Abstract

Abstract 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 inhibited the Cl− pump biochemical and transport characteristics. However, bafilomycin, azide, DCCD or efrapeptin had no effect on the Cl− pump characteristics suggesting that this Cl− pump was a P-type ATPase.

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