Institut für Biophysik und physikalische Biochemie, Universität Regensburg, 93040 Regensburg (Germany).
Angew Chem Int Ed Engl. 2015 Sep 14;54(38):11270-4. doi: 10.1002/anie.201505063.
Chorismate-utilizing enzymes play a vital role in the biosynthesis of metabolites in plants as well as free-living and infectious microorganisms. Among these enzymes are the homologous primary metabolic anthranilate synthase (AS) and secondary metabolic isochorismate synthase (ICS). Both catalyze mechanistically related reactions by using ammonia and water as nucleophiles, respectively. We report that the nucleophile specificity of AS can be extended from ammonia to water by just two amino acid exchanges in a channel leading to the active site. The observed ICS/AS bifunctionality demonstrates that a secondary metabolic enzyme can readily evolve from a primary metabolic enzyme without requiring an initial gene duplication event. In a general sense, these findings add to our understanding how nature has used the structurally predetermined features of enzyme superfamilies to evolve new reactions.
支链氨基酸利用酶在植物以及自由生活和感染性微生物的代谢物生物合成中起着至关重要的作用。这些酶包括同源的初级代谢色氨酸合酶 (AS) 和次级代谢异分支酸合酶 (ICS)。这两种酶都通过分别使用氨和水作为亲核试剂催化具有机制相关性的反应。我们报告说,通过在通向活性位点的通道中仅进行两次氨基酸交换,就可以将 AS 的亲核特异性从氨扩展到水。观察到的 ICS/AS 双功能表明,次级代谢酶可以很容易地从初级代谢酶进化而来,而无需最初的基因复制事件。从广义上讲,这些发现增加了我们对自然如何利用酶超家族的结构预定特征来进化新反应的理解。