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首页> 外文期刊>Legume research >Salicylic acid improves salinity tolerance in field pea (Pisum sativum L.) by intensifying antioxidant defense system and preventing salt-induced nitrate reductase (NR) activity loss
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Salicylic acid improves salinity tolerance in field pea (Pisum sativum L.) by intensifying antioxidant defense system and preventing salt-induced nitrate reductase (NR) activity loss

机译:水杨酸通过增强抗氧化防御系统并防止盐诱导的硝酸还原酶(NR)活性损失,提高了豌豆(Pisum sativum L.)的耐盐性

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摘要

To improve the antioxidant system and protect the nitrate reductase (NR) activity of two field pea genotypes (DDR 61 and HUDP 15) by seed hardening through optimum concentration salicylic acid (SA) @ 1.0 mM under salinity stress condition. Salinity was imposed by NaCl @ 50,100 and 150 mM with their corresponding EC 4.0, 8.2 and 10.6 dSm(-1) respectively. Nitrate reductase (NR) activity significantly reduced under stress at the reproductive (i.e. post anthesis) stage but was maintained higher in 1.0 mM SA treated plants upto the level of 100 mM NaCl. In addition to NR, membrane stability index (MSI) also decreased significantly under salinity stress. In DDR 61 MSI was found to be more as compared to HUDP 15. On the other hand, activities of antioxidant enzymes superoxide dismutase (SOD), ascorbate peroxidase (APX) and catalase (CAT) were up-regulated by salinity stress and further enhanced remarkably by 1.0 mM SA treatment. DDR 61 genotype was found to be more responsive to SA application as compared to HUDP 15. Salt stress was found to have more damaging effects during the pre-anthesis phase than the post-anthesis phase of development. Hence, results signify the role of SA in protecting NR metabolic activity along with regulating salinity response of plants.
机译:通过在盐分胁迫条件下通过最佳浓度的水杨酸(SA)@ 1.0 mM的种子硬化来改善两种豌豆基因型(DDR 61和HUDP 15)的抗氧化系统并保护其硝酸还原酶(NR)活性。盐度分别由NaCl @ 50,100和150 mM加上其相应的EC 4.0、8.2和10.6 dSm(-1)施加。硝酸盐还原酶(NR)活性在生殖(即花后)阶段在胁迫下显着降低,但在1.0 mM SA处理的植物中维持较高水平,直至100 mM NaCl的水平。除了NR,在盐胁迫下膜稳定性指数(MSI)也显着降低。在DDR 61中,与HUDP 15相比,MSI的含量更高。另一方面,盐分胁迫上调了抗氧化酶超氧化物歧化酶(SOD),抗坏血酸过氧化物酶(APX)和过氧化氢酶(CAT)的活性,并进一步增强了该活性。通过1.0 mM SA处理显着。与HUDP 15相比,发现DDR 61基因型对SA的应用更具响应性。发现盐胁迫在花前期阶段比花后阶段更具有破坏作用。因此,结果表明SA在保护NR代谢活性以及调节植物盐度反应中的作用。

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