Performing the paradoxical: how plant peroxidases modify the cell wall.
By F. Passardi, C. Penel, Christophe Dunand. Trends in Plant Science, 2004
909 citations recorded by the source corpus.
Since their appearance in the first land plants, genes encoding class III peroxidases have been duplicated many times during evolution and now compose a large multigene family. The reason for these many genes is elusive, and we are still searching for the specific function of every member of the family. Nevertheless, our current understanding implicates peroxidases as key players during the whole life cycle of a plant, and particularly in cell wall modifications, in roles that can be antagonistic depending on the developmental stage. This diversity of functions derives in part from two possible catalytic cycles of peroxidases involving the consumption or release of H(2)O(2) and reactive oxygen species (e.g. O(2)(-), H(2)O(2), OH).
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/5b3263b24500b2733b4b2c5f95dbb9bcdde31424
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Citations in the corpus
- Peroxidases have more functions than a Swiss army knife (2005, background): “1) (Liszkay et al. 2003; Passardi et al. 2004b).”
- A Comprehensive Review on Function and Application of PlantPeroxidases (2017, background): “Thus, they are involved in wide range of physiological processes such as cell wall metabolism [20], lignification [21], suberization [22], auxins metabolism [23], wound healing [24], reactive oxygen species (ROS) and reactive nitrogen species (RNS) metabolism [25,26], fruit growth and ripening [27] ”
- Hydrogen Peroxide: A Signaling Messenger (2006, neutral): “Plant cells in particular perform numerous oxidative biosynthetic processes in building and maintaining their cell walls, including the formation of diferulic linkages and the cross-linking of hydroxyproline-rich proteins named extensions, possibly through isodityrosine cross-links (160).”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “There is evidence that apoplastic ROS can regulate cell expansion, and that these activities are regulated in a spatial manner (Fry, 2004; Passardi et al., 2004).”
- Class III peroxidases in plant defence reactions. (2009, background): “Pectins would act as an anchor for Prxs, which would then crosslink extensins to create a dense and solid network in the host plant cell wall, with the aim of limiting pathogen colonization (Passardi et al., 2004b).”
- Functional leaf traits, plant communities and acclimation processes in relation to oxidative stress in trees: a critical overview (2008, background): “Resistance derives from the very nature of the reactions triggered in the subcellular region by oxidative stresses, and especially by peroxidases, favouring the formation of compounds improving mechanical and defence performance, such as lignins and phenolic compounds (Passardi et al., 2004, 2005).”
- The cell biology of lignification in higher plants. (2015, background): “…of peroxidases was further supported as they can form rigid cross-links between lignin, hemicelluloses and extensins in the secondary cell wall (Mäder et al., 1977, 1980; Lamport, 1986; Lagrimini et al., 1987; Passardi et al., 2004) once the initial lignin polymers/oligomers are made by laccases.”
- Reactive oxygen species as signals that modulate plant stress responses and programmed cell death (2006, background): “Involved in lignin biosynthesis, hormone metabolism, cross-linking of cell wall polymers, pathogen defense, plant development, senescence and symbiotic interactions cw, cyt, mit, vac (21, 24)”
- Plant peroxidases: biomarkers of metallic stress (2011, background): “Multigene family From the appearance of the first class III peroxidases, just before the emergence of terrestrial plants, to the emergence of angiosperms, the number of gene copies has increased greatly (Passardi et al. 2004).”