School of Food Sciences and Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510641, China.
Int J Mol Sci. 2023 Apr 1;24(7):6606. doi: 10.3390/ijms24076606.
Excess ammonium imposes toxicity and stress response in cyanobacteria. How cyanobacteria acclimate to NH stress is so far poorly understood. Here, sp. PCC6803 S2P homolog Slr1821 was identified as the essential regulator through physiological characterization and transcriptomic analysis of its knockout mutant. The proper expression of 60% and 67% of the NH activated and repressed genes, respectively, were actually Slr1821-dependent since they were abolished or reversed in ∆. 6803 suppressed nitrogen uptake and assimilation, ammonium integration and mobilization of other nitrogen sources upon NH stress. Opposite regulation on genes for assimilation of nitrogen and carbon, such as repression of nitrogen regulatory protein PII, PII interactive protein PirC and activation of carbon acquisition regulator RcbR, demonstrated that 6803 coordinated regulation to maintain carbon/nitrogen homeostasis under increasing nitrogen, while functional Slr1821 was indispensable for most of this coordinated regulation. Additionally, knockout disrupted the proper response of regulators and transporters in the ammonium-specific stimulon, and resulted in defective photosynthesis as well as compromised translational and transcriptional machinery. These results provide new insight into the coordinated regulation of nutritional fluctuation and the functional characterization of S2Ps. They also provide new targets for bioengineering cyanobacteria in bioremediation and improving ammonium tolerance in crop plants.
过量的氨会对蓝藻造成毒性和应激反应。目前,蓝藻对 NH 胁迫的适应机制还知之甚少。本研究通过生理特性分析和敲除突变体的转录组分析,鉴定 sp. PCC6803 S2P 同源物 Slr1821 为必需调控因子。由于在 ∆ 中这些基因的表达被完全抑制或逆转,因此,约 60%和 67%的 NH 激活和抑制基因的正常表达实际上依赖于 Slr1821。敲除 Slr1821 会抑制 6803 对氮的吸收和同化、铵同化以及其他氮源的动员。此外,氮和碳同化基因的表达受到相反的调控,如氮调节蛋白 PII、PII 相互作用蛋白 PirC 的抑制以及碳获取调节因子 RcbR 的激活,这表明 6803 在增加氮的情况下协调调节以维持碳/氮平衡,而功能性 Slr1821 对于这种协调调节是不可或缺的。另外,敲除 Slr1821 破坏了铵特异性刺激物中调控因子和转运蛋白的正常响应,导致光合作用缺陷以及翻译和转录机制受损。这些结果为营养波动的协调调控以及 S2P 的功能特征提供了新的见解。它们还为生物修复和提高作物植物对铵的耐受性的蓝藻生物工程提供了新的靶点。