Terada T, Kohno T, Samejima T, Hosomi S, Mizoguchi T, Uehara K
J Biochem. 1985 Jan;97(1):79-87. doi: 10.1093/oxfordjournals.jbchem.a135070.
An aldehyde reductase catalyzing the NADPH-dependent reduction of D-erythrose 4-phosphate to D-erythritol 4-phosphate was purified from beef liver. It was proved to be homogeneous by polyacrylamide gel electrophoresis, sodium dodecyl sulfate polyacrylamide gel electrophoresis and ultracentrifugation analysis. The enzyme was proved to be a monomeric enzyme and its molecular weight was about 40,000. The enzyme was able to reduce not only tetroses but also trioses, aromatic aldehydes, D-glucuronate and succinic semialdehyde. Apparent Km-values for aromatic aldehydes were lower than those for tetroses, trioses, D-glucuronate and succinic semi-aldehyde. Barbiturates and valproate were potent inhibitors of the enzyme and their apparent K1-values were in the range of 80-180 microM. Quercitrin was the most potent inhibitor and its K1-value was about 7 microM. From the viewpoint of substrate specificity and inhibitor sensitivity, it seems that the enzyme belongs to the high-Km type aldehyde reductases.
从牛肝脏中纯化出一种醛还原酶,该酶催化磷酸D - 赤藓糖的NADPH依赖性还原反应生成磷酸D - 赤藓醇。通过聚丙烯酰胺凝胶电泳、十二烷基硫酸钠聚丙烯酰胺凝胶电泳和超速离心分析,证明该酶是纯一的。该酶被证明是一种单体酶,其分子量约为40,000。该酶不仅能够还原丁糖,还能还原丙糖、芳香醛、D - 葡萄糖醛酸和琥珀酸半醛。芳香醛的表观Km值低于丁糖、丙糖、D - 葡萄糖醛酸和琥珀酸半醛的表观Km值。巴比妥酸盐和丙戊酸盐是该酶的强效抑制剂,它们的表观K1值在80 - 180 microM范围内。槲皮苷是最有效的抑制剂,其K1值约为7 microM。从底物特异性和抑制剂敏感性的角度来看,该酶似乎属于高Km型醛还原酶。