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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1618-0860
    Keywords: Bsr-REMI ; Dictyostelium discoideum ; Insertional mutagenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Using a plasmid pBsr2 which carries a blasticidin S-resistant gene, we have improved the method of REMI (restriction enzyme-mediated integration) provided for insertional mutagenesis inDictyostelium discoideum (bsr-REMI). To confirm usefulness of thebsr-REMI, transformation efficiency, copy number of integrated DNA, and randomness of integration into genome were examined.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The X-ray crystal structure of the molecular complex of penicillin G with a deacylation-defective mutant of the RTEM-1 β-lactamase from Escherichia coli shows how these antibiotics are recognized and destroyed. Penicillin G is covalently bound to Ser 70 Oγ as an ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 1211-1229 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Intrinsic spectral and kinetic parameters have been measured for the ethylperoxy radical, which was formed in the gas phase by the flash photolysis of azoethane in the presence of an adequate excess of oxygen. Absolute values of the extinction coefficient ∊(λ) were derived from complementary measurements of the yield of nitrogen and the absorbance of an equivalent concentration of ethylperoxy radicals. The absorption spectrum is broad, structureless and comparatively weak; ∊(236) = 1.02 × 103 liter mole-1 cm-1 at the maximum, and the oscillator strength is 3.4 × 10-2. This spectrum resembles the spectrum of the methylperoxy radical closely in form, but it is less intense; the ratio of the values of oscillator strength is 0.5. The bimolecular reactions of mutual interaction of ethylperoxy radicals are not exclusively terminating, and ethoxy and hydroperoxy radicals are formed in kinetically significant quantities. A computer program was designed to simulate the rise and fall of the concentration of each radical species, and to perform the related kinetic analysis. This program predicted that a second-order plot of the decline of the absorbance of the ethylperoxy radical during the dark period would not show a significant departure from linearity, a conclusion which was confirmed by experiment. Accordingly, the gradient of each such plot yielded a value of k'/∊(λ), where k' is the apparent value of the rate constant for the collective reactions of mutual interaction. This rate constant was evaluated from the product of corresponding values of k'/∊(λ) and ∊(λ); individual values are independent of the wavelength of measurement, and the mean value is k' = (6.6 ± 0.5) × 107 liter mole-1 sec-1. Further kinetic analysis yielded the corresponding absolute value: k = (6.0 ± 0.6) × 107 liter mole-1 sec-1. This value fits the pattern of a relationship between rate constant and structure shown by the methylperoxy, isopropylperoxy, and tert-butylperoxy radicals. Adequate sensitivity for the characterization of the spectrum of the ethylperoxy radical was achieved by the use of a pulsed xenon arc as the monitoring light source in conjunction with a dual beam detection system with twin cells and balanced photomultipliers, and the apparatus is described in detail.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 1243-1251 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants for the reactions have been measured directly by flash photolysis and kinetic spectroscopy. At room temperature, k3 = (3.4 ± 0.1) × 109 L/mol·s, independent of pressure in the range of 55-400 torr, and k6 = (2.1 ± 0.2) × 109 L/mol·s.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 995-1005 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Intrinsic spectral and kinetic parameters have been measured for the ethyl radical, which was formed in the gas phase by the flash photolysis of azoethane. Absolute values of the extinction coefficient ε(λ) were derived from complementary measurements of the yield of nitrogen and the absorbance of an equivalent concentration of the ethyl radical. The absorption spectrum is broad, structureless, and comparatively weak; ε(247) = 4.8 × 102 l/mol·cm at the maximum, and the oscillator strength is (9.1 ± 0.5) × 10-3. This is in good qualitative agreement with a spectrum obtained independently using the technique of molecular modulation spectrometry.The biomolecular reactions of mutual interaction were the only significant reactions of the ethyl radical in this system; kinetic analysis of the second-order decline of the absorbance during the dark period yielded a value of k/ε(λ) for each experiment. The rate constant for mutual interaction was evaluated from the product of corresponding measurements of k/ε(λ) and ε(λ) individual values are independent of the wavelength of measurement, and the mean value is k = (1.40 ± 0.27) × 1010 l/mol·sec. The rate constant for mutual combination was derived with the aid of product analysis as k2 = (1.24 ± 0.23) × 1010 l/mol·sec; it stands in close agreement with the set of “high” values obtained by direct measurement using a variety of methods.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 949-977 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decadic extinction coefficient of the methyl radical at 216.4 nm and the rate constant for mutual combination were redetermined as: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} \varepsilon (216.4) = (9.5 \pm 0.4) \times 10^3 1./mol\,cm \\ k_2 = (3.2 \pm 0.4) \times 10^{10} 1./mol\sec \\ \end{array} $$\end{document}. The application of the Beer-Lambert law to these measurements was justified experimentally. The absorption spectrum of the methylperoxy radical was characterized as a weak, broad, structureless band, having a maximum at 240 nm with ∊(240) = 1.55 × 103 l./mol cm. The mutual interaction of methylperoxy radicals leads to the generation of methoxy and hydroperoxy radicals as a consequence of the nonterminating interaction\documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} 2{\rm CH}_{\rm 3} {\rm OO}^{\rm .} \to 2{\rm CH3O}^{\rm .} + {\rm O}_{\rm 2} \\ {\rm CH}_{\rm 3} {\rm O}^{\rm .} + {\rm O}_2 \to {\rm HCHO + HOO}^{\rm .} \\ \end{array} $$\end{document}. Each derivative radical may consume a significant fraction of the methylperoxy radicals, and either of these cross interactions may be made predominant by a suitable choice of oxygen pressure. The mutual interaction was studied under both conditions. The overall mechanism was analyzed by a precise computational method, and the rate constant of the total mutual interaction \documentclass{article}\pagestyle{empty}\begin{document}$$ 2{\rm CH3O}^{\rm .} \to {\rm all}\,{\rm products} $$\end{document} was estimated as \documentclass{article}\pagestyle{empty}\begin{document}$$ k_4 = (3.5 \pm 0.3) \times 10^8 1./mol\sec $$\end{document}.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 1-16 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constant for the reaction CH3O2 + NO2 → (products) has been measured directly by flash photolysis and kinetic spectroscopy. At room temperature and at total pressures between 53 and 580 Torr, k3 = (9.2 ± 0.4) × 108 liter/mole sec so that the rate of formation of the probable primary product peroxymethyl nitrate (CH3O2NO2) may be significant in urban atmospheres.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 367-384 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis of azo-n-propane and of azoisopropane has been studied by kinetic spectroscopy. Transient absorption spectra in theregion of 220-260 nm have been assigned to the n-propyl and isopropyl radicals. For the n-propyl radical, ∊max = 744 ± 39 l/mol cm at 245 nm and the rate constants for the mutual reactions were measured to be kc = (1.0 ± 0.1) × 1010 l/mol sec (combination) and kd = (1.9 ± 0.2) × 109 l/mol sec (disproportionation). For the isopropyl radical, ∊max = 1280 ± 110 l/mol cm at 238 nm, with kc = (7.7 ± 1.6) × 109 l/mol sec and kd = (5.0 ± 1.2) × 109 l/mol secThe rate constant for the dissociation of the vibrationally excited triplet state of the azopropanes into radicals was measured from the variation in the quantum yield of radicals with pressure. For azo-n-propane kdT = (6.6 ± 1.3) × 107 sec-1, and for azoisopropane kdT = (1.6 ± 0.4) × 108 sec-1. Collisional deactivation of the vibrationally excited singlet and triplet states was found to occur on every collision for n-pentane; but nitrogen and argon were inefficient with a rate constant of 1.1 × 1010 l/mol sec.Spectra observed in the region of 220-260 and 370-400 nm areattributed to the cis isomers of the parent trans-azopropanes. These are formed, as permanent products, in increasing amounts as the pressure is increased.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 1251-1276 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ultraviolet absorption spectra have been characterized for the acetyl-h3 and acetyl-d3 radicals, which were generated by the flash photolysis of the corresponding acetones. The spectra are broad and intense, with values of the extinction coefficient at the respective maxima estimated as: εCH3CO(215) = (1.0 ± 0.1) × 104 L/mol·cm and εCD3CO(207.5) = (1.0 ± 0.05) × 104 L/mol·cm. Rate constants for the reactions of mutual interaction were estimated as: k4H = 3.5 × 1010 L/mol·s and k4D = 3.4 × 1010 L/mol·s. Rate constants for the reactions of cross interaction were estimated as: k3H = 8.6 × 1010 L/mol·s and k3D = 5.2 × 1010 L/mol·s. The related values of the cross interaction ratios k3H/(k2Hk4H)1/2 = 2.6 and k3D/(k2Dk4D)1/2 = 1.6 do not differ significantly from the statistical value of 2. The participation of the radical displacement reactions was estimated in terms of the fractions k3bH/k3H = 0.38 and k3bD/k3D = 0.47.Corroborative spectra were obtained from the flash photolysis of methyl ethyl ketone and biacetyl, and the relative rates of the competing primary processes were estimated from the relative peak heights of the acetyl and methyl radicals in each system.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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