχ regions were obtained for both ionic forms. For both forms the anti conformation was more stable than the syn, and barriers of ∼4 kcal/mol were obtained for the anti → syn transition. Str…

chemistry.chemical_classificationRibonucleotideGuanosineStereochemistryProtein ConformationHydrolysisGuanosineGlycosidic bondRibonucleotidesBiochemistryEnzyme structureReaction coordinatechemistry.chemical_compoundDeprotonationRibonucleaseschemistryBacterial ProteinsStructural BiologyAlkane stereochemistryRiboseThermodynamicsGlycosidesMolecular BiologyProteins
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Contact sites of peptide-oligoribonucleotide cross-links identified by a combination of peptide and nucleotide sequencing with MALDI MS.

1997

We have investigated peptide–oligoribonucleotide complexes isolated from cross-linked Escherichia coli 30S ribosomal subunits in order to identify the contact sites of these complexes at the molecular level. For this purpose, reversed-phase (RP) HPLC-purified peptide–oligoribonucleotide complexes were submitted to N-terminal amino acid sequencing in order to determine the cross-linked peptide moiety and were analyzed using matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) for calculation of the nucleotide composition of the cross-linked complex. Subsequently, for nucleotide sequence information the complexes were partially hydrolyzed or treated with exonucleases and a…

chemistry.chemical_classificationRibosomal ProteinsBinding SitesBase SequenceChemistryMolecular Sequence DataNucleic acid sequencePeptideRibosomal RNABiochemistryRibosomeAmino acidRNA BacterialBiochemistryBacterial ProteinsRibosomal proteinRNA RibosomalSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationEscherichia coli30SAmino Acid SequencePeptide sequenceJournal of protein chemistry
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Polymer-induced phase separation in suspensions of bacteria

2010

We study phase separation in suspensions of two unrelated species of rod-like bacteria, Escherichia coli and Sinorhizobium meliloti, induced by the addition of two different anionic polyelectrolytes, sodium polystyrene sulfonate or succinoglycan, the former being synthetic and the latter of natural origin. Comparison with the known behaviour of synthetic colloid-polymer mixtures and with simulations show that "depletion" (or, equivalently, "macromolecular crowding") is the dominant mechanism: exclusion of the non-adsorbing polymer from the region between two neighbouring bacteria creates an unbalanced osmotic force pushing them together. The implications of our results for understanding phe…

chemistry.chemical_classificationSinorhizobium melilotiADSORPTIONbiologyBiofilmMIXTURESfood and beveragesGeneral Physics and AstronomyPolymerAGGREGATIONbiology.organism_classificationmedicine.disease_causeLIGHT-SCATTERINGSUCCINOGLYCANPolyelectrolytechemistryESCHERICHIA-COLImedicineBiophysicsMacromolecular crowdingSodium Polystyrene SulfonateEscherichia coliBEHAVIORBacteriaEPL (Europhysics Letters)
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Modulation of Fatty Acid Patterns During Protoplast Isolation

1983

Protoplast isolation and regeneration is known from numerous plant species (Binding et al. 1). But there are plant species which show very unconstant regeneration or no reaction at all, even if the isolation showed high viability of the protoplasts. Does this lacking response only depend on medium composition and effectors or are there other unknown conditions? The procedure of protoplast isolation and the use of strong hypertonic media is a dramatic disturbance of cell metabolism and might be a stress situation, which cannot be overcome by the cell. Fleck et al. (2) reported “osmotic-stress proteins” in Nicotiana sylvestris protoplasts and Kaiser et al. (3) showed a remarkable influence of…

chemistry.chemical_classificationSpinaciabiologyEffectorRegeneration (biology)fungiCellfood and beveragesFatty acidbiochemical phenomena metabolism and nutritionProtoplastequipment and suppliesPhotosynthesisbiology.organism_classificationmedicine.anatomical_structurechemistryBiochemistrymedicinebacteriaNicotiana sylvestris
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Biogas Cleaning by Hydrogen Sulfide Scrubbing and Bio-oxidation of Captured Sulfides

2015

Hydrogen sulfide and partially carbon dioxide can be absorbed into alkaline washing liquid with nitrates for upgrading a quality of biogas. Sulfides captured into the washing liquid are consequently biologically oxidized in an anoxic bioreactor by autotrophic denitrifying bacteria. Nitrates in the washing liquid serve as electron acceptors for sulfide bio-oxidation. Washing of hydrogen sulfide from biogas was examined in a lab-scale countercurrent scrubber that was packed with plastic carriers and operated at different biogas and washing liquid flows. The hydrogen sulfide concentration in treated biogas was investigated in the range from 3 to 12.3 g m–3. The influence of the hydrogen sulfid…

chemistry.chemical_classificationSulfideChemistryGeneral Chemical EngineeringHydrogen sulfideInorganic chemistryEnergy Engineering and Power TechnologyScrubberAnoxic watersDenitrifying bacteriachemistry.chemical_compoundFuel TechnologyBiogasBioreactorData scrubbingEnergy &amp; Fuels
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Identification of the 3-amino-3-carboxypropyl (acp) transferase enzyme responsible for acp3U formation at position 47 in Escherichia coli tRNAs

2019

AbstracttRNAs from all domains of life contain modified nucleotides. However, even for the experimentally most thoroughly characterized model organism Escherichia coli not all tRNA modification enzymes are known. In particular, no enzyme has been found yet for introducing the acp3U modification at position 47 in the variable loop of eight E. coli tRNAs. Here we identify the so far functionally uncharacterized YfiP protein as the SAM-dependent 3-amino-3-carboxypropyl transferase catalyzing this modification and thereby extend the list of known tRNA modification enzymes in E. coli. Similar to the Tsr3 enzymes that introduce acp modifications at U or m1Ψ nucleotides in rRNAs this protein conta…

chemistry.chemical_classificationTRNA modificationAlkyl and Aryl TransferasesNucleic Acid EnzymesNucleotidesRNASaccharomyces cerevisiaeBiologymedicine.disease_causePhenotypeEnzymechemistryBiochemistryBacterial ProteinsRNA TransferTransfer RNAGeneticsmedicineEscherichia coliTransferaseNucleic Acid ConformationNucleotideEscherichia coliNucleic Acids Research
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