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对假单胞菌属M1菌株中苯酚和苯分解代谢所需基因簇的独特组织和协同调控的表征。

Characterization of the unique organization and co-regulation of a gene cluster required for phenol and benzene catabolism in Pseudomonas sp. M1.

作者信息

Santos Pedro M, Sá-Correia Isabel

机构信息

IBB, Institute for Biotechnology and Bioengineering, Centre for Biological and Chemical Engineering, Instituto Superior Técnico, Av Rovisco Pais, 1049-001, Lisboa, Portugal.

出版信息

J Biotechnol. 2007 Sep 30;131(4):371-8. doi: 10.1016/j.jbiotec.2007.07.941. Epub 2007 Jul 26.

Abstract

This work describes a new genetic organization and co-regulation of a cluster of genes involved in the first steps of phenol and benzene catabolic pathways in Pseudomonas sp. M1, different from the established models for Pseudomonas upper pathway. Pseudomonas sp. M1 was isolated by others from the sediments of the Rhine River and exhibits an exceptional biodegradation ability towards a wide range of toxic and/or recalcitrant compounds. Although the taxonomic classification of strain M1 could not be determined, we found in a previous study that Pseudomonas citronellolis is the closest species. The genetic organization characterized in this study, the phc (phenol catabolism) genes, includes eight clustered genes, encoding a catechol 1,2-dioxygenase (phcA), a multicomponent phenol hydroxylase (phcKLMNOP) and the transcriptional regulator PhcR (phcR). PhcR controls the transcription of the referred seven clustered genes from two catabolic promoters: Pa (for phcA) and Pk (for phcKLMNOP). In agreement with in silico prediction, the activity of Pa and Pk promoters was proved to depend on the presence of sigma(54). Both promoters are phenol and benzene inducible and evidence supporting the unique sigma(54)-dependent co-regulation of the phenol/benzene inducible genes phcA and phcKLMNOP, mediated by PhcR, was obtained.

摘要

这项研究描述了假单胞菌属M1菌株中参与苯酚和苯分解代谢途径第一步的一组基因的新遗传组织和共调控,这与假单胞菌属上途径的既定模型不同。假单胞菌属M1菌株是其他人从莱茵河沉积物中分离出来的,对多种有毒和/或难降解化合物具有特殊的生物降解能力。尽管无法确定菌株M1的分类地位,但我们在之前的一项研究中发现,香茅假单胞菌是最接近的物种。本研究中表征的遗传组织,即phc(苯酚分解代谢)基因,包括八个成簇基因,编码一种儿茶酚1,2-双加氧酶(phcA)、一种多组分苯酚羟化酶(phcKLMNOP)和转录调节因子PhcR(phcR)。PhcR从两个分解代谢启动子控制上述七个成簇基因的转录:Pa(用于phcA)和Pk(用于phcKLMNOP)。与计算机预测一致,Pa和Pk启动子的活性被证明依赖于sigma(54)的存在。两个启动子均为苯酚和苯诱导型,并且获得了支持由PhcR介导的苯酚/苯诱导基因phcA和phcKLMNOP独特的sigma(54)依赖性共调控的证据。

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