Search results for "Escher"

showing 10 items of 728 documents

Der Einflu� von Antibiotica auf die �berlebensrate von Mikroorganismen bei tiefen Temperaturen

1959

Die Lebendkeimzahl in einer Suspension vonE. coli nimmt bei +4°C langsam zu, nimmt bei-5°C wenig ab und fallt bei-19°C innerhalb von 24 Std stark, wahrend die Verringerung in den folgenden Tagen nur noch gering ist. Streptomycin und Penicillin vermindern in allen 3 Temperaturbereichen die Keimkonzentration in Abhangigkeit von der Antibioticumkonzentration. Subbakteriostatische Konzentrationen von Streptomycin haben bei-19°C eine zusatzliche Wirkung. Die Resistenz der in uberbakteriostatischen Antibioticakonzentrationen bei diesen Temperaturen uberlebenden Keime ist gegenuber dem Ausgangsstamm weder erhoht noch vermindert.

Cold effectsmedicine.drug_classMicroorganismAntibioticsMicrococcusGeneral MedicineBiologymedicine.disease_causebiology.organism_classificationBiochemistryMicrobiologyMicrobiologyMicrobial ecologyStaphylococcus aureusStreptomycinGeneticsmedicineMolecular BiologyEscherichia colimedicine.drugArchiv f�r Mikrobiologie
researchProduct

Behavior of four main dairy pathogenic bacteria during manufacturing and ripening of pecorino siciliano cheese

2020

Background: Consumption of raw cheese may be associated with different diseases. This study aimed to evaluate behavior of four pathogenic bacteria during manufacture and ripening of Protected Designation of Origin (PDO) Pecorino Siciliano cheese.
 Methods: The experimental cheese groups were inoculated with pathogenic bacteria, including Escherichia coli O157, Listeria monocytogenes, Salmonella Enteritidis, and Staphylococcus aureus. The cheese making processes were monitored from milk curdling until 3 months ripened cheeses and the levels of Lactic Acid Bacteria (LAB) and the four dairy pathogens were evaluated by plate counts. Randomly Amplified Polymorphic DNA (RAPD)-Polymerase Chai…

Colony-forming unitStaphylococcus aureuslcsh:TP368-456Curdlingbiologylisteria monocytogenesfood and beveragesPathogenic bacteriaRipeningmedicine.disease_causebiology.organism_classificationSalmonella enteritidiRAPDFood safetylcsh:Food processing and manufactureListeria monocytogenesCheesemedicineEscherichia coliFood sciencesalmonella enteritidisBacteriaFood ScienceMesophileListeria monocytogene
researchProduct

Bacterial endosymbionts of insects: insights from comparative genomics.

2004

The development of molecular techniques for the study of uncultured bacteria allowed the extensive study of the widespread association between insects and intracellular symbiotic bacteria. Most of the bacterial endosymbionts involved in such associations are gamma-proteobacteria, closely related to Escherichia coli. In recent years, five genomes from insect endosymbionts have been sequenced, allowing the performance of extensive genome comparative analysis that, as a complement of phylogenetic studies, and analysis on individual genes, can help to understand the different traits of this particular association, including how the symbiotic process is established, the explanation of the specia…

Comparative genomicsInsectaBacteriaEcologyfungiAdaptation BiologicalBacterial Physiological PhenomenaBiologymedicine.disease_causeBacterial Physiological PhenomenaMicrobiologyGenomeBiological EvolutionSymbiosisEvolutionary biologymedicinebacteriaAnimalsAdaptationSymbiosisEscherichia coliGeneEcology Evolution Behavior and SystematicsGenome BacterialSymbiotic bacteriaEnvironmental microbiology
researchProduct

Differentiation of DctA and DcuS function in the DctA/DcuS sensor complex ofEscherichia coli: function of DctA as an activity switch and of DcuS as t…

2014

Summary The C4-dicarboxylate responsiveness of the sensor kinase DcuS is only provided in concert with C4-dicarboxylate transporters DctA or DcuB. The individual roles of DctA and DcuS for the function of the DctA/DcuS sensor complex were analysed. (i) Variant DctA(S380D) in the C4-dicarboxylate site of DctA conferred C4-dicarboxylate sensitivity to DcuS in the DctA/DcuS complex, but was deficient for transport and for growth on C4-dicarboxylates. Consequently transport activity of DctA is not required for its function in the sensor complex. (ii) Effectors like fumarate induced expression of DctA/DcuS-dependent reporter genes (dcuB–lacZ) and served as substrates of DctA, whereas citrate ser…

Concentration dependentBiochemistryTransport activitymedicineBiologymedicine.disease_causeMolecular BiologyMicrobiologyEscherichia coliFunction (biology)Molecular Microbiology
researchProduct

Decipher the mechanisms of protein conformational changes induced by nucleotide binding through free-energy landscape analysis: ATP binding to Hsp70.

2013

ATP regulates the function of many proteins in the cell by transducing its binding and hydrolysis energies into protein conformational changes by mechanisms which are challenging to identify at the atomic scale. Based on molecular dynamics (MD) simulations, a method is proposed to analyze the structural changes induced by ATP binding to a protein by computing the effective free-energy landscape (FEL) of a subset of its coordinates along its amino-acid sequence. The method is applied to characterize the mechanism by which the binding of ATP to the nucleotide-binding domain (NBD) of Hsp70 propagates a signal to its substrate-binding domain (SBD). Unbiased MD simulations were performed for Hsp…

Conformational changeProtein ConformationAllosteric regulationPlasma protein bindingMolecular Dynamics SimulationCellular and Molecular NeuroscienceProtein structureAdenosine TriphosphateGeneticsHSP70 Heat-Shock ProteinsMolecular Biologylcsh:QH301-705.5Nuclear Magnetic Resonance BiomolecularEcology Evolution Behavior and SystematicsEcologybiologyChemistryEscherichia coli ProteinsEnergy landscapeComputational Theory and MathematicsBiochemistrylcsh:Biology (General)Docking (molecular)Modeling and SimulationChaperone (protein)Biophysicsbiology.proteinBinding domainProtein BindingResearch ArticlePLoS computational biology
researchProduct

Interaction ofEscherichia colihemolysin with biological membranes

2001

Escherichia coli hemolysin (HlyA) is a membrane-permeabilizing protein belonging to the family of RTX-toxins. Lytic activity depends on binding of Ca2(+) to the C-terminus of the molecule. The N-terminus of HlyA harbors hydrophobic sequences that are believed to constitute the membrane-inserting domain. In this study, 13 HlyA cysteine-replacement mutants were constructed and labeled with the polarity-sensitive fluorescent probe 6-bromoacetyl-2-dimethylaminonaphthalene (badan). The fluorescence emission of the label was examined in soluble and membrane-bound toxin. Binding effected a major blue shift in the emission of six residues within the N-terminal hydrophobic domain, indicating inserti…

Conformational changeProtein ConformationPlasma protein bindingBiologymedicine.disease_causeHemolysisBiochemistryHemolysin ProteinsProtein structureBacterial Proteins2-NaphthylamineEscherichia colimedicineCysteineCloning MolecularLipid bilayerEscherichia coliFluorescent DyesEscherichia coli ProteinsCell MembraneErythrocyte MembraneBiological membraneProtein Structure TertiarySpectrometry FluorescenceMembraneBiochemistryMutagenesisLiposomesChromatography GelCalciumElectrophoresis Polyacrylamide GelProtein BindingBinding domainEuropean Journal of Biochemistry
researchProduct

Inducible Genetic Code Expansion in Eukaryotes

2020

Abstract Genetic code expansion (GCE) is a versatile tool to site‐specifically incorporate a noncanonical amino acid (ncAA) into a protein, for example, to perform fluorescent labeling inside living cells. To this end, an orthogonal aminoacyl‐tRNA‐synthetase/tRNA (RS/tRNA) pair is used to insert the ncAA in response to an amber stop codon in the protein of interest. One of the drawbacks of this system is that, in order to achieve maximum efficiency, high levels of the orthogonal tRNA are required, and this could interfere with host cell functionality. To minimize the adverse effects on the host, we have developed an inducible GCE system that enables us to switch on tRNA or RS expression whe…

Context (language use)Computational biology010402 general chemistry01 natural sciencesBiochemistryInsert (molecular biology)Amino Acyl-tRNA SynthetasesRNA TransferEscherichia coliHumansunnatural amino acidAmino AcidsMolecular BiologyT-RExchemistry.chemical_classificationTet-On010405 organic chemistryChemistryCommunicationOrganic ChemistryEukaryotaGenetic codeamber suppressionCommunications0104 chemical sciencesAmino acidMaximum efficiencyFluorescent labellingHEK293 CellsGenetic CodePylRSTransfer RNAMolecular MedicineAmber Stop CodonChemBioChem
researchProduct

Removal of Escherichia coli from Saturated Sand Columns Supplemented with Hydrochar Produced from Maize

2014

Despite numerous studies on hydrochar use, its application in water treatment for pathogen removal remains unexplored. In this study, we evaluated the efficiency of hydrochar produced from crop residue of maize for water treatment by determining Escherchia coli breakthrough from sand columns supplemented with hydrochar. To enhance the adsorptive capacity, raw hydrochar was activated by 1 mol L⁻¹ KOH at room temperature. The experiments conducted in a 10-cm sand bed with 1.5% (w/w) activated and raw hydrochar supplements, not activated by KOH, showed 93 and 72% of E. coli removal efficiencies, respectively. Activation of KOH not only enhanced the E. coli removal but also increased the streng…

Crop residueEnvironmental EngineeringChemistryScanning electron microscopeManagement Monitoring Policy and Lawmedicine.disease_causePollutionAgronomyparasitic diseasesmedicineSurface structureWater treatmentFourier transform infrared spectroscopyPorosityWaste Management and DisposalEscherichia coliWater Science and TechnologyNuclear chemistryJournal of Environmental Quality
researchProduct

Cell inactivation and membrane damage after long-term treatments at sub-zero temperature in the supercooled and frozen states.

2008

The survival of cells subjected to cooling at sub-zero temperature is of paramount concern in cryobiology. The susceptibility of cells to cryopreservation processes, especially freeze-thawing, stimulated considerable interest in better understanding the mechanisms leading to cell injury and inactivation. In this study, we assessed the viability of cells subjected to cold stress, through long-term supercooling experiments, versus freeze-thawing stress. The viability of Escherichia coli, Saccharomyces cerevisiae, and leukemia cells were assessed over time. Supercooled conditions were maintained for 71 days at -10 degrees C, and for 4 h at -15 degrees C, and -20 degrees C, without additives or…

CryobiologyCell Membrane PermeabilityTime FactorsMembrane permeabilityOsmotic shockCell Survival[SDV]Life Sciences [q-bio]BioengineeringSaccharomyces cerevisiaeApplied Microbiology and BiotechnologyCryopreservation03 medical and health sciences[SPI]Engineering Sciences [physics]Cell Line TumorCongelation[ SPI ] Engineering Sciences [physics]Escherichia coliHumansViability assayComputingMilieux_MISCELLANEOUS030304 developmental biologyCryopreservation0303 health sciencesMicrobial Viability[ SDV ] Life Sciences [q-bio]Chemistry030302 biochemistry & molecular biologyCell MembraneMembraneBiophysicsWater of crystallizationBiotechnologyBiotechnology and bioengineering
researchProduct

Three-dimensional structure of hepatitis B virus core particles determined by electron cryomicroscopy

1994

Human hepatitis B virus core protein expressed in E. coli assembles into two sizes of particle. We have determined their three-dimensional structures by electron cryomicroscopy and image processing. The large and small particles correspond to triangulation number T = 4 and T = 3 dimer clustered packings, containing 240 and 180 protein subunits, respectively. The local packing of subunits is very similar in the two sizes of particle and shows holes or channels through the shell. The native viral core particle packages RNA and is active in reverse transcription to DNA. The holes we observe may provide access for the necessary small molecules. Shells assembled from the intact core protein cont…

CryopreservationHepatitis B virusProtein ConformationCryo-electron microscopyProtein subunitDimerShell (structure)RNABiologyHepatitis B Core AntigensVirologyRecombinant ProteinsGeneral Biochemistry Genetics and Molecular BiologyMicroscopy Electronchemistry.chemical_compoundCrystallographyProtein structurechemistryEscherichia coliImage Processing Computer-AssistedHumansParticleDNACell
researchProduct