Bauer Judith S, Hauck Nils, Christof Lisa, Mehnaz Samina, Gust Bertolt, Gross Harald
Department of Pharmaceutical Biology, Pharmaceutical Institute, University of Tuebingen, Tuebingen, Germany.
German Centre for Infection Research (DZIF), Partner site Tuebingen, Tuebingen, Germany.
PLoS One. 2016 Nov 18;11(11):e0167002. doi: 10.1371/journal.pone.0167002. eCollection 2016.
The shoot endophytic biocontrol strain Pseudomonas chlororaphis subsp. aurantiaca PB-St2 produces a wide range of exoproducts, including enzymes and antibiotics. The production of exoproducts is commonly tightly regulated. In order to get a deeper insight into the regulatory network of PB-St2, the strain was systematically investigated regarding its quorum sensing systems, both on the genetic and metabolic level. The genome analysis of PB-St2 revealed the presence of four putative acyl homoserine lactone (AHL) biosynthesis genes: phzI, csaI, aurI, and hdtS. LC-MS/MS analyses of the crude supernatant extracts demonstrated that PB-St2 produces eight AHLs. In addition, the concentration of all AHL derivatives was quantified time-resolved in parallel over a period of 42 h during the growth of P. aurantiaca PB-St2, resulting in production curves, which showed differences regarding the maximum levels of the AHLs (14.6 nM- 1.75 μM) and the production period. Cloning and heterologous overexpression of all identified AHL synthase genes in Escherichia coli proved the functionality of the resulting synthases PhzI, CsaI, and AurI. A clear AHL production pattern was assigned to each of these three AHL synthases, while the HdtS synthase did not lead to any AHL production. Furthermore, the heterologous expression study demonstrated unequivocally and for the first time that AurI directs the synthesis of two 3-oxo-AHLs.
芽内生生物防治菌株嗜氯假单胞菌亚种aurantantiaca PB-St2产生多种胞外产物,包括酶和抗生素。胞外产物的产生通常受到严格调控。为了更深入地了解PB-St2的调控网络,从遗传和代谢水平对该菌株的群体感应系统进行了系统研究。PB-St2的基因组分析揭示了四个假定的酰基高丝氨酸内酯(AHL)生物合成基因的存在:phzI、csaI、aurI和hdtS。对粗上清提取物的LC-MS/MS分析表明,PB-St2产生八种AHL。此外,在嗜氯假单胞菌PB-St2生长的42小时内,对所有AHL衍生物的浓度进行了时间分辨的平行定量,得到了生产曲线,这些曲线显示了AHL的最大水平(14.6 nM - 1.75 μM)和生产期的差异。在大肠杆菌中对所有鉴定出的AHL合酶基因进行克隆和异源过表达,证明了所得合酶PhzI、CsaI和AurI的功能。为这三种AHL合酶中的每一种都确定了明确的AHL产生模式,而HdtS合酶未导致任何AHL产生。此外,异源表达研究首次明确证明AurI指导两种3-氧代-AHL的合成。