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Peroxisomal enzyme activities in attached senescing leaves
L Pistelli1, L De Bellis, A Alpi
1Dipartimento di Biologia delle Piante Agrarie, Università di Pisa, Viale delle Piagge 23, I-56124, Pisa, Italy.
Planta
|November 7, 2013
Summary
Plant leaves can exhibit glyoxysomal enzyme activity, particularly during senescence. This study found higher glyoxylate-cycle enzyme activity in dark-treated rice and wheat leaves, suggesting peroxisomes may revert to glyoxysomes.
Area of Science:
- Plant Biology
- Biochemistry
- Molecular Biology
Background:
- Detached leaves can exhibit glyoxysomal enzyme activities when incubated in darkness.
- Glyoxysomes are crucial for lipid metabolism in germinating seedlings.
- The presence and function of glyoxysomal enzymes in senescing leaves are not well understood.
Purpose of the Study:
- To investigate the presence and activity of glyoxylate-cycle enzymes in rice and wheat leaves during senescence.
- To compare glyoxysomal enzyme activity in naturally senescing versus dark-induced senescing leaves.
- To explore the potential role of peroxisomes in leaf senescence.
Main Methods:
- Enzyme assays for isocitrate lyase and malate synthase.
- Measurement of beta-oxidation activities.
- Isolation and characterization of leaf peroxisomes from rice (Oryza sativa L.) and wheat (Triticum durum L.).
- Comparison of enzyme activities in naturally senescing and dark-treated leaves.
Main Results:
- Glyoxylate-cycle enzymes (isocitrate lyase, malate synthase) and beta-oxidation activities were detected in isolated leaf peroxisomes of rice and wheat.
- Dark-induced senescing leaves exhibited 2-4 times higher glyoxylate-cycle enzyme activities compared to naturally senescing leaves.
- These findings indicate the presence of glyoxysomal functions in senescing plant leaves.
Conclusions:
- Leaf peroxisomes in rice and wheat possess glyoxysomal enzyme activities.
- Dark treatment enhances these glyoxysomal activities in senescing leaves.
- The observed glyoxysomal activities during foliar senescence may indicate a reverse transition of peroxisomes into glyoxysomes.
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