Xu Haijin, Lin Weili, Xia Huiming, Xu Shuwa, Li Yingli, Yao Hongming, Bai Fang, Zhang Xiuming, Bai Yanling, Saris Per, Qiao Mingqiang
Tianjin Key Laboratory of Microbiology, College of Life Sciences, Nankai University, Tianjin 300071, PR China.
FEMS Microbiol Lett. 2005 Dec 1;253(1):103-9. doi: 10.1016/j.femsle.2005.09.027. Epub 2005 Oct 5.
A pyocyanin overproducer with insertional inactivation of ptsP gene was isolated from a mini-Mu insertion library in Pseudomonas aeruginosa PA68. The mutation was complemented by a functional ptsP gene in trans. The pyocyanin-overproducing phenotype was also found in a ptsP mutant constructed by gene replacement in the P. aeruginosa PAO1 strain. Reporter plasmids with P(qscR)-lacZ, P(lasI)-lacZ and P(rhlI)-lacZ were constructed and the beta-galactosidase activity in the ptsP mutant/wild-type background was measured. The results showed that lack of Enzyme I(Ntr) (EI(Ntr), encoded by ptsP) decreased transcription from the P(qscR) promoter and increased the activity of the P(lasI) and P(rhlI) promoters. Normally, QscR represses the quorum-sensing LasR-LasI and RhlR-RhlI systems involved in pyocyanin regulation. Our results showed that the ptsP gene has an important role in the regulation of pyocyanin production and that two quorum-sensing systems and their repressor QscR are involved in this regulation.
从铜绿假单胞菌PA68的mini-Mu插入文库中分离出一株ptsP基因插入失活的绿脓菌素过量产生菌。该突变通过转导功能性ptsP基因得到互补。在通过基因置换构建的铜绿假单胞菌PAO1菌株的ptsP突变体中也发现了绿脓菌素过量产生的表型。构建了带有P(qscR)-lacZ、P(lasI)-lacZ和P(rhlI)-lacZ的报告质粒,并测定了ptsP突变体/野生型背景中的β-半乳糖苷酶活性。结果表明,缺乏由ptsP编码的酶I(Ntr)(EI(Ntr))会降低P(qscR)启动子的转录,并增加P(lasI)和P(rhlI)启动子的活性。正常情况下,QscR会抑制参与绿脓菌素调节的群体感应LasR-LasI和RhlR-RhlI系统。我们的结果表明,ptsP基因在绿脓菌素产生的调节中具有重要作用,并且两个群体感应系统及其阻遏物QscR参与了这一调节。