Effect of physiological electron donors and acceptors on F1-ATPase

Abstract
The hydrolytic activity of F1-ATPase isolated from rat liver was enhanced in the presence of NADH, FADH2, QH2 or reduced cyt c.The extent of this activation depended largely on substrate concentration.F1-ATPase sensitivity to bicarbonate or dinitrophenol activators decreased in the presence of any of those electron donors, which originated as well a slight sensitivity to oligomycin and a sensitivity increase to the inhibitory anion OCN-.In the presence of oxidized carriers the sensitivity to bicarbonate, dinitrophenol, or OCN- was not modified, and the enzyme remained oligomycin insensitive.
Keywords:
Adenosine Triphosphatases/metabolism, Animals, Cyanates/pharmacology, Cytochrome c Group/metabolism, Dinitrophenols/pharmacology, Enzyme Activation, Flavin-Adenine Dinucleotide/metabolism, Liver/enzymology, Mitochondria, NAD/metabolism, Oligomycins/pharmacology, Proton-Translocating ATPases, Rats, Ubiquinone/metabolism
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