Kahn A, Esters A, Habedank M
Hum Genet. 1976 May 19;32(2):171-80. doi: 10.1007/BF00291500.
A deficient G-6PD variant was discovered in 4 males of one family from northwestern Germany. Five generations of this family could be studied. The deficient G-6PD was a new variant, called "Gd (--) Aachen". Its main characteristics are the following: severe enzyme deficiency in erythrocytes (3% of normal), contrasting with an almost normal activity in leukocytes; normal molecular specific activity (i.e., normal ratio enzyme activity/cross-reacting material); slow mobility in starch gel electrophoresis (92-94% of normal); increased Michaelis constant for glucoes-6-phosphate (60-70 muM) and NADP+ (20-25 muM); decreased inhibition constant by NADPH with respect to NADP+ (7 muM); increased inhibition by ATP; normal utilization of the substrate analogues; slightly biphasic pH curve; thermal instability, and normal activation energy of the enzymatic reaction. The relationships between the hematologic disorders (severe and frequent hemolytic crises) and the unfavorable kinetic modifications are discussed.
在德国西北部一个家族的4名男性中发现了一种缺陷型葡萄糖-6-磷酸脱氢酶(G-6PD)变体。该家族五代人可供研究。这种缺陷型G-6PD是一种新变体,称为“Gd (--) 亚琛”。其主要特征如下:红细胞中酶严重缺乏(为正常水平的3%),而白细胞中的活性几乎正常;分子比活性正常(即酶活性/交叉反应物质的正常比率);在淀粉凝胶电泳中迁移率较慢(为正常水平的92 - 94%);葡萄糖-6-磷酸(60 - 70 μM)和NADP⁺(20 - 25 μM)的米氏常数增加;NADPH对NADP⁺的抑制常数降低(7 μM);ATP抑制作用增强;底物类似物的利用正常;pH曲线略呈双相;热不稳定,酶促反应的活化能正常。讨论了血液学疾病(严重且频繁的溶血危机)与不利的动力学改变之间的关系。