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Plant Physiology 63:1123-1132 (1979)
© 1979 American Society of Plant Biologists

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Articles

Hydrolytic Enzymes in the Central Vacuole of Plant Cells 1

Thomas Boller2 and Hans Kende

a MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824

The hydrolase content of vacuoles isolated from protoplasts of suspension-cultured tobacco cells, of tulip petals, and of pineapple leaves, and the sedimentation behavior of tobacco tonoplasts were studied. Three precautions were found to be important for the analysis of vacuolar hydrolases and of the tonoplast. (a) Purification of protoplasts in a Ficoll gradient was necessary to remove cell debris which contained contaminating hydrolases adsorbed from the fungal cell-wall-degrading enzyme preparation. (b) Hydrolase activities in the homogenates of the intact cells or the tissue used and of the purified protoplasts had to be compared to verify the absence of contaminating hydrolases in the protoplast preparation. (c) Vacuoles obtained from the protoplasts by an osmotic shock had to be purified from the lysate in a Ficoll gradient. Since the density of the central vacuole approximates that of the protoplasts, about a 10% contamination of the vacuolar preparation by surviving protoplasts could not be eliminated and had to be taken into account when the distribution of enzymes and of radioactivity was calculated.

The intracellular activities of the following acid hydrolases were primarily localized in the vacuole of tobacco cells: {alpha}-mannosidase, {beta}-N-acetylglucosaminidase, {beta}-fructosidase, nuclease, phosphatase, phosphodiesterase. A similar composition of acid hydrolases was found in vacuoles obtained from protoplasts of tulip petals. Proteinase, a hydrolase with low activity in tobacco cells and tulip petals and therefore difficult to localize unequivocally, was found to be vacuolar in pineapple leaves, a tissue containing high levels of this enzyme. Our data support the hypothesis that the central vacuole of higher plant cells has an enzyme composition analogous to that of the animal lysosome.

None of the vacuolar enzymes investigated was found to be bound to the tonoplast. When vacuoles were isolated from cells labeled with radioactive choline, the vacuolar membrane was found to contain radioactivity. On sucrose gradients, the label incorporated into tonoplasts banded around a density of 1.10 grams per cubic centimeter (24% sucrose, w/w).


2 Present address: Botanisches Institut der Universität Basel, Schönbeinstr. 6, CH-4056 Basel, Switzerland.

1 This research was supported by United States Department of Energy Contract EY-76-C-02-1338, by National Science Foundation Grant PCM 77-08522 to H. K., and by a fellowship of the Swiss National Science Foundation to T. B.




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