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  • Chemistry  (7)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 35 (1959), S. 549-552 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. S21 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 18 (1979), S. 1073-1079 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Raman spectra from 800 to 1850 cm-1 of aqueous solutions of ovalbumin and its more heat-stable form, S-ovalbumin, are presented. A Raman difference spectrum (ovalbumin minus S-ovalbumin) shows differences in intensity in the amide I and III regions. These intensity differences lead us to postulate that the conversion of ovalbumin to S-ovalbumin involves a conformation change of a small part (∼3-4%) of the protein from α-helix to antiparallel β-sheet geometry. This small difference in the three-dimensional arrangement of the peptide chain may contribute to the large difference in the thermodynamic stability between ovalbumin and S-ovalbumin.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 3 (1965), S. 509-517 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Optical rotatory dispersions (ORD) of ovalbumin, conalbumin, ovomucoid, and lysozyme (muramidase) were measured in aqueous solution over a wavelength range of 195-600 mμ. The dispersion curves obeyed a one-term Drude equation above 300 mμ. The strong Cotton effects in the ultraviolet showed peaks and troughs at about the same wavelength for all four proteins, but the crossover point for the 225 mμ Cotton effect for ovomucoid was appreciably lower than for the other proteins. Helical contents calculated by using the Moffitt equation, the trough value of the 225 mμ Cotton effect, and the expressions for helical content recently proposed by Schechter and Blout ranged from 5 to 34%. Except for ovomucoid, the trough value of the 225 mμ Cotton effect gave the lowest helical content.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 2 (1964), S. 275-277 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proper correction of angular light-scattering data for reflection effects results in agreement between determinations by light scattering and by sedimentation equilibrium of the molecular weight of rabbit myosin A prepared in the same manner. This leaves the question of molecular weight dependence on the method of sample preparation unsettled. Reflection corrections for angular light-scattering measurements by the more exact Tomimatsu-Palmer (T-P) method are compared to those by the less adequate Sheffer-Hyde (S-H) method.
    Additional Material: 1 Ill.
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  • 6
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight of sugar beet araban fractions prepared by fractionation of the araban acetates on a charcoal column have been determined. Light-scattering measurements using 2 M NaCl and aqueous 1% N,N-dimethylformamide (DMF) as solvents gave, weight average molecular weights which did not agree, the values in the latter solvent being about half of those in the former. Other experimental observations, such as, number average and sedimentation-viscosity molecular weights favor the results in salt solution; the low results in 1% DMF are presumably due to the interaction between araban and DMF. Arabans exhibited appreciable fluorescence when incident light of wavelength 436 mμ was used, but none at λ = 546 mμ. Sample limitations prevented measurements at the higher wavelength, and an alternate procedure for correcting for fluorescence is presented. The weight average molecular weights in 2 M NaCI which ranged from 18,400 to 37,000 for this study are appreciably higher than the previously reported value of 10,000. Number-average molecular weights determined by the chlorous acid end-group method ranged from 8700 to 24,200 for the various fractions. No simple relationship between molecular weight and fraction number was observed, and most of the fractions showed appreciable molecular weight heterogeneity.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 1005-1014 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The discrepancy in the light-scattering molecular weight of sugar beet araban in two solvent systems, 2M NaCl and 1% (v/v) DMF, is explained as being due to a charge effect in the latter solvent. The previously reported explanation of a multicomponent effect in 1% (v/v) DMF, based on the assumption that araban is uncharged, is shown to be incorrect by equilibrium dialysis experiments. Titration and sodium analysis indicate a total charge of about 20 per araban molecule, while the limiting slope of the Debye plot of light-scattering data in low ionic strength solvent indicate an effective charge of 10. Attempts to explain the observed curvature in the Debye plot for araban in low ionic strength buffer on the basis of the Stigter-Hill method was unsatisfactory, probably due to the inadequacy of the solid sphere-diffuse double layer model for araban and/or the inapplicability of the Stigter-Hill virial expansion method at high ratios of macromolecule to salt in low ionic strength solvent. Molecular weight measurements on araban acetate prepared for purification purposes indicate considerable degradation during deacetylation but not during acetylation. This suggests that araban in situ has a molecular weight considerably greater than that observed for the purified araban.
    Additional Material: 4 Ill.
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