Shen V, Bremer H
J Bacteriol. 1977 Jun;130(3):1109-16. doi: 10.1128/jb.130.3.1109-1116.1977.
In Escherichia coli B/r growing in glucose-amino acids medium, the radioactive labeling of 5S ribosomal ribonucleic acid (rRNA) and transfer RNA (tRNA) was measured after the simultaneous addition to the bacteria of chloramphenicol (CAM) (100 mug/ml), rifampin (200 mug/ml), and radioactive uracil. Accumulation of 5S rRNA ceased 85 s after the addition of rifampin, independent of the presence or absence of CAM; this indicates that CAM did not affect the rRNA chain growth rate. Together with previous measurements of the synthesis of rRNA and messenger RNA under these conditions, the results imply that CAM caused a redistribution of RNA polymerase which greatly favored stable RNA synthesis (77 to 97% of total functioning RNA polymerase engaged in synthesis of rRNA and tRNA). Further, it is inferred that RNA polymerase molecules were activated that were inactive during exponential growth. The labeling of tRNA observed under these conditions suggests the existence of clusters of tRNA genes at the 3' end of long transcripts that resemble the rRNA precursor in length and response to CAM and may be parts of rRNA transcripts.
在葡萄糖 - 氨基酸培养基中生长的大肠杆菌B/r中,在向细菌同时添加氯霉素(CAM)(100μg/ml)、利福平(200μg/ml)和放射性尿嘧啶后,测定了5S核糖体核糖核酸(rRNA)和转运RNA(tRNA)的放射性标记。添加利福平85秒后,5S rRNA的积累停止,这与CAM的存在与否无关;这表明CAM不影响rRNA链的生长速率。结合之前在这些条件下对rRNA和信使RNA合成的测量结果,结果表明CAM导致了RNA聚合酶的重新分布,极大地有利于稳定RNA的合成(77%至97%的总功能性RNA聚合酶参与rRNA和tRNA的合成)。此外,据推测,在指数生长期间无活性的RNA聚合酶分子被激活。在这些条件下观察到的tRNA标记表明,在长转录本的3'端存在tRNA基因簇,其长度和对CAM的反应类似于rRNA前体,可能是rRNA转录本的一部分。