Popp J L, Berliner C, Bentley R
Department of Biological Sciences, University of Pittsburgh, Pennsylvania 15260.
Anal Biochem. 1989 May 1;178(2):306-10. doi: 10.1016/0003-2697(89)90643-x.
An early enzyme in menaquinone (vitamin K2) biosynthesis is the synthase forming 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylic acid (SHCHC) from isochorismic acid. In turn, SHCHC is aromatized to o-succinylbenzoic acid (OSB) by OSB synthase. An assay for the combined activity of these two enzymes ("overall OSB synthesis") has been developed using a high-performance liquid chromatographic method for the quantitation of OSB. The assay, which measures as little as 0.1 nmol of OSB, is vastly superior to the radiogas chromatographic method previously used to estimate overall OSB synthesis. To measure SHCHC synthase activity separately, the enzymatically formed SHCHC is converted nonenzymatically to OSB (heating to 80 degrees C, pH 10, 10 min), which is then quantitated by the HPLC assay. The preparation of the substrate, isochorismic acid, and its purification by preparative HPLC are also described.
甲萘醌(维生素K2)生物合成过程中的一种早期酶是由异分支酸形成2-琥珀酰-6-羟基-2,4-环己二烯-1-羧酸(SHCHC)的合酶。反过来,SHCHC通过OSB合酶芳构化为邻琥珀酰苯甲酸(OSB)。已开发出一种使用高效液相色谱法定量OSB的方法来检测这两种酶的联合活性(“总OSB合成”)。该检测方法可检测低至0.1 nmol的OSB,大大优于先前用于估计总OSB合成的放射性气相色谱法。为了单独测量SHCHC合酶的活性,将酶促形成的SHCHC非酶促转化为OSB(在80℃、pH 10条件下加热10分钟),然后通过HPLC检测进行定量。还描述了底物异分支酸的制备及其通过制备型HPLC的纯化方法。