Stimulation of an N-ethylmaleimide-sensitive ATPase in the collecting duct segments of the rat nephron by metabolic acidosis

1985 ◽  
Vol 63 (10) ◽  
pp. 1291-1296 ◽  
Author(s):  
Lal C. Garg ◽  
Neelam Narang

A plasma membrane ATPase sensitive to inhibition by N-ethylmaleimide (NEM) and insensitive to inhibition by oligomycin and ouabain has been shown to be involved in acidification of urine in the turtle bladder. The activity of this NEM-sensitive ATPase was determined in four types of distal nephron segments of normal rats and in rats treated with ammonium chloride. The enzyme activity was determined by a fluorometric micromethod in which ATP hydrolysis was coupled to NADH oxidation. Significant activities (10–35 pmol ADP∙min−1∙mm−1) of NEM-sensitive ATPase were present in the distal convoluted tubule (DCT) and in the cortical and outer and inner medullary collecting duet segments of normal rats. In metabolic acidosis produced by ammonium chloride treatment (plasma CO2 content = 15.3 ± 0.8 mequiv./L), the NEM-sensitive ATPase activity was increased significantly (60–100%) in the collecting duct segments without showing a significant change in the enzyme activity in the DCT. Our data are consistent with the hypothesis that a plasma membrane H+-ATPase (inhibited by NEM but not by oligomycin or ouabain) is involved in H+ secretion in the mammalian collecting duct.

1984 ◽  
Vol 62 (9) ◽  
pp. 865-877 ◽  
Author(s):  
Antonio Villalobo

A highly purified plasma membrane ATPase from the yeast Schizosaccharomyces pombe incorporated into liposomes was able to carry out translocation of H+ and K+ in the absence of the substrate ATP, when a membrane potential of appropriate polarity was applied. In the absence of ATP, the membrane potential induced K+ translocation was strongly inhibited by the ATPase inhibitor vanadate. [Formula: see text], but not [Formula: see text], stimulated the rate of ATP hydrolysis in the absence, but not in the presence, of the H+-conducting agent carbonylcyanide m-chlorophenylhydrazone. Sodium ion on either side of the membrane did not have any stimulatory effect. The potassium ion translocation driven by ATP hydrolysis appeared to have two different kinetic components. Although the ATP-dependent K+ transport strictly required the presence of a membrane potential, the rate of K+ translocation was not affected by a broad modulation of the degree of coupling (q) between ATP hydrolysis and the electrogenic H+ translocation. These experiments support the view that the yeast plasma membrane ATPase not only uses the membrane potential generated by the electrogenic H+ translocation, but also uses part of the free energy of the hydrolysis of ATP (ΔGP) to translocate potassium ion across the cytoplasmic cell membrane.


1984 ◽  
Vol 62 (10) ◽  
pp. 998-1005 ◽  
Author(s):  
Jan Ahlers

The effect of various inorganic and organic salts on the plasma membrane ATPase from the yeast Saccharomyces cerevisiae and on its proton transport were studied. We observed up to 460% stimulation of ATPase activity depending on the type of salt. The anion had a major effect and the monovalent cation a minor effect. These activations were the consequence of an increase in the affinity of the ATPase for activating Mg2+ ions and of an enhancement of Vmax. The mechanism of the reaction between enzyme, substrate, and Mg2+ ions was not altered by these salts. Similary, several salts stimulated the proton transport through the plasma membranes of Saccharomyces cerevisiae as evidenced by fluorescence quench of the dye 9-amino-6-chloro-2-methoxyacridine in plasma membrane vesicles. It is proposed that this effect is due to a stimulation of ATPase activity and in addition to charge compensation by membrane permeating anions.


1985 ◽  
Vol 37 (3) ◽  
pp. 189-193 ◽  
Author(s):  
Maria Cecilia Cocucci ◽  
Maria Ida De Michelis ◽  
Maria Chiara Pugliarello ◽  
Franca Rasi-Caldogno

2018 ◽  
Vol 10 (1) ◽  
Author(s):  
Sabine Ottilie ◽  
Gregory M. Goldgof ◽  
Andrea L. Cheung ◽  
Jennifer L. Walker ◽  
Edgar Vigil ◽  
...  

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