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探索铜绿假单胞菌中与 γ-氨基丁酸和 5-氨基戊酸结合的溶质结合蛋白及其在激活传感器激酶中的作用。

Exploring solute binding proteins in Pseudomonas aeruginosa that bind to γ-aminobutyrate and 5-aminovalerate and their role in activating sensor kinases.

机构信息

Department of Biotechnology and Environmental Protection, Estación Experimental del Zaidín, Consejo Superior de Investigaciones Científicas, Granada, Spain.

Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria/Consejo Superior de Investigaciones Científicas, Parque Científico y Tecnológico de la Universidad Politécnica de Madrid, Pozuelo de Alarcón, Madrid, Spain.

出版信息

Microbiologyopen. 2024 Jun;13(3):e1415. doi: 10.1002/mbo3.1415.

Abstract

The standard method of receptor activation involves the binding of signals or signal-loaded solute binding proteins (SBPs) to sensor domains. Many sensor histidine kinases (SHKs), which are activated by SBP binding, are encoded adjacent to their corresponding sbp gene. We examined three SBPs of Pseudomonas aeruginosa PAO1, encoded near the genes for the AgtS (PA0600) and AruS (PA4982) SHKs, to determine how common this arrangement is. Ligand screening and microcalorimetric studies revealed that the SBPs PA0602 and PA4985 preferentially bind to GABA (KD = 2.3 and 0.58 μM, respectively), followed by 5-aminovalerate (KD = 30 and 1.6 μM, respectively) and ethanoldiamine (KD = 2.3 and 0.58 μM, respectively). In contrast, AgtB (PA0604) exclusively recognizes 5-aminovaleric acid (KD = 2.9 μM). However, microcalorimetric titrations did not show any binding between the AgtS sensor domain and AgtB or PA0602, regardless of the presence of ligands. Similarly, bacterial two-hybrid assays did not demonstrate an interaction between PA4985 and the AruS sensor domain. Therefore, sbp and shk genes located nearby are not always functionally linked. We previously identified PA0222 as a GABA-specific SBP. The presence of three SBPs for GABA may be linked to GABA's role as a trigger for P. aeruginosa virulence.

摘要

受体激活的标准方法涉及信号或信号加载的溶质结合蛋白 (SBP) 与传感器结构域的结合。许多 SBP 结合可激活的传感器组氨酸激酶 (SHK) ,它们与相应的 sbp 基因相邻编码。我们检查了铜绿假单胞菌 PAO1 的三个 SBP,它们靠近 AgtS (PA0600) 和 AruS (PA4982) SHK 的基因编码,以确定这种排列方式有多常见。配体筛选和微量热研究表明,SBP PA0602 和 PA4985 优先结合 GABA (KD = 2.3 和 0.58 μM),其次是 5-氨基戊酸 (KD = 30 和 1.6 μM) 和乙二胺 (KD = 2.3 和 0.58 μM)。相比之下,AgtB (PA0604) 专门识别 5-氨基戊酸 (KD = 2.9 μM)。然而,微量热滴定实验表明,无论是否存在配体,AgtS 传感器结构域与 AgtB 或 PA0602 之间均没有任何结合。同样,细菌双杂交测定也没有显示 PA4985 与 AruS 传感器结构域之间存在相互作用。因此,附近的 sbp 和 shk 基因并不总是具有功能关联。我们之前鉴定出 PA0222 是一种 GABA 特异性 SBP。存在三种 GABA 的 SBP 可能与 GABA 作为铜绿假单胞菌毒力的触发物有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57d3/11113362/d18b0a851e0c/MBO3-13-e1415-g007.jpg

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