Subrahmanyam Y V, Padayatty J D
Department of Biochemistry, Indian Institute of Science, Bangalore.
Biochem Int. 1988 Apr;16(4):701-12.
The 2.3 kb BamHI fragment from the colitis bacteriophage DNA was transcribed and translated into a 20 kd structural protein P6, in a coupled transcription-translation system derived from Escherichia coli. This protein was expressed in vivo by the 2.3 kb DNA cloned in pBR322. The gene with the regulatory elements for this protein was located on the 680 bp AvaII fragment of the insert DNA. It hybridized with two RNAs of sizes 520 and 1630 nucleotides indicating that both are messengers for the 20 kd protein. Dot-blot hybridization showed that the transcripts for P6 reached a maximum level at 12 min after phage infection.
在源自大肠杆菌的偶联转录-翻译系统中,来自结肠炎噬菌体DNA的2.3 kb BamHI片段被转录并翻译成一种20 kd的结构蛋白P6。该蛋白通过克隆在pBR322中的2.3 kb DNA在体内表达。编码该蛋白的带有调控元件的基因位于插入DNA的680 bp AvaII片段上。它与大小分别为520和1630个核苷酸的两种RNA杂交,表明这两种都是20 kd蛋白的信使RNA。斑点印迹杂交显示,P6的转录本在噬菌体感染后12分钟达到最高水平。