Norman H A, Smith L A, Lynch D V, Thompson G A
Arch Biochem Biophys. 1985 Oct;242(1):157-67. doi: 10.1016/0003-9861(85)90489-8.
Two-minute exposures to exogenous [14C]palmitic, [14C]oleic, or [14C]lauric acid differentially labeled the lipids of Dunaliella salina microsomes and chloroplasts. Changes in fatty acid desaturation and intracellular movement during a subsequent 16-h incubation in nonradioactive medium indicated a slow transfer of lipids into the chloroplast from other organelles. Since Dunaliella lacks the massive traffic of microsomally produced glycerolipids into chloroplast galactolipids that dominates chloroplast-microsome lipid relations in most plant cells, it affords a sensitive system for studying more subtle intracellular lipid fluxes. Lowering the culture temperature from 30 to 12 degrees C was more inhibitory toward glycerolipid biosynthesis in chloroplasts than in microsomes. The ability of Dunaliella chloroplasts to utilize microsomal lipids may be essential for their systematic acclimation to low temperature.
用外源性[14C]棕榈酸、[14C]油酸或[14C]月桂酸进行两分钟的处理,对盐生杜氏藻微粒体和叶绿体的脂质进行了不同程度的标记。在随后于无放射性培养基中进行的16小时孵育期间,脂肪酸去饱和作用和细胞内移动的变化表明脂质从其他细胞器缓慢转移到叶绿体中。由于盐生杜氏藻缺乏大多数植物细胞中占主导地位的微粒体产生的甘油脂质向叶绿体半乳糖脂质的大量转运,它为研究更细微的细胞内脂质通量提供了一个敏感的系统。将培养温度从30℃降至12℃对叶绿体中甘油脂质生物合成的抑制作用比对微粒体的抑制作用更大。盐生杜氏藻叶绿体利用微粒体脂质的能力可能对其系统适应低温至关重要。