Keyhani E, Keyhani J
Biochim Biophys Acta. 1980 Dec 1;633(2):211-27. doi: 10.1016/0304-4165(80)90407-9.
Heme a was not detected either in mitochondria isolated from copper-deficient yeast or in the intact cells. Nevertheless, the intracellular concentration of free porphyrins indicated that the pathway of porphyrin and heme synthesis was not impaired in copper-deficient cells. The immunoprecipitated apo-oxidase from copper-deficient cells revealed an absorption spectrum with maxima at 645, 592, 559, 519 and 423 nm, similar to that of purified porphyrin a. When solubilized mitochondria from [3H]leucine and delta-amino[14C]levulinic acid-labeled copper-deficient yeast cells were incubated with rabbit antiserum against cytochrome c oxidase, a precipitate was obtained. Sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis of this immunoprecipitate showed [3H]leucine associated with six bands and delta-amino[14C]levulinic acid resolved in a single band. HCl fractionation of copper-deficient mitochondria labeled with delta amino[14C]levulinic acid showed a high specific radioactivity in the fraction extracted by 20% HCl, a solvent which extracts porphyrin a. Thin-layer chromatography of the radioactivity found in 20% HCl showed an RF value identical to that of purified porphyrin a. When delta-amino[3H]levulinic acid-labeled, copper-deficient yeast cells are grown in copper-supplemented medium, the porphyrin a accumulated in copper-deficient cells was converted into heme a, and this conversion was prevented by cycloheximidine. These observations suggest that porphyrin a is present in the apo-oxidase of copper-deficient cells, but that the conversion to heme a does not occur. This conversion reaction appears to be a point in the biosynthetic pathway of cytochrome c oxidase which is blocked by copper deficiency.
在从缺铜酵母中分离出的线粒体或完整细胞中均未检测到血红素a。然而,游离卟啉的细胞内浓度表明,缺铜细胞中卟啉和血红素的合成途径并未受损。从缺铜细胞中免疫沉淀得到的脱辅基氧化酶显示出在645、592、559、519和423nm处有最大吸收峰的吸收光谱,类似于纯化的卟啉a的吸收光谱。当将来自用[³H]亮氨酸和δ-氨基[¹⁴C]戊酸标记的缺铜酵母细胞的可溶线粒体与抗细胞色素c氧化酶的兔抗血清一起孵育时,得到了沉淀物。该免疫沉淀物的十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳显示[³H]亮氨酸与六条带相关,而δ-氨基[¹⁴C]戊酸在一条带中分离。用δ-氨基[¹⁴C]戊酸标记的缺铜线粒体的盐酸分级分离显示,在由20%盐酸提取的级分中有高比放射性,20%盐酸是一种能提取卟啉a的溶剂。在20%盐酸中发现的放射性物质的薄层色谱显示其RF值与纯化的卟啉a相同。当用δ-氨基[³H]戊酸标记的缺铜酵母细胞在补充铜的培养基中生长时,缺铜细胞中积累的卟啉a会转化为血红素a,而环己酰亚胺可阻止这种转化。这些观察结果表明,卟啉a存在于缺铜细胞的脱辅基氧化酶中,但不会发生向血红素a的转化。这种转化反应似乎是细胞色素c氧化酶生物合成途径中被铜缺乏阻断的一个点。