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谷氨酸棒杆菌 ATCC 13032 的 MocR 型调控蛋白 PdxR 对磷酸吡哆醛生物合成基因 pdxST 的正转录调控。

Positive transcriptional control of the pyridoxal phosphate biosynthesis genes pdxST by the MocR-type regulator PdxR of Corynebacterium glutamicum ATCC 13032.

机构信息

International NRW Graduate School in Bioinformatics and Genome Research, Centrum für Biotechnologie, Universität Bielefeld, Universitätsstraße 25, D-33615 Bielefeld, Germany.

Institut für Genomforschung und Systembiologie, Centrum für Biotechnologie, Universität Bielefeld, Universitätsstraße 27, D-33615 Bielefeld, Germany.

出版信息

Microbiology (Reading). 2011 Jan;157(Pt 1):77-88. doi: 10.1099/mic.0.044818-0. Epub 2010 Sep 16.

DOI:10.1099/mic.0.044818-0
PMID:20847010
Abstract

The pdxR (cg0897) gene of Corynebacterium glutamicum ATCC 13032 encodes a regulatory protein belonging to the MocR subfamily of GntR-type transcription regulators and consisting of an amino-terminal winged helix-turn-helix DNA-binding domain and a carboxy-terminal aminotransferase-like domain. A defined deletion in the pdxR gene resulted in the decreased expression of the divergently orientated pdxST genes coding for the subunits of pyridoxal 5'-phosphate synthase. The pdxST mutant C. glutamicum NJ0898 and the pdxR mutant C. glutamicum AMH17 showed vitamin B(6) auxotrophy that was restored by supplementing the growth medium with either pyridoxal, pyridoxal 5'-phosphate or pyridoxamine. The genetic organization of the 89 bp pdxR-pdxST intergenic region was elucidated by mapping the 5' ends of the respective transcripts, followed by detection of typical promoter sequences. Bioinformatic pattern searches and comparative genomics revealed three DNA motifs with the consensus sequence AAAGTGGW(-/T)CTA, overlapping the deduced promoter sequences and serving as candidate DNA-binding sites for PdxR. DNA band shift assays with the purified PdxR protein demonstrated the specific binding of the transcription regulator to double-stranded 40-mer sequences containing the detected motifs, thereby confirming the direct regulatory role of PdxR in activating the expression of the pdxST genes.

摘要

谷氨酸棒杆菌 ATCC 13032 的 pdxR(cg0897)基因编码一种调节蛋白,属于 GntR 型转录调节子的 MocR 亚家族,由氨基端翼螺旋-转角-螺旋 DNA 结合域和羧基端氨基转移酶样结构域组成。pdxR 基因的明确缺失导致编码吡哆醛 5'-磷酸合酶亚基的 divergently orientated pdxST 基因的表达降低。pdxST 突变体 C. glutamicum NJ0898 和 pdxR 突变体 C. glutamicum AMH17 表现出维生素 B(6)营养缺陷型,可通过在生长培养基中添加吡哆醛、吡哆醛 5'-磷酸或吡哆胺来恢复。通过映射各自转录物的 5' 末端,并检测典型的启动子序列,阐明了 89 个碱基对的 pdxR-pdxST 基因间区的遗传组织。生物信息学模式搜索和比较基因组学揭示了三个具有一致序列 AAAGTGGW(-/T)CTA 的 DNA 基序,重叠推断的启动子序列,并作为 PdxR 的候选 DNA 结合位点。用纯化的 PdxR 蛋白进行 DNA 带迁移测定证明了转录调节剂与含有检测到的基序的双链 40 -mer 序列的特异性结合,从而证实了 PdxR 在激活 pdxST 基因表达中的直接调节作用。

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