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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 108 (1976), S. 203-209 
    ISSN: 1432-072X
    Keywords: Enzymology ; Thiobacilli ; Regulation ; Quaternary structure ; Ribulose bisphos-phate carboxylase ; Sub-units
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Purified ribulose-bisphosphate carboxylase (EC 4.1.1.39) was strongly and equally inhibited either by ADP or GDP and to a lesser extent by IDP. AMP or ATP exerted little effect on activity. Inhibition by the nucleotide diphosphates was competitive with respect to RuBP and non-competitive with respect to “CO2” and Mg2+, respectively. Treatment of the enzyme with urea or guanidine-HCl resulted in rapid loss of activity that was not restored by dialysis even in the presence of Mg2+ and cysteine. Sodium dodecyl sulfate electrophoresis of 8.0 M urea treated enzyme revealed the presence of a fast-moving (small) sub-unit with molecular weight 14150 and a slower moving (large) sub-unit with molecular weight 68000. Examination of native enzyme by sodium dodecyl sulfate electrophoresis gave sub-units of 13700 and 55500 respectively. The amino acid content standardized to phenylalanine was essentially similar to that from other sources. Arrhenius plots showed a “break” at 29°C with an E a of 12.34 kcal per mole for the steeper part of the curve and a ΔH of 11.43 kcal per mole while for the less steep region, the E a was 1.04 kcal per mole and the ΔH 1.92 kcal per mole.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 108 (1976), S. 195-202 
    ISSN: 1432-072X
    Keywords: Enzymology ; CO2 fixation ; Thiobacilli ; Ribulose bisphosphate carboxylase ; Regulation ; Chemolithotrophy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ribulose bisphosphate carboxylase (EC 4.1.1.39) from Thiobacillus A2 has been purified to homogeneity on the basis of polyacrylamide gel electrophoresis and U.V. analysis during sedimentation velocity studies. The enzyme had an optimum pH of about 8.2 with Tris-HCl buffers. The molecular weight was about 521000 with an S rel. of 16.9. K m for RuBP was 122 μM, for total “CO2” it was 4.17 mM, and for Mg2+ 20.0 μM. The absolute requirement for a divalent cation was satisfied by Mg2+ which was replaceable to a certain extent by Mn2+. Activity was not significantly affected by SO 4 2- , SO 3 2- , or S2O 3 2- at 1.0 mM. At this concentration S2- caused a 27% stimulation. All mercurials tested were inhibitory. pHMB was the most potent causing about 60% inhibition at 0.01 mM. This inhibition was reversible by low concentrations of cysteine. Cyanide was also inhibitory. Its mode of inhibition with respect to RuBP was un-competitive and with a K i of 20 μM. Lost activity could be restored partially by GSH or Cu2+. Although azide at the concentration tested had no significant effect on enzyme activity, 2,4-dinitrophenol at 1.0 mM caused 91% inhibition. Finally, activity was also affected by energy charge.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 1513-1520 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Continuum approximation is often used to treat problems involving reaction mixtures of a vast number of species. Previous studies predicted that in many situations the lumped kinetics of a continuum of reactions, regardless of their kinetics, are of the power law form after a long time. In this article we present experimental support for such asymptotic power law kinetics. The system considered is catalytic deep desulfurization of a petroleum distillate. In addition, a theoretical analysis is made to establish the condition under which the continuum approximation is valid in the long-time limit. The condition turns out not to be very stringent for practical purposes.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 685-700 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The kinetics of lumped nth-order reactions are examined both asymptotically and numerically. The lumped kinetics in most cases are Mth order at large times. There exist two critical values for n, denoted by n* and n*, which are expressed explicitly as functions of the feed properties. It is shown that (1) M = n when n 〉 n*, (2) M is linear in n when n* 〈 n 〈 n*, and (3) M does not exist when n = n* or n ≤ n*. Whenever the feed contains some unconvertibles, M is independent of n for -∞ 〈 n 〈 n*. The overall effective rate constant is not continuous at n = n* nor at n = n*. Unexpectedly, when n 〉 n* the lump's long-time behavior is governed by all species, not just by the most refractory species. Although the asymptotic kinetics are developed for long times, they are useful for fitting the whole-time behavior of the lump by an mth-order model. This is true even when M does not exist in the asymptotic regime. Numerical experiments show that M and m behave similarly in many respects. For example, as n increases, they both become closer to n and less dependent on the feed properties. Some published data are rationalized in light of the present results.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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