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The IclR-Type Transcriptional Repressor LtbR Regulates the Expression of Leucine and Tryptophan Biosynthesis Genes in the Amino Acid Producer Corynebacterium glutamicum▿

机译:IclR型转录阻遏物LtbR调节氨基酸生产者谷氨酸棒杆菌中亮氨酸和色氨酸生物合成基因的表达▿

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摘要

The transcriptional regulator Cg1486 of Corynebacterium glutamicum ATCC 13032 is a member of the IclR protein family and belongs to the conserved set of regulatory proteins in corynebacteria. A defined deletion in the cg1486 gene, now designated ltbR (leucine and tryptophan biosynthesis regulator), led to the mutant strain C. glutamicum IB1486. According to whole-genome expression analysis by DNA microarray hybridizations, transcription of the leuB and leuCD genes encoding enzymes of the leucine biosynthesis pathway was enhanced in C. glutamicum IB1486 compared with the wild-type strain. Moreover, the genes of the trpEGDCFBA operon involved in tryptophan biosynthesis of C. glutamicum showed an enhanced expression in the cg1486 mutant strain. Bioinformatics pattern searches in the upstream regions of the differentially expressed genes revealed the common 12-bp motif CA(T/C)ATAGTG(A/G)GA that is located downstream of the −10 region of the mapped promoter sequences. DNA band shift assays with a streptavidin-tagged LtbR protein demonstrated the specific binding of the purified protein to 40-mers containing the 12-bp motif localized in front of leuB, leuC, and trpE, thereby confirming the direct regulatory role of LtbR in the expression of the leucine and tryptophan biosynthesis pathway genes of C. glutamicum. Genes homologous with ltbR were detected upstream of the leuCD genes in almost all sequenced genomes of bacteria belonging to the taxonomic class Actinobacteria. The ltbR-like genes of Corynebacterium diphtheriae, Corynebacterium jeikeium, Mycobacterium bovis, and Bifidobacterium longum were cloned and shown to complement the deregulation of leuB, leuCD, and trpE gene expression in C. glutamicum IB1486.
机译:谷氨酸棒杆菌ATCC 13032的转录调节子Cg1486是IclR蛋白家族的成员,属于棒杆菌中的保守调节蛋白集。 cg1486基因的明确缺失(现称为ltbR(亮氨酸和色氨酸生物合成调节剂))导致了突变菌株谷氨酸棒杆菌IB1486。根据DNA微阵列杂交的全基因组表达分析,与野生型菌株相比,谷氨酸棒杆菌IB1486增强了亮氨酸生物合成途径的酶leuB和leuCD基因的转录。此外,参与谷氨酸棒杆菌色氨酸生物合成的trpEGDCFBA操纵子基因在cg1486突变株中显示出增强的表达。在差异表达基因上游区域的生物信息学模式搜索显示位于映射的启动子序列-10区域下游的常见12 bp基元CA(T / C)ATAGTG(A / G)GA。用链霉亲和素标记的LtbR蛋白进行的DNA带移分析表明,纯化的蛋白与40个聚体具有特异性结合,该40个聚体包含位于leuB,leuC和trpE前面的12 bp的基序,从而证实了LtbR在该蛋白中的直接调控作用。谷氨酸棒杆菌亮氨酸和色氨酸生物合成途径基因的表达在属于分类学放线菌的几乎所有测序细菌基因组中,在leuCD基因上游检测到与ltbR同源的基因。克隆了白喉棒状杆菌,耶氏棒状杆菌,牛分枝杆菌和长双歧杆菌的ltbR样基因,并显示出它们可以补充谷氨酸棒杆菌IB1486中leuB,leuCD和trpE基因表达的失调。

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