Scopes R K, Griffiths-Smith K
Anal Biochem. 1984 Feb;136(2):530-4. doi: 10.1016/0003-2697(84)90257-4.
Using differential dye-ligand chromatography and affinity elution with a substrate analog, 6-phosphogluconate dehydratase (EC 4.2.1.12) has been isolated from extracts of Zymomonas mobilis in a one-step procedure with 50% recovery. The specific activity of freshly isolated enzyme was 245 units mg-1. The enzyme contains iron, and it is rapidly inactivated in oxidizing conditions. It is inhibited by glycerophosphates, most strongly by the D-alpha-isomer which structurally corresponds to half of the substrate molecule.
使用差示染料配体色谱法和用底物类似物进行亲和洗脱,已通过一步法从运动发酵单胞菌提取物中分离出6-磷酸葡萄糖酸脱水酶(EC 4.2.1.12),回收率为50%。新分离酶的比活性为245单位mg-1。该酶含铁,在氧化条件下会迅速失活。它受到甘油磷酸酯的抑制,其中D-α-异构体抑制作用最强,其结构相当于底物分子的一半。