Bolund C
J Virol. 1973 Jul;12(1):49-57. doi: 10.1128/JVI.12.1.49-57.1973.
In Escherichia coli B infected with phage T4 with mutations in gene 55 the shut-off of synthesis of two early enzymes was found to be delayed 10 to 15 min as compared to wild-type T4 infection. The kinetics of early enzyme formation was very similar to that obtained after DNA-negative mutant infection. The transcription of gene 1 (one of the genes coded for early enzymes) ceased at 9 to 12 min after infection whether the gene 55 product was active or not, as determined by the time dependence of fluorouracil rescuability of DNA synthesis in cells infected with a gene 1 amber mutant. The synthesis of the major part of the early RNA species, determined by pulse-labeling with uracil-5-(3)H, was furthermore found to be regulated independently of gene 55. An explanation for the extended early enzyme synthesis in DNA-negative and gene 55 mutant infection is offered: translation of early messengers is restricted after about 12 min in wild-type infection, whereas in cells infected with DNA-negative or gene 55 mutants, i.e., the absence of late protein synthesis, early messengers direct the formation of early enzymes for a longer time.
在感染了基因55发生突变的噬菌体T4的大肠杆菌B中,与野生型T4感染相比,两种早期酶合成的关闭被发现延迟了10到15分钟。早期酶形成的动力学与DNA阴性突变体感染后获得的动力学非常相似。通过感染基因1琥珀突变体的细胞中DNA合成的氟尿嘧啶拯救能力的时间依赖性确定,无论基因55产物是否有活性,感染后9到12分钟基因1(编码早期酶的基因之一)的转录都会停止。此外,通过用尿嘧啶-5-(3)H脉冲标记确定,大部分早期RNA种类的合成被发现是独立于基因55进行调节的。对于DNA阴性和基因55突变体感染中早期酶合成延长的情况给出了一种解释:在野生型感染中,大约12分钟后早期信使的翻译受到限制,而在感染DNA阴性或基因55突变体的细胞中,即不存在晚期蛋白质合成的情况下,早期信使在更长的时间内指导早期酶的形成。