Sinclair R B, Bibb M J
John Innes Institute, Norwich, UK.
Mol Gen Genet. 1988 Aug;213(2-3):269-77. doi: 10.1007/BF00339591.
The nucleotide sequence of the 3.4 kb SphI-G fragment that contained the repressor gene (c) of the temperate Streptomyces phage phi c31 was determined. Analysis of this sequence revealed a large open reading frame with protein coding character and sequence changes in c gene point and deletion mutants identified this as the coding region of the repressor. Two of the mutants studied had undergone deletions of 1.1 kb and 1.4 kb that had occurred across short direct repeats of 6 bp and 11 bp, respectively. Coupled in vitro transcription-translation experiments using the cloned SphI-G fragment and Streptomyces lividans cell free extracts identified a protein product of approximately 72 kDa, in close agreement with that predicted from the nucleotide sequence. A strongly predicted helix-turn-helix motif that may be involved in DNA binding occurred towards the carboxy-terminus of the amino acid sequence. Initial attempts to clone the SphI-G fragment in Streptomyces failed; using information gained from the sequence analysis a smaller segment of this DNA fragment was cloned in S. lividans and conferred immunity to a clear plaque mutant (c1) of phi c31.
测定了包含温和型链霉菌噬菌体φc31阻遏基因(c)的3.4 kb SphI-G片段的核苷酸序列。对该序列的分析揭示了一个具有蛋白质编码特征的大开放阅读框,并且c基因点突变体和缺失突变体中的序列变化表明这是阻遏蛋白的编码区。所研究的两个突变体分别在6 bp和11 bp的短直接重复序列上发生了1.1 kb和1.4 kb的缺失。使用克隆的SphI-G片段和天蓝色链霉菌无细胞提取物进行的体外转录-翻译偶联实验鉴定出一种约72 kDa的蛋白质产物,这与从核苷酸序列预测的结果非常一致。在氨基酸序列的羧基末端出现了一个强烈预测的可能参与DNA结合的螺旋-转角-螺旋基序。最初在链霉菌中克隆SphI-G片段的尝试失败了;利用从序列分析中获得的信息,将该DNA片段的一个较小片段克隆到天蓝色链霉菌中,并赋予其对φc31的一个清亮噬菌斑突变体(c1)的免疫性。