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使用超临界流体色谱-中真空化学电离串联质谱法对番茄叶中生育酚及其氧化产物进行快速分析。

Rapid Analysis for -Tocopherol and Its Oxidative Products in the L. Leaf Using Supercritical Fluid Chromatography-Medium Vacuum Chemical Ionization Tandem Mass Spectrometry.

作者信息

Hondo Toshinobu, Miyake Yumi, Toyoda Michisato

机构信息

Forefront Research Center, Graduate School of Science, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043, Japan.

MS-Cheminformatics LLC, 2-13-21 Sasao-nishi, Toin, Inabe, Mie 511-0231, Japan.

出版信息

Mass Spectrom (Tokyo). 2024;13(1):A0153. doi: 10.5702/massspectrometry.A0153. Epub 2024 Oct 12.

DOI:10.5702/massspectrometry.A0153
PMID:39411199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11474449/
Abstract

A method for the rapid determination of -tocopherol (-T) and its oxidative products in plant tissue has been developed using supercritical fluid extraction (SFE) coupled with supercritical fluid chromatography (SFC) and medium vacuum chemical ionization (MVCI) with tandem mass spectrometry. The method is designed to study changes in levels for -T and its oxidative products in plant cells during photosynthesis, aiming to observe the light response curves. -T oxidation is a non-enzymatic self-defense mechanism in plant cells. Unlike enzyme-involved reactions, it cannot be stopped, so the oxidation continues in crude extracts even after extraction. Therefore, a real-time method is essential for tracking the light response curves. To optimize the selective reaction monitoring method, the reaction mixture of -T and singlet oxygen (O), generated by rose Bengal under light illumination, was used as the source of oxidative products. The relative abundance changes in -tocopherylquinone and 8a-hydroperoxy tocopherone in L. (Pea) leaves under excessive light illumination have been preliminarily analyzed as part of the light response curve study. The method archives a throughput of 10-15 minutes for analyzing duplicate leaf samples. This process includes cutting off the leaf, sectioning it, placing the sample in a frozen SFE vessel, and conducting SFE/SFC analysis. Consequently, the average throughput is approximately 5-7 minutes per sample.

摘要

已开发出一种使用超临界流体萃取(SFE)结合超临界流体色谱(SFC)以及中真空化学电离(MVCI)和串联质谱法快速测定植物组织中生育酚(-T)及其氧化产物的方法。该方法旨在研究光合作用过程中植物细胞内-T及其氧化产物水平的变化,以观察光响应曲线。-T氧化是植物细胞中的一种非酶促自我防御机制。与酶参与的反应不同,它无法停止,因此即使在提取后,粗提物中的氧化仍会继续。所以,一种实时方法对于追踪光响应曲线至关重要。为优化选择性反应监测方法,以孟加拉玫瑰红在光照下产生的-T与单线态氧(O)的反应混合物作为氧化产物来源。作为光响应曲线研究的一部分,已初步分析了豌豆叶片在强光照射下生育醌和8a-氢过氧化生育酚的相对丰度变化。该方法分析重复叶片样品的通量为10至15分钟。此过程包括切下叶片、切片、将样品放入冷冻的SFE容器中以及进行SFE/SFC分析。因此,每个样品的平均通量约为5至7分钟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/35003cfaefd6/massspectrometry-13-1-A0153-figure08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/e2fe5ceebd72/massspectrometry-13-1-A0153-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/ee78f35ef11e/massspectrometry-13-1-A0153-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/74ce06c19592/massspectrometry-13-1-A0153-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/88919b6c3e2e/massspectrometry-13-1-A0153-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/d1fcaa3bf94d/massspectrometry-13-1-A0153-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/093ccd3b06e1/massspectrometry-13-1-A0153-figure06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/986eb53849cb/massspectrometry-13-1-A0153-figure07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/35003cfaefd6/massspectrometry-13-1-A0153-figure08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/e2fe5ceebd72/massspectrometry-13-1-A0153-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/ee78f35ef11e/massspectrometry-13-1-A0153-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/74ce06c19592/massspectrometry-13-1-A0153-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/88919b6c3e2e/massspectrometry-13-1-A0153-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/d1fcaa3bf94d/massspectrometry-13-1-A0153-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/093ccd3b06e1/massspectrometry-13-1-A0153-figure06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/986eb53849cb/massspectrometry-13-1-A0153-figure07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8381/11474449/35003cfaefd6/massspectrometry-13-1-A0153-figure08.jpg

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