Baumert A, Hieke M, Gröger D
Institute of Plant Biochemistry of the Academy of Sciences of the GDR, Halle (Saale), GDR.
Planta Med. 1983 Aug;48(8):258-62. doi: 10.1055/s-2007-969929.
Cell-free extracts from acridone synthesizing cell suspension cultures of RUTA GRAVEOLENS L. catalyze the N-methylation of anthranilic acid using S-adenosyl-L-methionine as methyl donor. The stability of enzyme preparations was remarkably high during storage at -20 degrees C. Optimum activity was exhibited at pH 8.2, Mg (2+) was not required for maximum activity and EDTA did not affect the reaction rate. The rate of N-methylanthranilic acid formation was shown to be linear for about 45 min and was proportional to the protein concentration up to at least 0.350 mg of the enzyme preparation. In a number of suspension cultures of plant species not belonging to the Rutaceae this particular N-methyltransferase was not found. Apparantly N-methylation of anthranilic acid is the first pathway-specific reaction in acridone alkaloid biosynthesis.
从芸香(RUTA GRAVEOLENS L.)吖啶酮合成细胞悬浮培养物中获得的无细胞提取物,以S-腺苷-L-甲硫氨酸作为甲基供体,催化邻氨基苯甲酸的N-甲基化反应。酶制剂在-20℃储存期间稳定性极高。在pH 8.2时表现出最佳活性,最大活性不需要Mg(2+),EDTA不影响反应速率。N-甲基邻氨基苯甲酸的形成速率在约45分钟内呈线性,并且与酶制剂的蛋白质浓度成正比,至少达到0.350 mg。在许多不属于芸香科的植物物种的悬浮培养物中未发现这种特定的N-甲基转移酶。显然,邻氨基苯甲酸的N-甲基化是吖啶酮生物碱生物合成中的第一个途径特异性反应。