Voelker D R, Snyder F
J Biol Chem. 1979 Sep 10;254(17):8628-33.
The site of synthesis of 1,2-disaturated-(diacyl)-sn-glycero-3-phosphocholine (Sat2PC) in mouse alveolar type II cell adenomas has been studied by conducting pulse-chase experiments. Isolation of microsomal and lamellar body fractions from adenomas after a 20-min pulse with [methyl-3H]choline demonstrates that Sat2PC first appears in the microsomal fraction, and after a short lag subsequently appears in the lamellar body fraction. The kinetics of labeling of Sat2PC are consistent with the microsomal membranes functioning as the subcellular site of synthesis for this pulmonary surfactant phospholipid. Short term labeling experiments with [9,10-3H]palmitate demonstrate that this fatty acid is incorporated into the sn-2 position of Sat2PC at a faster rate than its incorporation into the sn-1 position. This finding indicates that the synthesis of Sat2PC occurs by a deacylation-reacylation mechanism.
通过进行脉冲追踪实验,对小鼠肺泡II型细胞腺瘤中1,2 - 二饱和 - (二酰基)-sn - 甘油 - 3 - 磷酸胆碱(Sat2PC)的合成位点进行了研究。用[甲基 - ³H]胆碱进行20分钟脉冲后,从腺瘤中分离微粒体和板层小体组分,结果表明Sat2PC首先出现在微粒体组分中,经过短暂延迟后随后出现在板层小体组分中。Sat2PC的标记动力学与微粒体膜作为这种肺表面活性物质磷脂的亚细胞合成位点的功能一致。用[9,10 - ³H]棕榈酸进行的短期标记实验表明,该脂肪酸掺入Sat2PC的sn - 2位的速率比掺入sn - 1位的速率快。这一发现表明Sat2PC的合成是通过脱酰基 - 再酰基化机制进行的。