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斯氏假单胞菌OX1甲苯-邻二甲苯单加氧酶调控基因(touR)及其同源启动子的鉴定。

Identification of the Pseudomonas stutzeri OX1 toluene-o-xylene monooxygenase regulatory gene (touR) and of its cognate promoter.

作者信息

Arenghi F L, Pinti M, Galli E, Barbieri P

机构信息

Dipartimento di Genetica e di Biologia dei Microrganismi, Università degli Studi di Milano, 20133 Milan, Italy.

出版信息

Appl Environ Microbiol. 1999 Sep;65(9):4057-63. doi: 10.1128/AEM.65.9.4057-4063.1999.

Abstract

Toluene-o-xylene monooxygenase is an enzymatic complex, encoded by the touABCDEF genes, responsible for the early stages of toluene and o-xylene degradation in Pseudomonas stutzeri OX1. In order to identify the loci involved in the transcriptional regulation of the tou gene cluster, deletion analysis and complementation studies were carried out with Pseudomonas putida PaW340 as a heterologous host harboring pFB1112, a plasmid that allowed regulated expression, inducible by toluene and o-xylene and their corresponding phenols, of the toluene-o-xylene monooxygenase. A locus encoding a positive regulator, designated touR, was mapped downstream from the tou gene cluster. TouR was found to be similar to transcriptional activators of aromatic compound catabolic pathways belonging to the NtrC family and, in particular, to DmpR (83% similarity), which controls phenol catabolism. By using a touA-C2,3O fusion reporter system and by primer extension analysis, a TouR cognate promoter (P(ToMO)) was mapped, which showed the typical -24 TGGC, -12 TTGC sequences characteristic of sigma(54)-dependent promoters and putative upstream activating sequences. By using the reporter system described, we found that TouR responds to mono- and dimethylphenols, but not the corresponding methylbenzenes. In this respect, the regulation of the P. stutzeri system differs from that of other toluene or xylene catabolic systems, in which the hydrocarbons themselves function as effectors. Northern analyses indicated low transcription levels of tou structural genes in the absence of inducers. Basal toluene-o-xylene monooxygenase activity may thus transform these compounds to phenols, which then trigger the TouR-mediated response.

摘要

甲苯-邻二甲苯单加氧酶是一种酶复合物,由touABCDEF基因编码,负责施氏假单胞菌OX1中甲苯和邻二甲苯降解的早期阶段。为了鉴定参与tou基因簇转录调控的基因座,以恶臭假单胞菌PaW340作为异源宿主进行了缺失分析和互补研究,该宿主携带pFB1112质粒,该质粒允许甲苯-邻二甲苯单加氧酶在甲苯、邻二甲苯及其相应酚类诱导下进行调控表达。一个编码正调控因子的基因座,命名为touR,被定位在tou基因簇的下游。发现TouR与属于NtrC家族的芳香化合物分解代谢途径的转录激活因子相似,特别是与控制苯酚分解代谢的DmpR(相似度83%)相似。通过使用touA-C2,3O融合报告系统和引物延伸分析,定位了一个TouR同源启动子(P(ToMO)),其显示出典型的-24 TGGC、-12 TTGC序列,这是σ(54)依赖启动子和推定的上游激活序列的特征。通过使用所述的报告系统,我们发现TouR对单甲基酚和二甲基酚有反应,但对相应的甲基苯没有反应。在这方面,施氏假单胞菌系统的调控与其他甲苯或二甲苯分解代谢系统不同,在其他系统中,碳氢化合物本身作为效应物。Northern分析表明,在没有诱导剂的情况下,tou结构基因的转录水平较低。因此,基础甲苯-邻二甲苯单加氧酶活性可能将这些化合物转化为酚类,然后引发TouR介导的反应。

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