Linder C H, Fast R
J Virol. 1975 Sep;16(3):463-9. doi: 10.1128/JVI.16.3.463-469.1975.
Regulation of T4-specific mRNA synthesis was studied during leucine starvation of a leucine-requiring stringent Escherichia coli B strain. This was done by imposing starvation prior to T4 infection and then letting RNA synthesis proceed for different time periods. Rifampin or streptolydigin was added to stop further RNA synthesis, and protein synthesis was restored by addition of leucine. Samples were withdrawn at different times, and the enzyme-forming capacities found that, during conditions which elicit the stringent response in uninfected bacteria, immediate early mRNA is not stringently regulated. This conclusion contradicts the earlier conclusion of others, obtained by measuring incorporation of radioactive uracil; this is explained by the observation of Edlin and Neuhard (1967), confirmed and extended by us to the T4-infected cell, that the incorporation of uracil into RNA of a stringent strain is virtually blocked by amino acid starvation, whereas that of adenine continues at 30 to 50% of the rate seen in the presence of the required amino acid.
在一株需要亮氨酸的严谨型大肠杆菌B菌株亮氨酸饥饿期间,对T4特异性mRNA合成的调控进行了研究。具体做法是在T4感染前施加饥饿状态,然后让RNA合成持续不同的时间段。加入利福平或利迪链菌素以停止进一步的RNA合成,并通过添加亮氨酸恢复蛋白质合成。在不同时间点取样,酶形成能力表明,在引发未感染细菌严谨反应的条件下,立即早期mRNA不受严谨调控。这一结论与其他人通过测量放射性尿嘧啶掺入得出的早期结论相矛盾;这可以通过埃德林和纽哈德(1967年)的观察结果来解释,我们对T4感染细胞进行了证实和扩展,即氨基酸饥饿几乎会阻止严谨菌株中尿嘧啶掺入RNA,而腺嘌呤的掺入则以所需氨基酸存在时所见速率的30%至50%继续进行。