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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyridoxylated adult human hemoglobin (HbAo) was prepared using a one molar equivalent of pyridoxal 5-phosphate (PLP) per heme and reduced with either NaCNBH3 or NaBH4. A separate sample was pyridoxylated and passed through a mixed-bed ion exchange column without reduction. All three preparations had a P50 of 29 ± 2 torr and a cooperativity of n = 2.4 ± 0.1. These preparations, in both the oxy and deoxy forms, were then treated with 7 equivalents of glutaraldehyde per tetramer at pH 6.8 at 4°C and at room temperature. The polymerization invariably reduced the P50 to 18 ± 2 torr with Hill coefficients of less than 2. These solutions, with or without further reduction using NaCNBH3, all retained the PLP in differing amounts (2-3 moles/tetramer). Methemoglobin concentrations were increased during the polymerization reaction. The normal pyridoxylation procedure, using sodium borohydride reduction, resulted in a number of different molecular species. Polymerization with glutaraldehyde caused a further proliferation of molecular species that could not be separated by anion exchange chromatography or by isoelectric focusing. The extent of polymerization, estimated by gel exclusion chromatography and SDS polyacrylamide gel electrophoresis, was from 40 to 50%. Analysis of the reverse phase chromatograms, which separate the heme and the α- and β-chains, showed extensive polymerization and distribution of the radioactively labeled PLP on the protein for all preparations. All of the polymerized and pyridoxylated samples were unstable, and showed different chromatographic patterns after storage at 4°C for 1 month. Attempts to stabilize these preparations by further reduction with NaCNBH3 gave products with a lower P50 and lower cooperativity. When the reactions were conducted with a purified HbAo, heterogeneity was somewhat decreased compared to the normally used stroma-free hemoglobin, but a large number of molecular species were still formed.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 38 (1996), S. 535-552 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Static and dynamic light scattering measurements were made of solutions of pGem1a plasmids (3730 base pairs) in the relaxed circular (nicked) and supercoiled forms. The static structure factor and the spectrum of decay modes in the autocorrelation function were examined in order to determine the salient differences between the behaviors of nicked DNA and supercoiled DNA. The concentrations studied are within the dilute regime, which is to say that the structure and dynamics of an isolated DNA molecule were probed. Static light scattering measurements yielded estimates for the molecular weight M, second virial coefficient A2, and radius of gyration RG. For the nicked DNA, M = (2.8 ± 0.4) × 106g/mol, A2 = (0.9 ± 0.2) × 10-3 mol cm3/g2, and RG = 90 ± 3 nm were obtained. For the supercoiled DNA, M = (2.5 ± 0.4) × 106 g/mol, A2 = (1.2 ± 0.2) × 10-3 mol cm3/g2, and RG = 82 ± 2.5 nm were obtained. The static structure factors for the nicked and supercoiled DNA were found to superpose when they were scaled by the radius of gyration. The intrinsic stiffness of DNA was evident in the static light scattering data.Homodyne intensity autocorrelation functions were collected for both DNAs at several angles, or scattering vectors. At the smallest scattering vectors the probe size was comparable to the longest intramolecular distance, while at the largest scattering vectors the probe size was smaller than the persistence length of the DNA. Values of the self-diffusion coefficients D were obtained from the low-angle data. For the nicked DNA, D = (2.9 ± 0.3) × 10-8 cm2/s, and for the supercoiled DNA, D = (4.11 ± 0.21) × 10-8 cm2/s. The contribution to the correlation function from the internal dynamics of the DNA was seen to result in a strictly bimodal decay function. The rates of the faster mode Γint, reached plateau values at low angles. For the nicked DNA, Γint = 2500 ± 500 s-1, and for the supercoiled DNA, Γint = 5000 ± 500 s-1. These rates correspond to the slowest internal relaxation modes of the DNAs. The dependence of the relaxation rates on scattering vector was monitored with the aid of cumulants analysis and compared with theoretical predictions for the semiflexible ring molecule. The internal mode rates and the dependence of the cumulants moments reflected the difference between the nicked DNA and the supercoiled DNA dynamical behavior. The supercoiled DNA behavior seen here indicates that conformational dynamics might play a larger role in DNA behavior than is suggested by the notion of a branched interwound structure. © 1996 John Wiley & Sons, Inc.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyridoxylated normal adult human hemoglobin (HbAo) has been prepared using both oxygenated and deoxygenated HbAo at pH 6.8 and room temperature without the addition of Tris to produce a mixture with P50 of 30 ± 2 torr and a Hill coefficient of 2.3 ± 0.1 similar to that of the isolated adult human hemoglobin from the red blood cell. Reduction of the pyridoxylated HbAo in the oxygen-ligated form by sodium borohydride gives unacceptable levels of methemoglobin (i.e., 〉 10%). Exessive foaming and methemoglobin formation can be partially avoided using deoxyHbAo. Reduction with sodium cyanoborohydride is much gentler and gives solutions with 〈 5% methemoglobin. Both reducing agents give products with multiple components as shown by analytical chromatography. Radioautography on the isoelectric focusing gels of HbAo treated with 14C pyridoxal 5-phosphate (PLP) shows three major bands for the cyanoborohydride-reduced derivatives and a much more complex mixture of labeled molecules after the sodium borohydride reduction. When pyridoxylated hemoglobin is prepared without reduction, the preparation, after passage through a mixed-bed resin, contains 0.4 equivalents of PLP per heme, and has a P50 of 30 ± 2 torr and an n value of 2.3 similar to the values found after reduction. Upon anion exchange resin chromatography, the PLP is removed, indicating that the reaction forms a reversible Schiff base. On standing at 4°C for one month, this preparation produces a mixture of HbAo and pyridoxylated HbAo with the original P50. Methemoglobin increased to 3% during this incubation. After four months in the cold, the yield of a single chromatographic species is 70% with 20% methemoglobin. This fraction appears to be stable and can be passed through an anion exchange column without release of the PLP. Separation of the individual chains by reverse-phase chromatography indicates that the addition of PLP to HbAo is directed solely to the β-chains. This is also the case for the cyanoborohydride reduced derivatives. When NaBH4 is used for the reduction, radioactively labeled PLP is found on both the α- and β-chains.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 4 (1966), S. 77-84 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The theory of kinetics of polynucleotide synthesis at oligomeric templates is developed. It is shown that the dependence of oligomer efficacy on its size cannot be explained without taking into account the probability of separation of the oligomer from the growing chain. If such a possibility exists, the maximal size which can be achieved by the growing chain is determined by the ratio of the probability of proposed propagation and of the probability of separation. Without any models of the separation mechanism, the study of experimental kinetic data shows that two such mechanisms exist. Very short oligomers can be easily separated from the growing chain, but there is a critical size of oligomer after which the probability of separation is much smaller. The oligomers whose size is equal to or greater than the critical one form helices with growing chains.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 663-670 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Films were made from blends of high methoxy pectin and high amylose starch gelatinized in a microwave oven in the presence and absence of glycerol at times ranging from 10 to 105 s. Three thermodynamic transitions were observed when storage modulus, loss modulus, and loss tangent were plotted against temperature. All three transitions gave minima when the transition temperature was plotted against time of gelatinization. Overall, there were only modest changes in these moduli over the range of gelatinization times studied, with little difference between films made with the starch gelatinized in either the presence or absence of glycerol. Starch granules were found to disappear at gelatinization times between 20 and 30 s, although much smaller starch particles seemed to recur at gelatinization times of 75 s and above. The minima found in the transition temperature and modulus plots were believed to result from a minimum in the amount of intermolecular interactions between the starch molecules. © 1995 John Wiley & Sons, Inc.This article is a US Government work and, as such, is in the public domain in the United States of America.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 54 (1994), S. 1311-1320 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Blends of citrus pectin and high amylose starch plasticized with glycerine were investigated to determine the effect of compositional variables on film properties. Several films with representative compositions were made from sugar beet and almond pectin, and tested for comparison. The films were cast from water onto glass plates, dried, and removed. Mechanical analysis was done using a Rheometrics RSA II solids analyzer. Increasing the glycerine concentration led to decreases in static modulus, dynamic modulus, and tensile strength, but to increases in elongation. Increasing levels of starch in the blend lowered the effect of glycerine on mechanical properties. Oxygen permeability of the films was extremely low. Sugar-beet pectin and almond pectin gave films with mechanical properties comparable to those made with citrus pectin. © 1994 John Wiley & Sons, Inc. This article is a US Government work and, as such, is in the public domain in the United States of America.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 71-79 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Blends of citrus pectin and several types of poly(vinyl alcohol) were investigated to determine the effects of compositional variables and polymer type on film properties. Some films were also plasticized with glycerol. Films were cast from water onto Lexan™ plates, dried, and removed. Thermomechanical properties were obtained using a dynamic mechanical analyzer, and thermodynamic transitions were also obtained using a differential scanning calorimeter. Increasing the amount of poly(vinyl alcohol) in the blends reduced the storage and loss modulus of the films above the glass transition temperature (Tg). The Tg values observed decreased as the amount of PVOH in the blend increased. Addition of glycerol depressed the PVOH Tg and merged it into the Tg of the pectin/glycerol blend. Changes in the molecular weight and degree of ester hydrolysis of poly(vinyl alcohol) exerted a rather small effect on the blends. © 1996 John Wiley & Sons, Inc.Reference to a brand or firm name does not constitute an endorsement by the U.S. Department of Agriculture over others of a similar nature.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 3 (1991), S. 899-907 
    ISSN: 1040-0397
    Keywords: Microelectrodes ; electrochemical treatment ; carbon ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical anodic treatment at ultrasmall carbon ring electrodes appears to result in the formation of an oxide film that displays charge-selective and pH-dependent enhancements following treatment. Voltammetry after treatment in pH 7.4 citrate-phosphate buffer is more Nernstian for dopamine (DA) and less Nernstian for 3,4-dihydroxyphenylacetic acid (DOPAC). However, oxidation in pH 2.8 buffer gives rise to voltammetry that is less Nernstian for both DA and DOPAC. Extensive surface oxidation in potassium hydroxide apparently forms a thick layer that acts like a thin layer reservoir for adsorbed analyte. Voltammetry following extensive treatment is attenuated and peak shaped. Minimal surface oxidation in KOH results in more Nernstian sigmoidal voltammetry with only light current attenuation. The data suggest that an oxide layer formed following anodic treatment is non-uniform and leaves sites of activated carbon exposed on the surface. Furthermore, it appears that this layer has cation-exchange properties giving rise to charge transfer selectivity. A model of the surface formed following anodic oxidation is consistent with previous models involving both surface cleanliness and carbon structure orientation.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 899-901 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
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