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眼虫叶绿体早期发育相关事件:14. 野生型和突变体细胞中细胞色素c-552的生物合成

Events Surrounding the Early Development of Euglena Chloroplasts: 14. Biosynthesis of Cytochrome c-552 in Wild Type and Mutant Cells.

作者信息

Freyssinet G, Harris G C, Nasatir M, Schiff J A

机构信息

Institute for Photobiology of Cells and Organelles, Brandeis University, Waltham, Massachusetts 02154.

出版信息

Plant Physiol. 1979 May;63(5):908-15. doi: 10.1104/pp.63.5.908.

Abstract

Lack of a suitable assay has thwarted attempts to measure cytochrome c-552 in dark-grown wild type cells of Euglena gracilis var. bacillaris in mutants and in other situations where the concentrations are low. Purification methods are described based on electrofocusing which provide a cytochrome c-552 preparation homogeneous enough to elicit a single reactive antibody in rabbits; this antibody is then used as a specific and sensitive assay for cytochrome c-552. Dark-grown cells of wild type and of mutants O(1)BS, O(2)BX, G(1)BU and P(1)BXL (which make normal sized chloroplasts with abnormal internal structure in the light) have 0.02 to 0.1 x 10(-11) micromoles of cytochrome c-552 per cell, 10 to 150 times less than light-grown cells. Light-grown cells of these mutants and of wild type show a ratio of chlorophyll to cytochrome of about 300 (mole to mole). Cytochrome c-552 is undetectable in dark-grown Y(1)BXD, Y(3)BUD, and W(34)ZUD which cannot carry plastid development beyond the proplastid in light; the light-grown cells of these mutants have levels of cytochrome similar to or lower than dark-grown wild type cells. Cytochrome c-552 is undetectable in light- and dark-grown mutants in which plastid DNA is undetectable (such as Y(2)BUL, W(3)BUL, W(8)BHL, and W(10)BSmL) consistent with the view, but not proving, that this molecule may be coded, at least in part, in plastid DNA. During light-induced chloroplast development in resting cells, cytochrome c-552 formation behaves in all respects like chlorophyll except that the dark-grown cells contain low amounts of the cytochrome c-552 but lack chlorophyll. Thus, both cytochrome c-552 and chlorophyll show the same lag period even when the length is changed by nutritional manipulation; preillumination largely eliminates the lag in the formation of both molecules, cycloheximide and streptomycin both inhibit the biosynthesis of chlorophyll and cytochrome c-552 in the same manner, and the formation of both during chloroplast development is strictly light-dependent. It is shown that chloroplasts isolated from Euglena by methods thought to give intact organelles, lack 95% of the cytochrome c-552; this and the loss of similar molecules may explain why these isolated chloroplasts are not photosynthetically active.

摘要

由于缺乏合适的检测方法,人们一直无法在纤细裸藻杆状变种的黑暗培养野生型细胞、突变体以及其他浓度较低的情况下测量细胞色素c - 552。本文描述了基于电聚焦的纯化方法,该方法所制备的细胞色素c - 552足够纯,能在兔子体内引发单一反应性抗体;然后将此抗体用作细胞色素c - 552的特异性灵敏检测方法。野生型以及突变体O(1)BS、O(2)BX、G(1)BU和P(1)BXL(这些突变体在光照下能形成内部结构异常的正常大小叶绿体)的黑暗培养细胞,每个细胞含有0.02至0.1×10⁻¹¹微摩尔的细胞色素c - 552,比光照培养细胞少10至150倍。这些突变体和野生型的光照培养细胞中叶绿素与细胞色素的摩尔比约为300。在黑暗培养的Y(1)BXD、Y(3)BUD和W(34)ZUD中检测不到细胞色素c - 552,这些突变体在光照下质体发育不能超过前质体阶段;这些突变体的光照培养细胞中细胞色素水平与黑暗培养的野生型细胞相似或更低。在质体DNA检测不到的光照和黑暗培养突变体(如Y(2)BUL、W(3)BUL、W(8)BHL和W(10)BSmL)中检测不到细胞色素c - 552,这与该分子可能至少部分由质体DNA编码的观点相符,但并未证实。在静止细胞的光诱导叶绿体发育过程中,细胞色素c - 552的形成在各方面表现都与叶绿素相似,只是黑暗培养细胞中细胞色素c - 552含量低但缺乏叶绿素。因此,即使通过营养调控改变滞后期的长度,细胞色素c - 552和叶绿素的滞后期仍相同;预光照在很大程度上消除了这两种分子形成过程中的滞后期,环己酰亚胺和链霉素都以相同方式抑制叶绿素和细胞色素c - 552的生物合成,并且在叶绿体发育过程中这两种物质的形成都严格依赖光照。结果表明,用被认为能得到完整细胞器的方法从裸藻中分离出的叶绿体,其细胞色素c - 552含量缺失95%;这以及类似分子的缺失可能解释了为什么这些分离出的叶绿体没有光合活性。

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