Enhancement of nitrate efflux and the plasma membrane hydrogen ion‐transport activity of barley roots by nitrate treatment

1997 ◽  
Vol 20 (6) ◽  
pp. 657-668
Author(s):  
Kousei Yamashita ◽  
Minobu Kasai ◽  
Yoko Yamamoto ◽  
Hideaki Matsumoto
1967 ◽  
Vol 33 (2) ◽  
pp. 395-410 ◽  
Author(s):  
David W. Deamer ◽  
Antony Crofts

Addition of Triton X-100 to chloroplast suspensions to a final concentration of 100–200 µM causes an approximate tripling of chloroplast volume and complete inhibition of light-induced conformational changes, light-dependent hydrogen ion transport, and photophosphorylation. Electron microscopic studies show that chloroplasts treated in this manner manifest extensive swelling in the form of vesicles within their inner membrane structure. Triton was adsorbed to chloroplast membranes in a manner suggesting a partition between the membrane phase and the suspending medium, rather than a strong, irreversible binding. This adsorption results in the production of pores through which ions may freely pass, and it is suggested that the inhibition of conformational changes, hydrogen ion transport, and photophosphorylation by Triton is due to an inability of treated chloroplast membranes to maintain a light-dependent pH gradient. The observed swelling is due to water influx in response to a fixed, osmotically active species within the chloroplasts, after ionic equilibrium has occurred. This is supported by the fact that chloroplasts will shrink upon Triton addition if a nonpenetrating, osmotically active material such as dextran or polyvinylpyrrolidone is present externally in sufficient concentration (>0.1 mM) to offset the osmotic activity of the internal species.


1967 ◽  
Vol 20 (12) ◽  
pp. 2575 ◽  
Author(s):  
R Arnold ◽  
DA Swift

Hydrogen-ion transport numbers, water transference numbers, and acid absorption are reported for some cation-exchange membranes in presence of 0.1N, 1.0N, and 5.0N sulphuric acid. The transport numbers of hydrogen ion remain fairly close to unity even at the highest acid concentration; this is largely due to the retardation of the anions by the electro-osmotic water flux. With increasing acid concentration the water transference number falls to a lower limit of 1.0 mole per faraday; with the driest membrane used this value is obtained at all acid concentrations used. This behaviour suggests that when there are less than about 11 moles of water available per hydrogen ion in the membrane, association occurs between sulphonate groups and hydrogen ions, with consequent immobilization of the latter.


FEBS Letters ◽  
1982 ◽  
Vol 140 (1) ◽  
pp. 145-146
Author(s):  
R.J. Naftalin

2000 ◽  
Vol 203 (1) ◽  
pp. 127-135 ◽  
Author(s):  
H. Wieczorek ◽  
G. Grber ◽  
W.R. Harvey ◽  
M. Huss ◽  
H. Merzendorfer ◽  
...  

H(+) V-ATPases (V-ATPases) are found in two principal locations, in endomembranes and in plasma membranes. The plasma membrane V-ATPase from the midgut of larval Manduca sexta is the sole energizer of all transepithelial secondary transport processes. At least two properties make the lepidopteran midgut a model tissue for studies of general aspects of V-ATPases. First, it is a rich source for purification of the enzyme and therefore for structural studies: 20 larvae provide up to 0.5 mg of holoenzyme, and soluble, cytosolic V(1) complexes can be obtained in even greater amounts of up to 2 mg. Second, midgut ion-tranport processes are strictly controlled by the regulation of the V-ATPase, which is the sole energizer of all ion transport in this epithelium. Recent advances in our understanding the structure of the V(1) and V(o) complexes and of the regulation of the enzyme's biosynthesis and ion-transport activity will be discussed.


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