Nicholls N J, Lampen J O
FEBS Lett. 1987 Aug 31;221(1):179-83. doi: 10.1016/0014-5793(87)80375-7.
The repressor gene, blaI, for the beta-lactamase of Bacillus licheniformis 749 was functional when cloned in Escherichia coli, but addition of a beta-lactam did not lead to induction. One plasmid contained fragments from the inducible strain (source of repressor), the other carried fragments from the blaI- mutant 749/C (target). blaI lies just 5' to the promoter for the structural gene, blaP, and the target is the promoter region between the two genes. Interaction with both promoters seemed necessary for full repression. BlaI is a hydrophilic protein (Mr 15036) with the some structural similarities to repressors from Gram-negative bacteria.
地衣芽孢杆菌749的β-内酰胺酶阻遏基因blaI克隆到大肠杆菌中时具有功能,但添加β-内酰胺并不会导致诱导。一个质粒含有来自可诱导菌株(阻遏物来源)的片段,另一个携带来自blaI突变体749/C(靶标)的片段。blaI位于结构基因blaP启动子的5'端,靶标是两个基因之间的启动子区域。与两个启动子相互作用似乎是完全阻遏所必需的。BlaI是一种亲水蛋白(Mr 15036),与革兰氏阴性菌中的阻遏物有一些结构相似性。