Wang C, Xu C, Yu H, Pan L
Department of Biomedical Engineering, Chongqing University of Medical Sciences, Chongqing 400016.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2000 Sep;17(3):363-5.
This paper presents a modified method of enzymatic assay for Fructose-1,6-diphosphate(FDP). FDP is split to dihydroxyacetone phosphate (DAP) and glyceraldehyde-3-phosphate (GAP) by the action of aldolase. DAP is hydrolyzed at room temperature to free triose. Under alkaline conditions, the free triose is reacted with 2,4-dinitrophenylhydrazine (DNPH), yielding a 2,4-dinitrophenylhydrazine derivative which dissolve in alkali forming a purple color mixture, with maximum absorption at 540.nm. It is proportional to the contents of FDP. Because the method depends on the colorimetric determination of triose formed from fructose-1,6-diphosphate only by aldolase, glycerophosphate dehydrogenase/triosephosphate isomerase (GDH/TIM) and reduced nicotinamide adenine dinucleotide (NADH) which usually applied in multienzymatic method, are omitted in the modified method. The method is specific, convenient and accuracy for the determination of FDP.
本文介绍了一种改良的果糖-1,6-二磷酸(FDP)酶法测定方法。在醛缩酶的作用下,FDP分解为磷酸二羟丙酮(DAP)和3-磷酸甘油醛(GAP)。DAP在室温下水解为游离的丙糖。在碱性条件下,游离丙糖与2,4-二硝基苯肼(DNPH)反应,生成一种2,4-二硝基苯肼衍生物,该衍生物溶解于碱中形成紫色混合物,在540nm处有最大吸收。其与FDP的含量成正比。由于该方法仅依赖于通过醛缩酶由果糖-1,6-二磷酸生成的丙糖的比色测定,因此改良方法中省略了通常用于多酶法的甘油磷酸脱氢酶/磷酸丙糖异构酶(GDH/TIM)和还原型烟酰胺腺嘌呤二核苷酸(NADH)。该方法对于FDP的测定具有特异性、便利性和准确性。