Laboratory of Plant Physiology and Biochemistry, Department of Botany, University of Delhi, Delhi-11007, India.
Laboratory of Plant Physiology and Biochemistry, Department of Botany, University of Delhi, Delhi-11007, India; and Corresponding author. Email:
Funct Plant Biol. 2021 May;48(6):573-587. doi: 10.1071/FP20334.
Among abiotic stresses, salt stress is a major threat to crop production all over the world. Present work demonstrates the profuse accumulation of Na+ in 2-day-old, dark-grown sunflower (Helianthus annuus L.) seedlings roots in response to salt stress (NaCl). The pattern of K+ accumulation in response to salt stress is similar to that of Na+ but on relatively lower scale. Application of nitric oxide (NO) donor (DETA) scales down Na+ accumulation in salt-stressed seedlings. The impact of NO donor on K+ accumulation is, however, different in control and salt-stressed seedling roots. In control seedlings, it enhances K+ accumulation, whereas, it gets reduced in salt-stressed seedlings. Specialised channels called 'aquaporins' (AQPs) play a major role maintaining the water status and transport across plant parts under salt-stress. Thus, accumulation of plasma-membrane intrinsic proteins (PIPs) and tonoplast-intrinsic proteins (TIPs), localised on plasma-membrane and vacuolar-membrane, respectively was undertaken in 2-day-old, dark-grown seedling roots. Salt stress increased the abundance of these isoforms, whereas, NO application resulted in decreased accumulation of PIP2 and TIP1. PIP1 and TIP2 isoforms remained undetectable. Present work thus, puts forward a correlation between AQP expression and ions (Na+ and K+) homeostasis in response to salt stress and NO.
在非生物胁迫中,盐胁迫是全世界作物生产的主要威胁。本工作表明,在盐胁迫(NaCl)下,2 天大、黑暗生长的向日葵(Helianthus annuus L.)幼苗根中大量积累 Na+。对盐胁迫的 K+积累模式与 Na+相似,但规模相对较小。一氧化氮(NO)供体(DETA)的应用减少了盐胁迫幼苗中 Na+的积累。然而,NO 供体对对照和盐胁迫幼苗根中 K+积累的影响不同。在对照幼苗中,它增强了 K+的积累,而在盐胁迫幼苗中则减少了。称为“水通道蛋白”(AQPs)的专门通道在盐胁迫下维持植物部分的水状态和运输中起着重要作用。因此,在 2 天大、黑暗生长的幼苗根中,对质膜内在蛋白(PIPs)和液泡膜内在蛋白(TIPs)进行了研究,它们分别位于质膜和液泡膜上。盐胁迫增加了这些同工型的丰度,而 NO 处理导致 PIP2 和 TIP1 的积累减少。PIP1 和 TIP2 同工型仍无法检测到。因此,本工作提出了在盐胁迫和 NO 响应中,AQP 表达与离子(Na+和 K+)稳态之间的相关性。