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  • 1
    ISSN: 1572-8927
    Schlagwort(e): Activity coefficients ; osmotic coefficients ; aqueous electrolytes ; elevated temperatures
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract It was found over a wide concentration and temperature range that differences between osmotic coefficients of a given electrolyte and a standard electrolyte, φ - φst , can be approximated by a linear relation. Sodium chloride, calcium chloride and sodium sulfate were chosen as standard electrolytes for 1:1, 2:1 and 1:2 electrolytes, respectively. Special numerical procedures were developed for the prediction and estimation of activity and osmotic coefficients at elevated temperatures based on data at two temperatures or on data at room temperature only. Reasonable agreement was found between activity coefficients estimated by the present procedure and those correlated by Pitzer's and Meissner's equations.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 9 (1980), S. 535-551 
    ISSN: 1572-8927
    Schlagwort(e): Activity coefficients ; electrolyte mixtures ; Harned coefficient ; Pitzer's equations ; ionic interactions ; hydrochloric acid ; manganous chloride
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Activity coefficients of hydrochloric acid in mixed solutions of manganous chloride at twelve ionic strengths, from 0.1 to 5.0 mole-kg−1, were obtained from emf measurements of cells without liquid junction at five temperatures from 5 to 45°C. The data were interpreted in terms of the simple and convenient Pitzer treatment. Activity coefficients for manganous chloride in the mixtures were also derived using Pitzer's equations. Hydrochloric acid follows Harned's rule fromI=0.1 to 3.0 mole-kg−1, as concluded by Downes, whereas quadratic terms are warranted fromI=3.5 to 5.0 mole-kg−1. Contrary to Downes' conclusion, Harned's rule clearly does not hold true for manganous chloride at most ionic strengths.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1572-8927
    Schlagwort(e): Activity coefficients ; emf ; hydrochloric acid ; magnesium chloride ; Pitzer's equations ; Harned interaction coefficients ; Brönsted-Guggenheim parameters ; Higher-order electrostatic effects
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Electromotive-force measurements have been made on HCl−MgCl2−H2O mixtures at 5, 15, 25, 35 and 45°C at eleven different ionic strengths from 0.1–5.0 mol-kg −1 . The results are interpreted in terms of the simple Harned's equations, as well as the more complicated Pitzer ion-component treatment of multicomponent electrolyte mixtures. Activity coefficients for HCl in the salt mixtures obey Harned's rule up to and including I=5.0. For the salt in the acid mixtures, Harned's rule holds true up to and including I=0.5. The contribution of higher-order electrostatic terms (Eθ and E'θ) in the Pitzer equations is important for accurate evaluations of unlike cation-cation interactions (θH,Mg), and cation-anion-cation interactions (ΨH,Mg,Cl). The values ofSθH,Mg and ΨH,Mg,Cl (determined with Eθ and E'θ), θH,Mg and ΨH,Mg,Cl (determined without Eθ and E'θ), as well as the trace activity coefficients of HCl, γ tr A , in solutions of MgCl2 (where ionic strength fraction of the salt,y B = 1) at all the experimental temperatures and ionic strengths, are reported. Results of this study are compared with those for similar systems. At I=0.1 and 25°C, the results of the Brönsted-Guggenheim specific interaction theory are discussed briefly.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 11 (1979), S. 563-577 
    ISSN: 0091-7419
    Schlagwort(e): plasma membrane ; lectin receptors ; affinity chromatography ; membrane proteins ; hybridoma ; monoclonal antibody ; Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: Concanavalin A-binding (Con A)-binding cell surface glycoproteins were isolated, via Con A-affinity chromatography, from Triton X-100-solubilized Chinese hamster ovary (CHO) cell plasma membranes. The Con A binding glycoproteins isolated in this manner displayed a significantly different profile on sodium dodecyl sulfate-polyacrylamide gels than did the Tritonsoluble surface components, which were not retarded by the Con A-Sepharose column. [125I]-Con A overlays of the pooled column fractions displayed on sodium dodecyl sulfate-polyacrylamide gel electro-phoresis (SDS-PAGE) demonstrated that there were virtually no Con A receptors associated with the unretarded peak released by the Con A-Sepharose column, whereas the material which was bound and specifically eluted from the Con A-Sepharose column with the sugar hapten α-methyl-D-mannopyranoside contained at least 15 prominent bands which bound [125I]-Con A.In order to produce monoclonal antibodies against various cell surface Con A receptors, Balb/c mice were immunized with the pooled Con A receptor fraction. Following immunization spleens were excised from the animals and single spleen cell suspensions were fused with mouse myeloma P3/X63-Ag8 cells. Numerous hybridoma clones were subsequently picked on the basis of their ability to secrete antibody which could bind to both live and glutaraldehyde-fixed CHO cells as well as to the Triton-soluble fraction isolated from the CHO plasma membrane fraction. Antibody from two of these clones was able to precipitate a single [125I]-labeled CHO surface component of ∼265,000 daltons.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 14 (1980), S. 305-311 
    ISSN: 0091-7419
    Schlagwort(e): in vitro synthesis ; branched-chain amino acid binding proteins ; precursors ; processing ; periplasmic proteins ; Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: The synthesis of the leucine-specific and LIV-binding proteins was examined in vitro in a coupled transcription/translation system using the hybrid plasmids pOX7 and pOX13 as templates. Plasmid pOX7 contains the livK gene coding for the leucine-specific binding protein, and pOX13 contains the liv J gene coding for the LIV-binding protein. Both binding proteins were synthesized in vitro as precursor forms with molecular weights approximately 2,500 greater than their respective mature forms. Conversion of the precursor forms to their mature forms occurred during post-translational incubation following synthesis in the presence of membrane. The precursor of the LIV-binding protein was processed more rapidly than the leucine-specific binding protein precursor. Processing activity could be removed from the in vitro synthesis system by centrifugation, suggesting that the processing activity was membrane associated. Restoration of post-translational processing activity was achieved by adding inside-out membrane vesicles to membrane-depleted reaction mixtures.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 1 (1973), S. 368-379 
    ISSN: 0091-7419
    Schlagwort(e): Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: 1In the stimulation of rat hepatic adenylyl cyclase by glucagon or epinephrine we observe an abrupt change in the energy of activation at 32°C (seen as an increase in the slope of the Arrhenius plot). The energy of activation for the cyclase reaction above 32°C is about 1.7 times that found below this temperature. Cyclase activity stimulated by fluoride, prostaglandin E1, or 1-propanol, or activity in the absence of added stimulators does not show this change. The structural differences between the hormones suggest that they interact with the cyclase system at different loci. But the mechanism by which they stimulate cyclase activity appears to involve a common, temperature-dependent step.2In the presence of 1-propanol the change at 32°C in the energy of activation of the hormone-stimulated activity is not observed.3In view of the relatively large mole fraction of cholesterol present in the rat liver plasma membrane (which appears to inhibit phase transitions in bulk membrane lipids), it is suggested that this thermal sensitivity resides in protein rather than lipid components or that the cyclase is restricted to cholesterol-poor membrane regions.4The occurrence of anomalous Arrhenius plots of enzyme activities (with abrupt changes of slope) for both membrane-bound and soluble enzymes is reviewed.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 14 (1980), S. 527-537 
    ISSN: 0091-7419
    Schlagwort(e): leucine transport genes ; cloning ; regulation ; rho factor ; Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: Leucine is transported into E coli by two osmotic shock-sensitive, high-affinity systems (LIV-I and leucine-specific systems) and one membrane bound, low-affinity system (LIV-II). Expression of the high-affinity transport systems is altered by mutations in liv R and 1st R, genes for negatively acting regulatory elements, and by mutations in rho, the gene for transcription termination. All four genes for high-affinity leucine transport (livJ, livK, livH, and livG) are closely linked and have been cloned on a plasmid vector, pOX1. Several subcloned fragments of this plasmid have been prepared and used in complementation and regulation studies. The results of these studies suggest that livJ and livK are separated by approximately one kilobase and give a gene order of livJ-livK-livH. livJ and livK appear to be regulated in an interdependent fashion; livK is expressed maximally when the livJ gene is inactivated by mutation or deletion. The results support the existence of separate promoters for the livJ and livK genes. The effects of mutations in the rho and livR genes are additive on one another and therefore appear to be involved in independent regulatory mechanisms. Mutations in the rho gene affect both the LIV-I and leucinespecific transport systems by increasing the expression of livJ and livK, genes for the LIV-specific and leucine-specific binding proteins, respectively.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, N.Y. : Wiley-Blackwell
    Journal of Supramolecular Structure 6 (1977), S. 419-431 
    ISSN: 0091-7419
    Schlagwort(e): regulation ; amino acid transport ; mutants ; leucine sensitivity ; leucine ; isoleucine ; valine ; Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Chemie und Pharmazie , Medizin
    Notizen: Leucine is transported into E. coli cells by high-affinity transport systems (LIV-I and leucine-specific systems) which are sensitive to osmotic shock and require periplasmic binding proteins. In addition leucine is transported by a low-affinity system (LIV-II) which is membrane bound and retained in membrane vesicle preparations. The LIV-I system serves for threonine and alanine in addition to the 3 branched-chain amino acids. The LIV-II system is more specific for leucine, isoleucine, and valine while the high-affinity leucine-specific system has the greatest specificity.A regulatory locus, livR at minute 22 on the E. coli chromosome produces negatively regulated leucine transport and synthesis of the binding proteins. Valine-resistant strains have been selected to screen for transport mutants. High-affinity leucine transport mutants that have been identified include a LIV-binding protein mutant, livJ, a leucine-specific binding protein mutant livK and a nonbinding protein component of the LIV-I system, livH. A fourth mutant, livP, appears to be required only for the low-affinity LIV-II system. The existence of this latter mutant indicates that LIV-I and LIV-II are parallel transport systems. The 4 mutations concerned with high-affinity leucine transport form a closely linked cluster of genes on the E. coli chromosome at minute 74.The results of recent studies on the regulation of the high-affinity transport systems suggests that an attenuator site may be operative in its regulation. This complex regulation appears to require a modified leucyl-tRNA along with the transcription termination factor rho. Regulation of leucine transport is also defective in relaxed strains.Among the branched-chain amino acids only leucine produces regulatory changes in LIV-I activity suggesting a special role of this amino acid in the physiology of E. coli. It was shown that the rapid exchange of external leucine for intracellular isoleucine via the LIV-I system could create an isolucine pseudoauxotrophy and account for the leucine sensitivity of E. coli.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 14 (1996), S. 49-55 
    ISSN: 0263-6484
    Schlagwort(e): redox state ; protein disulfide isomerase ; AP1 ; NF-κB ; electromobility shift assay ; Life Sciences ; Molecular Cell Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: Most transcription factors are multimeric complexes whose subunits depend on strict conformational requirements to form the active unit. Among these requirements is the presence of appropriate sulfhydryl interactions that are critical to transcription factor binding to cognate DNA recognition sites. Our experiments now suggest that modulation of these sulfhydryls may involve the action of thiol-modifying oxido-reductases such as protein disulfide isomerase (PDI). Electrophoretic mobility shift titration experiments incorporating different ratios of GSH:GSSG indicated that changes in GSH and GSSG concentrations corresponding to redox potential differences of as little as ±15 mV enabled or abolished binding of NF-κB and AP1 to their cognate DNA sites. Moreover, this binding range was modulated significantly by the addition of purified protein disulfide isomerase (PDI). Collectively, these results suggest that a reversible oxidation/reduction signalling pathway may exist in the cell whereby localized changes in redox potentials and/or oxido-reductase activity can be functionally relevant in the regulation of critical gene expression events.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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