Plant Physiology 1991
DOI: 10.1016/b978-0-12-668610-4.50011-2
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Physiological Mechanisms of Plant Senescence

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Cited by 21 publications
(11 citation statements)
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“…It appears that normal enzymatic defenses against activated oxygen diminish during senescence: While the glutathione (GSH) level, activities of catalase and superoxide dismutase decrease, the activity of peroxidase, a scavenger for hydrogen peroxide increases during senescence (Brown et al 1991). In parallel, mRNA levels for gluthatione-S-transferase (Smart et al 1995) and for a metallothionein possibly involved in protection of DNA from oxidative damage by free radicals (Buchanan-Wollaston 1994) increase during leaf senescence.…”
Section: Discussionmentioning
confidence: 98%
“…It appears that normal enzymatic defenses against activated oxygen diminish during senescence: While the glutathione (GSH) level, activities of catalase and superoxide dismutase decrease, the activity of peroxidase, a scavenger for hydrogen peroxide increases during senescence (Brown et al 1991). In parallel, mRNA levels for gluthatione-S-transferase (Smart et al 1995) and for a metallothionein possibly involved in protection of DNA from oxidative damage by free radicals (Buchanan-Wollaston 1994) increase during leaf senescence.…”
Section: Discussionmentioning
confidence: 98%
“…ABA has also been reported to be an important regulator in transporting assimilates to the developing seeds or fruits (Tietz et al 1981;Clifford et al 1986;Brenner and Cheikh 1995;Yang et al 1999). However, the proposal that ABA is involved in regulating both senescence and assimilate mobilization has remained disputable (Jones and Brenner 1987;Nooden 1988; Barratt et al 1989;Ober and Setter 1990;Brown et al 1991;Schussler et al 1991;de Bruijn and Vreugdenhil 1992;Yang et al 2000).…”
Section: Introductionmentioning
confidence: 98%
“…Studies involving a non-yellowing mutant of Festuca pratensis support the idea that the hydrolysis of thylakoid galacto lipids plays an important role in the regulation of leaf senescence (Thomas 1987;Gepstein 1988). Since lipolytic enzymes are found in membranes of non-senescent tissues (Brown et al 1991), the protein synthesis in cytoplasm, which is necessary for chloroplast degradation (Stoddart & Thomas 1982;Cuello et al 1984) might lead to an increase in the activity of these enzymes.…”
Section: Resultsmentioning
confidence: 89%
“…High levels of LNA are esterified in thylakoid galactolipids (Douce & Joyard 1980) and it has been shown that the galactolipid LNA and/or linoleic acid content of thylakoids of chloroplasts in oat leaves increases during senescence in the dark (Dalgarn & Newman 1979). In addition, phospholipid-degrading enzymes in senescing membranes show a preference to degrade molecular species containing polyunsaturated fatty acids (Brown et al 1991) which, if extended to include the galactolipids, would lead to the liberation of LNA. The in vitro release of LNA from thylakoids through thylakoid-associated galactolipase activity has been demonstrated (O'Sullivan et al 1987;O'Sullivan & Dalling 1989),although in our case the quantity of LNA released must be very low since the SDS of the reaction medium inhibits galactolipase activity (O'Sullivan et al 1987).…”
Section: Resultsmentioning
confidence: 99%