Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling.

By G. Noctor, L. Gomez, H. Vanacker, Christine H. Foyer. Journal of Experimental Botany, 2002

903 citations recorded by the source corpus.

Subfields: Biochemistry, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/73a5b66dee4ce6077e7869e419f514aa490d08c2

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Citations in the corpus

Glutathione (2011, positive): “In wheat leaves, γ-ECS activities are strongly associated with chloroplasts (Noctor et al., 2002) and subcellular localization studies of the Arabidopsis protein have convincingly demonstrated that the enzyme is restricted to plastids (Wachter et al., 2005).”
Salinity stress and hydrogen peroxide regulation of antioxidant defense system in Ulva fasciata (2006, background): “Because it has been documented that GSH functions as an antioxidant to react nonenzymatically with singlet oxygen, superoxide and hydroxyl radical and also protects proteins against denaturation caused by the oxidation of protein thiol groups ( Noctor et al. 2002 ), GSH can be non-enzymatically used”
Allicin: Chemistry and Biological Properties (2014, neutral): “Illustration was redrawn from [116].”
Reactive oxygen species: metabolism, oxidative stress, and signal transduction. (2004, background): “In response to chilling, heat shock, pathogen attack, and drought stress, plants increase the activity of GSH biosynthetic enzymes (123, 125) and GSH levels (93).”
Oxidative stress homeostasis in grapevine (Vitis vinifera L.) (2015, background): “…2015 | Volume 3 | Article 20 a major reservoir of non-protein reduced sulfur, and a crucial element in cellular defense and protection, preventing the denaturation of proteins caused by oxidation of thiol groups during stress, reacting chemically with a wide range of ROS (Noctor et al., 2002).”
Glutathione in plants: an integrated overview. (2012, positive): “This observation provides further evidence that GSH can be imported from the cytosol into the plastid, consistent with radiolabelling studies of isolated wheat chloroplasts (Noctor et al. 2002a).”
RESPONSES OF PROLINE, LIPID PEROXIDATION AND ANTIOXIDATIVE ENZYMES IN TWO VARIETIES OF PISUM SATIVUM L. UNDER SALT STRESS (2008, background): “Nonetheless, two molecules of MDHA can also be converted non-enzymatically to MDHA and dehydroascorbate, which in turn is reduced to ascorbate via the dehydroascorbate reductase and GR cycle ( Noctor et al., 2002 ).”
Physiology and molecular biology of stress tolerance in plants (2006, background): “…2002; Noctor et al., 2002), considering the relative specificity of plant RuBisCO and CO 2 19Water Stress and O 2 concentrations in chloroplasts during photosynthesis (Noctor et al., 2002), the rate of energy utilization of photorespiration does not exceed that under non-drought conditions.”