Department of Botany, Faculty of Agriculture and Horticulture, Technical University of Munich, D-8050, Freising 12, Germany.
Planta. 1986 Jan;167(1):87-93. doi: 10.1007/BF00446373.
A heterologous in-vitro system is described for the import of the precursor to glyoxysomal malate dehydrogenase from watermelon (Citrullus vulgaris Schrad., cv. Kleckey's Sweet No. 6) cotyledons into glyoxysomes from castor-bean (Ricinus communis L.) endosperm. The 41-kDa precursor is posttranslationally sequestered and correctly processed to the mature 33-kDa subunit by a crude glyoxysomal fraction or by glyoxysomes purified on a sucrose gradient. The import and the cleavage of the extrasequence is not inhibited by metal chelators such as 1,10-phenanthroline and ethylenediaminetetraacetic acid. Uncouplers (carbonylcyanide m-chlorophenylhydrazone), ionophores (valinomycin), or inhibitors of oxidative phosphorylation (oligomycin) and ATP-ADP translocation (carboxyatractyloside) do not interfere, thus indicating the independence of the process of import by the organelle from the energization of the glyoxysomal membrane.
一种异源体外系统被描述用于将西瓜(Citrullus vulgaris Schrad.,cv. Kleckey's Sweet No. 6)子叶中的乙醛酸体苹果酸脱氢酶前体导入到蓖麻(Ricinus communis L.)胚乳中的乙醛酸体中。41kDa 的前体通过粗乙醛酸体部分或通过在蔗糖梯度上纯化的乙醛酸体被翻译后隔离并正确加工成熟为 33kDa 的亚基。金属螯合剂(如 1,10-邻菲啰啉和乙二胺四乙酸)不会抑制外显子序列的导入和切割。解偶联剂(羰基氰化物 m-氯代苯腙)、离子载体(缬氨霉素)或氧化磷酸化抑制剂(寡霉素)和 ATP-ADP 转运抑制剂(羧基三甲氧苄啶)不会干扰,因此表明细胞器的导入过程与乙醛酸体膜的能量供应无关。