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

1986 ◽  
Vol 247 (1) ◽  
pp. 40-48 ◽  
Author(s):  
G.A. Peschek ◽  
B. Hinterstoisser ◽  
M. Riedler ◽  
R. Muchl ◽  
W.H. Nitschmann
1982 ◽  
Vol 9 (4) ◽  
pp. 399 ◽  
Author(s):  
AB Hope ◽  
D Ranson ◽  
PG Dixon

Measurements of ATP (luciferase assay) formed by class C pea chloroplasts in illumination times varying from 10 ms to 30 s are reported for control, + valinomycin and + nigericin conditions. ATP was made at a constant rate in controls following a time lag of a few milliseconds which varied with the illumination. Valinomycin increased the time lag to ~100 ms after which therate approached controls. Nigericin caused a gradual decrease in rate of ATP synthesis over a period of ~1s . In the steady state the rate was a different function of the transthylakoid pH difference (ΔpH) with nigericin and with valinomycin, with thresholds at ΔpH = 2.9 and 3.5 respectively. The time lags and thresholds are shown to be consistent with a threshold proton motive force (PMF) of 140-190 mV in various experiments. It is argued that this PMF corresponds to that required to poise the phosphorylation reaction to the point of ATP net synthesis at the prevailing dark phosphorylation potential. The experiments could not decide between a stoichiometry of 2 or 3 protons per ATP. Data suitable for use in constructing a kinetic model are briefly discussed. The findings generally are interpreted as showing a close correlation between phosphorylation and the PMF estimated as the mean potential energy of protons in the intrathylakoid spaces relative to the outside. It is concluded that Mitchellian coupling between bulk protons and the ATP synthetase is not yet to be discarded.


Microbiology ◽  
1986 ◽  
Vol 132 (2) ◽  
pp. 369-377 ◽  
Author(s):  
C. P. Cartwright ◽  
J.-R. juroszek ◽  
M. J. Beavan ◽  
F. M. S. Ruby ◽  
S. M. F. De Morais ◽  
...  

1997 ◽  
Vol 321 (2) ◽  
pp. 487-495 ◽  
Author(s):  
Peter J. A. van den BROEK ◽  
Angeline E. van GOMPEL ◽  
Marijke A. H. LUTTIK ◽  
Jack T. PRONK ◽  
Carla C. M. van LEEUWEN

Transport of glucose and maltose was studied in plasma-membrane vesicles from Candida utilis. The yeast was grown on a mixture of glucose and maltose in aerobic carbon-limited continuous cultures which enabled transport to be studied for both sugars with the same vesicles. Vesicles were prepared by fusion of isolated plasma membranes with proteoliposomes containing bovine heart cytochrome coxidase as a proton-motive-force-generating system. Addition of reduced cytochrome cgenerated a proton-motive force, consisting of a membrane potential, negative inside, and a pH gradient, alkaline inside. Energization led to accumulation of glucose and maltose in these vesicles, reaching accumulation ratios of about 40Ő50. Accumulation also occurred in the presence of valinomycin or nigericin, but was prevented by a combination of the two ionophores or by uncoupler, showing that glucose and maltose transport are dependent on the proton-motive force. Comparison of sugar accumulation with quantitative data on the proton-motive force indicated a 1:1 H+/sugar stoichiometry for both transport systems. Efflux of accumulated glucose was observed on dissipation of the proton-motive force. Exchange and counterflow experiments confirmed the reversible character of the H+Őglucose symporter. In contrast, uncoupler or a mixture of valinomycin plus nigericin induced only a slow efflux of accumulated maltose. Moreover under counterflow conditions, the expected transient accumulation was small. Thus the H+Őmaltose symporter has some characteristics of a carrier that is not readily reversible. It is concluded that in C. utilisthe transport systems for glucose and maltose are both driven by the proton-motive force, but the mechanisms are different.


1994 ◽  
Vol 196 (1) ◽  
pp. 361-373 ◽  
Author(s):  
A Lepier ◽  
M Azuma ◽  
W R Harvey ◽  
H Wieczorek

The midgut of the tobacco hornworm secretes K+ across the apical plasma membrane of its goblet cells. This secondary K+ transport results from K+/H+ antiport energized by the proton-motive force generated by a primary, H(+)-transporting plasma membrane V-ATPase. Thus, the lepidopteran midgut constitutes a well-established example of the emerging concept that the proton-motive force is an alternative to the classical sodium-motive force for the energization of animal plasma membranes. K+/H+ antiport in the tobacco hornworm midgut is electrophoretic, exchanging 2H+ for 1K+. Under physiological conditions, it is energized by the voltage component of the proton-motive force. The strong coupling of electrophoretic K+/2H+ antiport with the electrogenic V-ATPase provides, in principle, the minimal device for the alkalization of the midgut lumen to pH values higher than 11. K+/H+ antiport is insensitive to bafilomycin A1, but is inhibited by amiloride or Concanavalin A. Lectin staining of blots after SDS-PAGE revealed several glycosylated polypeptides in the goblet cell apical membrane which are not part of the V-ATPase and thus are candidates for the antiporter protein. Current efforts are focused on the isolation of the K+/H+ antiporter.


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