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Expression of the mau gene cluster of Paracoccus denitrificans is controlled by MauR and a second transcription regulator

机译:反硝化副球菌的mau基因簇的表达受MauR和第二个转录调节因子控制

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摘要

The mau gene cluster of Paracoccus denitrificans constitutes 11 genes (10 are located in the transcriptional order mauFBEDACJGMN; the 11th, mauR, is located upstream and divergently transcribed from these genes) that encode a functional methylamine-oxidizing electron transport branch. The mauR gene encodes a LysR-type transcriptional activator essential for induction of the mau operon. In this study, the characteristics of that process were established. By using lacZ transcriptional fusions integrated into the genome of P. denitrificans, it was found that the expression of the mauR gene during growth on methylamine and/or succinate was not autoregulated, but proceeded at a low and constant level. The mauF promoter activity was shown to be controlled by MauR and a second transcriptional regulator. This activity was very high during growth on methylamine, low on succinate plus methylamine, and absent on succinate alone. MauR was overexpressed in Escherichia coli by using a T7 RNA polymerase expression system. Gel shift assays indicated that MauR binds to a 403 bp DNA fragment spanning the mauR-mauF promoter region. It is concluded from these results that the expression of the structural mau genes is dependent on MauR and its inducer, methylamine, as well as on another transcription factor. Both activators are required for high-level transcription from the mauF promoter. It is hypothesized that the two activators act synergistically to activate transcription: the effects of the two activators are not additive and either one alone activates the mauF promoter rather weakly.
机译:反硝化副球菌的mau基因簇构成11个基因(编码10个位于mauFBEDACJGMN的转录顺序中;第11个mauR位于这些基因的上游并从这些基因中有差异地转录),它们编码功能性甲胺氧化电子转运分支。 mauR基因编码诱导mau操纵子所必需的LysR型转录激活因子。在这项研究中,建立了该过程的特征。通过使用整合到反硝化假单胞菌基因组中的lacZ转录融合,发现在甲胺和/或琥珀酸盐上生长期间,mauR基因的表达不是自动调节的,而是以恒定的低水平进行的。已显示mauF启动子活性受MauR和第二个转录调节因子控制。在甲胺上生长期间,该活性非常高,在琥珀酸盐加甲胺上则较低,而仅在琥珀酸盐上则不存在。通过使用T7 RNA聚合酶表达系统,MauR在大肠杆菌中过表达。凝胶位移分析表明,MauR与跨过mauR-mauF启动子区域的403 bp DNA片段结合。从这些结果可以得出结论,结构性mau基因的表达依赖于MauR及其诱导剂甲胺,以及另一种转录因子。这两种激活剂都是从mauF启动子进行高级转录所必需的。假设这两种激活剂协同作用来激活转录:这两种激活剂的作用不是累加的,并且任一个单独激活mauF启动子的能力都较弱。

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