Tellis C, Tsoukatos D C, Lekka M E
Department of Chemistry, University of Ioannina, Greece.
J Biochem. 1996 Apr;119(4):823-7. doi: 10.1093/oxfordjournals.jbchem.a021314.
1-O-Hexadecyl-2-acetyl-sn-glycerol, the immediate precursor of platelet- activating factor (PAF) in its de novo formation, was detected in the protozoon Tetrahymena pyriformis. It was purified from the total lipid extract by TLC, after successive developments in two different solvent systems. Characterization was assessed by (a) gas-liquid chromatography with electron capture detection, and (b) gas chromatography combined with mass spectrometry in selected ion monitoring mode, after derivatization with heptafluorobutyric acid anhydride and tert-butyldimethylchlorosilane/imidazole, respectively. Its quantity was found to be 0.1 nmol/10(7) cells from the GC-MS, using authentic alkylacetylglycerol as external standard. Cell fractionation revealed that alkylacetylglycerol is located exclusively in the microsomal fraction of the protozoon. Previously, we have reported the occurrence of PAF in the microsomal fraction, as well as a dithiothreitol-insensitive CDP-choline: cholinephosphotransferase activity that utilizes exogenous alkylacetylglycerol as substrate in the mitochondrial and microsomal fractions. The above findings indicate that PAF can be formed in the cell by the de novo pathway.
1-十六烷基-2-乙酰基-sn-甘油,即血小板活化因子(PAF)从头合成过程中的直接前体,在梨形四膜虫原生动物中被检测到。在两种不同溶剂系统中连续展开后,通过薄层色谱法从总脂质提取物中对其进行纯化。表征通过以下方式进行评估:(a)采用电子捕获检测的气相色谱法,以及(b)分别用七氟丁酸酐和叔丁基二甲基氯硅烷/咪唑衍生化后,在选择离子监测模式下的气相色谱-质谱联用。使用纯烷基乙酰甘油作为外标,通过气相色谱-质谱联用发现其含量为0.1 nmol/10⁷个细胞。细胞分级分离显示烷基乙酰甘油仅位于原生动物的微粒体部分。此前,我们已报道微粒体部分存在PAF,以及一种对二硫苏糖醇不敏感的CDP-胆碱:胆碱磷酸转移酶活性,该活性在线粒体和微粒体部分利用外源性烷基乙酰甘油作为底物。上述发现表明PAF可在细胞中通过从头合成途径形成。