Shingler V, Bartilson M, Moore T
Department of Cell and Molecular Biology, University of Umeå, Sweden.
J Bacteriol. 1993 Mar;175(6):1596-604. doi: 10.1128/jb.175.6.1596-1604.1993.
The catabolic plasmid pVI150 of Pseudomonas sp. strain CF600 encodes all the genetic information required for the regulated metabolism of phenol and some of its methyl-substituted derivatives. The structural dmp genes of the pathway are clustered in a single operon that lies just downstream of a -24 TGGC, -12 TTGC nif/ntr-like promoter sequence. Promoters of this class are recognized by a minor form of RNA polymerase utilizing sigma 54 (NtrA, RpoN). Primer extension analysis demonstrated that the dmp operon transcript initiates downstream of the -24, -12 promoter. Transposon insertion mutants, specifically defective in the regulation of the dmp operon, were isolated, and complementation of a phenol-utilization regulatory mutant was used to identify the regulatory locus, dmpR. The 67-kDa dmpR gene product alone was shown to be sufficient for activation of transcription from the dmp operon promoter. Nucleotide sequence determination revealed that DmpR belongs to the NtrC family of transcriptional activators that regulate transcription from -24, -12 promoters. The deduced amino acid sequence of DmpR has high homology (40 to 67% identity) with the central and carboxy-terminal regions of these activators, which are believed to be involved in the interaction with the sigma 54 RNA polymerase and in DNA binding, respectively. The amino-terminal region of DmpR was found to share 64% identity with the amino-terminal region of XylR, which is also a member of this family of activators. This region has been implicated in effector recognition of aromatic compounds that is required for the regulatory activity of XylR.
假单胞菌属CF600菌株的分解代谢质粒pVI150编码了苯酚及其一些甲基取代衍生物的调节代谢所需的所有遗传信息。该途径的结构dmp基因聚集在一个单一操纵子中,该操纵子位于-24 TGGC、-12 TTGC nif/ntr样启动子序列的下游。这类启动子由利用σ54(NtrA,RpoN)的一种次要形式的RNA聚合酶识别。引物延伸分析表明,dmp操纵子转录本在-24、-12启动子的下游起始。分离出在dmp操纵子调节方面存在特异性缺陷的转座子插入突变体,并利用苯酚利用调节突变体的互补来鉴定调节基因座dmpR。单独的67 kDa dmpR基因产物被证明足以激活dmp操纵子启动子的转录。核苷酸序列测定表明,DmpR属于调节-24、-12启动子转录的NtrC转录激活因子家族。推导的DmpR氨基酸序列与这些激活因子的中央和羧基末端区域具有高度同源性(40%至67%的同一性),据信这些区域分别参与与σ54 RNA聚合酶的相互作用和DNA结合。发现DmpR的氨基末端区域与XylR的氨基末端区域具有64%的同一性,XylR也是该激活因子家族的成员。该区域与XylR调节活性所需的芳香族化合物的效应物识别有关。