Rosenthal L J, Martin S E, Pariza M W, Iandolo J J
J Bacteriol. 1972 Jan;109(1):243-9. doi: 10.1128/jb.109.1.243-249.1972.
Thermally shocked cells of Staphylococcus aureus rapidly synthesized ribonucleic acid (RNA) during the early stages of recovery. During this period, protein synthesis was not observed and occurred only after RNA had reached a maximum level. Even in the absence of coordinated protein synthesis, a large portion of the RNA appeared in newly synthesized ribosomes. Although the 30S subunit was specifically destroyed by the heating process, both ribosomal particles were reassembled during recovery. The addition of chloramphenicol did not inhibit the formation of the ribosomal subunits, nor was the presence of immature chloramphenicol particles detected. Extended recovery with highly prelabeled cells showed that the original ribosomal proteins present before heating are conserved and recycled. Furthermore, the data indicate that the 50S subunit is turned over and used as a source of protein for new ribosome assembly. Kinetic studies of the assembly process by pulse labeling have not revealed the presence of the normally reported precursor particles. Rather, the data suggest that assembly may occur, in this system, in a manner similar to that reported for in vitro assembly of Escherichia coli subunits.
金黄色葡萄球菌经热休克处理后的细胞在恢复初期迅速合成核糖核酸(RNA)。在此期间,未观察到蛋白质合成,蛋白质合成仅在RNA达到最高水平后才发生。即使在没有协调的蛋白质合成的情况下,大部分RNA也出现在新合成的核糖体中。尽管30S亚基在加热过程中被特异性破坏,但在恢复过程中两个核糖体颗粒都重新组装。氯霉素的添加并未抑制核糖体亚基的形成,也未检测到未成熟氯霉素颗粒的存在。对高度预标记细胞的延长恢复表明,加热前存在的原始核糖体蛋白得以保留并循环利用。此外,数据表明50S亚基被周转并用作新核糖体组装的蛋白质来源。通过脉冲标记对组装过程进行的动力学研究未发现通常报道的前体颗粒的存在。相反,数据表明,在该系统中,组装可能以类似于报道的大肠杆菌亚基体外组装的方式发生。