Quinlan D C, Hochstadt J
J Biol Chem. 1976 Jan 25;251(2):344-54.
Plasma membrane vesicles are isolated from Simian virus 40-transformed Balb/c mouse 3T3 (SV-3T3) cells. These membrane vesicles contain no significant contamination by mitochondria, endoplasmic reticulum, or lysosomes as determined by marker enzyme analysis. The use of [U-14C] inosine as a transport substrate results in the accumulation of labeled ribose-1P as transport product by the plasma membrane vesicles. This suggests the action of purine nucleoside phosphorylase (the enzyme which mediates the phosphorolysis of inosine to ribose-1-P and hypoxanthine0 before, during, or after the transport step. Neither inosine nor significant amounts of hypoxanthine are found intravesicularly. The Km for inosine, the substrate in this reaction which leads to the accumulation of ribose-1-P by the plasma membrane vesicles, is 35 to 45 muM while the Vmax for ribose-1-P accumulation is 100 to 120 pmol/min/mg of plasma membrane protein...
从猿猴病毒40转化的Balb/c小鼠3T3(SV - 3T3)细胞中分离出质膜囊泡。通过标记酶分析确定,这些膜囊泡没有受到线粒体、内质网或溶酶体的显著污染。使用[U - 14C]肌苷作为转运底物,质膜囊泡会积累标记的核糖 - 1 - 磷酸作为转运产物。这表明嘌呤核苷磷酸化酶(该酶在转运步骤之前、期间或之后介导肌苷磷酸解为核糖 - 1 - 磷酸和次黄嘌呤)发挥了作用。在囊泡内未发现肌苷或大量次黄嘌呤。导致质膜囊泡积累核糖 - 1 - 磷酸的该反应底物肌苷的米氏常数为35至45μM,而核糖 - 1 - 磷酸积累的最大反应速率为100至120 pmol/分钟/毫克质膜蛋白……