Michigan State University-Department of Energy Plant Research Laboratory, East Lansing, Michigan 48824-1312.
Plant Physiol. 1991 Dec;97(4):1487-93. doi: 10.1104/pp.97.4.1487.
The profile of major ribonuclease (RNase) activities of Arabidopsis thaliana has been identified and characterized using a substrate-based gel assay. Following sodium dodecyl sulfatepolyacrylamide gel electrophoresis, as many as 16 RNases, varying in size from 9 to 41 kilodaltons can be detected. Most of the RNase activities exhibit a pH optimum of about 6.5; however, the activity of a 22.6-kilodalton RNase is greatly enhanced at low pH. A number of the RNases in the 30- to 41-kilodalton range are sensitive to ethylenediaminetetraacetic acid, and their activities are enhanced by the presence of a low concentration of zinc during renaturation. At least one RNase appears to comigrate with a major DNase activity. The differential accumulation of several RNases in stems versus leaves indicates that some RNases are controlled in an organ-specific manner in A. thaliana.
利用基于底物的凝胶分析,鉴定并描述了拟南芥中主要核糖核酸酶(RNase)的活性分布。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后,可检测到多达 16 种大小在 9 至 41 千道尔顿之间的 RNase。大多数 RNase 活性的 pH 最佳值约为 6.5;然而,22.6 千道尔顿 RNase 的活性在低 pH 值下大大增强。30 至 41 千道尔顿范围内的一些 RNase 对乙二胺四乙酸敏感,并且在复性过程中存在低浓度锌时,其活性增强。至少有一种 RNase 似乎与主要的 DNA 酶活性共迁移。茎与叶中几种 RNase 的差异积累表明,一些 RNase 在拟南芥中以器官特异性方式受到调控。