Takenoshita R, Nomura Y, Toki S
Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, 814-0180, Fukuoka, Japan.
Chem Biol Interact. 2001 Jan 30;130-132(1-3):863-70. doi: 10.1016/s0009-2797(00)00241-6.
Using RACE techniques we have cloned and sequenced one of the hamster liver 3-hydroxy-hexobarbital dehydrogenases which catalyze not only cyclic alcohols but also 17beta-hydroxy-steroids and 3alpha-hydroxysteroids. The gene specific primers to 3-hydroxyhexobarbital dehydrogenase 1 (G2) were synthesized on the basis of its partial peptide sequences. The sequence of full length cDNA generated by 3'- and 5'-RACE PCR consisted of 1225 nucleotides including an open reading frame of 972 nucleotides encoding a protein of 323 amino acids. The deduced amino acid sequence matched exactly with the partial peptide sequences of hamster liver 3-hydroxyhexobarbital dehydrogenase 1 (G2). The sequence showed 84.5% identity to mouse liver 17beta-dehydrogenase(A-specific), and 74-76% identity to human liver bile acid binding protein/3alpha-hydroxysteroid dehydrogenase (DD2), human liver 3alpha-hydroxysteroid dehydrogenase type I (DD4) and type II (DD3), and rabbit ovary 20alpha-hydroxysteroid dehydrogenase. The protein contains catalytic residues of aldo-keto reductases, Asp50, Tyr55, Lys84, His117. These results suggest that the hamster liver 3-hydroxyhexobarbital/17beta(3alpha)-hydroxysteroid dehydrogenase belongs to aldo-keto reductase superfamily. The insert containing the full-length cDNA of 3-hydroxyhexobarbital dehydrogenase and vector specific overhang produced by PCR was annealed with pET-32 Xa/LIC vector. The plasmid was transformed into BL21 (DE3) cells containing pLysS. The recombinant enzyme was induced 1 mM IPTG. The expressed enzyme was produced as fusion protein and purified by nickel chelating affinity chromatography followed by POROS CM column chromatography and superdex 75 gel filtration. Molecular weight of the recombinant enzyme fused thioredoxin and his*tag was about 55000 and that was 35000 after Factor Xa protease treatment. The recombinant enzyme dehydrogenated 3-hydroxy-hexobarbital, 1-acenaphthenol, 2-cyclohexen-1-ol, testosterone, glycolithocholic acid as well as the native enzyme purified from hamster liver.
利用RACE技术,我们克隆并测序了仓鼠肝脏中的一种3-羟基己巴比妥脱氢酶,该酶不仅能催化环醇,还能催化17β-羟基类固醇和3α-羟基类固醇。基于其部分肽序列合成了3-羟基己巴比妥脱氢酶1(G2)的基因特异性引物。通过3'-和5'-RACE PCR产生的全长cDNA序列由1225个核苷酸组成,包括一个972个核苷酸的开放阅读框,编码一个323个氨基酸的蛋白质。推导的氨基酸序列与仓鼠肝脏3-羟基己巴比妥脱氢酶1(G2)的部分肽序列完全匹配。该序列与小鼠肝脏17β-脱氢酶(A特异性)的同一性为84.5%,与人类肝脏胆汁酸结合蛋白/3α-羟基类固醇脱氢酶(DD2)、人类肝脏I型(DD4)和II型(DD3)3α-羟基类固醇脱氢酶以及兔卵巢20α-羟基类固醇脱氢酶的同一性为74-76%。该蛋白质含有醛酮还原酶的催化残基,Asp50、Tyr55、Lys84、His117。这些结果表明仓鼠肝脏3-羟基己巴比妥/17β(3α)-羟基类固醇脱氢酶属于醛酮还原酶超家族。将含有3-羟基己巴比妥脱氢酶全长cDNA的插入片段和PCR产生的载体特异性突出端与pET-32 Xa/LIC载体退火。将质粒转化到含有pLysS的BL21(DE3)细胞中。用1 mM IPTG诱导重组酶。表达的酶以融合蛋白形式产生,并通过镍螯合亲和层析,随后进行POROS CM柱层析和Superdex 75凝胶过滤进行纯化。融合硫氧还蛋白和his*标签的重组酶的分子量约为55000,经Xa因子蛋白酶处理后为35000。重组酶与从仓鼠肝脏纯化的天然酶一样,能使3-羟基己巴比妥、1-苊醇、2-环己烯-1-醇、睾酮、甘氨石胆酸脱氢。