Rowlett R S, Gargiulo N J, Santoli F A, Jackson J M, Corbett A H
Department of Chemistry, Colgate University, Hamilton, New York 13346.
J Biol Chem. 1991 Jan 15;266(2):933-41.
We have found that many dianionic species, at millimolar concentrations, significantly activate or inhibit the bovine carbonic anhydrase III-catalyzed hydration of CO2. Dianionic species such as HPO2-4 and SO2-3, with pKb values near 7, are activators, whereas weakly basis species such as SO2-4 act as inhibitors. Both activation and inhibition are partial hyperbolic in nature and do not appear to compete with monoanionic linear inhibitors like N-3. Our kinetic data are consistent with a formal mechanism of action for carbonic anhydrase III that is directly analogous to that of carbonic anhydrase II, in which Lys-64 of carbonic anhydrase III can act as an intramolecular H+ transfer group during CO2 hydration. Our data suggest that dianionic inhibitors depress the rate of H+ transfer during turnover by stabilizing the protonated form of Lys-64. We postulate that dianionic activators enhance the rate of a rate-limiting H+ transfer step in the mechanism, probably by acting directly as H+ acceptors.
我们发现,许多二价阴离子物种在毫摩尔浓度下能显著激活或抑制牛碳酸酐酶III催化的CO₂水合反应。pKb值接近7的二价阴离子物种,如HPO₄²⁻和SO₃²⁻,是激活剂,而弱碱性物种如SO₄²⁻则起抑制剂的作用。激活和抑制本质上都是部分双曲线型的,似乎并不与像N₃⁻这样的单阴离子线性抑制剂竞争。我们的动力学数据与碳酸酐酶III的一种形式作用机制一致,该机制与碳酸酐酶II的机制直接类似,其中碳酸酐酶III的Lys-64在CO₂水合过程中可作为分子内H⁺转移基团。我们的数据表明,二价阴离子抑制剂通过稳定Lys-64的质子化形式来降低周转过程中H⁺转移的速率。我们推测,二价阴离子激活剂可能通过直接作为H⁺受体来提高该机制中限速H⁺转移步骤的速率。