Utilizing a basolateral membrane vesicle preparation containing Cl--ATPase
from Aplysia foregut, it was shown that orthovanodate inhibited Cl--ATPase
activity, ATP-dependent Cl- transport and ATP-dependent membrane potential
change. N-ethylmalemide (NEM) and p-chloromercurobenzoate (PCMBS) also inhi
bited the Cl- pump biochemical and transport characteristics. However, bafi
lomycin, azide, DCCD or efrapeptin had no effect on the Cl- pump characteri
stics suggesting that this Cl- pump was a P-type ATPase.