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MALDI-based intact spore mass spectrometry of downy and powdery mildews

机译:基于MALDI的霜霉病和白粉病完整孢子质谱

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摘要

Fast and easy identification of fungal phytopathogens is of great importance in agriculture. In this context, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) has emerged as a powerful tool for analyzing microorganisms. This study deals with a methodology for MALDI-TOF MS-based identification of downy and powdery mildews representing obligate biotrophic parasites of crop plants. Experimental approaches for the MS analyses were optimized using Bremia lactucae, cause of lettuce downy mildew, and Oidium neolycopersici, cause of tomato powdery mildew. This involved determining a suitable concentration of spores in the sample, selection of a proper MALDI matrix, looking for the optimal solvent composition, and evaluation of different sample preparation methods. Furthermore, using different MALDI target materials and surfaces (stainless steel vs polymer-based) and applying various conditions for sample exposure to the acidic MALDI matrix system were investigated. The dried droplet method involving solvent evaporation at room temperature was found to be the most suitable for the deposition of spores and MALDI matrix on the target and the subsequent crystallization. The concentration of spore suspension was optimal between 2 and 5 × 10 ~9 spores per ml. The best peptide/protein profiles (in terms of signal-to-noise ratio and number of peaks) were obtained by combining ferulic and sinapinic acids as a mixed MALDI matrix. A pretreatment of the spore cell wall with hydrolases was successfully introduced prior to MS measurements to obtain more pronounced signals. Finally, a novel procedure was developed for direct mass spectra acquisition from infected plant leaves.
机译:快速简便地鉴定真菌性植物病原体在农业中非常重要。在这种情况下,基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)已成为分析微生物的强大工具。这项研究涉及一种基于MALDI-TOF MS的霜霉病和白粉病鉴定方法,这些霜霉病和白粉病代表农作物的专性生物营养寄生虫。 MS分析的实验方法使用莴苣霜霉病的致病菌Bremia lactucae和番茄霜霉病的致病菌Oidium neolycopersici进行了优化。这涉及确定样品中合适的孢子浓度,选择合适的MALDI基质,寻找最佳的溶剂组成以及评估不同的样品制备方法。此外,研究了使用不同的MALDI目标材料和表面(不锈钢vs聚合物基),并应用了各种条件使样品暴露于酸性MALDI基质系统。发现在室温下涉及溶剂蒸发的干滴法最适合在目标上沉积孢子和MALDI基质,以及随后的结晶。孢子悬浮液的浓度在每毫升2至5×10〜9个孢子之间为最佳。通过将阿魏酸和芥子酸混合成混合MALDI基质,可获得最佳的肽/蛋白质谱(就信噪比和峰数而言)。在进行MS测量之前,成功地采用了水解酶对孢子细胞壁进行了预处理,从而获得了更明显的信号。最后,开发了一种新方法,可从受感染的植物叶片中直接进行质谱采集。

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