Lane A B
Biochem Genet. 1985 Feb;23(1-2):61-72. doi: 10.1007/BF00499113.
Essential pentosuria is the result of a partial deficiency of L-xylulose reductase. Red blood cells of normal individuals have been found to contain two L-xylulose reductases: a major and a minor isozyme. Red cells from pentosurics contain only one isozyme. The residual enzyme of pentosurics and the normal minor isozyme have similar Michaelis constants for L-xylulose and xylitol, similar activity responses to pH, and similar rates of migration when electrophoresed or subjected to ion-exchange chromatography. It is suggested that homozygosity for the pentosuria allele results in the absence of the major isozyme and that the residual isozyme of pentosurics is identical to the minor isozyme of normal individuals.
原发性戊糖尿是L-木酮糖还原酶部分缺乏的结果。已发现正常个体的红细胞含有两种L-木酮糖还原酶:一种主要同工酶和一种次要同工酶。戊糖尿患者的红细胞仅含有一种同工酶。戊糖尿患者的残留酶与正常次要同工酶对L-木酮糖和木糖醇具有相似的米氏常数,对pH具有相似的活性反应,并且在进行电泳或离子交换色谱分析时具有相似的迁移速率。有人提出,戊糖尿等位基因的纯合性导致主要同工酶缺失,并且戊糖尿患者的残留同工酶与正常个体的次要同工酶相同。