Harshey R M, Ramakrishnan T
J Bacteriol. 1977 Feb;129(2):616-22. doi: 10.1128/jb.129.2.616-622.1977.
Two methods were employed to measure the rate of ribonucleic acid (RNA) chain growth in vivo in Mycobacterium tuberculosis H37Rv cultures growing in Sauton medium at 37 degrees C, with a generation time of 10 h. In the first, the bacteria were allowed to assimilate [3H]uracil or [3H]guanine into their RNA for short time periods. The RNA was then extracted and hydrolyzed with alkali, and the radioactivity in the resulting nucleotides and nucleosides was measured. The data obtained by this method allowed the calculation of the individual nucleotide step times during the growth of RNA chains, from which the average rate of RNA chain elongation was estimated to be about 4 nucleotides per s. The second method employed the antibiotic rifampin, which specifically inhibits the initiation of RNA synthesis without interfering with the elongation and completion of nascent RNA chains. Usint this method, the transcription time of the 16S, 23S, and 5S ribosomal RNA genes was estimated to be 7.6 min, which corresponds to a ribosomal RNA chain growth rate of 10 nucleotides per s.
采用两种方法来测定在37摄氏度的苏通培养基中生长、代时为10小时的结核分枝杆菌H37Rv培养物在体内的核糖核酸(RNA)链生长速率。第一种方法是让细菌在短时间内将[3H]尿嘧啶或[3H]鸟嘌呤掺入其RNA中。然后提取RNA并用碱水解,测量所得核苷酸和核苷中的放射性。通过该方法获得的数据可以计算RNA链生长过程中各个核苷酸步移时间,据此估计RNA链延伸的平均速率约为每秒4个核苷酸。第二种方法使用抗生素利福平,它特异性抑制RNA合成的起始,而不干扰新生RNA链的延伸和完成。使用这种方法,16S、23S和5S核糖体RNA基因的转录时间估计为7.6分钟,这相当于核糖体RNA链的生长速率为每秒10个核苷酸。