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首页> 外文期刊>Journal of bacteriology >GenR, an IclR-Type Regulator, Activates and Represses the Transcription of gen Genes Involved in 3-Hydroxybenzoate and Gentisate Catabolism in Corynebacterium glutamicum
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GenR, an IclR-Type Regulator, Activates and Represses the Transcription of gen Genes Involved in 3-Hydroxybenzoate and Gentisate Catabolism in Corynebacterium glutamicum

机译:GenR,一种IclR型调节剂,激活和抑制谷氨酸棒杆菌中3-羟基苯甲酸和Gentisate分解代谢相关基因的转录。

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摘要

The genes required for 3-hydroxybenzoate and gentisate catabolism in Corynebacterium glutamicum are closely clustered in three operons. GenR, an IclR-type regulator, can activate the transcription of genKH and genDFM operons in response to 3-hydroxybenzoate and gentisate, and it can repress its own expression. Footprinting analyses demonstrated that GenR bound to four sites with different affinities. Two GenR-binding sites (DFMn01 and DFMn02) were found to be located between positions ?41 and ?84 upstream of the ?35 and ?10 regions of the genDFM promoter, which was involved in positive regulation of genDFM transcription. The GenR binding site R-KHn01 (located between positions ?47 and ?16) overlapped the ?35 region of the genKH promoter sequence and is involved in positive regulation of its transcription. The binding site R-KHn02, at which GenR binds to its own promoter, was found within a footprint extending from position ?44 to ?67. It appeared to be involved in negative regulation of the activity of the genR promoter. A consensus motif with a 5-bp imperfect palindromic sequence [ATTCC-N7(5)-GGAAT] was identified among all four GenR binding sites and found to be necessary to GenR regulation through site-directed mutagenesis. The results reveal a new regulatory function of the IclR family in the catabolism of aromatic compounds.
机译:谷氨酸棒杆菌中3-羟基苯甲酸酯和龙胆酸酯分解代谢所需的基因紧密地聚集在三个操纵子中。 GenR是一种IclR型调节剂,可响应3-羟基苯甲酸酯和龙胆酸酯来激活 genKH genDFM 操纵子的转录,并且可以抑制其自身表达。足迹分析表明GenR绑定到四个具有不同亲和力的位点。发现两个GenR结合位点(DFMn01和DFMn02)位于 genDFM 启动子的第35位和第10位区域上游的第41位和第84位之间,这些位点参与了正向调控。 genDFM 转录。 GenR结合位点R-KHn01(位于α47和β16之间)与 genKH 启动子序列的β35区域重叠,并参与其转录的正调控。发现在GenR与其自身的启动子结合的结合位点R-KHn02位于从α44至α67位置的足迹内。它似乎参与了 genR 启动子活性的负调控。在所有四个GenR结合位点中均鉴定出具有5 bp不完美回文序列[ATTCC-N 7(5) -GGAAT]的共有基序,并发现这是通过定点诱变进行GenR调控所必需的。结果揭示了IclR家族在芳香化合物分解代谢中的新调控功能。

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