ANALYSIS OF MOLECULAR-SPECIES OF PLANT POLAR LIPIDS BY HIGH-PERFORMANCE AND GAS-LIQUID CHROMATOGRAPHY
ANALYSIS OF MOLECULAR-SPECIES OF PLANT POLAR LIPIDS BY HIGH-PERFORMANCE AND GAS-LIQUID CHROMATOGRAPHY
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DOI:
10.1016/s0031-9422(00)80752-9
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发表时间:
1985-01-01
期刊:
影响因子:
3.8
通讯作者:
MAZLIAK, P
中科院分区:
文献类型:
--
作者:
DEMANDRE, C;TREMOLIERES, A;MAZLIAK, P
Total lipid extracts from potato tubers and tobacco leaves are separated into lipid classes by 2 step HPLC [high performance liquid chromatography] using a silicic column. Elution is first performed for 20 min with a programmed linear gradient of 2 mixed solvents running from 100% of solution A (isopropanol-hexane, 4:3) to 100% of solution B (isopropanol-hexane-water, 8:6:1.5); the column is then eluted with pure solution B in an isocratic mode for 20 min more. The main polar lipids (MGDG, DGDG, PC, PE, PG) from both plant tissues can be collected and further separated into component molecular species on a simplified HPLC system with a C18 column eluted in an isocratic mode with a polar solvent. Molecular species separations are achieved within 35 min; quantifications are made through GLC analysis of attached fatty acids. Three to five main molecular species are thus clearly identified in each lipid class. In potato tuber, phospholipids (PC, PE) 18:2/18:2 species are predominant. In tobacco leaf, 6 double bond species (18:3/18:3 and 16:3/18:3) are predominant in galactolipids; PC contains a greater number of molecular species varying by their degree of unsaturation (from 18:3/18:3 to 16:0/18:2). Only certain molecular species of PG contain .DELTA.3-trans-hexadecenoic acid.