Cho S H, Thompson G A
J Biol Chem. 1987 Jun 5;262(16):7586-93.
Dunaliella salina cells were pulse-labeled for 2 min with [14C]palmitic acid, [14C]oleic acid, or [14C]lauric acid in order to trace the pathway of galactolipid biosynthesis and desaturation. Through the use of high performance liquid chromatography it was possible to follow the movement of radioactivity through many individual molecular species of monogalactosyldiacylglycerol (MGDG) and digalactosyldiacylglycerol (DGDG) for periods of 24 h and, in some cases, as much as 120 h. Analysis of the fatty acid fluxes permitted us to refine current views regarding biosynthesis of the predominantly "prokaryotic" galactolipids. The initial D. salina MGDG molecular species, containing paired oleate and palmitate (18:1/16:0), can follow two metabolic routes. If the palmitoyl chain is desaturated to 16:1, the resulting 18:1/16:1 MGDG is subject to rapid further desaturation to varying degrees, and a part of these products is subsequently galactosylated to DGDG. Contrary to widely held opinions, these DGDG molecular species can themselves be further desaturated toward a 18:3/16:4 final product. In a separate series of reactions, a smaller portion of the nascent 18:1/16:0 MGDG is directly galactosylated to 18:1/16:0 DGDG. This molecular species can then be sequentially desaturated to 18:2/16:0 DGDG and 18:3/16:0 DGDG. However, there is only very limited desaturation of the palmitoyl group attached to these molecular species.
为了追踪半乳糖脂生物合成与去饱和的途径,用[14C]棕榈酸、[14C]油酸或[14C]月桂酸对盐生杜氏藻细胞进行了2分钟的脉冲标记。通过高效液相色谱法,可以在24小时内,在某些情况下长达120小时,追踪放射性在许多单半乳糖基二酰基甘油(MGDG)和双半乳糖基二酰基甘油(DGDG)的单个分子种类中的移动情况。对脂肪酸通量的分析使我们能够完善目前关于主要“原核”半乳糖脂生物合成的观点。最初的盐生杜氏藻MGDG分子种类,含有成对的油酸酯和棕榈酸酯(18:1/16:0),可以遵循两条代谢途径。如果棕榈酰链去饱和为16:1,生成的18:1/16:1 MGDG会在不同程度上迅速进一步去饱和,并且这些产物的一部分随后会被半乳糖基化形成DGDG。与广泛持有的观点相反,这些DGDG分子种类自身可以进一步去饱和形成最终产物18:3/16:4。在另一系列反应中,新生的18:1/16:0 MGDG的一小部分直接被半乳糖基化形成18:1/16:0 DGDG。然后这种分子种类可以依次去饱和形成18:2/16:0 DGDG和18:3/16:0 DGDG。然而,连接在这些分子种类上的棕榈酰基团的去饱和非常有限。