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  • Branched respiratory chain  (1)
  • Lysoamidase bacteriolytic complex  (1)
  • 1
    ISSN: 1432-072X
    Keywords: Staphylococcus aureus ; Electron transport ; Branched respiratory chain ; Cytochrome oxidase ; Ethanol oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Addition of ethanol and some other primary alcohols, except methanol, to cells and protoplasts (but not membrane particles) considerably stimulated the rate of oxygen consumption. This additional respiration was strongly inhibited by 0.1 mM KCN. The cyanide inhibition curve of endogenous substrate oxidation was slightly biphasic while in the presence of ethanol it became clearly biphasic having K i values of approx. 0.1 and 0.5 mM. Based on the steady-state cytochrome spectra in the presence of 0.1 mM KCN, we attributed the lower K i to cytochrome a 602. Proteolysis of protoplasts external membrane proteins did not change the rate of endogeneous substrate oxidation but prevented the inhibition of this respiration by low concentrations of KCN and stimulation of oxygen consumption by ethanol. The activity of NAD+-dependent ethanol dehydrogenase in the cytoplasm was found to be 520 nmol NADH-x min−1 x mg−1 protein. Proteolysis of external membrane proteins apparently inhibits the operation of the cytochrome a 602-containing electron transport branch inducing the suppression of electron flow from NADH to oxygen.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-072X
    Keywords: Lysoamidase bacteriolytic complex ; Staphylococcus aureus protoplasts ; α-Glycerophosphate oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The action of the lysoamidase bacteriolytic complex on Staphylococcus aureus VKM B-209P cells has been studied to obtain protoplasts. The cells in the midlogarithmic phase were the most sensitive to lysoamidase action. It led to local destruction of cell wall due to hydrolysis of the peptidoglycan. Protoplast formation occurred in two steps in the presence of 1 M sucrose. First, osmotically fragile spheroplasts were formed. Then, the protoplasts were released from the destructed cell wall. The protoplast yield was about 80%. The protoplasts preserved the intact ultrastructure and were able to synthesize peptidoglycan fibrillae. Mainly the spheroplasts that maintained the cell-wall residues reversed into bacterial forms. The protoplasts had respiratory activity similar to cells. Respiration of cells and protoplasts was stimulated by various substrates. High rates of oxygen consumption were observed with α-glycerophosphate and ethanol as substrates.
    Type of Medium: Electronic Resource
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