The apoplastic oxidative burst in response to biotic stress in plants: a three-component system.

By G. Bolwell, L. Bindschedler, K. Blee, V. S. Butt, D. Davies, S. Gardner, C. Gerrish, F. Minibayeva. Journal of Experimental Botany, 2002

709 citations recorded by the source corpus.

Subfields: Plant Science

View Paper: https://www.semanticscholar.org/paper/5e9e0015b1f1caac1491f8cb299897d98e00a1d1

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In Plant Science

1. M. Fujita
2. M. A. Hossain
3. S. Bhattacharjee
4. C. Bailly
5. C. Kao
6. Y. Hsu
7. R. Beckett
8. S. Lüthje

Citations in the corpus

• Class III peroxidases in plant defence reactions. (2009, background): “, 2003), although a role for Prxs has been also proposed (Bolwell et al., 2002).”
• Innate immunity in plants and animals: striking similarities and obvious differences (2004, background): “Other plant responses associated with pathogen defense result from allosteric enzyme activation initiating cell wall reinforcement by oxidative cross-linking of cell wall components, apposition of callose and lignins, and production of reactive oxygen intermediates (ROIs) (21, 22, 26, 27).”
• Class III peroxidases and ascorbate metabolism in plants (2004, background): “It has been estimated that chloroplasts dissipate between 3 and 27% of their total electron flow in the univalent reduction of di-oxygen, even under optimal conditions ( Badger, 1985 ).”
• Hydrogen peroxide and nitric oxide as signalling molecules in plants. (2002, background): “Potential sources include NADPH oxidase, cell wall peroxidases, amine oxidase, oxalate oxidase, and flavin-containing oxidases (Fig. 1; Bolwell and Wojtaszek, 1997; Bolwell et al., 2002).”
• The hypersensitive response; the centenary is upon us but how much do we know? (2008, background): “Plant NADPH oxidases could fulfil a similar role in the apoplast, thereby initiating ROS indirectly via alkalinization–responsive peroxidases (Bolwell et al., 2002).”
• Stress response, cell death and signalling: the many faces of reactive oxygen species (2003, background): “The enzymatic sources of ROS are both extracellular and intracellular (Bolwell et al. 1995, Allan and Fluhr 1997, Pellinen et al. 1999, Bolwell et al. 2002).”
• Molecular physiology of aluminum toxicity and tolerance in plants (2007, background): “The enzymatic sources of ROS are both extracellular and intracellular (Bolwell et al., 2002).”
• Roles of reactive oxygen species in interactions between plants and pathogens (2008, background): “Virulent pathogens that avoid or suppress host recognition induce only the transient, first phase of this response (Bolwell et al. 2002).”
• Hydrogen peroxide is involved in methyl jasmonate-induced senescence of rice leaves (2006, background): “Recently, a cell wall peroxidase has been identified in French bean (Bolwell et al. 1998, Blee et al. 2001), and a potentially peroxidase-mediated H2O2 production has been demonstrated in Arabidopsis cultures challenged with a fungal elicitor (Bolwell et al. 2002).”
• Reactive oxygen species: metabolism, oxidative stress, and signal transduction. (2004, background): “Plants also generate ROS by activating various oxidases and peroxidases that produce ROS in response to certain environmental changes (1, 13, 14, 35, 109).”
• Biotic elicitors: a boon for the in-vitro production of plant secondary metabolites (2021, background): “Few elicitors induce alkalization of apoplast which leads to an influx of protons and some elicitors induce acidification of apoplast which leads to efflux of vacuolar protons (Bolwell et al. 2002; Angelova et al. 2006).”