The mechanism of orotidine 5′-monophosphate decarboxylase:: Catalysis by destabilization of the substrate

被引:53
作者
Feng, WY [1 ]
Austin, TJ [1 ]
Chew, F [1 ]
Gronert, S [1 ]
Wu, WM [1 ]
机构
[1] San Francisco State Univ, Dept Chem & Biochem, San Francisco, CA 94132 USA
关键词
D O I
10.1021/bi992553w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanism of orotidine 5'-monophosphate decarboxylase (OMP decarboxylase, ODCase) was studied using the decarboxylation of orotic acid analogues as a model system, The rate of decarboxylation of 1,3-dimethylorotic acid and its analogues as well as the stability of their corresponding carbanion intermediates was determined. The results have shown that the stability of the carbanion intermediate is not a critical factor in the rate of decarboxylation. On the other hand, the reaction rate is largely dependent on the equilibrium constant for the formation of a zwitterion. Based on these results, we have proposed a new mechanism in which ODCase catalyzes the decarboxylation of OMP by binding the substrate in a zwitterionic form and providing a destabilizing environment for the carboxylate group of OMP.
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页码:1778 / 1783
页数:6
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