Boller T, Kende H
MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824.
Plant Physiol. 1979 Jun;63(6):1123-32. doi: 10.1104/pp.63.6.1123.
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).
对从悬浮培养的烟草细胞原生质体、郁金香花瓣和菠萝叶中分离出的液泡的水解酶含量,以及烟草液泡膜的沉降行为进行了研究。发现对于液泡水解酶和液泡膜的分析,有三点注意事项很重要。(a) 在菲可梯度中纯化原生质体,以去除含有从真菌细胞壁降解酶制剂中吸附的污染性水解酶的细胞碎片。(b) 必须比较完整细胞或所用组织匀浆以及纯化原生质体中的水解酶活性,以验证原生质体制备中不存在污染性水解酶。(c) 通过渗透休克从原生质体获得的液泡必须在菲可梯度中从裂解物中纯化。由于中央液泡的密度与原生质体相近,因此无法消除液泡制剂中约10% 的存活原生质体污染,在计算酶和放射性的分布时必须考虑到这一点。以下酸性水解酶的细胞内活性主要定位于烟草细胞的液泡中:α-甘露糖苷酶、β-N-乙酰葡糖胺糖苷酶、β-果糖苷酶、核酸酶、磷酸酶、磷酸二酯酶。从郁金香花瓣原生质体获得的液泡中发现了类似的酸性水解酶组成。蛋白酶在烟草细胞和郁金香花瓣中活性较低,因此难以明确其定位,在含有高水平这种酶的菠萝叶组织中发现其存在于液泡中。我们的数据支持这样的假设,即高等植物细胞的中央液泡具有与动物溶酶体类似的酶组成。所研究的液泡酶均未发现与液泡膜结合。当从用放射性胆碱标记的细胞中分离液泡时,发现液泡膜含有放射性。在蔗糖梯度上,掺入液泡膜的标记物在密度约为每立方厘米1.10克(24% 蔗糖,w/w)处形成条带。