Nitric oxide stimulates seed germination and counteracts the inhibitory effect of heavy metals and salinity on root growth of Lupinus luteus

By M. Kopyra, E. Gwóźdź. 2003

448 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/ac1e6193ca6172cb00dddb3fedf5ab5b290e5680

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In Plant Science

Citations in the corpus

Protective roles of nitric oxide on germination and antioxidant metabolism in wheat seeds under copper stress (2007, background): “For example, Kopyra and Gwóźdź (2003) provided evidence that NO could stimulate seed germination and counteract the inhibitory effect of heavy metals and salinity on root growth of Lupinus liteus.”
Mechanism of Salinity Tolerance in Plants: Physiological, Biochemical, and Molecular Characterization (2014, background): “Kopyra and Gwóźdź [148] further showed that the pretreatment of L. luteus seedlings for 24 h with 10 𝜇M SNP resulted in efficient reduction of the detrimental effect of the abiotic stressors on root growth and morphology.”
The cell wall in plant cell response to trace metals: polysaccharide remodeling and its role in defense strategy (2010, background): “It must be noted that these effects were triggered by the additional exposition of O. sativa to exogenous NO, one of the main stress-signaling molecules (e.g., Wojtaszek 2000; Kopyra and Gwo´z´dz´ 2003; Arasimowicz and Floryszak-Wieczorek 2007).”
Variation in response to heavy metals during vegetative growth in Dorycnium pentaphyllum Scop. (2009, background): “Kopyra and Gwozdz (2003) recently demonstrated that nitric oxide, which may be overproduced in response to heavy metals, could be involved in the hastening of germination through the stimulation of enzyme activities involved in the management of oxidative stress.”
Metals and seeds: Biochemical and molecular implications and their significance for seed germination (2011, background): “Lupinus luteus (Kopyra and Gwozdz, 2003) PbCl2 1500 No effect Lr reduced by ≥300 M CdCl2 500 No effect Lr reduced by ≥500 M”
Nitric oxide, stomatal closure, and abiotic stress. (2007, background): “In Arabidopsis guard cells this is likely to arise from superoxide generated by the isoforms of NAD(P)H oxidase encoded by the genes AtrbohD and AtrbohF (Kwak et al., 2003; Desikan et al., 2004b; She et al., 2004).”
Genotype-Dependent Effect of Exogenous Nitric Oxide on Cd-induced Changes in Antioxidative Metabolism, Ultrastructure, and Photosynthetic Performance in Barley Seedlings (Hordeum vulgare) (2010, background): “It has been reported that exogenously applied NO can enhance germination or break seed dormancy (Beligni and Lamattina 2000), and when no dormancy breakage is required, greater germination rates have been observed by supplementation with an NO donor (Kopyra and Gwóźdź 2003).”
Drought-Responsive Antioxidant Enzymes in Potato (Solanum tuberosum L.) (2010, background): “2002) and by several classes of peroxidases such as guaiacol peroxidase (GPOX) and ascorbate peroxidase (APX) (Kopyra and Gwóźdź 2003).”
Nitric oxide as a bioactive signalling molecule in plant stress responses (2007, background): “Literature data supply evidence showing that plant response to such stressors as drought, high or low temperature, salinity, heavy metals and oxidative stress, is regulated by NO [7,100– 103].”
Carbon monoxide counteracts the inhibition of seed germination and alleviates oxidative damage caused by salt stress in Oryza sativa (2007, background): “This effect was similar to the report from Kopyra and Gwóźdź [22].”
Antioxidants and Antioxidant Enzymes in Higher Plants (2018, background): “Furthermore, the exogenous application of NO donors reduced oxidative stress and increased the resistance to salinity in plants and germinating seeds (Kopyra and Gwózdz 2003).”