Tibell L, Lindskog S
Biochim Biophys Acta. 1984 Jul 17;788(1):110-6. doi: 10.1016/0167-4838(84)90302-9.
Cd2+ derivatives of human carbonic anhydrases I and II and bovine red cell carbonic anhydrase (carbonate hydro-lyase, EC 4.2.1.1) have been prepared. The metal ion in these derivatives is readily displaced by Zn2+. The Cd2+-carbonic anhydrases have appreciable 4-nitrophenyl acetate hydrolase activities. These activities increase with pH as if dependent on the basic form of a group with pKa near 10. The Cd2+-carbonic anhydrases also have significant CO2 hydration activities. The Cd2+ derivatives are strongly inhibited by monovalent anions. In particular, I- is a much more potent inhibitor of the Cd2+ enzymes than of the native enzymes. Acetazolamide (5-acetylamido-1,3,4-thiadiazole 2-sulfonamide) is also a strong inhibitor although its affinity for the Cd2+ enzyme is less than its affinity for the native enzyme.
已制备出人类碳酸酐酶I和II以及牛红细胞碳酸酐酶(碳酸水解酶,EC 4.2.1.1)的Cd2+衍生物。这些衍生物中的金属离子很容易被Zn2+取代。Cd2+ - 碳酸酐酶具有可观的对硝基苯乙酸酯水解酶活性。这些活性随pH升高,似乎依赖于pKa接近10的基团的碱性形式。Cd2+ - 碳酸酐酶也具有显著的CO2水合活性。Cd2+衍生物受到单价阴离子的强烈抑制。特别是,I-对Cd2+酶的抑制作用比对天然酶的抑制作用要强得多。乙酰唑胺(5 - 乙酰氨基 - 1,3,4 - 噻二唑 - 2 - 磺酰胺)也是一种强抑制剂,尽管它对Cd2+酶的亲和力小于对天然酶的亲和力。