Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 15 (1993), S. 42-49 
    ISSN: 0887-3585
    Schlagwort(e): X-ray structure ; ATP-binding proteins ; glycine-rich loop ; enzyme kinetics ; induced-fit ; H-ras-p21 relationship ; crystal packing contacts ; noncrystallographic symmetry ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: Two mutants of adenylate kinase from Escherichia coli have been crystallized and analyzed by X-ray diffraction at resolutions of 3.4 and 2.4 Å, respectively. These mutants are Pro-9→Leu and Gly-10→Val. They were selected for their positions in the highly conserved Gly-loop forming a giant anion hole for the β-phosphate of ATP (GTP) in adenylate kinases, H-ras-p21, and other nucleotide-binding proteins. Mutants at these positions of H-ras-p21 cause cancer. In adenylate kinase these mutations cause smallish changes at the active site. Relating the structural changes to the known changes in catalysis indicates that these mutants hinder the induced-fit movements. As a side result we find that mutant Pro-9→Leu and wild-type form one very similar crystal packing contact that is crystallographic in one case and noncrystallographic in the other, while all other packing contacts and the space groups are quite at variance. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 27 (1997), S. 438-449 
    ISSN: 0887-3585
    Schlagwort(e): α/β hydrolase fold ; catalytic triad ; cyanolysis ; heterologous expression ; Saccharomyces cerevisiae ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: (S)-Hydroxynitrile lyase (Hnl) from the tropical rubber tree Hevea brasiliensis is a 29 kDa single chain protein that catalyses the breakdown or formation of a C(SINGLE BOND)C bond by reversible addition of hydrocyanic acid to aldehydes or ketones. The primary sequence of Hnl has no significant homology to known proteins. Detailed homology investigations employing PROFILESEARCH and secondary structure prediction algorithms suggest that Hnl is a member of the α/β hydrolase fold protein family and contains a catalytic triad as functional residues for catalysis. The significance of the predicted catalytic residues was tested and confirmed by site-directed mutagenesis and expression of mutant and wild-type proteins in the yeast, Saccharomyces cerevisiae. Based on these data we suggest a mechanistic model for the (S)-cyanohydrin synthesis catalyzed by hydroxynitrile lyase from Hevea brasiliensis. Proteins 27:438-449, 1997. © 1997 Wiley-Liss, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Chicester [u.a.] : Wiley-Blackwell
    Journal of Molecular Recognition 10 (1997), S. 245-255 
    ISSN: 0952-3499
    Schlagwort(e): RY-repeat ; minor groove binders ; topoisomerase II cleavage ; footprinting ; microscopic binding constants ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: We present titrations of the human δβ-globin gene region with DNA minor groove binders netropsin, bisnetropsin, distamycin, chromomycin and four bis-quaternary ammonium compounds in the presence of calf thymus topoisomerase II and DNase I. With increasing ligand concentration, stimulation and inhibition of enzyme activity were detected and quantitatively evaluated. Additionally we show a second type of stimulation, the appearance of strong new topoisomerase II cleavage sites at high ligand concentrations. The specific binding sites of the minor groove binders of the DNA sequence and their microscopic binding constants were determined from DNase I footprints. A binding mechanism for minor groove binders is proposed in order to explain these results especially when ligand concentration is increased. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 49 (1996), S. 659-666 
    ISSN: 0006-3592
    Schlagwort(e): suspension culture ; insect cells ; baculovirus ; multiplicity of infection ; time of infection ; model ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: In vitro infection of insect cells with baculoviruses is increasingly considered a viable means for the production of biopesticides, recombinant veterinary vaccines, and other recombinant products. Batch fermentation processes traditionally employ intermediate to high multiplicities of infection necessitating two parallel scale-up processes - one for cells and one for virus. In this study, we consider the use of multiplicities of infection as low as 0.0001 plaque-forming units per cell, a virus level low enough to enable infection of even large reactors (e.g., 10 m3) directly from a frozen stock. Using low multiplicities in the Sf9/β-gal-AcNPV system, recombinant protein titers comparable with the maximum titer observed in high multiplicity infections were achieved. Cultures yielding the maximum titer were characterized by reaching a maximum cell density between 3 and 4 × 109 cell L-1. This optimal cell yield did not depend on the multiplicity of infection, supporting the existing view that batch cultures are limited by availability of substrate. Up to a certain cell density, product titer will increase almost linearly with availability of biocatalyst, that is, cells. Beyond this point any further cell formation comes at the expense of final product titer. Low multiplicity infections were found not to cause any significant dispersion of the protein production process. Hence, product stability is not a major issue of concern using low multiplicities of infection. The sensitivity to initial conditions and disturbances, however, remains an issue of concern for the commercial use of low multiplicity infections. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 28 (1986), S. 1735-1741 
    ISSN: 0006-3592
    Schlagwort(e): Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: The utilization of mixtures of methanol (C1) and glucose (C6) of different composition by the methylotrophic yeast Hansenula polymorpha was studied in carbon-limited chemostat culture. For all mixtures tested a similar utilization pattern was observed: At low dilution rates both carbon sources were utilized simultaneously, but at high dilution rates the cells used glucose only and the unutilized methanol accumulated in the culture medium. When grown with C1 only, the cells exhibited a critical dilution rate Dc(C1) of 0.19 h-1, but when C1-C6 mixtures were used as the carbon and energy substrate, the yeast was able to completely utilize C1 at dilution rates considerably higher than Dc(C1). The dilution rate at which the transition from C1-C6 growth to C6 growth occurred (Dt) was strictly dependent on the composition of the C1-C6 mixture in the feed, and Dt increased with decreasing proportions of C1 in the mixture. During mixed substrate growth the formation of biomass from the two substrates was additive. The results reported indicate that the utilization of C1-C6 mixtures and hence Dt in H. polymorpha are subject to two different regulatory regimes. When the cells were growing with C1-C6 mixtures containing more than 60% C1, the transition form C1-C6 to C6 growth was most probably influenced by the maximum C1 oxidizing capacity of the cells, whereas for growth with mixtures containing less than 40% C1, a growth rate of 0.28-0.30 h-1 seemed to be the limiting barrier for the simultaneous utilization of the components of the binary carbon and energy substrate mixture.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2219-2230 
    ISSN: 1434-193X
    Schlagwort(e): Retrodisproportionation ; Arenes ; EPR spectroscopy ; Thermochemistry ; Coal liquefaction ; Catalysis ; Hydrogen transfer ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The transfer of hydrogen from excess 9,10-dihydroanthracene (DHA) to acceptors such as α-methylstyrene is catalyzed, i.e. occurs at temperatures in the range 200-260 °C instead of 280-320 °C, when hydrocarbons with weaker C-H bonds than DHA, e.g. 6H-benzo[cd]pyrene (4), 7H-dibenzo[a,kl]anthracene (5), 4-methyl-7H-benzo[de]naphthacene (6) or 8H-dibenzo[b,fg]pyrene (7), are added to the reaction mixture. The reactions are initiated by bimolecular H-atom transfer from 4-7 to the acceptor (retrodisproportionation) and proceed by nonchain radical mechanisms. This is supported by isotopic labelling and kinetic isotope effects, substituent and solvent effects, EPR spectroscopy of intermediate radicals, and by a comparison of the thermochemical and kinetic characteristics of these reactions.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    ISSN: 0006-3592
    Schlagwort(e): aqueous two-phase systems ; partitioning of peptides ; liquid-liquid phase equilibrium ; Chemistry ; Biochemistry and Biotechnology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Notizen: Buffered aqueous two-phase systems are effective extraction systems for separating amphoteric hydrocarbons like, for example, polypeptides from aqueous phases. The design and basic engineering of such processes requires the knowledge of the liquid-liquid equilibrium. The study presented here aims to contribute to the development of methods to predict the partitioning of peptides in aqueous two-phase systems. Experimental results are reported for the partitioning of small amounts (≈0.001 g solute per gram of solution) of low molecular combination peptides of glycine, L-glutamic acid, L-phenylalanine, and L-lysine (9 dipeptides, gly-glu, gly-phe, gly-lys, glu-gly, phe-gly, phe-glu, lys-gly, lys-glu, lys-phe; 7 tripeptides, gly-gly-phe, gly-phe-gly, glu-gly-phe, phe-gly-gly, lys-gly-lys, lys-glu-gly, lys-phe-lys) in aqueous two-phase systems of high molecular weight dextran (molecular weight about 500,000) and poly(ethylene glycol) (molecular weight about 6,000 and 35,000, respectively) in the presence of small amounts (about 0.05 mol/kg) of K2HPO4/KH2PO4 buffer at about 293 K. The new data are compared to predictions. Partition coefficients are predicted applying a group contribution excess Gibbs energy model. The model is an osmotic virial equation. It uses surface fractions to encounter for the probability of interactions between solutes. All model parameters were taken from the literature. They were determined exclusively from experimental data for the phase forming systems and for the partitioning of amino acids and their di- and tripeptides (containing only a single amino acid), but no experimental data for the partitioning of combinations peptides were used. In most cases predicted partition coefficients agree favourably with the experimental data. © 1998 John Wiley & Sons, Inc. Biotechnol Bioeng 60: 699-711, 1998.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1996 (1996), S. 1529-1532 
    ISSN: 0947-3440
    Schlagwort(e): Retrodisproportionation ; Radicals ; Hydrogen transfer ; Molecule-induced formation of radicals ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1,3-Cyclohexadiene, 1,3-cycloheptadiene and cycloheptatriene are smoothly hydrogenated to cyclohexene and cycloheptene, respectively, when heated to 260-340°C with an excess of 9,10-dihydroanthracene (DHA) in diphenyl ether or benzonitrile. On the basis of a mechanistic study a nonchain three-step mechanism is proposed which is initiated by a transfer of a hydrogen atom from DHA to the polyenes (retrodisproportionation).
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    ISSN: 0947-3440
    Schlagwort(e): Hydrogen transfer ; Molecule-induced formation of radicals ; Retrodisproportionation ; Acridines, dihydro- ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Hydrogen is transferred from acridane (1c) and N-methylacridane (1d) to α-methyl-styrene (2) in a bimolecular uncatalyzed reaction at 260-300°C. On the basis of the activation parameters (for 1c: ΔH≠ = 29.0 kcal/mol, ΔS≠ = -23.5 e.u. in triglyme) the kinetic isotope effect (kH/kD = 2.0, in triglyme at 300°C) as well as the small solvent effects and from the observation of an EPR signal of N-methylhydroacridyl radicals a three-step radical mechanism is prosposed which is initiated by a retrodisproportionation between 1 and 2.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    ISSN: 0947-3440
    Schlagwort(e): Retrodisproportionation ; Molecule-induced radical formation ; Semiempirical calculations ; Hydrogen transfer ; Rearrangements ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: From the uncatalyzed transfer-hydrogenation of azulene 1 with the hydrogen donors 9,10-dihydroanthracene (4), 7H-benz[de]anthracene (5) and 9,9-diphenyl-10,10-dideuteroanthracene (6) at 340-375°C in diphenyl ether, two isomeric octahydroazulenes and, in addition, naphthalene and tetralin are obtained. From product studies, kinetics, isotopic labelling experiments and semiempirical MO calculations, a nonchain stepwise radical mechanism is proposed, which is initiated by H-atom transfer from the donor to azulene. The proposed mechanism for the formation of naphthalene and tetralin via azulene-naphthalene rearrangement under these conditions is a combination of the Scott mechanism and the Alder “walk” mechanism, which are initiated by the hydrogen-transfer step.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...