Cheng Minggen, Chen Kai, Guo Suhui, Huang Xing, He Jian, Li Shunpeng, Jiang Jiandong
Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China.
Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, China
Appl Environ Microbiol. 2015 Dec;81(23):8084-92. doi: 10.1128/AEM.02122-15. Epub 2015 Sep 18.
The 3-phenoxybenzoate (3-PBA) 1',2'-dioxygenase gene cluster (pbaA1A2B cluster), which is responsible for catalyzing 3-phenoxybenzoate to 3-hydroxybenzoate and catechol, is inducibly expressed in Sphingobium wenxiniae strain JZ-1(T) by its substrate 3-PBA. In this study, we identified a transcriptional activator of the pbaA1A2B cluster, PbaR, using a DNA affinity approach. PbaR is a 253-amino-acid protein with a molecular mass of 28,000 Da. PbaR belongs to the IclR family of transcriptional regulators and shows 99% identity to a putative transcriptional regulator that is located on the carbazole-degrading plasmid pCAR3 in Sphingomonas sp. strain KA1. Gene disruption and complementation showed that PbaR was essential for transcription of the pbaA1A2B cluster in response to 3-PBA in strain JZ-1(T). However, PbaR does not regulate the reductase component gene pbaC. An electrophoretic mobility shift assay and DNase I footprinting showed that PbaR binds specifically to the 29-bp motif AATAGAAAGTCTGCCGTACGGCTATTTTT in the pbaA1A2B promoter area and that the palindromic sequence (GCCGTACGGC) within the motif is essential for PbaR binding. The binding site was located between the -10 box and the ribosome-binding site (downstream of the transcriptional start site), which is distinct from the location of the binding site in previously reported IclR family transcriptional regulators. This study reveals the regulatory mechanism for 3-PBA degradation in strain JZ-1(T), and the identification of PbaR increases the variety of regulatory models in the IclR family of transcriptional regulators.
3-苯氧基苯甲酸酯(3-PBA)1',2'-双加氧酶基因簇(pbaA1A2B簇)负责催化3-苯氧基苯甲酸酯生成3-羟基苯甲酸酯和儿茶酚,在文氏鞘氨醇菌JZ-1(T)菌株中可被其底物3-PBA诱导表达。在本研究中,我们采用DNA亲和方法鉴定了pbaA1A2B簇的转录激活因子PbaR。PbaR是一种由253个氨基酸组成的蛋白质,分子量为28,000 Da。PbaR属于IclR家族转录调节因子,与鞘氨醇单胞菌属KA1菌株中位于咔唑降解质粒pCAR3上的假定转录调节因子具有99%的同一性。基因破坏和互补实验表明,PbaR对于JZ-1(T)菌株中pbaA1A2B簇响应3-PBA的转录至关重要。然而,PbaR并不调控还原酶组分基因pbaC。电泳迁移率变动分析和DNase I足迹分析表明,PbaR特异性结合pbaA1A2B启动子区域的29 bp基序AATAGAAAGTCTGCCGTACGGCTATTTTT,并且该基序内的回文序列(GCCGTACGGC)对于PbaR的结合至关重要。结合位点位于-10框和核糖体结合位点之间(转录起始位点下游),这与先前报道的IclR家族转录调节因子的结合位点位置不同。本研究揭示了JZ-1(T)菌株中3-PBA降解的调控机制,PbaR的鉴定增加了IclR家族转录调节因子的调控模式多样性。