Bohren K M, Grimshaw C E, Gabbay K H
Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030.
J Biol Chem. 1992 Oct 15;267(29):20965-70.
Human aldose reductase and aldehyde reductase are members of the aldo-keto reductase superfamily that share three domains of homology and a nonhomologous COOH-terminal region. The two enzymes catalyze the NADPH-dependent reduction of a wide variety of carbonyl compounds. To probe the function of the domains and investigate the basis for substrate specificity, we interchanged cDNA fragments encoding the NH2-terminal domains of aldose and aldehyde reductase. A chimeric enzyme (CH1, 317 residues) was constructed in which the first 71 residues of aldose reductase were replaced with first 73 residues of aldehyde reductase. Catalytic effectiveness (kcat/Km) of CH1 for the reduction of various substrates remained virtually identical to wild-type aldose reductase, changing a maximal 4-fold. Deletion of the 13-residue COOH-terminal end of aldose reductase, yielded a mutant enzyme (AR delta 303-315) with markedly decreased catalytic effectiveness for uncharged substrates ranging from 80- to more than 600-fold (average 300-fold). The KmNADPH of CH1 and AR delta 303-315 were nearly identical to that of the wild-type enzyme indicating that cofactor binding is unaffected. The truncated AR delta 303-315 displayed a NADPH/D isotope effect in kcat and an increased D(kcat/Km) value for DL-glyceraldehyde, suggesting that hydride transfer has become partially rate-limiting for the overall reaction. We conclude that the COOH-terminal domain of aldose reductase is crucial to the proper orientation of substrates in the active site.
人醛糖还原酶和醛还原酶是醛酮还原酶超家族的成员,它们共有三个同源结构域和一个非同源的羧基末端区域。这两种酶催化多种羰基化合物的NADPH依赖性还原反应。为了探究这些结构域的功能并研究底物特异性的基础,我们交换了编码醛糖还原酶和醛还原酶氨基末端结构域的cDNA片段。构建了一种嵌合酶(CH1,317个残基),其中醛糖还原酶的前71个残基被醛还原酶的前73个残基所取代。CH1对各种底物还原反应的催化效率(kcat/Km)与野生型醛糖还原酶几乎相同,最大变化为4倍。删除醛糖还原酶13个残基的羧基末端,产生了一种突变酶(AR delta 303 - 315),对于不带电荷的底物,其催化效率显著降低,降低幅度在80至600倍以上(平均300倍)。CH1和AR delta 303 - 315的KmNADPH与野生型酶几乎相同,表明辅因子结合未受影响。截短的AR delta 303 - 315在kcat中表现出NADPH/D同位素效应,并且对于DL - 甘油醛,D(kcat/Km)值增加,这表明氢化物转移已成为整个反应的部分限速步骤。我们得出结论,醛糖还原酶的羧基末端结构域对于底物在活性位点的正确定向至关重要。