Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Herman O. Str. 15, 1022 Budapest, Hungary.
Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Herman O. Str. 15, 1022 Budapest, Hungary.
J Chromatogr A. 2018 Mar 30;1543:73-80. doi: 10.1016/j.chroma.2018.02.038. Epub 2018 Feb 21.
The knowledge about the activity of polyacetylenes was extended by their new acetylcholinesterase inhibition and antibacterial activity against plant pathogenic bacteria. For this discovery, an utmost streamlined workflow, which we consider to be of high potential in the field of natural product or superfood search was developed. It demonstrates the combined power of biological, biochemical and chemical fingerprints. Bioactive components of tansy (Tanacetum vulgare L.) root extract were profiled and identified by high-performance thin-layer chromatography hyphenated with in situ effect-directed analysis, chemical derivatizations and high-resolution mass spectrometry (HPTLC-UV/Vis/FLD-EDA-HRMS). The effect-directed profiling was performed using four bacterial bioassays including two plant pathogens, an antioxidant assay and acetyl- and butyrylcholinesterase inhibitory assays. The chromatographic, spectral and powerful mass spectrometric study of zones that exerted substantial antibacterial and/or antioxidant and/or acetylcholinesterase inhibitory effects allowed these multi-potent zones to be identified as polyacetylenes. Five polyacetylene compounds were assigned to be 2-non-1-ene-3,5,7-triynyl-3-vinyl-oxirane, 2-(2,4-hexadiynylidene)-3,4-epoxy-1,6-dioxaspiro[4.5]decane, trans- and cis-2-(2,4-hexadiynylidene)-1,6-dioxaspiro[4.5]dec-3-ene and tetradeca-2,4,6-triine-8-en-12-one. This study clearly showed the advantage of the combined use of different ionization sources, i.e. electrospray ionization via an elution-head based interface and also the Direct Analysis in Real Time interface, for HRMS analysis of compounds from the same class with very similar chromatographic behavior and polarity.
多炔类化合物的新乙酰胆碱酯酶抑制和抗植物病原菌活性的发现,扩展了人们对其活性的认识。为了实现这一发现,我们开发了一种最为简化的工作流程,我们认为这种流程在天然产物或超级食品的研究领域具有很高的潜力。该流程展示了生物、生化和化学指纹图谱的综合力量。通过高效薄层色谱与原位效应导向分析、化学衍生化和高分辨率质谱联用(HPTLC-UV/Vis/FLD-EDA-HRMS),对艾菊(Tanacetum vulgare L.)根提取物的生物活性成分进行了分析和鉴定。采用四种细菌生物测定方法(包括两种植物病原菌、抗氧化测定和乙酰胆碱酯酶和丁酰胆碱酯酶抑制测定)进行效应导向分析。对具有显著抗菌和/或抗氧化和/或乙酰胆碱酯酶抑制作用的区域进行色谱、光谱和强大的质谱研究,这些多效区域被鉴定为多炔类化合物。鉴定出的五种多炔类化合物分别为:2-壬-1-烯-3,5,7-三炔基-3-乙烯基环氧化物、2-(2,4-己二炔基)-3,4-环氧-1,6-二恶螺[4.5]癸烷、反式和顺式-2-(2,4-己二炔基)-1,6-二恶螺[4.5]癸-3-烯和十四烷-2,4,6-三炔-8-烯-12-酮。这项研究清楚地表明,结合使用不同的电离源(即通过基于洗脱头的接口进行电喷雾电离和实时直接分析接口)进行 HRMS 分析,对于具有非常相似色谱行为和极性的同一类化合物具有优势。