de Bruijn I, Raaijmakers J M
Laboratory of Phytopathology, Wageningen University, Wageningen, The Netherlands.
Appl Environ Microbiol. 2009 Jul;75(14):4753-61. doi: 10.1128/AEM.00575-09. Epub 2009 May 15.
Cyclic lipopeptides (CLPs) are produced by many Pseudomonas species and have several biological functions, including a role in surface motility, biofilm formation, virulence, and antimicrobial activity. This study focused on the diversity and role of LuxR-type transcriptional regulators in CLP biosynthesis in Pseudomonas species and, specifically, viscosin production by Pseudomonas fluorescens strain SBW25. Phylogenetic analyses showed that CLP biosynthesis genes in Pseudomonas strains are flanked by LuxR-type regulators that contain a DNA-binding helix-turn-helix domain but lack N-acylhomoserine lactone-binding or response regulator domains. For SBW25, site-directed mutagenesis of the genes coding for either of the two identified LuxR-type regulators, designated ViscAR and ViscBCR, strongly reduced transcript levels of the viscABC biosynthesis genes and resulted in a loss of viscosin production. Expression analyses further showed that a mutation in either viscAR or viscBCR did not substantially (change of <2.5-fold) affect transcription of the other regulator. Transformation of the DeltaviscAR mutant of SBW25 with a LuxR-type regulatory gene from P. fluorescens strain SS101 that produces massetolide, a CLP structurally related to viscosin, restored transcription of the viscABC genes and viscosin production. The results further showed that a functional viscAR gene was required for heterologous expression of the massetolide biosynthesis genes of strain SS101 in strain SBW25, leading to the production of both viscosin and massetolide. Collectively, these results indicate that the regulators flanking the CLP biosynthesis genes in Pseudomonas species represent a unique LuxR subfamily of proteins and that viscosin biosynthesis in P. fluorescens SBW25 is controlled by two LuxR-type transcriptional regulators.
环脂肽(CLPs)由许多假单胞菌属物种产生,并具有多种生物学功能,包括在表面运动性、生物膜形成、毒力和抗菌活性方面发挥作用。本研究聚焦于假单胞菌属物种中LuxR型转录调节因子在CLP生物合成中的多样性和作用,特别是荧光假单胞菌菌株SBW25产生的黏性放线菌素。系统发育分析表明,假单胞菌菌株中的CLP生物合成基因两侧是LuxR型调节因子,这些调节因子含有DNA结合螺旋-转角-螺旋结构域,但缺乏N-酰基高丝氨酸内酯结合或应答调节结构域。对于SBW25,对编码两个已鉴定的LuxR型调节因子(分别命名为ViscAR和ViscBCR)之一的基因进行定点诱变,强烈降低了viscABC生物合成基因的转录水平,并导致黏性放线菌素产量丧失。表达分析进一步表明,viscAR或viscBCR中的突变对另一个调节因子的转录没有实质性影响(变化小于2.5倍)。用来自荧光假单胞菌菌株SS101的LuxR型调节基因转化SBW25的DeltaviscAR突变体,该基因产生与黏性放线菌素结构相关的CLP——马西菌素,恢复了viscABC基因的转录和黏性放线菌素的产生。结果还表明,功能性viscAR基因是菌株SS101的马西菌素生物合成基因在菌株SBW25中异源表达所必需的,从而导致黏性放线菌素和马西菌素的产生。总体而言,这些结果表明,假单胞菌属物种中CLP生物合成基因两侧的调节因子代表了一个独特的LuxR蛋白亚家族,荧光假单胞菌SBW25中的黏性放线菌素生物合成受两个LuxR型转录调节因子控制。