The Institute of Low Temperature Science, Hokkaido University, Sapporo 060, Japan.
Plant Physiol. 1986 Jan;80(1):187-95. doi: 10.1104/pp.80.1.187.
Plasma membranes were isolated from both unfrozen and frozen tissues of Jerusalem artichoke tubers (Helianthus tuberosus L.) in high purity utilizing an aqueous two-polymer phase partition system. Although the recovery of the plasma membranes was decreased significantly by freezing of tissues even at the nonlethal temperature (-5 degrees C), the isolated plasma membrane samples were considered to be representative of the plasma membranes in situ. Freezing of the tissues at sublethal temperatures resulted in marked changes in the chemical composition of the plasma membrane. Those are losses of sterols and phosphatidylethanolamine from the plasma membranes, and a change of specific proteins with relatively high molecular weights into low molecular weight peptides. These specific proteins were designated as frost susceptible proteins. The properties of the plasma membrane ATPase seem to be not affected so much by the in vivo freezing of cells. However, inhibition of the plasma membrane ATPase by N,N'-dicyclohexylcarbodiimide (DCCD) was relatively low before and after freezing in vivo at the nonlethal temperature at -5 degrees C, but was markedly enhanced by freezing in vivo at sublethal temperatures below -10 degrees C. From the results, it is assumed either that the enzyme molecule was partially modified, especially at the presumed DCCD binding sites or that the DCCD had become more accessible to the enzyme as a result of increased permeability of the plasma membranes. These observed changes are discussed in connection with the mechanism of cell injury.
采用双水相聚合物系统从未冷冻和冷冻的菊芋块茎(Helianthus tuberosus L.)组织中高度纯离地分离质膜。尽管即使在非致死温度(-5°C)下冷冻组织也会显著降低质膜的回收,但分离的质膜样品被认为是原位质膜的代表。在亚致死温度下冷冻组织会导致质膜的化学成分发生明显变化。这些变化包括质膜中的固醇和磷脂酰乙醇胺的损失,以及具有相对高分子量的特定蛋白质转变为低分子量肽。这些特定蛋白质被指定为易受冻蛋白。质膜 ATP 酶的性质似乎受细胞体内冷冻的影响不大。然而,在非致死温度-5°C下体内冷冻前后,N,N'-二环己基碳二亚胺(DCCD)对质膜 ATP 酶的抑制作用相对较低,但在亚致死温度(低于-10°C)下体内冷冻时显著增强。根据这些结果,可以假设酶分子部分发生了修饰,特别是在假定的 DCCD 结合部位,或者由于质膜通透性增加,DCCD 变得更容易接近酶。这些观察到的变化与细胞损伤的机制有关。