TABLE 1.
Abiotic stress response in relation with JA, Ca2+, and GSH among different plant species.
Stress type | Plant species | JA/GSH/Ca2+ | Response | Growth pattern | Cotyledon number | References | |
MeJA | |||||||
High salt concentration | Pisum sativum (L.) | 10–5 M | Osmoregulation, increased proline content | Annual | Dicot | Fedina and Tsonev, 1997 | |
Glycine max (L.) | 20 and 30 μM | Increase in growth and proline content | Annual | Dicot | Yoon et al., 2009 | ||
Arabidopsis thaliana (L.) | 5 and 10 μM | Compliments lox3 mutant rescues salt stress | Annual | Dicot | Ding H. et al., 2016 | ||
Triticum aestivum (L.) | 0.1 μM | Increases cytokinin production and plant growth | Annual | Monocot | Avalbaev et al., 2016 | ||
Solanum lycopersicum (L.) | 10, 20, 30, 40, 50, and 60 μM | Increase in levels of osmo-protectants and enzymatic antioxidants | Annual | Dicot | Manan et al., 2016 | ||
Brassica napus (L.) | 100 μM | Increases relative water content, soluble sugar, photosynthesis | Annual | Dicot | Ahmadi et al., 2018 | ||
JA | |||||||
Pisum sativum (L.) | 10–5 M | Decreased activity of sodium and chloride ions, increased endogenous level of proline | Annual | Dicot | Velitchkova and Fedina, 1998 | ||
Oryza sativa (L.) | 30 μM | Increases ion uptake, growth, ABA levels | Annual | Monocot | Kang et al., 2005 | ||
Hordeum vulgare (L.) | 12 μM | Induction of genes having role in imparting salt tolerance | Annual | Monocot | Walia et al., 2007 | ||
Brassica napus (L.) | 10–6, 10–9, and 10–12 M | Sugar accumulation | Annual | Dicot | Kaur et al., 2013 | ||
Triticum aestivum (L.) | 2 mM | Increase in concentration of GSH, enhanced activity of SOD, CAT, APX | Annual | Monocot | Qiu et al., 2014 | ||
GSH | |||||||
Oryza sativa (L.) | 2 mM | Positive influence on yield contributing traits | Annual | Monocot | Wang et al., 2014 | ||
Arabidopsis thaliana (L.) | 400 μM | Abscisic acid, auxin and jasmonic acid biosynthesis | Annual | Dicot | Cheng et al., 2015 | ||
Vigna radiata (L.) | 1 mM | Activation of glyoxalase system and improved antioxidant system | Annual | Dicot | Nahar et al., 2015b | ||
Solanum lycopersicum (L.) | 5 mM | Increased GSH biosynthesis, improved activity of SOD, CAT, POD | Annual | Dicot | Zhou et al., 2017 | ||
Glycine max (L.) | 2 mM | Improved stress tolerance and yield attributes | Annual | Dicot | Akram et al., 2017 | ||
Ca2+ | |||||||
Solanum lycopersicum (L.) | 5 and 10 mM | Increased growth, physiology and fruit production | Annual | Dicot | Parvin et al., 2015 | ||
Glycine max (L.) | 6 mM | Positive effect on growth and metabolic activities. | Annual | Dicot | Yin et al., 2015 | ||
Oryza sativa (L.) | 3 and 5 mM | Elevated antioxidant enzyme levels | Annual | Monocot | Tahjib-Ul-Arif et al., 2018 | ||
Lead | JA | ||||||
Heavy metal stresses | Wolffia arrhiza (L.) | 0.1 μM | Preventing Pb accumulation by restoring plant growth and primary metabolite level | Perennial | Monocot | Piotrowska et al., 2009 | |
Solanum lycopersicum (L.) | 0.1, 1, and 100 μM | Increase osmolytes concentration and ascorbate glutathione cycle | Annual | Dicot | Bali et al., 2018 | ||
GSH | |||||||
Gossypium sp. (L.) | 50 μM | Stabilized ultra-structure and increased antioxidant activity | Perennial | Dicot | Khan M. et al., 2016 | ||
Triticum aestivum (L.) | 1 mM | Enhancement of enzymatic and non-enzymatic antioxidant activities and improved seedling growth | Annual | Monocot | Hasanuzzaman et al., 2018 | ||
Cadmium | JA | ||||||
Glycine max (L.) | 20 μM | Increased antioxidant response | Annual | Dicot | Noriega et al., 2012 | ||
Vicia faba (L.) | 0.01 mM | Restoration of growth and pigment system | Annual | Dicot | Ahmad et al., 2017 | ||
Brassica napus (L.) | 25 μM | Osmolytes and antioxidant activity increased | Annual | Dicot | Ali et al., 2018 | ||
MeJA | |||||||
Oryza sativa (L.) | 5 μM | GSH homeostasis, JA biosynthesis | Annual | Monocot | Singh and Shah, 2014 | ||
Arabidopsis thaliana (L.) | 0.01 μM | Suppression of genes involved in Cd uptake | Annual | Dicot | Lei et al., 2020 | ||
GSH | |||||||
Hordeum vulgare (L.) | 20 mg/L | Improved photosynthesis | Annual | Monocot | Chen et al., 2010 | ||
Oryza sativa (L.) | 50 μM | Enhanced photosynthetic performance | Annual | Monocot | Cai et al., 2011a | ||
Gossypium sp. (L.) | 50 μM | Reverses stressful effects, leaf ultra-morphology revived | Perennial | Monocot | Daud et al., 2016 | ||
Populus sp. (L.) | 100 μM | Increased Cd detoxifying gene transcript | Perennial | Monocot | Ding et al., 2017 | ||
Ca2+ | |||||||
Vicia faba (L.) | 2% | Antioxidant enzyme up regulation | Annual | Dicot | Siddiqui et al., 2012 | ||
Brassica juncea (L.) | 50 mM | Improved photosynthesis | Annual | Dicot | Ahmad et al., 2015 | ||
Arabidopsis thaliana (L.) | 3 mM | Alleviated the inhibition of Cd on the root growth | Annual | Dicot | Li P. et al., 2016 | ||
Sesamum indicum (L.) | 50 mM | Improved growth and proline levels | Annual | Dicot | Abd-Allah et al., 2017 | ||
Copper | JA | ||||||
Oryza sativa (L.) | 0.5 mM | Phytoalexin production | Annual | Monocot | Rakwal et al., 1996 | ||
Cajanus cajan (L.) | 1 μM, 1 nM, | Osmolytes and antioxidant enzyme increased | Perennial | Dicot | Poonam et al., 2013 | ||
Triticum Aestivum (L.) | 5 mM | Increased transcript of glutathione–s- transferase | Annual | Monocot | Li et al., 2013 | ||
MeJA | |||||||
Phaseolus coccineus (L.) | 10–5 M | Promoted plant growth and development | Perennial | Dicot | Hanaka et al., 2015 | ||
GSH | |||||||
Triticum aestivum (L.) | 2.5 mM/L | Accumulation of nitrogen, sulfur, and phosphorous | Annual | Monocot | Peng et al., 2012 | ||
Glycine Max (L.) | 0.16 and 0.32 Mm/L | Enhances amylase activity | Annual | Dicot | Chen, 2012 | ||
Oryza Sativa (L.) | 100 mg/L | Increased germination rate and vigor index | Annual | Monocot | Mostofa et al., 2015 | ||
Ca2+ | |||||||
Drought | JA | ||||||
Water stress | Glycine Max (L.) | 4.5 and 9 mM/L | Maintenance of membrane integrity | Annual | Dicot | Chen et al., 2008 | |
Vigna radiata (L.) | 5 mM | Solution improved the growth of Cu-treated seedling and lowering the concentration of Polyamines putrescine and increased concentrations of spermine and spermidine in epicotyl of plants | Annual | Dicot | Shen et al., 1998 | ||
Brassica sp. (L.) | 0.5 mM | Increase in physiological, antioxidant and glyoxalase system activities | Annual | Dicot | Alam et al., 2014 | ||
Allium cepa (L.) | 25, 50, and 100 μM | Pigment and compatible solute enhancement | Annual | Monocot | Ahmad and Murali, 2015 | ||
Beta vulgaris (L.) | 5 and 10 μM | Increased germination rate | Annual | Dicot | Ghafari and Tadayon, 2019 | ||
MeJA | |||||||
Brassica oleracea (L.) | 10 μM | Increased Net photosynthetic rate and antioxidant machinery activation | Annual | Dicot | Wu et al., 2012 | ||
Triticum aestivum (L.) | 0.25 μM | Water status and antioxidant capacity increased | Annual | Monocot | Ma et al., 2014 | ||
Satureja hortensis (L.) | 75, 150, and 225 μM | Improved many characteristics of plant like growth, water content, proline level, antioxidant activity | Annual | Dicot | Miranshahi and Sayyari, 2016 | ||
GSH | |||||||
Arabidopsis thaliana (L.) | 400 μM | Changes at translational level of numerous hormones | Annual | Dicot | Cheng et al., 2015 | ||
Vigna radiata (L.) | 1 mM | Improved their antioxidant components under drought stress | Annual | Dicot | Nahar et al., 2015a | ||
Ca2+ | |||||||
Zoysia japonica (L.) | 5 and 10 mM | Improved photosynthesis, growth and antioxidant response | Perennial | Monocot | Xu et al., 2013 | ||
Zea mays (L.) | 5 mg/L | Improved photosynthesis, growth and soluble sugar content | Annual | Monocot | Naeem et al., 2018 | ||
Nicotiana tabacum (L.) | 10 mM/L | Stabilization of gaseous exchange and photosynthetic organelles | Annual | Dicot | Hu et al., 2018 | ||
Flooding | JA | ||||||
Citrus spp. (L.) | 1 mM | Increase in abscisic acid levels | Perennial | Dicot | de Ollas et al., 2013 | ||
Ca2+ | |||||||
Zea mays (L.) | 0.75% (W/V) | Regulates the cell wall integrity and mitigates effect of oxidative stress during flood stress conditions | Annual | Monocot | Porto et al., 2013 | ||
Glycine max (L.) | 50 mM | Increase the root elongation and inhibited the cell death of root tip of under flood stress | Annual | Dicot | Oh et al., 2014 | ||
JA | |||||||
Ozone stress | Capsicum annuum (L.) | 10 mM | Regulates osmotic and antioxidant metabolism | Annual | Dicot | Yang et al., 2016 | |
Arabidopsis thaliana (L.) | 1.4 μM | Inhibited cell death and lesion containment | Annual | Dicot | Overmyer et al., 2000 | ||
Arabidopsis thaliana (L.) (JA insensitive mutants) | 10 μM | Extremely susceptible to ozone | Annual | Dicot | Kanna et al., 2004 | ||
GSH | |||||||
Transgenic Nicotiana tabacum (L.) | Overexpression of glutathione synthetase in plastid | Ozone tolerance developed | Annual | Dicot | Wellburn et al., 1998 | ||
Populus sp. (L.) | Overexpression of Glutathione reductase | Ozone tolerance developed | Perennial | Monocot | Foyer et al., 1995 | ||
Heat | JA | ||||||
Temperature stress | Vitis sp (L.) seedling | 50 μM/L | Thermotolerance | Perennial | Dicot | Chen et al., 2006 | |
Ca2+ | |||||||
Solanum lycopersicum (L.) | 1 Mm | Operating efficiency of photosystem II increased | Annual | Dicot | Sakhonwasee and Phingkasan, 2017 | ||
Nicotiana tabacum (L.) | 20 Mm | Improved stomatal conductance and thermostablity | Annual | Dicot | Tan et al., 2011 | ||
Cold | JA | ||||||
Prunus persica (L.) | 0.1 Mm/L | Maintenance of fruit quality | Perennial | Dicot | Meng et al., 2009 | ||
MeJA | |||||||
Cucumis sativus (L.) | 100 μM | Enhances chilling tolerance by regulating antioxidant enzymes | Annual | Dicot | Li et al., 2012 | ||
Arabidopsis thaliana (L.) | 30 μM | Induced freezing tolerance | Annual | Dicot | Hu et al., 2013 | ||
Eriobotrya japonica (L.) | 10 μM | Alleviates the chilling injury in the fruits of plants | Perennial | Dicot | Cai et al., 2011b | ||
Ca2+ | |||||||
Solanum lycopersicum (L.) | 27 mM | Improvement carbon fixation, electron transport, etc. | Annual | Dicot | Zhang G. et al., 2014 | ||
Cynodon dactylon (L.) | 1, 5, 10, and 20 mM | Antioxidant activation and metabolic homeostasis | Perennial | Monocot | Shi et al., 2014 | ||
GSH | |||||||
Eriobotrya japonica (L.) | 50, 100, and 300 mg/L | Increase in membrane fluidity and decrease in lipid peroxidation | Perennial | Dicot | Wu et al., 2010 |