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Autoregulation of subtilin biosynthesis in Bacillus subtilis:the role of the spa-box in subtilin-responsive promoters

机译:枯草芽孢杆菌中枯草杆菌素生物合成的自动调节:spa-box在枯草杆菌素响应启动子中的作用

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摘要

The production of the type I antimicrobial peptide (AMP) subtilin by Bacillus subtilis is regulated in a cell-density-dependent manner. Three subtilin-responsive promoter elements within the spaBTCSIFEGRK are controlled by the specific cis-acting sequence element called the spa-box, which represents the binding site of the subtilin regulator SpaR. Here, we describe the functional characterization of the spaB, spaS and spaI promoters by transcriptional fusion with a promoterless β-glucuronidase encoding gusA gene. Within these gusA fusion constructs, transcription initiation start sites of the spaS and spaI promoters were mapped to be located downstream of the spa-box, which is in contrast to previous reports. Nevertheless, all spa-promoters displayed typical cell-density-dependent activity in a subtilin-producing strain B. subtilis ATCC6633. Moreover, analysis of β-glucuronidase activities in a spaB mutant of B. subtilis ATCC6633 and a derivative of strain 168 that harbors the spaRK genes integrated in the chromosomal amyE locus, confirmed that these promoters are activated by subtilin-triggered, SpaRK-mediated, quorum-sensing control. Quantitative analysis showed that the spaS promoter strength at a given subtilin concentration appeared to be approximately five-fold higher than the spaB promoter, which in turn is approximately two-fold higher than the spaI promoter. Finally, it is shown that the elementary components involved in subtilin-mediated regulation are the two-component system, SpaRK, and a spa-box containing promoter.
机译:枯草芽孢杆菌以细胞密度依赖性方式调节I型抗菌肽(AMP)枯草杆菌蛋白酶的产生。 spaBTCSIFEGRK中的三个枯草杆菌素响应性启动子元件由称为spa-box的特定顺式作用序列元件控制,它代表枯草杆菌素调节剂SpaR的结合位点。在这里,我们描述了通过与无启动子的编码gusA基因的β-葡萄糖醛酸苷酶的转录融合来实现spaB,spaS和spaI启动子的功能表征。在这些gusA融合构建体中,spaS和spaI启动子的转录起始起始位点被定位为位于spa-box的下游,这与以前的报道相反。然而,所有的spa启动子在产生枯草杆菌的菌株枯草芽孢杆菌ATCC6633中显示出典型的细胞密度依赖性活性。此外,对枯草芽孢杆菌ATCC6633的spaB突变体和带有整合在染色体amyE基因座中的spaRK基因的菌株168的衍生物进行的β-葡萄糖醛酸苷酶活性分析表明,这些启动子是由枯草蛋白酶触发的,SpaRK介导的,群体感应控制。定量分析表明,在给定的枯草杆菌蛋白酶浓度下,spaS启动子强度似乎比spaB启动子高约5倍,而spaB启动子则比spaI启动子高约2倍。最后,显示了枯草杆菌蛋白酶介导的调控中涉及的基本成分是两成分系统SpaRK和一个含有启动子的spa盒。

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