Camadro J M, Labbe P
Laboratoire de Biochimie des Porphyrines, Institut Jacques Monod, Université Paris VII, France.
J Biol Chem. 1988 Aug 25;263(24):11675-82.
Ferrochelatase was purified to homogeneity from yeast mitochondrial membranes and found to be a 40-kDa polypeptide with a pI at 6.3. Fatty acids were absolutely necessary to measure the activity in vitro. The Michaelis constants for protoporphyrin IX (9 x 10(-8) M), ferrous iron (1.6 x 10(-7) M), and zinc (9 x 10(-6) M) were determined on purified enzyme preparations in the presence of dithiothreitol. However, the Km for zinc was lower when measured in the absence of dithiothreitol (K-m(Zn2+) = 2.5 x 10(-7) M, Km(protoporphyrin) unchanged). The maximum velocities of the enzyme were 35,000 nmol of heme/h/mg of protein and 27,000 nmol of zinc-protoporphyrin/h/mg of protein. Antibodies against yeast ferrochelatase were raised in rabbits and used in studies on the biogenesis of the enzyme. Ferrochelatase is synthesized as a higher molecular weight precursor (Mr = 44,000) that is very rapidly matured in vivo to the Mr = 40,000 membrane-bound form. This precursor form of ferrochelatase was immunoprecipitated from in vitro translation (in a rabbit reticulocyte lysate system) of total yeast RNAs. The antibodies were used to characterize two yeast mutant strains deficient in ferrochelatase activity as being devoid of immunodetectable protein in vivo and ferrochelatase mRNA in vitro translation product. The N-terminal amino acid sequence of the purified protein has been established and was found to be frayed.
从酵母线粒体膜中纯化出均一的铁螯合酶,发现它是一种40 kDa的多肽,其pI为6.3。脂肪酸对于体外测定该酶活性是绝对必需的。在二硫苏糖醇存在的情况下,在纯化的酶制剂上测定了原卟啉IX(9×10⁻⁸ M)、亚铁(1.6×10⁻⁷ M)和锌(9×10⁻⁶ M)的米氏常数。然而,在没有二硫苏糖醇的情况下测量时,锌的Km较低(K-m(Zn²⁺) = 2.5×10⁻⁷ M,原卟啉的Km不变)。该酶的最大反应速度分别为每小时每毫克蛋白质35000 nmol血红素和每小时每毫克蛋白质27000 nmol锌原卟啉。针对酵母铁螯合酶的抗体在兔体内产生,并用于该酶生物合成的研究。铁螯合酶最初以较高分子量的前体形式(Mr = 44000)合成,在体内迅速成熟为Mr = 40000的膜结合形式。这种铁螯合酶的前体形式是从酵母总RNA的体外翻译(在兔网织红细胞裂解物系统中)中免疫沉淀得到的。这些抗体被用于鉴定两种缺乏铁螯合酶活性的酵母突变株,发现它们在体内缺乏可免疫检测的蛋白质,并且在体外翻译产物中缺乏铁螯合酶mRNA。已确定纯化蛋白质的N端氨基酸序列,发现其已磨损。