Miller L S, Holt S C
Arch Microbiol. 1977 Nov 18;115(2):185-98. doi: 10.1007/BF00406374.
The effect of carbon dioxide on pigment and membrane content in Synechococcus lividus was studied by depriving cells of CO2 and examining cell populations biochemically and by electron microscopy. After 120 h of CO2 deprivation, S. lividus lost all detectable chlorophyll a and C-phycocyanin. Such bleached cultures were "mustard yellow", the result of approximately 1.8 times more carotenoid per cell than green control cultures. Although cells from beached cultures appeared morphologically identical to control green cells when examined by light microscopy, electron microscopic examination revealed them to be devoid of detectable thylakoid membrane. Thylakoid membrane could not be recovered by physical isolation or revealed by freeze etching of bleached S. lividus. In addition, inclusion bodies characteristically found in S. lividus were also absent. Reintroduction of CO2 into bleached cultures resulted in a rapid resynthesis of both chlorophyll a and C-phycocyanin. Electron microscopic examination of these regreening cultures revealed that thylakoid membrane was also rapidly resynthesized. Growth of regreened cultures did not occur until there was the synthesis of a full complement of chlorophyll a, C-phycocyanin, and thylakoid membrane. A time course study of the cytological events occurring during bleaching and regreening is presented.
通过剥夺细胞的二氧化碳并对细胞群体进行生化检测和电子显微镜检查,研究了二氧化碳对蓝绿色集胞藻色素和膜成分的影响。在剥夺二氧化碳120小时后,蓝绿色集胞藻失去了所有可检测到的叶绿素a和C-藻蓝蛋白。这种漂白的培养物呈“芥末黄”色,每个细胞的类胡萝卜素含量比绿色对照培养物多约1.8倍。尽管在光学显微镜下观察时,来自漂白培养物的细胞在形态上与对照绿色细胞相同,但电子显微镜检查显示它们没有可检测到的类囊体膜。通过物理分离无法回收类囊体膜,对漂白的蓝绿色集胞藻进行冷冻蚀刻也无法显示类囊体膜。此外,蓝绿色集胞藻中特有的包涵体也不存在。将二氧化碳重新引入漂白培养物中会导致叶绿素a和C-藻蓝蛋白迅速重新合成。对这些重新变绿的培养物进行电子显微镜检查发现,类囊体膜也迅速重新合成。直到合成了完整的叶绿素a、C-藻蓝蛋白和类囊体膜,重新变绿的培养物才开始生长。本文展示了漂白和重新变绿过程中发生的细胞学事件的时间进程研究。