Kim Jihan, Park Jaehyun, Lee Keondo, Chung Wan Kyun, Nam Ki Hyun, Cho Yunje
Department of Life Sciences, Pohang University of Science and Technology, Pohang, 37673, Kyungbook, Republic of Korea.
Pohang Accelerator Laboratory, Pohang University of Science and Technology, Pohang, 37673, Kyungbook, Republic of Korea.
Sci Rep. 2024 Dec 28;14(1):31442. doi: 10.1038/s41598-024-83045-8.
Alanine racemase (Alr) catalyzes the pyridoxal 5'-phosphate (PLP)-dependent racemization between L- and D-alanine in bacteria. Owing to the potential interest in targeting Alr for antibacterial drug development, several studies have determined the structures of Alr from different species, proposing models for the reaction mechanism. Insights into its reaction dynamics may be conducive to a better understanding of the Alr reaction mechanism. In this study, we determined the structures of the apo and reaction states of Bacillus subtilis Alr (BsAlr) at room temperature using a fixed-target based X-ray free-electron laser. The 2.3 Å resolution structures revealed the alanine substrate or intermediate in various positions at the active site. Conformational change between the N- and C-terminal domains of BsAlr expanded the entryway for substrate binding. In the reaction state of BsAlr, two main alanine binding states were observed: one alanine molecule is positioned away from PLP, whereas the other alanine molecule is covalently bonded to PLP. These structures might represent the dynamic states of the substrate for entrance into, reaction with, or exit from the active site. Our approach provides a simple and rapid method for elucidating the intermediate structure of Alr, which can be expanded to other enzymes.
丙氨酸消旋酶(Alr)催化细菌中L-丙氨酸和D-丙氨酸之间依赖于磷酸吡哆醛(PLP)的消旋反应。由于靶向Alr用于抗菌药物开发具有潜在的研究价值,多项研究已确定了来自不同物种的Alr结构,并提出了反应机制模型。深入了解其反应动力学可能有助于更好地理解Alr反应机制。在本研究中,我们使用基于固定靶标的X射线自由电子激光在室温下确定了枯草芽孢杆菌Alr(BsAlr)的无底物状态和反应状态的结构。分辨率为2.3 Å的结构揭示了丙氨酸底物或中间体在活性位点的不同位置。BsAlr的N端和C端结构域之间的构象变化扩大了底物结合的入口。在BsAlr的反应状态下,观察到两种主要的丙氨酸结合状态:一种丙氨酸分子远离PLP,而另一种丙氨酸分子与PLP共价结合。这些结构可能代表了底物进入、与活性位点反应或从活性位点离开的动态状态。我们的方法为阐明Alr的中间结构提供了一种简单快速的方法,该方法可扩展到其他酶。