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优化生物营养型原生动物植物病原体的孢子纯化和蛋白质提取技术。

Optimisation of Sporosori Purification and Protein Extraction Techniques for the Biotrophic Protozoan Plant Pathogen .

机构信息

Tasmanian Institute of Agriculture, New Town Research Laboratories, University of Tasmania, New Town, Tasmania 7008, Australia.

Central Science Laboratory, University of Tasmania, Hobart, Tasmania 7001, Australia.

出版信息

Molecules. 2020 Jul 8;25(14):3109. doi: 10.3390/molecules25143109.

Abstract

is a soil-borne plant pathogen responsible for the economically significant root and powdery scab diseases of potato. However, the obligate biotrophic nature of has made the detailed study of the pathogen problematic. Here, we first compared the benefits of sporosori partial purification utilizing Ludox gradient centrifugation. We then undertook optimization efforts for protein isolation comparing the use of a urea buffer followed by single-pot solid-phase-enhanced sample preparation (SP3) and a sodium dodecyl sulphate (SDS) buffer followed by suspension-trapping (S-Trap). Label-free, quantitative proteomics was then used to evaluate the efficiency of the sporosori purification and the protein preparation methods. The purification protocol produced a highly purified suspension of sporosori without affecting the viability of the spores. The results indicated that the use of a combination of SDS and S-Trap for sample clean-up and digestion obtained a significantly higher number of identified proteins compared to using urea and SP3, with 218 and 652 proteins identified using the SP3 and S-Trap methods, respectively. The analysis of proteins by mass spectrometry showed that the number of identified proteins increased by approximately 40% after the purification of spores by Ludox. These results suggested a potential use of the described spore purification and protein preparation methods for the proteomics study of obligate biotrophic pathogens such as .

摘要

是一种土传植物病原体,可导致马铃薯的重要根和粉状痂疾病。然而, 的专性活体营养性质使得对病原体的详细研究变得成问题。在这里,我们首先比较了利用 Ludox 梯度离心法对孢子体进行部分纯化的好处。然后,我们比较了使用脲缓冲液然后进行单罐固相增强样品制备(SP3)和十二烷基硫酸钠(SDS)缓冲液然后进行悬浮陷阱(S-Trap)的方法,以优化蛋白质分离。然后使用无标记定量蛋白质组学来评估孢子体的纯化和蛋白质制备方法的效率。该纯化方案产生了高度纯化的 孢子体悬浮液,而不会影响孢子的活力。结果表明,与使用脲和 SP3 相比,SDS 和 S-Trap 组合用于样品净化和消化可获得明显更多的鉴定蛋白,分别使用 SP3 和 S-Trap 方法可鉴定出 218 和 652 种蛋白质。通过质谱法分析蛋白质表明,用 Ludox 纯化孢子后,鉴定出的蛋白质数量增加了约 40%。这些结果表明,所描述的孢子纯化和蛋白质制备方法可用于研究专性活体营养病原体,如 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc8c/7397026/b57cb46790d5/molecules-25-03109-g001.jpg

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