Castellaneta Andrea, Losito Ilario, Losacco Valentina, Leoni Beniamino, Santamaria Pietro, Calvano Cosima D, Cataldi Tommaso R I
Dipartimento di Chimica, Università degli Studi di Bari "Aldo Moro", Bari, Italy.
Centro Interdipartimentale SMART, Università degli Studi di Bari "Aldo Moro", Bari, Italy.
J Mass Spectrom. 2021 Aug 28;56(10):e4784. doi: 10.1002/jms.4784.
The uncontrolled activation of endogenous enzymes may introduce both qualitative and quantitative artefacts when lipids are extracted from vegetal matrices. In the present study, a method based on hydrophilic interaction liquid chromatography coupled either to high-resolution/accuracy Fourier-transform mass spectrometry (HILIC-ESI-FTMS) or to linear ion trap multiple stage mass spectrometry (HILIC-ESI-MS , with n = 2 and 3) with electrospray ionization was developed to unveil one of those artefacts. Specifically, the artificial generation of methyl esters of phosphatidic acids (MPA), catalysed by endogenous phospholipase D (PLD) during lipid extraction from five oleaginous microgreen crops (chia, soy, flax, sunflower and rapeseed), was studied. Phosphatidylcholines (PC) and phosphatidylglycerols (PG) were found to be the most relevant precursors of MPA among glycerophospholipids (GPLs), being involved in a transphosphatidylation process catalysed by PLD and having methanol as a coreactant. The combination of MS and MS measurements enabled the unambiguous recognition of MPA from their fragmentation pathways, leading to distinguish them from isobaric PA including a further CH group on their side chains. PLD was also found to catalyse the hydrolysis of PC and PG to phosphatidic acids (PAs). The described transformations were confirmed by the remarkable decrease of MPA abundance observed when isopropanol, known to inhibit PLD, was tentatively adopted instead of water during the homogenization of microgreens. The unequivocal identification of MPA might be exploited to assess if GPL alterations are actually triggered by endogenous PLD during lipid extractions from specific vegetal tissues.
当从植物基质中提取脂质时,内源性酶的失控激活可能会引入定性和定量假象。在本研究中,开发了一种基于亲水相互作用液相色谱与高分辨率/高精度傅里叶变换质谱(HILIC-ESI-FTMS)或线性离子阱多级质谱(HILIC-ESI-MS,n = 2和3)联用并结合电喷雾电离的方法,以揭示其中一种假象。具体而言,研究了在从五种富油微型蔬菜作物(奇亚籽、大豆、亚麻、向日葵和油菜籽)中提取脂质期间,内源性磷脂酶D(PLD)催化产生的磷脂酸甲酯(MPA)的人工生成情况。在甘油磷脂(GPL)中,磷脂酰胆碱(PC)和磷脂酰甘油(PG)被发现是MPA最相关的前体,它们参与由PLD催化的转磷脂酰基过程,并以甲醇作为共反应物。MS和MS测量的结合使得能够从MPA的碎裂途径明确识别MPA,从而将它们与侧链上还含有一个-CH基团的等压PA区分开来。还发现PLD催化PC和PG水解为磷脂酸(PA)。当在微型蔬菜匀浆过程中尝试用已知可抑制PLD的异丙醇代替水时,观察到MPA丰度显著降低,这证实了上述转化。MPA的明确鉴定可用于评估在从特定植物组织提取脂质期间,GPL的改变是否实际上是由内源性PLD触发的。