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
Filter
  • Biochemistry and Biotechnology  (39)
  • Geminal substituents, energetic interaction of  (7)
  • 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
    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 ...
  • 7
    ISSN: 0947-3440
    Schlagwort(e): Anomeric effect ; Enthalpies of formation ; Geminal substituents, energetic interaction of ; Increments, thermochemical, of orthoesters ; Group increments, interpretation of ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: New enthalpies of formation ΔHf^(g) are provided for the series of orthoesters 2a-2f, 3 and 4 from their enthalpies of combustion ΔHc^ and their enthalpies of vaporization ΔHvap^ or enthalpies of sublimation ΔHsub^. From these data and from literature data the following new thermochemical increments were calculated [kJ · mol-1]: CH[O3] - 106.4, C[O3, C] -103.7, and C[O3, Ph] -124.5. In addition the increment C[O4] - 167.1 was calculated from literature data for ΔHf^(g) of the orthocarbonates 9a and 9b. The anomeric stabilization derived from these results and from previous results for acetals and ketals are reported in Table 3. - A new concept of additive structural increments for the quantitative analysis of the group increments of hydrocarbons, ethers, acetals, and ketals is proposed. It is shown that the increments for CH3, CH2, CH, and C groups with their different neighboring atoms (see Table 4) are determined by the number of hydrogen atoms in the group and by the number of pairwise geminal interactions between all atoms attached to the central carbon atom. - Using this procedure for orthoesters and orthocarbonates, deviations from additivity for the geminal interaction between oxygen atoms, i.e. the anomeric effect, are observed.
    Zusätzliches Material: 10 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    ISSN: 0947-3440
    Schlagwort(e): Radicals, stability of ; C—C bond cleavage, kinetics of ; Enthalpies of combustion ; Geminal substituents, energetic interaction of ; Capto-dative effect ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The thermolysis reactions of 3a and 2a, b were studied over a temperature range of 40°C and the activation parameters were determined. They were compared with the activation parameters of structurally comparable hydrocarbons of similar strain in order to obtain the radical stabilization enthalpies RSEs of the cyano(dimethylamino)methyl radical 1a. For this comparison the geminal interaction enthalpies of the cyano and the dimethylamino groups in the ground state had to be determined for the series of amino nitriles 4a-4c and 4j-4n by thermochemical methods. The geminal interaction in the ground state varies between -0.6 kcal/mol stabilization in 4a and a destabilization of +10.7 and +7.0 kJ mol-1 for secondary and tertiary α-dialkylaminonitriles, respectively. A synergistic (i.e. more than additive) stabilization enthalpy of 26 kJ mol-1 of 1a was found in contrast to predictions in the literature. This stabilization is interpreted by conjugation between the substituents, which are separated by the radical center.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    ISSN: 0947-3440
    Schlagwort(e): Enthalpies of formation ; Geminal substituents, energetic interaction of ; Bond cleavage, C—C, kinetics of ; Radicals, stability of ; Increments, thermochemical ; Bond strength, substituent effects on ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Substituent Effects on the CC Bond Strength, 16.  -  Thermal Stability and Enthalpies of Formation of β-Dicarbonyl Compounds.  -  Stabilisation Enthalpies of α,α′-Diketoalkyl RadicalsThe geminal interactions of the two carbonyl groups in seven β-diketones of the type 8-9 and 11-13 were estimated from their enthalpies of formation, which were deduced from their heats of combustion and enthalpies of vaporization. The radical stabilisation enthalpies RSE of the α,α′-diketoalkyl radicals 9-13 were obtained from the enthalpies of activation ΔH≠ of thermal CC bond cleavage of eight model compounds of the type 9-13 by their comparison with ΔH≠ of comparable hydrocarbons of similar strain. For non-cyclic α,α′-diacyl-alkyl radicals and six-membered cyclic ones RSE = 54.8 ± 1.3 kJ mol-1 was determined, which indicates an additive stabilisation by two carbonyl groups.
    Zusätzliches Material: 11 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 10
    ISSN: 0947-3440
    Schlagwort(e): Enthalpies of formation ; Geminal substituents, energetic interaction of ; Bond cleavage, C-C, kinetics of ; Radicals, stabilization of ; Increments, thermochemical, of esters ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Heats of formation ΔHf0(g) were determined from enthalpies of combustion ΔHf0(c) and enthalpies of vaporization ΔHvap0 or enthalpies of sublimation ΔHsub0 for the eight substituted methanetricarboxylates 2a-h. From these data and from previously determined enthalpies of formation Δf0 of substituted malonic esters new thermochemical group increments were derived. From these increments and from the recently published improved increments for carboxylic acid esters the gem. interaction enthalpies of two and three COOR groups were calculated. The radical stabilization enthalpies RSE of α,α-bis(methoxycarbonyl)alkyl (18.2 kJ mol-1, 1a) and tris-(methoxycarbonyl)methyl radicals (5.2 kJ mol-1, 1b) were derived from kinetic data obtained by means of our previously developed protocol. They were corrected for the gem. interaction energies of the ester groups in the ground state and are satisfactorily explained by an additive stabilizing effect of the ester substituents and by dipolar substituent interactions in the radicals. The dipolar energies were taken from MM2 calculations.
    Zusätzliches Material: 10 Tab.
    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...