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The Two-Component GacS-GacA System Activates lipA Translation by RsmE but Not RsmA in Pseudomonas protegens Pf-5

机译:两组分GacS-GacA系统通过RsmE激活lipA翻译,但不激活RsemAs假单胞菌Pf-5。

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In Pseudomonas spp., the Gac-Rsm signal transduction system is required for the production of lipases. The current model assumes that the system induces lipase gene transcription mediated through the quorum-sensing (QS) system. However, there are no reports of a QS system based upon N -acyl homoserine lactones or the regulation of lipase gene expression in Pseudomonas protegens . In this study, we investigated the regulatory mechanism acting on lipA expression activated by the Gac-Rsm system in P. protegens Pf-5 through deletion and overexpression of gacA , overexpression of rsmA or rsmE , expression of various lacZ fusions, reverse transcription-PCR analysis, and determination of whole-cell lipase activity. The results demonstrated that the GacS-GacA (GacS/A) system activates lipA expression at both the transcriptional and the translational levels but that the translational level is the key regulatory pathway. Further results showed that the activation of lipA translation by the GacS/A system is mediated through RsmE, which inhibits lipA translation by binding to the ACAAGGAUGU sequence overlapping the Shine-Dalgarno (SD) sequence of lipA mRNA to hinder the access of the 30S ribosomal subunit to the SD sequence. Moreover, the GacS/A system promotes lipA transcription through the mediation of RsmA inhibiting lipA transcription via an unknown pathway. Besides the transcriptional repression, RsmA mainly activates lipA translation by negatively regulating rsmE translation. In , in P. protegens Pf-5, the Gac-RsmE system mainly and directly activates lipA translation and the Gac-RsmA system indirectly enhances lipA transcription.
机译:在假单胞菌属(Pseudomonas spp。)中,需要Gac-Rsm信号转导系统来生产脂肪酶。当前模型假设该系统诱导通过群体感应(QS)系统介导的脂肪酶基因转录。然而,没有关于基于N-酰基高丝氨酸内酯的QS系统或蛋白质假单胞菌中脂肪酶基因表达的调节的报道。在这项研究中,我们研究了通过缺失和过度表达gacA,过度表达rsmA或rsmE,多种lacZ融合蛋白的表达,逆转录-PCR对Gac-Rsm系统激活的Gac-Rsm系统激活的lipA表达的调控机制。分析,并确定全细胞脂肪酶活性。结果表明,GacS-GacA(GacS / A)系统在转录和翻译水平上都激活了lipA表达,但翻译水平是关键的调控途径。进一步的结果表明,GacS / A系统激活的lipA翻译是通过RsmE介导的,RsmE通过与与lipA mRNA的Shine-Dalgarno(SD)序列重叠的ACAAGGAUGU序列结合来抑制lipA翻译,从而阻碍了30S核糖体的进入。 SD序列的亚基。此外,GacS / A系统通过RsmA介导通过未知途径抑制lipA转录来促进lipA转录。除了转录抑制,RsmA主要通过负向调节rsmE翻译来激活lipA翻译。在P.protegens Pf-5中,Gac-RsmE系统主要直接激活lipA翻译,而Gac-RsmA系统间接增强lipA转录。

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