Vaca G, Medina C, Wunsch C, Garcia-Cruz D, Sanchez-Corona J, Gonzalez-Quiroga G, Cantu J M
Ann Genet. 1981;24(4):251-3.
A simple screening procedure for the detection of glucose-phosphate isomerase (GPI), phosphofructokinase (PFK), aldolase (AL) and glyceraldehyde-3-phosphate dehydrogenase (GAPD) deficiencies in blood, is described. These enzymes catalyze the second, third, fourth, and sixth reactions in the Embden-Meyerhof pathway. The procedure is based on the conversion of glucose-6-phosphate to 1,3-diphosphoglycerate (1,3-DPG) which is catalyzed by the sequential action of the GPI, PFK, AL and GAPD. The presence of the enzyme activities is visually estimated by the reduction of NAD+ (non-fluorescent) to NADH (fluorescent) which occurs when 1,3-DPG is formed. Absence of fluorescence indicates the deficiency of anyone of the four enzymes, which are specified by using separately the PFK, AL and GAPD respective substrates.
本文描述了一种简单的血液筛查程序,用于检测葡萄糖磷酸异构酶(GPI)、磷酸果糖激酶(PFK)、醛缩酶(AL)和甘油醛-3-磷酸脱氢酶(GAPD)缺乏症。这些酶催化糖酵解途径中的第二、第三、第四和第六步反应。该程序基于葡萄糖-6-磷酸在GPI、PFK、AL和GAPD的顺序作用下转化为1,3-二磷酸甘油酸(1,3-DPG)。通过将NAD⁺(非荧光)还原为NADH(荧光)来目测酶活性的存在,这一过程发生在1,3-DPG形成时。无荧光表明四种酶中任何一种缺乏,通过分别使用PFK、AL和GAPD各自的底物来确定具体缺乏的酶。