Liu Fei, Zhao Yi-Lei, Wang Xiaolei, Hu Hongbo, Peng Huasong, Wang Wei, Wang Jing-Fang, Zhang Xuehong
State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Key Laboratory of Systems Biomedicine (Ministry of Education), Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.
PLoS One. 2015 Sep 28;10(9):e0139081. doi: 10.1371/journal.pone.0139081. eCollection 2015.
The phenazine biosynthetic pathway is of considerable importance for the pharmaceutical industry. The pathway produces two products: phenazine-1,6-dicarboxylic acid and phenazine-1-carboxylic acid. PhzF is an isomerase that catalyzes trans-2,3-dihydro-3-hydroxyanthranilic acid isomerization and plays an essential role in the phenazine biosynthetic pathway. Although the PhzF crystal structure has been determined recently, an understanding of the detailed catalytic mechanism and the roles of key catalytic residues are still lacking. In this study, a computational strategy using a combination of molecular modeling, molecular dynamics simulations, and quantum mechanics/molecular mechanics simulations was used to elucidate these important issues. The Apo enzyme, enzyme-substrate complexes with negatively charged Glu45, enzyme-transition state analog inhibitor complexes with neutral Glu45, and enzyme-product complexes with negatively charged Glu45 structures were optimized and modeled using a 200 ns molecular dynamics simulation. Residues such as Gly73, His74, Asp208, Gly212, Ser213, and water, which play important roles in ligand binding and the isomerization reaction, were comprehensively investigated. Our results suggest that the Glu45 residue at the active site of PhzF acts as a general base/acid catalyst during proton transfer. This study provides new insights into the detailed catalytic mechanism of PhzF and the results have important implications for PhzF modification.
吩嗪生物合成途径对制药行业具有相当重要的意义。该途径产生两种产物:吩嗪 -1,6 - 二羧酸和吩嗪 -1 - 羧酸。PhzF是一种异构酶,催化反式 -2,3 - 二氢 -3 - 羟基邻氨基苯甲酸异构化,在吩嗪生物合成途径中起关键作用。尽管最近已确定了PhzF的晶体结构,但仍缺乏对详细催化机制和关键催化残基作用的了解。在本研究中,采用了一种结合分子建模、分子动力学模拟和量子力学/分子力学模拟的计算策略来阐明这些重要问题。使用200纳秒的分子动力学模拟对无配体酶、带负电荷的Glu45的酶 - 底物复合物、中性Glu45的酶 - 过渡态类似物抑制剂复合物以及带负电荷的Glu45的酶 - 产物复合物结构进行了优化和建模。全面研究了在配体结合和异构化反应中起重要作用的Gly73、His74、Asp208、Gly212、Ser213等残基以及水。我们的结果表明,PhzF活性位点的Glu45残基在质子转移过程中充当通用碱/酸催化剂。本研究为PhzF的详细催化机制提供了新的见解,其结果对PhzF的修饰具有重要意义。