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Plant Physiology 64:1114-1120 (1979)
© 1979 American Society of Plant Biologists

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Articles

Isolation and Partial Characterization of Vacuoles from Tobacco Protoplasts 1

Irvin J. Mettler2 and Robert T. Leonard

a Department of Botany and Plant Sciences, University of California, Riverside, California 92521

Protoplasts from suspension-cultured cells of Nicotiana glutinosa L. were lysed in 0.3 molar sorbitol in 2 millimolar ethylenediaminetetraacetate-tris(hydroxymethyl) aminomethane (pH 7.5) to release intact vacuoles. The vacuoles were purified by centrifugation in a Ficoll step gradient. About 11% of the vacuoles and 13% of the acid phosphatase activity was recovered in the purified vacuole fraction, suggesting that the vacuole is the major site for acid phosphatase in these cells. NADH-cytochrome c reductase, malate dehydrogenase, and cytochrome c oxidase activities were reduced during vacuole purification. The majority of the adenosine 5'-triphosphate (ATP) hydrolytic activity of purified vacuoles was associated with nonspecific acid phosphatase and not with a transport ATPase. As judged by acid phosphatase distribution and electron microscopy, the effective density of vacuoles in a sucrose gradient was low (less than 1.1 grams per cubic centimeter), although an unequivocal estimate of the vacuole or tonoplast density was not possible from the experiments conducted.


2 Present address: Department of Biology, Thimann Laboratories, University of California, Santa Cruz, California 95064.

1 This research was supported by National Science Foundation Grant PCM 7680295.







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Copyright © 1979 by the American Society of Plant Biologists