Department of Pharmacy, College of Pharmacy, Pusan National University, Busan, 609-735, Korea.
Mol Cells. 2011 Jul;32(1):57-65. doi: 10.1007/s10059-011-2322-6. Epub 2011 May 23.
Pseudomonas quinolone signal (PQS) plays a role in the regulation of virulence genes and it is intertwined in the las/rhl quorum sensing (QS) circuits of Pseudomonas aeruginosa. PQS is synthesized from anthranilate by pqsA-D and pqsH whose expression is influenced by the las/rhl systems. Since anthranilate can be degraded by functions of antABC and catBCA, PQS synthesis might be regulated by the balance between the expression of the pqsA-D/phnAB, pqsH, antABC, and catBCA gene loci. antA and catA are repressed by LasR during log phase and activated by RhlR in late stationary phase, whereas pqsA-E/phnAB is activated by LasR in log phase and repressed by RhlR. QscR represses both but each repression occurs in a different growth phase. This growth phase-differential regulation appears to be accomplished by the antagonistic interplay of LasR, RhlR, and QscR, mediated by two intermediate regulators, AntR and PqsR, and their cofactors, anthranilate and PQS, where the expressions of antR and pqsR and the production of anthranilate and PQS are growth phase-differentially regulated by QS systems. Especially, the anthranilate level increases in an RhlR-dependent manner at late stationary phase. From these results, we suggest that RhlR and LasR regulate the anthranilate metabolism in a mutually antagonistic and growth phase-differential manner by affecting both the expressions and activities of AntR and PqsR, and that QscR also phase-differentially represses both LasR and RhlR functions in this regulation.
铜绿假单胞菌喹诺酮信号(PQS)在调节毒力基因方面发挥作用,并且与铜绿假单胞菌的 las/rhl 群体感应(QS)电路交织在一起。PQS 是由 pqsA-D 和 pqsH 从邻氨基苯甲酸合成的,其表达受 las/rhl 系统的影响。由于邻氨基苯甲酸可以被 antABC 和 catBCA 的功能降解,因此 PQS 的合成可能受到 pqsA-D/phnAB、pqsH、antABC 和 catBCA 基因座表达之间的平衡调节。antA 和 catA 在对数期受 LasR 抑制,在晚期稳定期受 RhlR 激活,而 pqsA-E/phnAB 在对数期受 LasR 激活,受 RhlR 抑制。QscR 抑制两者,但每种抑制作用发生在不同的生长阶段。这种生长阶段差异调节似乎是通过 LasR、RhlR 和 QscR 的拮抗相互作用来完成的,由两个中间调节剂 AntR 和 PqsR 及其辅因子邻氨基苯甲酸和 PQS 介导,其中 antR 和 pqsR 的表达以及邻氨基苯甲酸和 PQS 的产生受到 QS 系统的生长阶段差异调节。特别是,在晚期稳定期,RhlR 依赖的方式使邻氨基苯甲酸水平增加。从这些结果中,我们认为 RhlR 和 LasR 通过影响 AntR 和 PqsR 的表达和活性,以相互拮抗和生长阶段差异的方式调节邻氨基苯甲酸代谢,而 QscR 也以这种调节中相位差异的方式抑制 LasR 和 RhlR 的功能。