Paterniti J R, Beattie D S
J Biol Chem. 1979 Jul 10;254(13):6112-8.
delta-Aminolevulinic acid synthetase has been purified from liver mitochondria of young, uninduced rats. After nonionic detergent solubilization of mitochondrial inner membrane-matrix fractions, the enzyme was purified to a specific activity of approximately 2,000 nmol of delta-aminolevulinic acid formed/h/mg of protein at 30 degrees C, by means of ammonium sulfate precipitation, diethylaminoethyl cellulose chromatography, Sephacryl chromatography, and preparative gel electrophoresis. The purified enzyme preparation thus obtained was apparently homogeneous as judged by its migration as a single band with a molecular weight of 58,000 +/- 6,000 upon electrophoresis in sodium dodecyl sulfate polyacrylamide gels. The native enzyme probably exists as a dimer with a molecular weight of approximately 120,000. A pH optimum of 7.5 and an isoelectric point of 4.5 were also determined. Both monovalent cations and hemin strongly inhibited the activity of the purified enzyme.
δ-氨基乙酰丙酸合成酶已从幼年未诱导大鼠的肝线粒体中纯化出来。在用非离子去污剂溶解线粒体内膜-基质组分后,通过硫酸铵沉淀、二乙氨基乙基纤维素色谱法、Sephacryl色谱法和制备性凝胶电泳,将该酶纯化至在30℃下每小时每毫克蛋白质形成约2000 nmol δ-氨基乙酰丙酸的比活性。通过在十二烷基硫酸钠聚丙烯酰胺凝胶中电泳时作为一条分子量为58000±6000的单带迁移来判断,如此获得的纯化酶制剂显然是均一的。天然酶可能以分子量约为120000的二聚体形式存在。还确定了最适pH为7.5,等电点为4.5。单价阳离子和血红素均强烈抑制纯化酶的活性。