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在杀稻瘟菌素生物合成中,通过使用依赖磷酸吡哆醛的3-氨基苯甲酸合酶PctV的K276R突变体对醌类中间体进行基于机制的捕获。

Mechanism-Based Trapping of the Quinonoid Intermediate by Using the K276R Mutant of PLP-Dependent 3-Aminobenzoate Synthase PctV in the Biosynthesis of Pactamycin.

作者信息

Hirayama Akane, Miyanaga Akimasa, Kudo Fumitaka, Eguchi Tadashi

机构信息

Department of Chemistry and Materials Science, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo, 152-8551, Japan.

Department of Chemistry, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo, 152-8551, Japan.

出版信息

Chembiochem. 2015 Nov;16(17):2484-90. doi: 10.1002/cbic.201500426. Epub 2015 Oct 23.

Abstract

Mutational analysis of the pyridoxal 5'-phosphate (PLP)-dependent enzyme PctV was carried out to elucidate the multi-step reaction mechanism for the formation of 3-aminobenzoate (3-ABA) from 3-dehydroshikimate (3-DSA). Introduction of mutation K276R led to the accumulation of a quinonoid intermediate with an absorption maximum at 580 nm after the reaction of pyridoxamine 5'-phosphate (PMP) with 3-DSA. The chemical structure of this intermediate was supported by X-ray crystallographic analysis of the complex formed between the K276R mutant and the quinonoid intermediate. These results clearly show that a quinonoid intermediate is involved in the formation of 3-ABA. They also indicate that Lys276 (in the active site of PctV) plays multiple roles, including acid/base catalysis during the dehydration reaction of the quinonoid intermediate.

摘要

对依赖于磷酸吡哆醛(PLP)的酶PctV进行了突变分析,以阐明从3-脱氢莽草酸(3-DSA)形成3-氨基苯甲酸(3-ABA)的多步反应机制。引入突变K276R导致在磷酸吡哆胺5'-磷酸(PMP)与3-DSA反应后,积累了一种在580 nm处具有最大吸收的醌类中间体。K276R突变体与醌类中间体形成的复合物的X射线晶体学分析支持了该中间体的化学结构。这些结果清楚地表明,醌类中间体参与了3-ABA的形成。它们还表明,Lys276(在PctV的活性位点)发挥多种作用,包括在醌类中间体脱水反应过程中的酸碱催化作用。

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