Laakso S, Lilius E M, Turunen P
J Biochem Biophys Methods. 1984 Mar;9(1):61-8. doi: 10.1016/0165-022x(84)90066-6.
The chemiluminescent reaction of luminol during lipoxygenase-catalyzed oxygenations was studied with the purpose of developing a specific luminometric assay for cis,cis-1,4-pentadiene fatty acids directly in aqueous solutions. The addition of picomole levels of either linoleic or arachidonic acids to reaction systems containing 0.04 mM luminol and 40 micrograms/ml of purified soybean lipoxygenase-1 gave light emission curves with a single sharp maximum. Under these conditions the peak heights were linearly dependent on the fatty acid concentration and the detection limit for both of the fatty acids was 2 pmol with a signal to noise ratio of 2. For maximum reproducibility of the assays a procedure for the proper quantitation of the enzyme was developed. The fact that the assay proved to be relatively interference-free was ascribed to the high molar enzyme/substrate ratio (above 1).
为了开发一种能直接对水溶液中的顺,顺-1,4-戊二烯脂肪酸进行特异性发光测定的方法,研究了鲁米诺在脂氧合酶催化氧化过程中的化学发光反应。向含有0.04 mM鲁米诺和40微克/毫升纯化大豆脂氧合酶-1的反应体系中加入皮摩尔水平的亚油酸或花生四烯酸,得到的发光曲线有一个尖锐的单一最大值。在这些条件下,峰值高度与脂肪酸浓度呈线性相关,两种脂肪酸的检测限均为2皮摩尔,信噪比为2。为了使测定具有最大的可重复性,开发了一种对酶进行适当定量的方法。该测定方法相对无干扰这一事实归因于高摩尔酶/底物比(大于1)。