2018
DOI: 10.1007/s11738-018-2762-0
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Effects of drought stress on the antioxidant system, osmolytes and secondary metabolites of Saposhnikovia divaricata seedlings

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Cited by 34 publications
(24 citation statements)
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“…Under drought, accumulation of osmolytes like proline and sugars can maintain cell turgor through osmotic adjustments, protect proteins, organelles and membrane from oxidative damage (Krasensky and Jonak 2012). Proline accumulation under water deficit is a good marker of stress tolerance through osmoregulation and ROS scavenging in various stressed plants (Liu et al 2013;Men et al 2018). In the present study, increase in proline content indicates response of plants toward PEG-induced drought.…”
Section: Discussionmentioning
confidence: 61%
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“…Under drought, accumulation of osmolytes like proline and sugars can maintain cell turgor through osmotic adjustments, protect proteins, organelles and membrane from oxidative damage (Krasensky and Jonak 2012). Proline accumulation under water deficit is a good marker of stress tolerance through osmoregulation and ROS scavenging in various stressed plants (Liu et al 2013;Men et al 2018). In the present study, increase in proline content indicates response of plants toward PEG-induced drought.…”
Section: Discussionmentioning
confidence: 61%
“…Drought stress-induced exacerbated ROS generation is well-recognized at cellular level, and increased antioxidant system regulates ROS homeostasis at both the production and consumption levels in plants. Furthermore, droughtinduced overproduction of ROS leads to increase the concentration of MDA through lipid peroxidation (Men et al 2018). Hence, the MDA is suitable marker for membrane lipid peroxidation and its higher level in water-stressed plants is related to excess of ROS (Huang et al 2013;Khan et al 2019).…”
Section: Discussionmentioning
confidence: 99%
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“…For the roots tips, lipid peroxidation via MDA; the production of ROS, such as H 2 O 2 ; the activity of antioxidative enzymes, such as POD and CAT; the content of non-enzymatic antioxidants, such as GSH; and osmotic-adjusting substances, such as PRO, were determined using Comin Biochemical Test Kits (MDA-2-Y, H 2 O 2 -2-Y, POD-2-Y, CAT-2-Y, GSH-2-W and PRO-2-Y, respectively; Cominbio, Suzhou, China) in accordance with the manufacturer’s instructions. In brief, the MDA content was assayed based on the thiobarbituric acid-reactive substance assay according to the method of Castrejón and Yatsimirsky (1997) [73]; the H 2 O 2 content was determined by monitoring the absorbance of titanium-peroxide complex at 415 nm according to the method described by Men et al (2018) [74]; the POD activity was assayed based on the detection of the absorbance of the product at 470 nm in the reaction system according to the method of Toivonen and Sweeney (1998) [75]; the CAT activity was determined by measuring the rate of decomposition of H 2 O 2 (ε = 39.4 mM −1 cm −1 ) at 240 nm as described by Men et al (2018) [74]; the GSH content was measured by detecting the absorbance of 5,5′-Dithiobis-(2-nitrobenzoic acid)-GSH complex at 412 nm according to the method of Men et al (2018) [74] ; and the PRO content was measured using the acid ninhydrin method described by Vieira et al (2010) [76].…”
Section: Methodsmentioning
confidence: 99%