Du Shaoting, Zhang Yongsong, Lin Xianyong, Wang Yue, Tang Caixian
Ministry of Education Key Laboratory of Environmental Remediation and Ecosystem Health, College of Natural Resources and Environmental Science, Zhejiang University, Hangzhou, 310029, China.
Plant Cell Environ. 2008 Feb;31(2):195-204. doi: 10.1111/j.1365-3040.2007.01750.x. Epub 2007 Nov 20.
Nitrate reductase (NR), a committed enzyme in nitrate assimilation, involves generation of nitric oxide (NO) in plants. Here we show that the NR activity was significantly enhanced by the addition of NO donors sodium nitroprusside (SNP) and NONOate (diethylamine NONOate sodium) to the culturing solution, whereas it was decreased by NO scavenger 2-(4-carboxyphenyl)-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxide (cPTIO). Interestingly, both NO gas and SNP directly enhanced but cPTIO inhibited the NR activities of crude enzyme extracts and purified NR enzyme. The cPTIO terminated the interaction between NR-generated NO and the NR itself. Furthermore, the NR protein content was not affected by the SNP treatment. The investigation of the partial reactions catalysed by purified NR using various electron donors and acceptors indicated that the haem and molybdenum centres in NR were the two sites activated by NO. The results suggest that the activation of NR activity by NO is regulated at the post-translational level, probably via a direct interaction mechanism. Accordingly, the concentration of nitrate both in leaves and roots was decreased after 2 weeks of cultivation with SNP. The present study identifies a new mechanism of NR regulation and nitrate assimilation, which provides important new insights into the complex regulation of N-metabolism in plants.
硝酸还原酶(NR)是硝酸盐同化过程中的一种关键酶,参与植物体内一氧化氮(NO)的生成。在此我们表明,向培养液中添加NO供体硝普钠(SNP)和NONOate(二乙胺NONOate钠)可显著提高NR活性,而NO清除剂2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧基-3-氧化物(cPTIO)则会降低其活性。有趣的是,NO气体和SNP均可直接提高粗酶提取物和纯化的NR酶的活性,但cPTIO会抑制其活性。cPTIO终止了NR生成的NO与NR自身之间的相互作用。此外,SNP处理对NR蛋白含量没有影响。使用各种电子供体和受体对纯化的NR催化的部分反应进行研究表明,NR中的血红素和钼中心是被NO激活的两个位点。结果表明,NO对NR活性的激活是在翻译后水平上进行调节的,可能是通过直接相互作用机制实现的。因此,用SNP培养2周后,叶片和根中的硝酸盐浓度均降低。本研究确定了一种新的NR调节和硝酸盐同化机制,为植物氮代谢的复杂调节提供了重要的新见解。