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扁桃酸途径中的重组催化作用。

Restructuring catalysis in the mandelate pathway.

作者信息

Neidhart D C, Howell P L, Petsko G A, Gerlt J A, Kozarich J W, Powers V M, Kenyon G L

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Biochem Soc Symp. 1990;57:135-41.

PMID:2099737
Abstract

Mandelate racemase (MR) is the first enzyme in the bacterial pathway that converts mandelic acid to benzoic acid. The mandelate pathway can utilize either enantiomer of mandelate because this enzyme interconverts them. We have solved the structure of MR at 2.5 A resolution. The enzyme is almost identical in conformation to another bacterial enzyme, muconate lactonizing enzyme (MLE). Both enzymes are TIM-barrel proteins. This result has profound implications for the evolution of enzymic function and the origin of metabolic pathways. It also implies that it should be possible to transform one enzyme into the other by site-directed mutagenesis.

摘要

扁桃酸消旋酶(MR)是细菌将扁桃酸转化为苯甲酸途径中的第一种酶。扁桃酸途径可以利用扁桃酸的任何一种对映体,因为这种酶能使它们相互转化。我们已解析出分辨率为2.5埃的MR结构。该酶的构象与另一种细菌酶——粘康酸内酯化酶(MLE)几乎相同。这两种酶都是TIM桶状蛋白。这一结果对酶功能的进化和代谢途径的起源具有深远意义。它还意味着通过定点诱变有可能将一种酶转化为另一种酶。

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