The Roles of Reactive Oxygen Metabolism in Drought: Not So Cut and Dried[1][C][W]
By G. Noctor, Amna Mhamdi, Christine H. Foyer. Plant Physiology, 2014
642 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/4b96638b3539a5b9d3eb6cf2ad71a4b6a0965d3e
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Citations in the corpus
- Hydrogen peroxide priming modulates abiotic oxidative stress tolerance: insights from ROS detoxification and scavenging (2015, background): “…long life span and the small size of H2O2 molecules permit them to traverse through cellular membranes to different cellular compartments, facilitating signaling functions, including retrograde signaling (Apel and Hirt, 2004; Bienert et al., 2006; Maruta et al., 2012; Noctor et al., 2014).”
- Plant Growth Promoting Rhizobacterial Mitigation of Drought Stress in Crop Plants: Implications for Sustainable Agriculture (2019, background): “Excessive reduction in the electron transport causes the production of singlet oxygen ((1)O2) in Photosystem II (PSII), which elevates H2O2 production in the peroxisome while O2− and H2O2 or (1)O2 are produced in the chloroplast due to photorespiration [13,15,16].”
- Regulation of Ascorbate-Glutathione Pathway in Mitigating Oxidative Damage in Plants under Abiotic Stress (2019, background): “Ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), dehydroascorbate reductase (DHAR), glutathione reductase (GR), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), glutathione S-transferase (GST), and peroxiredoxin (PRX) are well known enzymatic antioxidant c”
- Ascorbic Acid-A Potential Oxidant Scavenger and Its Role in Plant Development and Abiotic Stress Tolerance (2017, methodology): “Nonetheless, APXs are often characterized primarily due to their subcellular localization (Shigeoka et al., 2002; Caverzan et al., 2012; Noctor et al., 2014; Ben Rejeb et al., 2014).”
- ROS Regulation During Abiotic Stress Responses in Crop Plants (2015, methodology): “…(GSH) regenerating cycle involved MDHAR, DHAR, and GR. GPX, GST, and PRX reduce H2O2 and organic hydroperoxides through ascorbate-independent thiol-mediated pathways using GSH, thioredoxin (TRX) or glutaredoxin (GRX) as nucleophile (Dietz et al., 2006; Meyer et al., 2012; Noctor et al., 2014).”
- Antioxidants and Antioxidant Enzymes in Higher Plants (2018, background): “However, in recent years, ROS/RNS involvement has been reported to activate the stress response including antioxidant pathways (Suzuki et al. 2012; Noctor et al. 2014).”
- Gene expression and activity of antioxidant enzymes in barley (Hordeum vulgare L.) under controlled severe drought (2015, background): “Furthermore, drought treatment that is based on water deficit in the soil stimulates distinct responses compared with that based on the use of osmoticum (Noctor et al. 2014).”
- Regulation of Photosynthesis during Abiotic Stress-Induced Photoinhibition. (2015, background): “Intracellular generation of 76 H2O2, the most stable ROS, has always been associated with chloroplasts but recent studies 77 suggest that peroxisomes may produce more H2O2 than other organelles (Noctor et al., 2014).”
- Effect of drought on growth, photosynthesis and total antioxidant capacity of the saharan plant Oudeneya africana (2020, background): “drought on plants, which may lead to oxidative damage to the photosynthetic apparatus (Noctor et al., 2014; Talbi et al., 2015).”