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来自土拉弗朗西斯菌的 II 类果糖-1,6-二磷酸酶的新结构为整个酶类提供了一个新颖的催化机制框架。

New structures of Class II Fructose-1,6-Bisphosphatase from Francisella tularensis provide a framework for a novel catalytic mechanism for the entire class.

机构信息

Institute for Tuberculosis Research, University of Illinois at Chicago, Chicago, Illinois, United States of America.

Department of Pharmaceutical Sciences, University of Illinois at Chicago, Chicago, Illinois, United States of America.

出版信息

PLoS One. 2023 Jun 23;18(6):e0274723. doi: 10.1371/journal.pone.0274723. eCollection 2023.

Abstract

Class II Fructose-1,6-bisphosphatases (FBPaseII) (EC: 3.1.3.11) are highly conserved essential enzymes in the gluconeogenic pathway of microorganisms. Previous crystallographic studies of FBPasesII provided insights into various inactivated states of the enzyme in different species. Presented here is the first crystal structure of FBPaseII in an active state, solved for the enzyme from Francisella tularensis (FtFBPaseII), containing native metal cofactor Mn2+ and complexed with catalytic product fructose-6-phosphate (F6P). Another crystal structure of the same enzyme complex is presented in the inactivated state due to the structural changes introduced by crystal packing. Analysis of the interatomic distances among the substrate, product, and divalent metal cations in the catalytic centers of the enzyme led to a revision of the catalytic mechanism suggested previously for class II FBPases. We propose that phosphate-1 is cleaved from the substrate fructose-1,6-bisphosphate (F1,6BP) by T89 in a proximal α-helix backbone (G88-T89-T90-I91-T92-S93-K94) in which the substrate transition state is stabilized by the positive dipole of the 〈-helix backbone. Once cleaved a water molecule found in the active site liberates the inorganic phosphate from T89 completing the catalytic mechanism. Additionally, a crystal structure of Mycobacterium tuberculosis FBPaseII (MtFBPaseII) containing a bound F1,6BP is presented to further support the substrate binding and novel catalytic mechanism suggested for this class of enzymes.

摘要

II 类果糖-1,6-二磷酸酶(FBPaseII)(EC:3.1.3.11)是微生物糖异生途径中高度保守的必需酶。先前对 FBPaseII 的晶体结构研究为不同物种中酶的各种失活状态提供了深入了解。本文呈现了第一个活性状态的 FBPaseII 晶体结构,该酶来自土拉弗朗西斯菌(FtFBPaseII),含有天然金属辅因子 Mn2+,并与催化产物果糖-6-磷酸(F6P)结合。由于晶体包装引起的结构变化,呈现了相同酶复合物的另一个失活状态的晶体结构。对酶催化中心中底物、产物和二价金属阳离子之间的原子间距离的分析导致对先前提出的 II 类 FBPase 催化机制的修订。我们提出,T89 在近端α-螺旋骨架(G88-T89-T90-I91-T92-S93-K94)中从底物果糖-1,6-二磷酸(F1,6BP)上裂解磷酸-1,其中底物过渡态由正α-螺旋骨架的偶极子稳定。一旦被裂解,位于活性位点的水分子将无机磷酸从 T89 上释放出来,完成催化机制。此外,还呈现了含有结合的 F1,6BP 的结核分枝杆菌 FBPaseII(MtFBPaseII)的晶体结构,以进一步支持该类酶的底物结合和新提出的催化机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be42/10289334/dc6004f3cf9c/pone.0274723.g001.jpg

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