Konno R, Isobe K, Niwa A, Yasumura Y
Department of Microbiology, Dokkyo University School of Medicine, Tochigi, Japan.
Metabolism. 1988 Dec;37(12):1139-42. doi: 10.1016/0026-0495(88)90190-4.
Thin-layer chromatography and amino acid analysis showed that mutant (ddY/DAO-) mice lacking D-amino-acid oxidase activity excreted about 3.5 times more methionine in urine than did normal (ddY/DAO+) mice. High-performance liquid chromatography using a chiral column showed that approximately 82% of urinary methionine of the ddY/DAO- mice had the D-configuration. Analysis revealed that the mouse diet used contained 0.04% free methionine and that approximately 46% of methionine was the D-isomer. When the ddY/DAO- mice were given a diet containing a low level of supplementary DL-methionine or a diet without D-methionine, they excreted the normal levels of methionine. These results indicate that the ddY/DAO- mice were unable to metabolize D-methionine and excrete it in urine.
薄层色谱法和氨基酸分析表明,缺乏D-氨基酸氧化酶活性的突变型(ddY/DAO-)小鼠尿液中蛋氨酸的排泄量比正常(ddY/DAO+)小鼠多约3.5倍。使用手性柱的高效液相色谱法表明,ddY/DAO-小鼠尿液中约82%的蛋氨酸具有D-构型。分析显示,所用的小鼠饲料含有0.04%的游离蛋氨酸,其中约46%的蛋氨酸是D-异构体。当给ddY/DAO-小鼠喂食含有低水平补充DL-蛋氨酸的饲料或不含D-蛋氨酸的饲料时,它们排泄的蛋氨酸水平正常。这些结果表明,ddY/DAO-小鼠无法代谢D-蛋氨酸并将其排泄到尿液中。