Gazeau M, Delort F, Dessen P, Blanquet S, Plateau P
Laboratoire de Biochimie, Unité de Recherche Associée 240 du Centre National de la Recherche Scientifique, Ecole Polytechnique, Palaiseau, France.
FEBS Lett. 1992 Apr 6;300(3):254-8. doi: 10.1016/0014-5793(92)80857-d.
Using random Tn10 insertion mutagenesis, we isolated an Escherichia coli mutant strain affected in the regulation of lysU, the gene encoding the inducible form of lysyl-tRNA synthetase. The transposon giving rise to the altered expression of lysU was found inserted within lrp. The latter gene codes for the leucine-responsive regulatory protein (Lrp) which mediates a global response of the bacterium to leucine. An involvement of Lrp in the regulation of lysU was searched for by using a lysU-lacZ operon fusion. The following conclusions were reached: (i) inactivation of lrp causes an increased activity of the lysU promoter, whatever the growth conditions assayed, (ii) insertion of a wild-type lrp gene into a multi-copy plasmid significantly reduces lysU expression, and (iii) sensitivity of the lysU promoter to the presence of leucine in the growth medium is abolished in the lrp context.
利用随机Tn10插入诱变技术,我们分离出了一株大肠杆菌突变株,该突变株在lysU(编码赖氨酸tRNA合成酶诱导形式的基因)的调控方面存在缺陷。导致lysU表达改变的转座子被发现插入到了lrp基因内部。后一个基因编码亮氨酸响应调节蛋白(Lrp),它介导细菌对亮氨酸的全局响应。我们通过使用lysU-lacZ操纵子融合来研究Lrp在lysU调控中的作用。得出了以下结论:(i)无论所检测的生长条件如何,lrp的失活都会导致lysU启动子活性增加;(ii)将野生型lrp基因插入多拷贝质粒会显著降低lysU的表达;(iii)在lrp背景下,lysU启动子对生长培养基中亮氨酸存在的敏感性消失。