Kardon Tamas, Noël Gaëtane, Vertommen Didier, Schaftingen Emile Van
Université catholique de Louvain and ICP, UCL 7539, Avenue Hippocrate 75, B-1200 Brussels, Belgium.
FEBS Lett. 2006 Apr 17;580(9):2347-50. doi: 10.1016/j.febslet.2006.02.082.
To identify the sequence of hydroxyacid-oxoacid transhydrogenase (HOT), responsible for the oxidation of 4-hydroxybutyrate in mammalian tissues, we have purified this enzyme from rat liver and obtained partial sequences of proteins coeluting with the enzymatic activity in the last purification step. One of the identified proteins was 'iron-dependent alcohol dehydrogenase', an enzyme encoded by a gene present on human chromosome 8q 13.1 and distantly related to bacterial 4-hydroxybutyrate dehydrogenases. The identification of this protein as HOT was confirmed by showing that overexpression of the mouse homologue in HEK cells resulted in the appearance of an enzyme catalyzing the alpha-ketoglutarate-dependent oxidation of 4-hydroxybutyrate to succinate semialdehyde.
为了鉴定负责哺乳动物组织中4-羟基丁酸氧化的羟酸-氧代酸转氢酶(HOT)的序列,我们从大鼠肝脏中纯化了这种酶,并获得了在最后纯化步骤中与酶活性共洗脱的蛋白质的部分序列。鉴定出的一种蛋白质是“铁依赖性乙醇脱氢酶”,该酶由人类染色体8q13.1上的一个基因编码,与细菌4-羟基丁酸脱氢酶有较远的亲缘关系。通过在HEK细胞中过表达小鼠同源物导致出现一种催化4-羟基丁酸以α-酮戊二酸依赖性方式氧化为琥珀酸半醛的酶,证实了该蛋白质就是HOT。