Sassa S
Enzyme. 1982;28(2-3):133-45. doi: 10.1159/000459097.
gamma-Aminolevulinic acid (ALA) dehydratase catalyzes the synthesis of porphobilinogen (PBG) from two molecules of ALA. A semimicro method for the colorimetric determination of ALA dehydratase is presented and applied to various tissues. The enzyme activity in adult male rat liver was 2.22 and 1.94 mumol PBG formed/g liver/h for homogenates assayed with or without dithiothreitol, respectively. The assay was linear for at least 2.5 h and for up to 2.5 mg tissue per assay. The Km for ALA was 4.0 X 10(-4)M and the pH optimum was 6.2-6.4. The effects of activators and inhibitors on enzyme activity are discussed.
γ-氨基乙酰丙酸(ALA)脱水酶催化由两分子ALA合成胆色素原(PBG)。本文介绍了一种用于比色法测定ALA脱水酶的半微量方法,并将其应用于各种组织。用或不用二硫苏糖醇测定成年雄性大鼠肝脏匀浆中的酶活性,分别为每克肝脏每小时形成2.22和1.94 μmol PBG。该测定方法至少在2.5小时内呈线性,每次测定的组织量可达2.5 mg。ALA的Km为4.0×10^(-4)M,最适pH为6.2 - 6.4。讨论了激活剂和抑制剂对酶活性的影响。