Rothmel R K, Aldrich T L, Houghton J E, Coco W M, Ornston L N, Chakrabarty A M
Department of Microbiology and Immunology, University of Illinois College of Medicine, Chicago 60612.
J Bacteriol. 1990 Feb;172(2):922-31. doi: 10.1128/jb.172.2.922-931.1990.
Pseudomonas putida utilizes the catBC operon for growth on benzoate as a sole carbon source. This operon is positively regulated by the CatR protein, which is encoded from a gene divergently oriented from the catBC operon. The catR gene encodes a 32.2-kilodalton polypeptide that binds to the catBC promoter region in the presence or absence of the inducer cis-cis-muconate, as shown by gel retardation studies. However, the inducer is required for transcriptional activation of the catBC operon. The catR promoter has been localized to a 385-base-pair fragment by using the broad-host-range promoter-probe vector pKT240. This fragment also contains the catBC promoter whose -35 site is separated by only 36 nucleotides from the predicted CatR translational start. Dot blot analysis suggests that CatR binding to this dual promoter-control region, in addition to inducing the catBC operon, may also regulate its own expression. Data from a computer homology search using the predicted amino acid sequence of CatR, deduced from the DNA sequence, showed CatR to be a member of a large class of procaryotic regulatory proteins designated the LysR family. Striking homology was seen between CatR and a putative regulatory protein, TfdS.
恶臭假单胞菌利用catBC操纵子以苯甲酸盐作为唯一碳源进行生长。该操纵子受到CatR蛋白的正调控,CatR蛋白由一个与catBC操纵子方向相反的基因编码。凝胶阻滞研究表明,无论有无诱导剂顺式-顺式-粘康酸,catR基因编码的32.2千道尔顿的多肽都能与catBC启动子区域结合。然而,catBC操纵子的转录激活需要诱导剂。通过使用广宿主范围的启动子探针载体pKT240,已将catR启动子定位到一个385碱基对的片段上。该片段还包含catBC启动子,其-35位点与预测的CatR翻译起始位点仅相隔36个核苷酸。斑点印迹分析表明,CatR与这个双重启动子控制区域的结合,除了诱导catBC操纵子外,还可能调节其自身的表达。利用从DNA序列推导的CatR预测氨基酸序列进行的计算机同源性搜索数据显示,CatR是一大类原核调节蛋白(称为LysR家族)的成员。在CatR和一种假定的调节蛋白TfdS之间发现了显著的同源性。