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  • 1990-1994  (16)
  • 1955-1959
  • 1920-1924
  • 1910-1914
  • Chemistry  (16)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 7 (1990), S. 16-31 
    ISSN: 0887-3585
    Keywords: BPTI ; dithiothreitol ; DTT-sensitive mutants ; protein folding ; random mutagenesis ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A genetic screening procedure has been developed to identify mutant forms of bovine pancreatic trypsin inhibitor (BPTI) that can fold to an active conformation but are inactivated more rapidly than the wild type protein. Small cultures of Escherichia coli containing plasmids with mutagenized BPTI genes were grown in microtiter plates, lysed, and treated with dithiothreitol (DTT). Under these conditions, unfolding and inactivation of wild-type protein has a half-time of about 10 hours. Variants of BPTI that are inactivated within 1 hour were identified by adding trypsin and a chromogenic substrate. Approximately 11,000 mutagenized clones were screened in this way and 75 clones that produce proteins that can fold but are inactivated by DTT were isolated. The genes coding for 68 “DTT-sensitive” mutant proteins were sequenced, and 25 different single amino acid substitutions at 15 of the 58 residues of the protein were identified. Most of the altered residues are largely buried in the core of the naive wild-type structure and are highly conserved among proteins homologous to BPTI. These results indicate that a large fraction of the sequence of the protein contributes to the kinetic stability of the active conformation, but it also appears that substitutions can be tolerated a most sites without completely preventing folding Because this genetics, further studies of the isolated mutants are expected to provide information about the roles of the altered residues in folding and unfolding.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 15 (1993), S. 322-329 
    ISSN: 0887-3585
    Keywords: unfolded proteins ; mutations ; BPTI ; gel electrophoresis ; disulfide-formation kinetics ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The effects of amino acid replacements on the hydrodynamic volume of reduced and unfolded bovine pancreatic trypsin inhibitor (BPTI) have been examined by gel electrophoresis. The electrophoretic mobilities of the reduced forms of 46 BPTI variants were compared at room temperature in the absence of denaturants. The single substitutions examined include many different types of replacements at sites throughout the polypeptide, and, collectively, alter 22 of the 58 residues of the wild-type protein. The only substitutions found to alter the electrophoretic mobility of the reduced protein by more than ∼3% are those that change the net charge of the protein. For nine mutants, the rates of disulfide formation in the reduced protein were also examined and found to be very similar to that of the wild-type protein. These results suggest that any structure that may be present in the reduced protein is either relatively insensitive to amino acid replacements or does not greatly influence the averaged properties of the polypeptide chain. © 1993 Wiley-Liss, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 39 (1992), S. 1151-1160 
    ISSN: 0006-3592
    Keywords: fluorescence ; monitoring ; methane ; fermentation ; NAD(P)H ; F420 ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: On-line in situ fluorescence measurements of the methanogenic fermentation were conducted with reactors receiving either glucose or a mixture of volatile fatty acids as the substrate. The reactors were perturbed from steady-state conditions in order to assess the response of fluorescencemonitoring probes. Two fluorescence-monitoring probes were evaluated over a period of 8 months; they performed in a consistent manner, and their response was not significantly affected by the changes in pH and redox potential encountered during routine reactor operation. A commercially available probe, designed to measure NAD(P)H, demonstrated particular promise for detecting imbalance caused by the entry of air, inhibitor addition and was capable of distinguishing between different substrates. This fluorescence-monitoring probe detected imbalance more rapidly than other on-line measurements such as pH, Eh, or gas production, or off-line measurements such as volatile fatty acid concentration or gas composition. An experimental fluorescence-monitoring probe, designed to measure coenzyme F420, also showed some promise in this regard. The response of the fluorescence-monitoring probes also revealed details of the metabolic routes in the reactors and the probes represent a useful research tool. For example, a failure to observe the characteristic response of the NAD(P)H-monitoring probe to formate addition during the metabolism of acetate, propionate, or glucose strongly suggests that any formate liberated during their catabolism is degraded via a different route to exogenously added formate.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 251-257 
    ISSN: 0887-6266
    Keywords: poly(aryl-ether-ether-ketone) (PEEK), solvent-induced crystallinity in ; crystallization of PEEK, solvent-induced ; sorption of solvents in PEEK, crystallinity induced by ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The amount and structure of the crystals formed by the solvent-induced crystallization (SIC) following a sorption-desorption cycle of five fluids (benzene, toluene, chloroform, methylene chloride, and carbon disulfide) in amorphous PEEK was determined by wideangle x-ray scattering (WAXS). The SIC crystal structure was compared with that produced by thermal methods, both those formed at low temperature by heating the amorphous material 10-20°C above Tg or by cooling from the melt. Although smaller in size, the SIC crystals are tighter and more organized than those produced thermally. The WAXS data indicates that all five fluids produce approximately 35% crystallinity in PEEK. Gravimetric data suggest that a low-density region, consisting of either microvoids or highly disordered amorphous region, surrounds the crystals.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 441-449 
    ISSN: 1040-7685
    Keywords: open-tubular columns ; supercritical fluid chromatography ; retention ; selectivity ; pressure ; temperature ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We studied solute retention for n-hydrocarbons, (low-molecular-weight) polystyrenes, an ethoxylated surfactant, and a selectivity test mix on open-tubular columns with methyl-, biphenyl-, and cyanopropyl-substituted stationary phases for pressures up to 680 atm and temperatures up to 240°C. The solute elution range varied tremendously with column choice, with the least retentive stationary phases providing the highest elution range. However, the best resolution and largest analysis range were obtained with the most retentive stationary phase and the highest pressures. Increasing the temperatures above 160°C did not cause a large increase in elution pressure for the solutes used in this study. Exceptionally large shifts in selectivity with temperatures up to about 160°C occurred for the biphenyl and cyanopropyl stationary phases. The availability of pressures higher than 680 atm, coupled with adequately retentive stationary phases used at optimal temperatures, would further increase the analysis scope of opentubular supercritical fluid chromatography.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 261-273 
    ISSN: 1040-7685
    Keywords: open-tubular columns ; supercritical fluid chromatography ; direct injection ; phase behavior ; critical mixture curves ; retention gap ; solvent effect ; phase-ratio focusing ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Open-tubular supercritical fluid chromatography (SFC) is a useful technique for many analyses, but is somewhat limited, in current practice, with respect to trace analysis of liquid samples. Direct injection of the volumes required for trace analysis with ordinary detectors creates a meter or more length of flooded zone and may lead to unacceptable band broadening. We studied solvent mass transfer on short, uncoated columns for several solvents forming Type I binary mixtures with CO2, and found evidence in the solvent peak shapes of distinct liquid and vapor phases, with the liquid present as a dynamically formed film. This study suggests that selecting an injection temperature and pressure to reduce, but not eliminate, the surface tension of the liquidvapor interface, and increasing the mobile phase velocity during injection increase the liquid film thickness and reduce the length of the resulting flooded zone. When a separate uncoated inlet tube (that is, a retention gap) is used to connect the injector with the column, decreasing the inlet tube radius improves the ratio of maximum effective injection volume to inlet tube volume.Just as in GC, dynamically formed films function as pseudo-stationary phases during injection. Without a liquid film, solutes can be transported by injection-solvent-modified mobile phase well beyond the length of a typical film, increasing the difficulty of refocusing the solutes before separation. Refocusing solutes from film-coated flooded zones is easily accomplished using either a solvent effect (specifically, solvent trapping) or phase-ratio focusing.We recommend the use of solvents with phase behavior like toluene and carbon tetrachloride, both of which form films at convenient temperatures and pressures. We discourage the use of solvents with phase behavior like n-pentane which tend to make single-phase, supercritical mixtures with CO2 under typical SFC injection conditions.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 127-133 
    ISSN: 1040-7685
    Keywords: supercritical fluid chromatography ; retention mechanism ; selectivity tuning ; stationary phase swelling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When temperature programming is performed in supercritical fluid chromatography (SFC) under conditions where the solute-mobile phase interactions are approximately fixed, that is, with the use of constant mobile phase density, then positive temperature programs can be used. The results resemble those in temperature-programmed gas chromatography (GC) except that chromatograms are compressed and solutes elute at lower temperatures. For a given temperature-program rat, the extent of this compression effect is controlled by the (fixed) mobile phase density. When a methylsilicone stationary phase is used along with CO2 mobile phase, the compression occurs with little change in selectivity. However, with a biphenyl-substituted polysiloxane stationary phase, selectivity shifts occur for some solutes (vs. hydrocarbons) as the density is varied. The effect is even greater and affects more solutes when a cyanopropyl-substituted polysiloxane stationary phase is used.This selectivity behavior differs from the temperature-dependent selectivity behavior known in GC. In GC only the forces between solutes and the stationary phase are involved. But in SFC, mobile phase interactions with both the solutes and the stationary phase are also important. The large selectivity shifts we observe in SFC most likely arise because of stationary phase swelling by the mobile phase. This is a function of the temperature and mobile phase density (or pressure) and can be tuned without changing the composition of the mobile phase. It is possible to use either temperature or density to adjust or fine-tune selectivity between a pair of solutes while using the other parameter to adjust retention of the pair.These experiments further suggest that GC is not only a special case of SFC (where the solute-mobile phase interactions are essentially zero), but that SFC possesses an additional and extremely powerful selectivity adjustment mechanism not available in GC.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 612-616 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Spin-lattice relaxation ; Chemical shift anisotropy ; Carbocations ; Superacids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The contributions to the 13C NMR spin-lattice relaxation rates of both protonated and non-protonated carbons of a range of carbocations in superacids were determined from the analysis of T1 values measured over a range of temperatures and at different field strengths. From the data for 1-adamantyl, 2-methyl-2-norbornyl, 3-methyl-3-nortricyclyl, 2-phenyl-2-norbornyl, cumyl (1-methyl-1-phenylethyl) and methylphenylcyclopropylcarbinyl (1-cyclopropyl-1-phenylethyl) cations, dipole-dipole interactions (both intra- and inter-molecular) were found to be entirely responsible for the relaxation of protonated carbons. However, for the cationic carbons, chemical shift anisotropy contributes significantly to their relaxation at low field strengths (2.3 T) and predominantly at high field strengths (5.8 T). The shielding anisotropies (Δσ) of the cationic carbons were determined as 410-540 ppm, which are amongst the largest reported for any carbon atoms.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 694-695 
    ISSN: 0749-1581
    Keywords: 15N ; NMR ; spectroscopy ; Carbolines ; Reduced β-carbolines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 15N NMR spectra of α-, β-, γ- and δ-carboline and a series of methyl, dihydro and tetrahydro derivatives are reported.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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