60 research outputs found

    Function of Lysosomes and Lysosomal Enzymes in the Senescing Corolla of the Morning Glory (Ipomoea purpurea)

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    The rapid senescence of the Ipomoea corolla is characterized by the breakdown of protein and nucleic acids. At the onset of wilting the activities of deoxyribonuclease (DNase), ribonuclease (RNase), and β-glucosidase are increased dramatically, while other hydrolytic activities such as the actions of protease, aminopeptidase, α-glucosidase, phosphatase, esterase, and α-amylase are only slightly changed. Isolated corolla discs show a course of senescence similar to that of the intact organ. When floating on solutions of cycloheximide the activities of DNase, RNase, and β-glucosidase do not increase. Actinomycin D inhibits the increase in RNase activity. It is concluded that protein synthesis is a prerequisite for the changes in these enzyme activities in the senescing corolla. The function of the lysosomal compartment in the process of senescence is illustrated by electron micrographs showing the autophagic activity of vacuoles. The last phase of senescence is characterized by the breakdown of the tonoplast and complete digestion of the cytoplasmic constituents in the autolysing cell

    Relationship between petal abscission and programmed cell death in Prunus yedoensis and Delphinium belladonna

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    Depending on the species, the end of flower life span is characterized by petal wilting or by abscission of petals that are still fully turgid. Wilting at the end of petal life is due to programmed cell death (PCD). It is not known whether the abscission of turgid petals is preceded by PCD. We studied some parameters that indicate PCD: chromatin condensation, a decrease in nuclear diameter, DNA fragmentation, and DNA content per nucleus, using Prunus yedoensis and Delphiniumbelladonna which both show abscission of turgid petals at the end of floral life. No DNA degradation, no chromatin condensation, and no change in nuclear volume was observed in P. yedoensis petals, prior to abscission. In abscising D.belladonna petals, in contrast, considerable DNA degradation was found, chromatin was condensed and the nuclear volume considerably reduced. Following abscission, the nuclear area in both species drastically increased, and the chromatin became unevenly distributed. Similar chromatin changes were observed after dehydration (24 h at 60°C) of petals severed at the time of flower opening, and in dehydrated petals of Ipomoea nil and Petunia hybrida, severed at the time of flower opening. In these flowers the petal life span is terminated by wilting rather than abscission. It is concluded that the abscission of turgid petals in D. belladonna was preceded by a number of PCD indicators, whereas no such evidence for PCD was found at the time of P. yedoensis petal abscission. Dehydration of the petal cells, after abscission, was associated with a remarkable nuclear morphology which was also found in younger petals subjected to dehydration. This nuclear morphology has apparently not been described previously, for any organism
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