The Role of Zinc in Angiotensin Converting Enzyme

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Abstract
Angiotensin converting enzyme is a chloride‐dependent zinc metalloexo‐peptidase. The zinc atom is essential for enzymatic activity. Removal of zinc by dialysis against the chelating agent 1,10‐phenanthroline abolishes activity toward the chromophoric substrates furanacryloyl‐Phe‐Gly‐Gly. Reconstitution of the resultant apoenzyme with either zinc, cobalt or manganese restores activity to 100, 55 or 25% of that of the native enzyme, respectively. Spontaneous dissociation of zinc from the enzyme occurs below pH 7 and this can be prevented by adding excess metal to the buffer. Radiationless energy transfer studies with a fluorescent substrate demonstrate that zinc is not required for substrate binding and does not mediate the activating effect of chloride. Thus, zinc functions solely in the hydrolytic step of catalysis.