首页> 外文OA文献 >Repression of Phenazine Antibiotic Production in Pseudomonas aureofaciens Strain 30-84 by RpeA
【2h】

Repression of Phenazine Antibiotic Production in Pseudomonas aureofaciens Strain 30-84 by RpeA

机译:RpeA抑制金黄色假单胞菌菌株30-84中的吩嗪抗生素生产

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pseudomonas aureofaciens strain 30-84 is a biological control bacterium that utilizes a two-component GacS/GacA regulatory system interconnected with the PhzR/PhzI quorum sensing system to positively regulate biosynthesis of phenazine antibiotics that contribute to its association with plant hosts. To date, no negative regulators of phenazine production have been identified, nor has the role of repression been studied. Here we describe a novel repressor of secondary metabolism in P. aureofaciens strain 30-84, RpeA, whose deduced amino acid sequence is similar to those of a group of putative two-component regulatory systems of unknown function found in several animal and plant-pathogenic bacteria. In minimal medium where phenazine production is very low, inactivation of the rpeA gene enhanced phenazine biosynthetic gene expression and increased phenazine production but did not increase quorum sensing signal accumulation. Furthermore, RpeA functioned to block phenazine biosynthetic gene transcription in minimal medium even when quorum-sensing signals were at a level that was sufficient for induction of phenazine gene expression in rich medium. Additionally, in the absence of rpeA, the quorum sensor PhzR was not required for phenazine production. Although repression plays a critical role in phenazine regulation, the rpeA mutation could not bypass the requirement for a functional GacS/GacA system, demonstrating that activation is required even in the absence of the RpeA repressor. This study reinforces that multiple signals, including nutrition and population density, are integrated to control the appropriate expression of phenazine antibiotics.
机译:金黄假单胞菌菌株30-84是一种生物防治细菌,利用两组分GacS / GacA调节系统与PhzR / PhzI群体感应系统互连,从而积极调节吩嗪抗生素的生物合成,从而有助于其与植物宿主的缔合。迄今为止,尚未鉴定出吩嗪产生的负调节剂,也未研究抑制作用。在这里,我们描述了一种新的阻遏金黄色葡萄球菌菌株30-84 RpeA的次级代谢新抑制剂,其推导的氨基酸序列与在几种动植物病原体中发现的一组未知功能的假定的两组分调节系统相似。菌。在吩嗪产量非常低的基本培养基中,rpeA基因的失活会增强吩嗪生物合成基因的表达并增加吩嗪的产量,但不会增加群体感应信号的积累。此外,即使群体感应信号处于足以诱导在丰富培养基中吩嗪基因表达的水平,RpeA仍能在最小培养基中阻断吩嗪生物合成基因的转录。此外,在不存在rpeA的情况下,吩嗪的生产不需要定额传感器PhzR。尽管阻抑在吩嗪调节中起着关键作用,但rpeA突变不能绕过功能性GacS / GacA系统的要求,这表明即使在没有RpeA阻遏物的情况下也需要激活。这项研究加强了包括营养和人口密度在内的多个信号的整合,以控制吩嗪抗生素的适当表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号