Jin Chong Wei, Du Shao Ting, Zhang Yong Song, Lin Xian Yong, Tang Cai Xian
Ministry of Education Key Laboratory of Environmental Remediation and Ecosystem Health, College of Natural Resources and Environmental Science, Zhejiang University, Hangzhou, China.
Ann Bot. 2009 Jul;104(1):9-17. doi: 10.1093/aob/mcp087. Epub 2009 Apr 17.
Nitric oxide (NO) has been demonstrated to stimulate the activity of nitrate reductase (NR) in plant roots supplied with a low level of nitrate, and to affect proteins differently, depending on the ratio of NO to the level of protein. Nitrate has been suggested to regulate the level of NO in plants. This present study examined interactive effects of NO and nitrate level on NR activity in roots of tomato (Solanum lycocarpum).
NR activity, mRNA level of NR gene and concentration of NR protein in roots fed with 0.5 mM or 5 mM nitrate and treated with the NO donors, sodium nitroprusside (SNP) and diethylamine NONOate sodium (NONOate), and the NO scavenger, 2-(4-carboxyphenyl)-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxide (cPTIO), were measured in 25-d-old seedlings.
Addition of SNP and NONOate enhanced but cPTIO decreased NR activity in the roots fed with 0.5 mm nitrate. The opposite was true for the roots fed with 5 mM nitrate. However, the mRNA level of the NR gene and the protein concentration of NR enzyme in the roots were not affected by SNP treatment, irrespective of nitrate pre-treatment. Nevertheless, a low rate of NO gas increased while cPTIO decreased the NR activities of the enzyme extracts from the roots at both nitrate levels. Increasing the rate of NO gas further increased NR activity in the enzyme extracts of the roots fed with 0.5 mM nitrate but decreased it when 5 mM nitrate was supplied. Interestingly, the stimulative effect of NO gas on NR activity could be reversed by NO removal through N(2) flushing in the enzyme extracts from the roots fed with 0.5 mM nitrate but not from those with 5 mM nitrate.
The effects of NO on NR activity in tomato roots depend on levels of nitrate supply, and probably result from direct interactions between NO and NR protein.
一氧化氮(NO)已被证明能刺激低硝酸盐供应条件下植物根系中硝酸还原酶(NR)的活性,并且根据NO与蛋白质水平的比例不同,对蛋白质产生不同影响。硝酸盐被认为可调节植物体内NO的水平。本研究考察了NO和硝酸盐水平对番茄(Solanum lycocarpum)根系中NR活性的交互作用。
在25日龄幼苗中,测定用0.5 mM或5 mM硝酸盐处理并分别用NO供体硝普钠(SNP)和二乙胺NONOate钠(NONOate)以及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)处理后的根系中NR活性、NR基因的mRNA水平和NR蛋白浓度。
添加SNP和NONOate可增强0.5 mM硝酸盐处理根系中的NR活性,但cPTIO则降低其活性。对于5 mM硝酸盐处理的根系,情况相反。然而,无论硝酸盐预处理如何,根系中NR基因的mRNA水平和NR酶的蛋白浓度均不受SNP处理的影响。不过,低浓度的NO气体可提高,而cPTIO可降低两种硝酸盐水平下根系酶提取物中的NR活性。进一步提高NO气体浓度可增加0.5 mM硝酸盐处理根系酶提取物中的NR活性,但在供应5 mM硝酸盐时则降低其活性。有趣的是,通过用N₂冲洗去除NO,可逆转0.5 mM硝酸盐处理根系酶提取物中NO气体对NR活性的刺激作用,但5 mM硝酸盐处理的根系则不能。
NO对番茄根系中NR活性的影响取决于硝酸盐供应水平,可能是由于NO与NR蛋白之间的直接相互作用所致。