Yoshida S
The Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan 060.
Plant Physiol. 1979 Aug;64(2):241-6. doi: 10.1104/pp.64.2.241.
The subcellular localization of phospholipase D in homogenates of living bark tissues of the black locust tree (Robinia pseudoacacia L.) was examined and found in both soluble and particulate fractions. At least some of the soluble enzyme was considered to be compartmentalized in vacuoles. Considerable amounts of phospholipase D seemed to be tightly bound on several membranes such as endoplasmic reticulum, tonoplast, and a membrane associated with potassium-stimulated ATPase (pH 6.1). The mitochondrial fraction banding at the 40 to 43% (w/w) sucrose layer, however, had the lowest specific activity. The soluble and the particulate phospholipase D were considered to be similar in nature. It is possible that the particulate enzyme, as a part, may be derived from the coexisting nonvesiculated materials visualized in the electron micrograph of each membrane fraction. An involvement of the soluble or the presumed membrane-bound phospholipase D in phospholipid degradation in vivo during freezing at sublethal temperatures was discussed with special reference to freezing injury of plant cells.
对刺槐(Robinia pseudoacacia L.)活体树皮组织匀浆中磷脂酶D的亚细胞定位进行了检测,发现其存在于可溶性组分和颗粒组分中。至少部分可溶性酶被认为是分隔在液泡中的。相当数量的磷脂酶D似乎紧密结合在几种膜上,如内质网、液泡膜以及与钾刺激的ATP酶(pH 6.1)相关的膜上。然而,在40%至43%(w/w)蔗糖层处的线粒体组分的比活性最低。可溶性磷脂酶D和颗粒性磷脂酶D在性质上被认为是相似的。颗粒性酶作为其中一部分,有可能来源于在每个膜组分的电子显微照片中可见的共存的非囊泡状物质。特别参照植物细胞的冻害,讨论了可溶性或推测的膜结合磷脂酶D在亚致死温度冷冻期间体内磷脂降解中的作用。