Centre of Microbial and Plant Genetics, KU Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee-Leuven, Belgium.
Environ Microbiol Rep. 2013 Feb;5(1):160-9. doi: 10.1111/1758-2229.12015. Epub 2012 Dec 4.
The interaction of WLIP (white line-inducing principle), a member of the viscosin group of Pseudomonas lipopeptides, with tolaasin, a lipopeptide mycotoxin secreted by Pseudomonas tolaasii, enables identification of the mushroom pathogen relying on formation of a lipopeptide coprecipitate between confronted colonies of an indicator strain (designated Pseudomonas 'reactans') and P. tolaasii. The WLIP non-ribosomal lipopeptide synthesis system of the mushroom isolate P. 'reactans' LMG 5329 (Wip) was identified and shown to be most similar to the Pseudomonas fluorescens SBW25 viscosin system (Visc), but remarkably different from the WLIP-generating Wlp system previously identified in the rice rhizosphere isolate Pseudomonas putida RW10S2. The Wlp machinery is composed of modules most similar to those recruited for biosynthesis of the non-viscosin-type lipopeptides putisolvin and entolysin by strains from the P. putida clade. In line with the pronounced synteny between the wip and visc flanking regions, strain LMG 5329 was identified as an authentic P. fluorescens closely related to strain SBW25. In both P. putida and P. fluorescens, WLIP production confers similar phenotypes of microbial antagonism and surface colonization. Genotypes other than wlp or wip were not identified among WLIP producers isolated from mushroom, maize rhizosphere or water.
WLIP(假单胞菌脂肽属中的白线诱导原理)与来自木霉假单胞菌的脂肽真菌毒素托拉菌素的相互作用,使我们能够根据指示菌株(指定为假单胞菌“反应型”)和木霉假单胞菌对峙菌落之间形成脂肽共沉淀来识别蘑菇病原体。蘑菇分离株 P. '反应型' LMG 5329(Wip)的 WLIP 非核糖体脂肽合成系统被鉴定出来,并显示出与荧光假单胞菌 SBW25 粘菌素系统(Visc)最相似,但与先前在水稻根际分离的假单胞菌 RW10S2 中发现的产生 WLIP 的 Wlp 系统有显著差异。Wlp 机械由与粘菌素型脂肽 PUT 合成相关的模块组成,而 PUT 合成由来自 P. putida 群的菌株产生。与 wip 和 visc 侧翼区域之间的明显同线性一致,LMG 5329 菌株被鉴定为与 SBW25 菌株密切相关的真正荧光假单胞菌。在 P. putida 和 P. fluorescens 中,WLIP 的产生赋予了相似的微生物拮抗和表面定植表型。在从蘑菇、玉米根际或水中分离的 WLIP 产生菌中,没有发现除 wlp 或 wip 以外的基因型。