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Development of Enzymes of the Glyoxylate Cycle during Senescence of Pumpkin Cotyledons
Authors:De Bellis  Luigi; Nishimura  Mikio
Institution:1Department of Cell Biology, National Institute for Basic Biology Myodaijicho, Okazaki, 444 Japan
2Dipartimento di Biologia delle Piante Agrarie Viale delle Piagge 23, 56124 Pisa, Italy
Abstract:The presence and activities of isocitrate lyase (EC 4.1.3.1 EC] )and malate synthase (EC 4.1.3.2 EC] ) were studied during senescenceof pumpkin cotyledons (Cucurbita sp. Amakuri Nankin). Afterincubation of detached cotyledons in permanent darkness, theactivities appeared and increased up to the eighth day and thendeclined, while the activities of catalase (EC 1.11.1.6 EC] ), glycolateox-idase (EC 1.1.3.1 EC] ), and hydroxypyruvate reductase (EC 1.1.1.81 EC] )decreased dramatically. After fractionation of cell organellesby sucrose density gradient, we detected isocitrate lyase andmalate synthase activities in peroxisomal fractions. The activityof the two key enzymes of the glyoxylate cycle also increasedduring senescence in vivo and we confirmed the presence of thetwo enzymes in the peroxisomal fractions after sucrose gradientcentrifugation. At every point examined, the level of malatesynthase was demonstrated by immunoblotting. It is concludedthat the development of isocitrate lyase and malate synthaseactivities represents the transition from leaf peroxisomes toglyoxysomes and that such a phenomenon is associated with senescence. (Received January 25, 1991; Accepted March 22, 1991)
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