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首页> 外文期刊>Environmental microbiology >The guanidinobutyrase GbuA is essential for the alkylquinolone-regulated pyocyanin production during parasitic growth of Pseudomonas aeruginosa in co-culture with Aeromonas hydrophila
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The guanidinobutyrase GbuA is essential for the alkylquinolone-regulated pyocyanin production during parasitic growth of Pseudomonas aeruginosa in co-culture with Aeromonas hydrophila

机译:在铜绿假单胞菌与嗜水气单胞菌共培养的寄生虫生长过程中,胍基丁酸水解酶GbuA对于烷基喹诺酮调节的绿脓素生成至关重要。

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摘要

The opportunistic pathogen Pseudomonas aeruginosa controls the production of virulence factors by quorum sensing (QS). Besides cell density, QS in P. aeruginosa is co-regulated by metabolic influences, especially nutrient limitation. Previously, a co-culture model system was established consisting of P. aeruginosa and the chitinolytic bacterium Aeromonas hydrophila, in which parasitic growth of P. aeruginosa is strictly dependent on the QS-controlled production of pyocyanin in response to nutrient limitation (Jagmann et al., 2010). In this study, the co-culture was employed to identify novel genes involved in the regulation of pyocyanin production. Via transposon mutagenesis, the gene gbuA encoding a guanidinobutyrase was identified, deletion of which led to a loss of pyocyanin production in co-cultures and to a reduced pyocyanin production in single cultures. Addition of the natural substrate of GbuA to the mutant strain enhanced the negative effect on pyocyanin production in single cultures. The gbuA mutant showed a reduced transcription of the pqsABCDE operon and could be complemented by PqsE overexpression and addition of alkylquinolone signal molecules. The strong effect of gbuA deletion on the QS-controlled pyocyanin production in co-cultures showed the value of this approach for the discovery of novel gene functions linking metabolism and QS in P. aeruginosa.
机译:机会性病原菌铜绿假单胞菌通过群体感应(QS)控制毒力因子的产生。除细胞密度外,铜绿假单胞菌的QS还受代谢影响(尤其是营养限制)的共同调节。以前,建立了由铜绿假单胞菌和几丁质分解细菌嗜水气单胞菌组成的共培养模型系统,其中铜绿假单胞菌的寄生生长严格依赖于QS控制的绿素的生产,以响应营养限制(Jagmann等(2010年)。在这项研究中,共培养被用于识别参与黄绿素生成调控的新基因。通过转座子诱变,鉴定出编码胍基丁酸酶的基因gbuA,其缺失导致共培养物中的花青素产量减少,而单培养物中的花青素产量降低。将GbuA的天然底物添加到突变菌株中,可增强单一培养物中对绿脓素生成的负面影响。 gbuA突变体显示pqsABCDE操纵子的转录减少,并且可以由PqsE过表达和烷基喹诺酮信号分子的添加来补充。 gbuA删除对共培养中QS控制的绿脓素产量的强烈影响表明,该方法对于发现将新陈代谢与QS铜绿假单胞菌联系起来的新型基因功能的价值。

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