Heavy metal ion inhibition studies of human, sheep and fish α-carbonic anhydrases

Abstract

Carbonic anhydrases (CAs, EC 4.2.1.1) were purified from sheep kidney (sCA IV), from the liver of the teleost fish Dicentrarchus labrax (dCA) and from human erythrocytes (hCA I and hCA II). The purification procedure consisted of a single step affinity chromatography on Sepharose 4B-tyrosine-sulfanilamide. The kinetic parameters of these enzymes were determined for their esterase activity with 4-nitrophenyl acetate as substrate. The following metal ions, Pb²⁺, Co²⁺, Hg²⁺, Cd²⁺, Zn²⁺, Se²⁺, Cu²⁺, Al³⁺ and Mn³⁺ showed inhibitory effects on these enzymes. The tested metal ions inhibited these CAs competitively in the low milimolar/submillimolar range. The susceptibility to various cations inhibitors differs significantly between these vertebrate α-CAs and is probably due to their binding to His64 or the histidine cluster.

Keywords::

• Carbonic anhydrase
• metal ion
• erythrocyte
• sheep kidney
• teleost fish