Chi M M, Pusateri M E, Carter J G, Norris B J, McDougal D B, Lowry O H
Anal Biochem. 1987 Mar;161(2):508-13. doi: 10.1016/0003-2697(87)90481-7.
Methods for 2-deoxyglucose (2-DG) and 2-deoxyglucose 6-phosphate (DG6P) are described which are based on the fact that DG6P is oxidized by glucose-6-phosphate dehydrogenase (G6PDH), but at a rate 1000-fold slower than for glucose 6-phosphate, whereas hexokinase phosphorylates 2DG and glucose at comparable rates. Therefore, by adding the two enzymes in a suitable order, and in appropriate concentrations, 2DG, glucose, DG6P, and glucose 6-P can all be separately measured. To avoid a side reaction from the use of a high level of G6PDH, when measuring DG6P, glucose is first removed with glucose oxidase plus aldose reductase.
描述了用于2-脱氧葡萄糖(2-DG)和6-磷酸-2-脱氧葡萄糖(DG6P)的方法,这些方法基于以下事实:DG6P被葡萄糖-6-磷酸脱氢酶(G6PDH)氧化,但速率比6-磷酸葡萄糖慢1000倍,而己糖激酶以相当的速率磷酸化2-DG和葡萄糖。因此,通过以合适的顺序和适当的浓度添加这两种酶,可以分别测量2-DG、葡萄糖、DG6P和6-磷酸葡萄糖。为避免因使用高浓度G6PDH而产生副反应,在测量DG6P时,先用葡萄糖氧化酶加醛糖还原酶去除葡萄糖。