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A novel assay for the detection of bioactive volatiles evaluated by screening of lichen-associated bacteria

机译:通过筛选地衣相关细菌来评估生物活性挥发物检测的新方法

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摘要

Volatile organic compounds (VOCs) produced by microorganisms are known both for their effect on pathogens and their role as mediators in various interactions and communications. Previous studies have demonstrated the importance of VOCs for ecosystem functioning as well as their biotechnological potential, but screening for bioactive volatiles remained difficult. We have developed an efficient testing assay that is based on two multi-well plates, separated by a sealing silicone membrane, two tightening clamps, and variable growth media, or indicators. The experiment design as presented here is a novel and robust technique to identify positive as well as negative VOC effects on the growth of a target organism and to test for specific substances e.g., hydrogen cyanide which can be detected with a suitable indicator. While the first pre-screening assay is primarily based on indicator color change and visible growth diameter reduction, we also introduce an advanced and quantitatively precise experiment design. This adaptation involves qPCR-based quantification of viable target cells after concluding the treatment with VOCs. Therefore, we chose preselected active isolates and compared the partial 16S rRNA gene copy number of headspace-exposed E. coli with non-treated controls. Separately obtained headspace SPME and GC/MS-based profiles of selected bacterial isolates revealed the presence of specific and unique signatures which suggests divergent modes of action. The assay was evaluated by screening 100 isolates of lung lichen-associated bacteria. Approximately one quarter of the isolates showed VOC-based antibacterial and/or antifungal activity; mainly Pseudomonas and Stenotrophomonas species were identified as producers of bioactive volatiles.
机译:微生物产生的挥发性有机化合物(VOC)既对病原体产生影响,又在各种相互作用和通讯中起中介作用。先前的研究表明,挥发性有机化合物对生态系统功能的重要性及其生物技术潜力,但对生物活性挥发物的筛查仍然很困难。我们已经开发了一种有效的测试分析方法,该方法基于两个多孔板,这些多孔板被密封的硅胶膜,两个紧固夹以及可变生长培养基或指示剂隔开。此处介绍的实验设计是一种新颖而强大的技术,可以识别对目标生物生长的正,负VOC效应,并测试可以用合适的指示剂检测到的特定物质,例如氰化氢。虽然第一个预筛选测定法主要基于指示剂颜色变化和可见的生长直径减小,但我们还引入了先进的定量精确实验设计。这种适应性包括在用VOC结束治疗后对活靶细胞进行基于qPCR的定量。因此,我们选择了预先选择的活性分离物,并将顶空暴露的大肠杆菌的16S rRNA基因部分拷贝数与未处理的对照进行了比较。单独获得的顶空SPME和基于GC / MS的选定细菌分离物谱揭示了特定和独特特征的存在,表明存在不同的作用方式。通过筛选100株与肺地衣相关细菌的分离株来评估该测定。大约四分之一的分离物显示出基于VOC的抗菌和/或抗真菌活性。主要鉴定出假单胞菌属和嗜单胞菌属物种是生物活性挥发物的产生者。

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