Research School of Biology, Australian National University, Canberra, ACT, Australia.
Isotopomics in Chemical Biology Group, School of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an, China.
Methods Mol Biol. 2021;2306:105-121. doi: 10.1007/978-1-0716-1410-5_8.
Fatty acids are an essential structural and energy storage component of cells and hence there is much interest in their metabolism, requiring identification and quantification with readily available instrumentation, such as GC-MS. Fatty acid methyl esters (FAMEs) can be generated and extracted directly from biological tissue, in a one-pot process, and following high resolution GC, their respective chain length, degrees of unsaturation, and other functionalities can be readily identified using EI-MS. Defining the positions of the double bonds in the alkyl chain requires conversion of the FAMEs into their respective dimethyloxazoline (DMOX) derivatives. Following EI, this derivative allows charge retention on the heterocycle, and concomitant charge remote fragmentation of the alkyl chain to yield key double bond position identifying ions. The protocols described herein have been applied to the identification and quantification of fatty acids harvested from microalgae grown to produce biofuels and to the screening of salt tolerant Arabidopsis mutants.
脂肪酸是细胞的必需结构和储能成分,因此人们对其代谢非常感兴趣,需要使用 GC-MS 等易于获得的仪器进行鉴定和定量。脂肪酸甲酯 (FAME) 可以直接从生物组织中生成和提取,在一锅法中,在进行高分辨率 GC 后,可以使用 EI-MS 轻松识别其各自的链长、不饱和度和其他官能团。定义烷基链中双键的位置需要将 FAME 转化为各自的二甲氧基恶唑啉 (DMOX) 衍生物。EI 后,该衍生物允许杂环上保留电荷,并伴随烷基链的电荷远程断裂,产生关键的双键位置鉴定离子。本文所述的方案已应用于从用于生产生物燃料的微藻中提取的脂肪酸的鉴定和定量,以及耐盐拟南芥突变体的筛选。