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Ultrastructural and Enzymic Studies of Cell Membranes from Ice-encased and Noniced Winter Wheat Seedlings

机译:冰封和非冰冬小麦幼苗细胞膜的超微结构和酶学研究

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摘要

A marked increase in the amount of cisternal-like cytoplasmic membranes was observed after ice encasement of winter wheat (Triticum aestivum L.) seedlings. Linear sucrose gradients were employed to separate the various membrane components of the microsomal membrane fraction. NADH- and NADPH-cytochrome c reductase, two specific enzyme markers for plant endoplasmic reticulum (ER) were used to locate the ER in the linear gradients. The identity of the ER fraction was confirmed by determining the effect of EDTA and Mg2+ in the preparative media on the distribution of NADH- and NADPH-cytochrome c reductase activity within the gradient. In the presence of EDTA which dissociates ribosomes from ER, peaks of activity for the two enzymes were observed at a density corresponding to that for “smooth” ER. When the media also contained an appropriate concentration of Mg2+ to maintain the attachment of ribosomes to the ER, the peaks of activity for the enzymes shifted to a density corresponding to that for “rough” ER. NADH-cytochrome c reductase activity was similar for 24 C-grown and 2 C-grown iced seedlings, but significantly lower for 2 C noniced seedlings. No preferential increase in uptake of radioactive leucine or choline in the ER was observed during ice encasement. The accumulation of electron microscopically visible membrane arrays was not inhibited by the presence of protein synthesis inhibitors at concentrations which severely inhibited incorporation of [1-14C]leucine into membrane protein, but did not affect survival and growth of the seedlings. These observations indicate that the apparent proliferation of ER during ice encasement does not result from net membrane synthesis, but rather from reorganization of existing membrane elements within the cell.
机译:冬小麦(Triticum aestivum L.)幼苗被冰包裹后,观察到脑池样细胞质膜的数量明显增加。使用线性蔗糖梯度来分离微粒体膜级分的各种膜成分。 NADH和NADPH细胞色素C还原酶是植物内质网(ER)的两个特定酶标记,用于在线性梯度中定位ER。通过确定制备介质中EDTA和Mg 2 + 对梯度内NADH-和NADPH-细胞色素c还原酶活性分布的影响,证实了ER组分的身份。在使核糖体与ER分离的EDTA存在下,以与“平滑” ER对应的密度观察到了两种酶的活性峰值。当培养基中还含有适当浓度的Mg 2 + 以维持核糖体与ER的结合时,酶的活性峰将移至与“粗糙” ER相对应的密度。对于24 C生长和2 C生长的冰苗,NADH-细胞色素C还原酶活性相似,但对于2 C非结冰幼苗,NADH-细胞色素C还原酶活性相似。在冰封期间,未观察到内质网对放射性亮氨酸或胆碱吸收的优先增加。蛋白质合成抑制剂的存在不会严重抑制[1- 14 C]亮氨酸掺入膜蛋白中的浓度,而不会抑制电子显微镜可见膜阵列的积累,但不会影响存活和生长。的幼苗。这些观察结果表明,冰包裹过程中ER的表观增殖不是由膜的净合成引起的,而是由细胞内现有膜元素的重组引起的。

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