Division of Environmental and Biomolecular Systems, Institute of Environmental Health, Oregon Health and Science University, 20000 NW Walker Rd, Beaverton, OR 97006, USA.
Microbiology (Reading). 2012 May;158(Pt 5):1268-1278. doi: 10.1099/mic.0.057661-0. Epub 2012 Feb 16.
Proteolytic control can govern the levels of specific regulatory factors, such as Spx, a transcriptional regulator of the oxidative stress response in Gram-positive bacteria. Under oxidative stress, Spx concentration is elevated and upregulates transcription of genes that function in the stress response. When stress is alleviated, proteolysis of Spx catalysed by ClpXP reduces Spx concentration. Proteolysis is enhanced by the substrate recognition factor YjbH, which possesses a His-Cys-rich region at its N terminus. However, mutations that generate H12A, C13A, H14A, H16A and C31/34A residue substitutions in the N terminus of Bacillus subtilis YjbH (BsYjbH) do not affect functionality in Spx proteolytic control in vivo and in vitro. Because of difficulties in obtaining soluble BsYjbH, the Geobacillus thermodenitrificans yjbH gene was cloned, which yielded soluble GtYjbH protein. Despite its lack of a His-Cys-rich region, GtYjbH complements a B. subtilis yjbH null mutant, and shows high activity in vitro when combined with ClpXP and Spx in an approximately 30 : 1 (ClpXP/Spx : GtYjbH) molar ratio. In vitro interaction experiments showed that Spx and the protease-resistant Spx(DD) (in which the last two residues of Spx are replaced with two Asp residues) bind to GtYjbH, but deletion of 12 residues from the Spx C terminus (SpxΔC) significantly diminished interaction and proteolytic degradation, indicating that the C terminus of Spx is important for YjbH recognition. These experiments also showed that Spx, but not GtYjbH, interacts with ClpX. Kinetic measurements for Spx proteolysis by ClpXP in the presence and absence of GtYjbH suggest that YjbH overcomes non-productive Spx-ClpX interaction, resulting in rapid degradation.
蛋白水解控制可以调节特定调节因子的水平,如 Spx,这是革兰氏阳性菌氧化应激反应的转录调节剂。在氧化应激下,Spx 浓度升高,并上调参与应激反应的基因的转录。当应激减轻时,ClpXP 催化的 Spx 蛋白水解将 Spx 浓度降低。蛋白水解通过具有其 N 端富含 His-Cys 区域的底物识别因子 YjbH 增强。然而,在 Bacillus subtilis YjbH(BsYjbH)的 N 端产生 H12A、C13A、H14A、H16A 和 C31/34A 残基取代的突变不会影响体内和体外 Spx 蛋白水解控制的功能。由于难以获得可溶性 BsYjbH,克隆了 Geobacillus thermodenitrificans yjbH 基因,该基因产生了可溶性 GtYjbH 蛋白。尽管缺乏富含 His-Cys 的区域,GtYjbH 仍能补充 B. subtilis yjbH 缺失突变体,并且在体外与 ClpXP 和 Spx 以大约 30:1(ClpXP/Spx:GtYjbH)的摩尔比组合时表现出高活性。体外相互作用实验表明,Spx 和蛋白酶抗性 Spx(DD)(其中 Spx 的最后两个残基被替换为两个 Asp 残基)与 GtYjbH 结合,但 Spx C 端缺失 12 个残基(SpxΔC)显著减少相互作用和蛋白水解降解,表明 Spx 的 C 端对于 YjbH 识别很重要。这些实验还表明,Spx 而不是 GtYjbH 与 ClpX 相互作用。在存在和不存在 GtYjbH 的情况下,通过 ClpXP 对 Spx 蛋白水解的动力学测量表明,YjbH 克服了非生产性的 Spx-ClpX 相互作用,导致快速降解。