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首页> 外文期刊>Microbiology >Isolation of regulatory mutants in photosynthesis gene expression in Rhodobacter sphaeroides 2.4.1 and partial complementation of a PrrB mutant by the HupT histidine-kinase
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Isolation of regulatory mutants in photosynthesis gene expression in Rhodobacter sphaeroides 2.4.1 and partial complementation of a PrrB mutant by the HupT histidine-kinase

机译:脱苯甲酸盐乳菌的光合作用基因表达中调节突变体的分离及脉冲组氨酸激酶PRRB突变体的部分互补

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The photosynthetic bacterium Rhodobacter sphaeroides responds to the transition from aerobiosis to anaerobic photosynthesis by increasing the expression of the photosynthesis genes. Mutants have been isolated based on their inability, following such a transition, to increase transcription of the puc operon encoding the apoproteins of the light-harvesting complex II. Mutant D5, a representative of one mutant class, described here, although remaining photosynthetically competent, produced only low levels of the photosynthetic spectral complexes. Complementation analysis revealed that either the gene for the photosynthesis response regulator prrA or the gene encoding its cognate sensor kinase, prrB, was capable of rescuing this mutant. However, partial complementation of this mutant was achieved by placing in trans additional copies of other defined genes from the cosmid library of R. sphaeroides. We describe this effect in detail, attributable to the hupT gene, which has been proposed to encode a histidine-kinase for the hydrogen uptake system in Rhodobacter capsulatus. The effect of HupT on the expression of the photosynthesis genes was mediated through PrrA and independent of a functioning hydrogen uptake system. Thus, we raise the possibility that HupT can participate in phosphorylation of the heterologous response regulator PrrA by so-called cross-talk and therefore partially compensate for the defect in the mutant described. The observation of cross-talk, together with the complementation analysis, allowed us to assign the original mutation to the prrB gene; this was confirmed by DNA sequencing. Analysis of cross-talk in the wild-type, prrB and prrA genetic backgrounds suggested that besides kinase activity, PrrB may possess phosphatase activity toward PrrA. We also report the cloning, organization and structure of some of the hup genes from R. sphaeroides and construction of a Hup- strain.
机译:光合细菌乳菌斯氏菌通过增加光合作用基因的表达来响应从有氧症到厌氧光合作用的过渡。在这种转变之后,基于它们的无法能力分离突变体,以增加编码光收获络合物II的诱导蛋白的PUC型术的转录。这里描述的一个突变类别的突变体D5,但这里描述的一个突变类别的代表性虽然剩余光合作用,但仅产生低水平的光合谱复合物。互补分析显示,光合作用响应调节剂PRRA或编码其同源传感器激酶PRRB的基因的基因能够抵押这种突变体。然而,通过放置来自R.Sphaeroides的粘性文库的其他定义基因的反式另外的基因的反式附加副本来实现该突变体的部分互补。我们详细描述了这种效果,其归因于抑制基因,该抑制基因已经提出为乳囊岩中的氢曲杆菌中的氢摄取系统编码组氨酸激酶。阻止对光合作用基因表达的影响通过PRRA介导并独立于功能氢吸收体系。因此,我们提出了通过所谓的串扰来参与异源反应调节剂PRRA的磷酸化的可能性,因此部分地补偿所描述的突变体中的缺陷。串扰的观察与互补分析一起允许我们将原始突变分配给PRRB基因;这通过DNA测序确认。野生型,PRRB和PRRA遗传背景中的串扰分析表明除了激酶活性,PRRB可能对PRRA具有磷酸酶活性。我们还报告了来自R. Sphaeroides的一些HUP基因的克隆,组织和结构。

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