Szalay A, Munsche D, Wolligiehn R, Parthier B
Biochem J. 1972 Aug;129(1):135-40. doi: 10.1042/bj1290135.
The RNA of the blue-green alga Anacystis nidulans contains three ribosomal RNA species with molecular weights of 0.56x10(6), 0.9x10(6), and 1.1x10(6) if the RNA is extracted in the absence of Mg(2+). The 0.9x10(6)mol.wt. rRNA is extremely slowly labelled in (32)P-incorporation experiments. This rRNA may be a cleavage product of the 1.1x10(6)mol.wt. rRNA from the ribosomes of cells in certain physiological states (e.g. light-deficiency during growth). The cleavage of the 1.1x10(6)mol.wt. rRNA during the extraction procedure can be prevented by the addition of 10mm-MgCl(2). (32)P-pulse-labelling studies demonstrate the rapid synthesis of two ribosomal precursor RNA species. One precursor RNA migrating slightly slower than the 1.1x10(6)mol.wt. rRNA appears much less stable than the other precursor RNA, which shows the electrophoretic behaviour of the 0.7x10(6)mol.wt. rRNA. Our observations support the close relationship between bacteria and blue-green algae also with respect to rRNA maturation. The conversion of the ribosomal precursor RNA species into 0.56x10(6)- and 1.1x10(6)-mol.wt. rRNA species requires Mg(2+) in the incubation medium.
如果在无镁离子的情况下提取蓝绿藻集胞藻6803的RNA,其RNA含有三种核糖体RNA,分子量分别为0.56×10⁶、0.9×10⁶和1.1×10⁶。在³²P掺入实验中,分子量为0.9×10⁶的rRNA标记极其缓慢。这种rRNA可能是处于某些生理状态(如生长期间光照不足)的细胞核糖体中分子量为1.1×10⁶的rRNA的裂解产物。在提取过程中,通过添加10mM MgCl₂可防止分子量为1.1×10⁶的rRNA裂解。³²P脉冲标记研究表明,有两种核糖体前体RNA快速合成。一种迁移速度略慢于分子量为1.1×10⁶的rRNA的前体RNA,其稳定性远低于另一种前体RNA,后者表现出分子量为0.7×10⁶的rRNA的电泳行为。我们的观察结果支持细菌和蓝绿藻在rRNA成熟方面也存在密切关系。核糖体前体RNA转化为分子量为0.56×10⁶和1.1×10⁶的rRNA需要在孵育培养基中加入镁离子。