Exogenous energy supply to the plasma membrane of dark anaerobic cyanobacterium Anacystis nidulans : Thermodynamic and kinetic characterization of the ATP synthesis effected by an artificial proton motive force
Archives of Biochemistry and Biophysics, ISSN: 0003-9861, Vol: 247, Issue: 1, Page: 40-48
1986
- 15Citations
- 1Captures
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Metrics Details
- Citations15
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- CrossRef15
- Captures1
- Readers1
Article Description
The net synthesis of ATP in dark anaerobic cells of Anacystis nidulans subjected to acid jumps and/or valinomycin pulses was characterized thermodynamically and kinetically. Maximum initial rates of 75 nmol ATP/min per mg dry weight at an applied proton motive force of −350 mV were obtained, the flow-force relationship (rate of ATP synthesis vs applied proton motive force) being linear between −240 and −320 mV irrespective of the source of the proton motive force. The pulse-induced ATP synthesis was inhibited by uncouplers (H + ionophores) and F 0 F 1 ATPase inhibitors but not by KCN or CO. In order to obtain maximum rates of pulse-induced ATP synthesis both a favorable stationary Δψ (−100 mV at pH o 9, preceding the acid jumps) and a favorable stationary ΔpH (+2 units at pH o 4.1, preceding the valinomycin pulse) of the plasma membrane were obligatory, the effects of Δψ and ΔpH being strictly additive. Moreover, the pulse-induced ATP synthesis required a minimum total proton motive force of −200 to −250 mV across the plasma membrane; it also required low preexisting phosphorylation potentials corresponding to −400 mV in dark anaerobic i.e., energy-depleted, cells. The results are discussed in terms of both a reversible H + -ATPase and a respiratory electron transport system occurring in the plasma membrane of intact Anacystis nidulans.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0003986186905308; http://dx.doi.org/10.1016/0003-9861(86)90530-8; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0022548597&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/3010879; https://linkinghub.elsevier.com/retrieve/pii/0003986186905308; http://dx.doi.org/10.1016/0003-9861%2886%2990530-8; https://dx.doi.org/10.1016/0003-9861%2886%2990530-8
Elsevier BV
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