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通过基质辅助激光解吸电离质谱成像技术观察真菌寄生相互作用过程中的真菌代谢产物。

Visualizing fungal metabolites during mycoparasitic interaction by MALDI mass spectrometry imaging.

作者信息

Holzlechner Matthias, Reitschmidt Sonja, Gruber Sabine, Zeilinger Susanne, Marchetti-Deschmann Martina

机构信息

Institute of Chemical Technologies and Analytics, Vienna University of Technology, Vienna, Austria.

Institute of Microbiology, University of Innsbruck, Innsbruck, Austria.

出版信息

Proteomics. 2016 Jun;16(11-12):1742-6. doi: 10.1002/pmic.201500510. Epub 2016 Apr 13.

DOI:10.1002/pmic.201500510
PMID:26959280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4982067/
Abstract

Studying microbial interactions by MALDI mass spectrometry imaging (MSI) directly from growing media is a difficult task if high sensitivity is demanded. We present a quick and robust sample preparation strategy for growing fungi (Trichoderma atroviride, Rhizoctonia solani) on glass slides to establish a miniaturized confrontation assay. By this we were able to visualize metabolite distributions by MALDI MSI after matrix deposition with a home-built sublimation device and thorough recrystallization. We present for the first time MALDI MSI data for secondary metabolite release during active mycoparasitism.

摘要

如果需要高灵敏度,通过基质辅助激光解吸电离质谱成像(MSI)直接从生长培养基中研究微生物相互作用是一项艰巨的任务。我们提出了一种快速且稳健的样品制备策略,用于在载玻片上培养真菌(深绿木霉、立枯丝核菌),以建立小型化对峙试验。通过这种方法,我们能够在使用自制升华装置沉积基质并进行彻底重结晶后,通过MALDI MSI可视化代谢物分布。我们首次展示了在活跃的真菌寄生过程中次生代谢物释放的MALDI MSI数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f293/4982067/45d09603fef2/PMIC-16-1742-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f293/4982067/0979a4e7ea16/PMIC-16-1742-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f293/4982067/45d09603fef2/PMIC-16-1742-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f293/4982067/0979a4e7ea16/PMIC-16-1742-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f293/4982067/45d09603fef2/PMIC-16-1742-g002.jpg

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