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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 104 (1975), S. 163-169 
    ISSN: 1432-072X
    Keywords: Azotobacter vinelandii ; Nitrogenase ; Glutamine Synthetase ; Ammonium Pool ; Ammonium Transport ; Citrate Transport ; Repression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Both the changes in the activities of nitrogenase, glutamine synthetase and glutamate dehydrogenase and in the extracellular and intracellular NH4 + concentrations were investigated during the transition from an NH4 + free medium to one containing NH4 + ions for a continuous culture of Azotobacter vinelandii. If added in amounts causing 80–100% repression of nitrogenase, ammonium acetate, lactate and phosphate are absorbed completely, whereas chloride, sulfate and citrate are only taken up to about 80%. After about 1–2 hrs the NH4 + remaining in the medium is absorbed too, indicating the induction or activation of a new NH4 + transport system. One of the new permeases allows the uptake of citrate in the presence of sucrose. Addition of inorganic NH4 + salts leads to acidification of the culture. Anaerobiosis suppresses NH4 + transport. A rise in the extracellular NH4 + level leads to a reversible rise in the glutamine synthetase activity, which is not prevented by chloramphenicol, and to a reversible decrease in nitrogenase activity. During these measurements glutamate dehydrogenase activity remains close to zero. The intracellular NH4 + level of about 0.6 mM does not change when extracellular NH4 + is taken up and repression of nitrogenase starts.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-072X
    Keywords: Azotobacter vinelandii ; Continuous culture ; Oxygen control ; Nitrogen fixation ; Respiratory protection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Azotobacter vinelandii strain OP was grown in continuous culture at various dissolved oxygen concentrations of air (100% air saturation of the medium=225 ±14 μM O2). Sucrose was added as carbon source and either dinitrogen or ammonia as nitrogen sources. Irrespective of the nitrogen source steady state cultures showed the following general responses with dissolved oxygen concentrations increasing from about 1% to 30% air saturation: (i) cell protein levels, (ii) the amount of cell protein formed per sucrose consumed as well as (iii) nitrogenase activity decreased by at least a factor of two while (iv) cellular respiration increased. At higher oxygen concentrations the parameters changed only slightly, if at all. Increasing the sucrose concentration in the inflowing medium (s R) from 3 g/l to 15 g/l increased the total level of cellular respiration with nitrogen-fixing cultures but was more pronounced with ammonium-assimilating cultures. With nitrogen-fixing cultures cell protein levels increased five-fold while the ratio of protein formed per sucrose consumed as well as cellular nitrogenase activity remained unaffected. With ammonium-assimilating cultures the cell protein level was only doubled and the level of cell protein formed per sucrose consumed was decreased at the higher s R. Increasing the dilution rate at a constant oxygen concentration of 45% air saturation resulted in an almost parallel increase of both cellular respiratory and nitrogenase activity at low and moderate dilution rates. At high dilution rates nitrogenase activity increased steeply over the respiratory activity. Nitrogen-fixing cultures adapted to various oxygen concentrations were subjected to oxygen stress by increasing the oxygen concentration for 7 min. In all cases, this resulted in a complete inhibition (‘switch-off’) of nitrogenase activity. Upon restoration of the original oxygen concentration nitrogenase activity returned to a decreased level. The discussion arrives at the conclusion that some of the results are incompatible with the concept of respiratory protection of nitrogenase.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 101 (1974), S. 153-159 
    ISSN: 1432-072X
    Keywords: Azotobacter vinelandii ; Nitrogenase ; Repression ; Ammonia Determination ; Oxygen Effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A method is described which allows the quantitative determination of small ammonia concentrations in the culture of nitrogen-fixing microorganisms. With this method the ammonia concentration range was estimated in which repression of nitrogenase synthesis in Azotobacter vinelandii occurs. Both in batch and continuous cultures there was no repression below 10 μM, whereas nitrogenase synthesis stopped completely if the ammonia concentration in the medium exceeded 25 μM.
    Type of Medium: Electronic Resource
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