Kong X F, Lovett P S, Kung S D
Gene. 1984 Nov;31(1-3):23-30. doi: 10.1016/0378-1119(84)90191-4.
The galK-expression plasmid vector system pKO1 has been used to clone Nicotiana chloroplast (ct) promoters that function in Escherichia coli. The randomly cloned promoter-containing restriction fragments have been located on the ct genome and originate both from those regions encoding ribosomal and transfer RNAs and from locations elsewhere on the ct genome. The results provide the first demonstration that sequences which function as prokaryotic promoters exist in the ct genome.
galK表达质粒载体系统pKO1已被用于克隆在大肠杆菌中起作用的烟草叶绿体(ct)启动子。随机克隆的含启动子的限制性片段已定位在ct基因组上,它们既来源于编码核糖体RNA和转运RNA的区域,也来源于ct基因组其他位置。这些结果首次证明ct基因组中存在起原核生物启动子作用的序列。