Willshaw G A, Smith H R, McConnell M M, Rowe B
Plasmid. 1985 Jan;13(1):8-16. doi: 10.1016/0147-619x(85)90051-4.
Molecular cloning from a plasmid encoding colonization factor antigen I (CFA/I) and heat-stable enterotoxin isolated two regions, 1 and 2, that are required for the production of CFA/I fimbriae. The level of CFA/I synthesis measured by ELISA was similar in an Escherichia coli K12 strain carrying regions 1 and 2 cloned separately on compatible plasmid vectors to that in the same strain containing the parental plasmid. The structural gene for the CFA/I fimbrial subunit was within region 1. This region directed production in E. coli minicells of at least six independent polypeptides, of which the fimbrial subunit and at least three others appeared to be synthesized as precursor molecules that underwent processing. Cloned DNA containing CFA/I region 2 specified three polypeptides in minicells. Attempts to reduce the size of the cloned region 1 resulted in a derivative plasmid that carried the CFA/I structural gene but did not complement a region-2 recombinant plasmid to restore production of CFA/I fimbriae.
从编码定居因子抗原I(CFA/I)和热稳定肠毒素的质粒中进行分子克隆,分离出两个区域,即区域1和区域2,它们是产生CFA/I菌毛所必需的。通过酶联免疫吸附测定(ELISA)测得的CFA/I合成水平,在携带分别克隆于相容质粒载体上的区域1和区域2的大肠杆菌K12菌株中,与在含有亲本质粒的同一菌株中的水平相似。CFA/I菌毛亚基的结构基因位于区域1内。该区域指导大肠杆菌微小细胞中至少六种独立多肽的产生,其中菌毛亚基和至少其他三种多肽似乎以前体分子的形式合成,这些前体分子会经历加工过程。含有CFA/I区域2的克隆DNA在微小细胞中指定了三种多肽。试图缩小克隆的区域1的大小,结果得到一种衍生质粒,该质粒携带CFA/I结构基因,但不能与区域2重组质粒互补以恢复CFA/I菌毛的产生。