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Enzymatic assay of metabolic substrates - by measuring reaction velocity when it has stabilised at low enzyme concn.

机译:代谢底物的酶促测定-通过在酶浓度较低时稳定反应速度来测量。

摘要

Enzymatic determination fo substrate, esp. metabolite concns., comprises starting the reaction by adding the enzyme then measuring teh reaction velocity (dE/dt), which is characteristic of the instantaneous substrate concn., only after the perturbation caused by introducing the enzyme has decayed and only during the period of time when the velocity at low enzyme concn. is practically constant e.g. 15-30 sec. Partic. for analysing blood glucose but also for blood alcohol, lactic acid or pyruvic acid. Analysis kis very rapid and method can be used where two enzymes are needed for reaction e.g. hexokinase and glucose-6-phosphate dehydrogenase in glucose assay.
机译:酶法测定底物,尤其是。代谢物浓度包括:仅在引入酶引起的扰动减弱后且仅在以下过程中,通过添加酶开始反应,然后测量反应速度(dE / dt),该速度是瞬时底物浓度的特征。低酶浓度时的时间。实际上是恒定的,例如15-30秒参加用于分析血糖,还用于分析血液中的酒精,乳酸或丙酮酸。分析非常快速并且可以在需要两种酶进行反应的情况下使用方法,例如葡萄糖测定法中的己糖激酶和6-磷酸葡萄糖脱氢酶。

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