Genetics and Experimental Bioinformatics, Faculty of Biology, Freiburg University, D-79104, Freiburg, Germany.
Department of Quantitative Proteomics, Interfaculty Institute for Cell Biology, University of Tübingen, D-72076, Tübingen, Germany.
Nat Commun. 2024 Mar 1;15(1):1911. doi: 10.1038/s41467-024-46253-4.
When the supply of inorganic carbon is limiting, photosynthetic cyanobacteria excrete nitrite, a toxic intermediate in the ammonia assimilation pathway from nitrate. It has been hypothesized that the excreted nitrite represents excess nitrogen that cannot be further assimilated due to the missing carbon, but the underlying molecular mechanisms are unclear. Here, we identified a protein that interacts with nitrite reductase, regulates nitrogen metabolism and promotes nitrite excretion. The protein, which we named NirP1, is encoded by an unannotated gene that is upregulated under low carbon conditions and controlled by transcription factor NtcA, a central regulator of nitrogen homeostasis. Ectopic overexpression of nirP1 in Synechocystis sp. PCC 6803 resulted in a chlorotic phenotype, delayed growth, severe changes in amino acid pools, and nitrite excretion. Coimmunoprecipitation experiments indicated that NirP1 interacts with nitrite reductase, a central enzyme in the assimilation of ammonia from nitrate/nitrite. Our results reveal that NirP1 is widely conserved in cyanobacteria and plays a crucial role in the coordination of C/N primary metabolism by targeting nitrite reductase.
当无机碳供应受到限制时,光合蓝细菌会排泄亚硝酸盐,这是硝酸盐同化途径中氨的有毒中间产物。据推测,排泄的亚硝酸盐代表了由于缺少碳而无法进一步同化的过量氮,但潜在的分子机制尚不清楚。在这里,我们鉴定了一种与亚硝酸盐还原酶相互作用的蛋白质,该蛋白质调节氮代谢并促进亚硝酸盐排泄。该蛋白名为 NirP1,由一个未注释的基因编码,该基因在低碳条件下上调,并受氮平衡中央调节剂 NtcA 转录因子的控制。在 Synechocystis sp. PCC 6803 中异位过表达 nirP1 导致出现黄化表型、生长迟缓、氨基酸库严重变化和亚硝酸盐排泄。共免疫沉淀实验表明,NirP1 与亚硝酸盐还原酶相互作用,亚硝酸盐还原酶是从硝酸盐/亚硝酸盐同化氨的中心酶。我们的结果表明,NirP1 在蓝细菌中广泛保守,通过靶向亚硝酸盐还原酶在协调 C/N 初级代谢中起着关键作用。