Centre de Physiologie Végétale de l'Université Paul Sabatier, Unité Associée au Centre National de la Recherche Scientifique, No. 241, 118 Route de Narbonne, F-31062 Toulouse, Cédex, France.
Plant Physiol. 1985 Dec;79(4):1090-3. doi: 10.1104/pp.79.4.1090.
Acer pseudoplatanus cell suspension cultures were used to examine the ability of vacuoles isolated from protoplasts to hydrolyze their endogenous proteins. Total cell proteins were labeled by addition of [(3)H]leucine to the culture medium. After preparation of the protoplasts, vacuoles were isolated and were shown to be essentially free from other cellular components. Up to 30% of the [(3)H]leucine-labeled newly synthesized proteins were recovered in the vacuoles. When incubated for 6 hours at 20 degrees C, the vacuoles degraded half of these proteins. The protein breakdown was temperature and pH dependent. Analysis by electrophoresis, in denaturing polyacrylamide gels, revealed that most of the vacuolar proteins were degraded. However, some vacuolar proteins were unaffected during a 6-hour incubation period. The results indicate that vacuoles are able to acquire and degrade intracellular proteins.
悬铃木细胞悬浮培养物被用来研究从原生质体分离的液泡是否能够水解其内源蛋白质。在培养基中添加 [(3)H]亮氨酸来标记总细胞蛋白。制备原生质体后,分离液泡,并证明其基本上不含其他细胞成分。多达 30%的 [(3)H]亮氨酸标记的新合成蛋白质被回收在液泡中。当在 20°C 下孵育 6 小时时,液泡降解了其中一半的蛋白质。蛋白质的降解依赖于温度和 pH 值。在变性聚丙烯酰胺凝胶中的电泳分析表明,大多数液泡蛋白被降解。然而,在 6 小时孵育期间,一些液泡蛋白不受影响。结果表明,液泡能够摄取和降解细胞内蛋白质。