Yoshimoto T, Miyamoto Y, Ochi K, Yamamoto S
Biochim Biophys Acta. 1982 Dec 13;713(3):638-46.
When arachidonic acid was incubated with porcine polymorphonuclear leukocytes, 12-hydroxy-5,8,10,14-eicosatetraenoic acid was produced as a major product. The production of this compound was not accounted for by contaminating platelets known to contain arachidonate 12-lipoxygenase. The enzyme was found predominantly in a cytosol fraction of leukocytes, and the cytosolic enzyme was purified about 30-fold by ammonium sulfate fractionation and DEAE-Sephadex column chromatography. The partially purified enzyme transformed arachidonic acid to a compound which was identified as 12-hydroperoxy-5,8,10,14-eicosatetraenoic acid. 5-Hydroxy-6,8,11,14-eicosatetraenoic acid as substrate was about 40% as active as arachidonic acid, and the reaction was inhibited by the addition of arachidonic acid. The reaction product which was further reduced by sodium borohydride was indistinguishable from authentic 5S, 12S-dihydroxy-(E,Z,E,Z)-6,8,10,14-eicosatetraenoic acid.
当花生四烯酸与猪多形核白细胞一起温育时,12-羟基-5,8,10,14-二十碳四烯酸作为主要产物生成。已知含有花生四烯酸12-脂氧合酶的污染血小板并不能解释该化合物的生成。该酶主要存在于白细胞的胞质溶胶部分,通过硫酸铵分级分离和DEAE-葡聚糖凝胶柱色谱法将胞质酶纯化了约30倍。部分纯化的酶将花生四烯酸转化为一种化合物,该化合物被鉴定为12-氢过氧基-5,8,10,14-二十碳四烯酸。以5-羟基-6,8,11,14-二十碳四烯酸作为底物时,其活性约为花生四烯酸的40%,并且该反应会因添加花生四烯酸而受到抑制。经硼氢化钠进一步还原的反应产物与 authentic 5S, 12S-二羟基-(E,Z,E,Z)-6,8,10,14-二十碳四烯酸无法区分。