Coupled oxidative phosphorylation in crude extracts of Azotobacter.
نویسندگان
چکیده
Two outstanding characteristics of azotobacter, their abilitv to fix nitrogen and unusually high rates of oxidation, have stimulated interest in obtaining cell free extracts suitable for biochemical analysis of these processes. Many difficulties have been encountered in obtaining such extracts. Attempts to obtain cell free extracts capable of nitrogen fixation have given extremely inconsistent results (reviewed by Burris, 1956, and Magee and Burris, 1956). The methods used for demonstrating coupled oxidative phosphorylation in crude and fractionated extracts of mycobacteria and corynebacteria (Brodie and Gray, 1955a, 1955b, 1956a, 1956b, 1956c) did not yield satisfactory results with azotobacter. Recently coupled oxidative phosphorylation has been demonstrated in fractionated extracts of azotobacter (Slater, 1955; Tissieres and Slater, 1955; Rose and Ochoa, 1956). Reinvestigation of the crude azotobacter svstem has revealed that the initial erratic results were largely due to the extremely labile nature of the crude system. The results achieved with extracts stabilized during preparation were reproducible. The nature and properties of this labile system are described and compared with other azotobacter and mycobacterial systems.
منابع مشابه
Protection of nitrogenase in Azotobacter vinelandii.
The site or sites that protect nitrogenase from O(2) inactivation in vivo are sensitive to sodium azide or 2,4-dinitrophenol. Both components of nitrogenase can be synthesized when oxidative phosphorylation is disrupted.
متن کاملRoles of nifF and nifJ gene products in electron transport to nitrogenase in Klebsiella pneumoniae.
Crude extracts of the wild-type Klebsiella pneumoniae reduced C2H2 with either pyruvate or formate as reductant (specific activity, 3 nmol min-1 mg of protein-1), whereas crude extracts of nifF mutant were almost inactive (specific activity, 0.05). However, activity in the latter extracts was stimulated by adding Azotobacter chroococcum flavodoxin (specific activity, 10). Thus, nifF mutants may...
متن کاملDihydrostreptomycin, Vitamin K2-coupled Tetrazolium Reduction, and Oxidative Phosphorylation in Escherichia Coli.
Bragg, P. D. (University of British Columbia, Vancouver, B.C., Canada). Dihydrostreptomycin, vitamin K(2)-coupled tetrazolium reduction, and oxidative phosphorylation in Escherichia coli. J. Bacteriol. 88:1019-1023. 1964.-Dihydrostreptomycin inhibited the vitamin K(2)-coupled pyruvate-triphenyltetrazolium (TTC) reductase system in extracts from antibiotic-sensitive cells, but stimulated this re...
متن کاملNitrite Inhibition of Bacterial Dinitrogen Fixation
Bacterial Nitrogenase, Nitrite Inhibition, Dinitrogenase Reductase Dinitrogen fixation by crude extracts from Rhodopseudomonas palustris and Rhodomicrobium vannielii and by purified nitrogenase preparations from Azotobacter vinelandii and Clostridium pasteurianum is inhibited by nitrite, whereas in the same preparations nitrate is without effect. In Clostridium nitrite seems to interact with di...
متن کاملReversibility of oxygen induced inactivation of nitrogenase in some enterobacteria.
Aerobic and microaerobic diazotrophs possess numerous oxygen restriction strategies to protect nitrogenase from inactivation by oxygen without interfering with energy generation through oxidative phosphorylation. Protection by conformational change in nitrogenase was first detected and described in Azotobacter. This strategy once considerd unique for Azotobacter has been shown in this study to ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine
دوره 101 1 شماره
صفحات -
تاریخ انتشار 1957