Bennett A, Bogorad L
J Cell Biol. 1973 Aug;58(2):419-35. doi: 10.1083/jcb.58.2.419.
Fluorescent and red light environments generate greatly different patterns of pigmentation and morphology in Fremyella diplosiphon. Most strikingly, red-illuminated cultures contain no measurable C-phycoerythrin and have a mean filament length about 10 times shorter than fluorescent-illuminated cultures. C-phycoerythrin behaves as a photoinducible constituent of this alga. Spectrophotometric and immunochemical procedures were devised so that C-phycoerythrin metabolism could be studied quantitatively with [(14)C]-phenylalanine pulse-chased cultures. Transfer of red-illuminated cultures to fluorescent light initiates C-phycoerythrin production by essentially de novo synthesis. C-phycoerythrin is not degraded to any significant extent in cultures continuously illuminated with fluorescent light. Transfer of fluorescent-illuminated cultures to red light causes an abrupt cessation of C-phycoerythrin synthesis. The C-phycoerythrin content of cultures adapting to red light decreases and subsequently becomes constant. Loss of C-phycoerythrin is not brought about by metabolic degradation, but rather by a decrease in mean filament length which is effected by transcellular breakage. In this experimental system, light influences intracellular C-phycoerythrin levels by regulating the rate of synthesis of the chromoprotein.
荧光和红光环境会在双岐藻(Fremyella diplosiphon)中产生截然不同的色素沉着和形态模式。最显著的是,红光照射下的培养物中检测不到C-藻红蛋白,其平均丝状体长度比荧光照射下的培养物短约10倍。C-藻红蛋白是这种藻类的一种光诱导成分。设计了分光光度法和免疫化学方法,以便用[¹⁴C]-苯丙氨酸脉冲追踪培养物对C-藻红蛋白的代谢进行定量研究。将红光照射下的培养物转移到荧光下会通过从头合成启动C-藻红蛋白的产生。在持续用荧光照射的培养物中,C-藻红蛋白不会有明显降解。将荧光照射下的培养物转移到红光下会导致C-藻红蛋白合成突然停止。适应红光的培养物中C-藻红蛋白含量下降,随后保持恒定。C-藻红蛋白的损失不是由代谢降解引起的,而是由跨细胞断裂导致的平均丝状体长度减少引起的。在这个实验系统中,光通过调节色素蛋白的合成速率来影响细胞内C-藻红蛋白的水平。