González-Cabanelas D, Hammerbacher A, Raguschke B, Gershenzon J, Wright L P
Max Planck Institute for Chemical Ecology, Jena, Germany.
Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.
Methods Enzymol. 2016;576:225-49. doi: 10.1016/bs.mie.2016.02.025. Epub 2016 Mar 24.
The 2-C-methyl-d-erythritol 4-phosphate (MEP) pathway occurs in the plastids of higher plants and in most economically important prokaryotes where it is responsible for the biosynthesis of the isoprenoid building blocks, isopentenyl diphosphate and dimethylallyl diphosphate. These five-carbon compounds are the substrates for the enormous variety of terpenoid products, including many essential metabolites and substances of commercial value. Increased knowledge of the regulation of the MEP pathway is critical to understanding many aspects of plant and microbial metabolism as well as in developing biotechnological platforms for producing these commercially valuable isoprenoids. To achieve this goal, researchers must have the ability to investigate the in vivo kinetics of the pathway by accurately measuring the concentrations of MEP pathway metabolites. However, the low levels of these metabolites complicate their accurate determination without suitable internal standards. This chapter describes a sensitive method to accurately determine the concentrations of MEP pathway metabolites occurring at trace amounts in biological samples using liquid chromatography coupled to triple quadrupole mass spectrometry. In addition, simple protocols are given for producing stable isotope-labeled internal standards for these analyses.
2-C-甲基-D-赤藓糖醇-4-磷酸(MEP)途径存在于高等植物的质体以及大多数具有重要经济意义的原核生物中,该途径负责类异戊二烯构建单元异戊烯基二磷酸和二甲基烯丙基二磷酸的生物合成。这些五碳化合物是种类繁多的萜类产物的底物,包括许多必需代谢物和具有商业价值的物质。深入了解MEP途径的调控对于理解植物和微生物代谢的诸多方面以及开发用于生产这些具有商业价值类异戊二烯的生物技术平台至关重要。为实现这一目标,研究人员必须具备通过准确测量MEP途径代谢物浓度来研究该途径体内动力学的能力。然而,这些代谢物含量较低,若无合适的内标,准确测定它们会变得复杂。本章介绍了一种灵敏的方法,该方法使用液相色谱-三重四极杆质谱联用技术准确测定生物样品中痕量存在的MEP途径代谢物的浓度。此外,还给出了用于这些分析的稳定同位素标记内标的简单制备方案。