Putrinš Marta, Tover Andres, Tegova Radi, Saks Ülle, Kivisaar Maia
Department of Genetics, Institute of Molecular and Cell Biology, Tartu University and Estonian Biocentre, 51010 Tartu, Estonia.
Microbiology (Reading). 2007 Jun;153(Pt 6):1860-1871. doi: 10.1099/mic.0.2006/003681-0.
Transcription of the plasmid-borne phenol catabolic operon pheBA in Pseudomonas putida is activated by the LysR-family regulator CatR in the presence of the effector molecule cis,cis-muconate (CCM), which is an intermediate of the phenol degradation pathway. In addition to the positive control of the operon, several factors negatively affect transcription initiation from the pheBA promoter. First, the activation of the pheBA operon depends on the extracellular concentration of phenol. The pheBA promoter is rapidly activated in the presence of micromolar concentrations of phenol in minimal growth medium, but the initiation of transcription from this promoter is severely delayed after sudden exposure of bacteria to 2.5 mM phenol. Second, the transcriptional activation from this promoter is impeded when the growth medium of bacteria contains amino acids. The negative effects of amino acids can be suppressed either by overproducing CatR or by increasing, the intracellular amount of CCM. However, the intracellular amount of CCM is a major limiting factor for the transcriptional activation of the pheBA operon, as accumulation of CCM in a P. putida catB-defective strain, unable to metabolize CCM (but expressing CatR at a natural level), almost completely relieves the negative effects of amino acids. The intracellular amount of CCM is negatively affected by the catabolite repression control protein via downregulating at the post-transcriptional level the expression of the pheBA-encoded catechol 1,2-dioxygenase and the phenol monooxygenase, the enzymes needed for CCM production.
恶臭假单胞菌中质粒携带的苯酚分解代谢操纵子pheBA的转录,在效应分子顺,顺-粘康酸(CCM)存在的情况下,由LysR家族调节因子CatR激活,CCM是苯酚降解途径的一个中间产物。除了对该操纵子的正调控外,还有几个因素对pheBA启动子的转录起始产生负面影响。首先,pheBA操纵子的激活取决于苯酚的细胞外浓度。在基本生长培养基中,微摩尔浓度的苯酚存在时,pheBA启动子会迅速被激活,但细菌突然暴露于2.5 mM苯酚后,该启动子的转录起始会严重延迟。其次,当细菌的生长培养基中含有氨基酸时,该启动子的转录激活会受到阻碍。氨基酸的负面影响可以通过过量表达CatR或增加细胞内CCM的量来抑制。然而,细胞内CCM的量是pheBA操纵子转录激活的主要限制因素,因为在恶臭假单胞菌catB缺陷菌株(无法代谢CCM,但以自然水平表达CatR)中CCM的积累几乎完全消除了氨基酸的负面影响。分解代谢物阻遏控制蛋白通过在转录后水平下调pheBA编码的儿茶酚1,2-双加氧酶和苯酚单加氧酶(CCM产生所需的酶)的表达,对细胞内CCM的量产生负面影响。