Ebina Y, Kishi F, Nakazawa T, Nakazawa A
Nucleic Acids Res. 1979 Oct 10;7(3):639-49. doi: 10.1093/nar/7.3.639.
Among eighteen polypeptides synthesized in vitro from colicin El plasmid, one of the major products with a molecular weight of 59,000 was identified as colicin El by its immunological property, molecular size, and biological activity. In addition to this polypeptide, seven other polypeptides reacted with colicin El antiserum. Using EcoRI-cleaved colicin El DNA, a 56,000 dalton polypeptide of truncated colicin El was synthesized, but no polypeptide that reacted with colicin El antiserum was produced from SmaI-cleaved colicin El DNA. This fact indicates that the direction of transcription of colicin El structural gene is from SmaI site to EcoRI site in vitro. The immunity protein of a molecular weight of 14,300 and a component of relaxation proteins of a molecular weight of 64,000 were deduced by comparing the results of the gene expression in vitro of one-half (pAO100) and a quarter (pAO2) of colicin El plasmid. The directions of transcription-translation in the genes on the plasmid were discussed. The colicin El plasmid appears to have at least three transcriptional units.
在从大肠杆菌素E1质粒体外合成的18种多肽中,一种分子量为59,000的主要产物通过其免疫特性、分子大小和生物活性被鉴定为大肠杆菌素E1。除了这种多肽外,还有七种其他多肽与大肠杆菌素E1抗血清发生反应。使用经EcoRI切割的大肠杆菌素E1 DNA,合成了截短的大肠杆菌素E1的一种56,000道尔顿的多肽,但经SmaI切割的大肠杆菌素E1 DNA未产生与大肠杆菌素E1抗血清发生反应的多肽。这一事实表明,在体外大肠杆菌素E1结构基因的转录方向是从SmaI位点到EcoRI位点。通过比较大肠杆菌素E1质粒的二分之一(pAO100)和四分之一(pAO2)的体外基因表达结果,推断出分子量为14,300的免疫蛋白和分子量为64,000的松弛蛋白成分。讨论了质粒上基因的转录-翻译方向。大肠杆菌素E1质粒似乎至少有三个转录单元。