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Plant Physiology 68:1081-1089 (1981)
© 1981 American Society of Plant Biologists

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Vacuole/Extravacuole Distribution of Soluble Protease in Hippeastrum Petal and Triticum Leaf Protoplasts 1

George J. Wagner, Peter Mulready and John Cutt

Biology Department, Upton, New York 11973, Brookhaven National Laboratory, Upton, New York 11973

The subcellular distribution of soluble protease in anthesis-stage, anthocyanin-containing Hippeastrum cv. Dutch Red Hybrid petal protoplasts has been reevaluated and that of Triticum aestivum L. var. Red Coat leaf protoplasts determined using 125I-fibrin as a protease substrate and improved methods for protoplast and vacuole volume estimation. Results indicate that about 20% of the Hippeastrum petal-soluble protease and about 90% of the wheat leaf-soluble protease can be assigned to the vacuole. Protoplast isolation enzyme labeled with 125I has been used to assess the efficiency of removing isolation enzyme from protoplasts by repeated washing and by separation of protoplasts from debris using density centrifugation. Results of these studies suggest that protoplasts prepared by both methods retain low levels of isolation enzyme. However, when protoplasts prepared by either method were lysed with washing medium lacking osmoticum, little isolation enzyme contaminated the lysates.


1 This research was carried out at the Brookhaven National Laboratory under the auspices of the United States Department of Energy.




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K. Wisniewski and B. Zagdanska
Genotype-dependent proteolytic response of spring wheat to water deficiency
J. Exp. Bot., July 1, 2001; 52(360): 1455 - 1463.
[Abstract] [Full Text] [PDF]




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Copyright © 1981 by the American Society of Plant Biologists