Phethean P D, Jervis L, Hallaway M
Biochem J. 1968 Jun;108(1):25-31. doi: 10.1042/bj1080025.
A method for isolating extensively purified cell walls from higher plants is described; the preparations contain no detectable chloroplast or nuclear material and the protein content (2-5% of the dry wt. of walls) indicates that there is little contamination with cytoplasm. Incubation of purified cell walls with 0.3n-potassium hydroxide for 17hr. at 37 degrees liberates ribonucleotides, which can be purified by adsorption on charcoal and by ion-exchange chromatography. Ribonucleotides are also liberated by incubating the walls with ribonuclease, but not with deoxyribonuclease. The RNA content varies from 0.5 to 6mg./g. dry wt. of walls, depending on the nature and age of the tissue, and at 3mg./g. dry wt. of walls accounts for about 7% of the total RNA of the tissue. Less than 0.2% of the RNA of the walls is due to the presence of bacteria in the preparation. The base composition of the cell-wall RNA is identical with that of ribosomal RNA.
本文描述了一种从高等植物中分离出高度纯化细胞壁的方法;制备物中未检测到叶绿体或核物质,蛋白质含量(占细胞壁干重的2 - 5%)表明几乎没有细胞质污染。将纯化的细胞壁与0.3N氢氧化钾在37℃下孵育17小时,可释放出核糖核苷酸,这些核糖核苷酸可通过吸附在木炭上和离子交换色谱法进行纯化。用核糖核酸酶孵育细胞壁也可释放核糖核苷酸,但用脱氧核糖核酸酶则不能。RNA含量因组织的性质和年龄而异,在细胞壁干重为3mg/g时,占组织总RNA的约7%。细胞壁RNA中不到0.2%是由于制备物中存在细菌所致。细胞壁RNA的碱基组成与核糖体RNA的碱基组成相同。