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碳酸酐酶催化作用的氢氧化锌机制的同位素效应证据。

Isotope effect evidence for the zinc hydroxide mechanism of carbonic anhydrase catalysis.

作者信息

Paneth P, O'Leary M H

出版信息

Biochemistry. 1987 Mar 24;26(6):1728-31. doi: 10.1021/bi00380a036.

Abstract

The carbon kinetic isotope effect on the enzymatic dehydration of HCO3- ion is k12/k13 = 1.011 and is independent, within experimental error, of the addition of sucrose, substitution of D2O for H2O, and substitution of enzyme-bound Zn2+ by Co2+. These results are consistent with a ping-pong mechanism in which proton transfer between enzyme and solvent is separated from HCO3- dehydration. For the dehydration half-reaction, diffusional processes are severalfold faster than dehydration, and the rate-determining step is the dehydration itself. The intrinsic isotope effect is approximately 1.011, indicating that hydration of CO2 occurs by reaction of zinc-bound OH-, rather than zinc-bound H2O.

摘要

碳动力学同位素效应作用于HCO₃⁻离子的酶促脱水反应时,k₁²/k₁³ = 1.011,并且在实验误差范围内,与蔗糖的添加、用D₂O替代H₂O以及用Co²⁺替代酶结合的Zn²⁺无关。这些结果与乒乓机制一致,在该机制中酶与溶剂之间的质子转移与HCO₃⁻脱水是分开的。对于脱水半反应,扩散过程比脱水快几倍,速率决定步骤是脱水本身。内在同位素效应约为1.011,表明CO₂的水合作用是通过锌结合的OH⁻反应发生的,而不是通过锌结合的H₂O。

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