Aix-Marseille University, CNRS, CEA, UMR7265, Biosciences and Biotechnologies Institute of Aix-Marseille, CEA/Cadarache, Saint-Paul-lez-Durance, France.
Methods Mol Biol. 2022;2526:181-189. doi: 10.1007/978-1-0716-2469-2_13.
Because they are highly unsaturated, plant lipids are sensitive to oxidation and constitute a primary target of reactive oxygen species. Therefore, quantification of lipid peroxidation provides a pertinent approach to evaluating oxidative stress in plants. Here, we describe a simple method to measure upstream products of the peroxidation of the major polyunsaturated fatty acids in plants, namely, linolenic acid (C18:3) and linoleic acid (C18:2). The method uses conventional HPLC with UV detection to measure hydroxy C18:3 and C18:2 after reduction of their respective hydroperoxides. The described experimental approach requires low amounts of plant material (a few hundred milligrams), monitors oxidation of both membrane and free fatty acids, and can discriminate between enzymatic and non-enzymatic lipid peroxidation.
由于植物脂质高度不饱和,容易受到氧化的影响,因此是活性氧物质的主要目标之一。因此,脂质过氧化的定量分析提供了一种评估植物氧化应激的有效方法。在这里,我们描述了一种简单的方法来测量植物中主要多不饱和脂肪酸(亚油酸(C18:3)和亚麻酸(C18:2))过氧化的上游产物。该方法使用常规 HPLC 结合 UV 检测,在还原各自的氢过氧化物后测量羟基 C18:3 和 C18:2。所描述的实验方法需要少量的植物材料(几百毫克),可监测膜和游离脂肪酸的氧化,并能区分酶促和非酶促脂质过氧化。