Tanner Martin E
Department of Chemistry, University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.
Acc Chem Res. 2002 Apr;35(4):237-46. doi: 10.1021/ar000056y.
Epimerases and racemases are enzymes that catalyze the inversion of stereochemistry in biological molecules. In this article, three distinct examples are used to illustrate the wide range of chemical strategies employed during catalysis, and the diverse set of ancestors from which these enzymes have evolved. Glutamate racemase is an example of an enzyme that operates at an "activated" stereocenter (bearing a relatively acidic proton) and employs a nonstereospecific deprotonation/reprotonation mechanism. UDP-N-Acetylglucosamine 2-epimerase acts at an "unactivated" stereocenter and uses a mechanism involving a nonstereospecific elimination/addition of UDP. L-Ribulose phosphate 4-epimerase also acts at an unactivated stereocenter and uses a nonstereospecific retroaldol/aldol mechanism.
差向异构酶和消旋酶是催化生物分子中立体化学翻转的酶。在本文中,使用了三个不同的例子来说明催化过程中所采用的广泛化学策略,以及这些酶所进化而来的多样祖先。谷氨酸消旋酶是一种作用于“活化”立体中心(带有相对酸性质子)并采用非立体特异性去质子化/再质子化机制的酶的例子。UDP-N-乙酰葡糖胺2-差向异构酶作用于“未活化”立体中心,并使用涉及UDP的非立体特异性消除/添加的机制。磷酸L-核糖ulose 4-差向异构酶也作用于未活化立体中心,并使用非立体特异性逆羟醛缩合/羟醛缩合机制。