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首页> 外文期刊>Microbiology >Iron regulation of the hcnABC genes encoding hydrogen cyanide synthase depends on the anaerobic regulator ANR rather than on the global activator GacA in Pseudomonas fluorescens CHA0
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Iron regulation of the hcnABC genes encoding hydrogen cyanide synthase depends on the anaerobic regulator ANR rather than on the global activator GacA in Pseudomonas fluorescens CHA0

机译:编码氰化氢合成酶的HCNABC基因的铁调节取决于厌氧调节剂ANR,而不是在假单胞菌荧光荧光素中的全球活化剂GACA

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Pseudomonas fluorescens CHA0 produces hydrogen cyanide (HCN), a secondary metabolite that substantially contributes to this strain’s biocontrol ability. Cyanogenesis is induced by oxygen-limiting conditions, but abolished by iron depletion. In P. fluorescens, the anaerobic regulator ANR and the global activator GacA are both required for the maximal expression of the HCN biosynthetic genes hcnABC. The molecular basis of this regulation by ANR and GacA was investigated under conditions of oxygen and iron limitation. A promoter deletion analysis using a translational hcnA′–′lacZ fusion revealed that a conserved FNR/ANR recognition sequence in the ?40 promoter region was necessary and sufficient for the regulation by ANR in response to oxygen limitation. Stimulation of hcnA′–′lacZ expression by the addition of iron also depended on the presence of ANR and the FNR/ANR box, but not on GacA, suggesting that in addition to acting as an oxygen-sensitive protein, ANR also responds to iron availability. Expression of the translational hcnA′–′lacZ fusion remained GacA-dependent in hcn promoter mutants that were no longer responsive to ANR, in agreement with earlier evidence for a post-transcriptional regulatory mechanism under GacA control. These data support a model in which cyanogenesis is sequentially activated by ANR at the level of transcription and by components of the GacA network at the level of translation.
机译:假单胞菌荧光荧光素CHA0产生氰化氢(HCN),次级代谢物显着促进这种菌株的生物防治能力。氰基通过氧气限制条件诱导,但通过铁耗尽诱导。在P.荧光型,厌氧调节剂ANR和全局活化剂GACA都需要HCN生物合成基因HCNABC的最大表达所需的。在氧气和铁限制条件下研究了ANR和GACA调节该调节的分子基础。使用平移HCNA' - 'LacZ融合的启动子缺失分析显示,α40启动子区域中的保守的FNR / ANR识别序列是必要的,并且足以通过ANR的调节响应于氧气限制。通过添加铁的加入HCNA' - 'LacZ表达也依赖于ANR和FNR / ANR盒的存在,但不在GACA上,表明除了用作氧敏感蛋白,ANR还应对铁可用性。翻译HCNA' - ' - 'Lacz融合的表达依赖于Gaca依赖于HCN启动子突变体,其不再对ANR响应于ANR,同意在GACA对照下的转录后调节机制的前述调节机制的早期证据。这些数据支持一种模型,其中在转录水平的ANR和GACA网络的组分在翻译水平下依次激活氰化物。

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