Department of Botany, University of Adelaide, Adelaide, Australia.
Planta. 1972 Sep;102(3):190-205. doi: 10.1007/BF00386890.
A soluble (supernatant) fraction from turnips catalyses the reduction of both FeCN and DCPIP but usually not cytochrome c in the presence of either NADH or NADPH. Slicing and aging turnip tissue induces an increase in these activities as well as the development of an NADH-cytochrome c reductase activity.(NH4)2SO4 and Sephadex fractionation indicated that at least three enzymes were involved: an NADH-cytochrome-c reductase, an NADH-FeCN reductase, and an NAD(P)H-DCPIP and FeCN reductase. While the latter reductase had an acid pH optimum, indicating vacuolar origin, the NADH-cytochrome-c and FeCN reductases both had neutral pH optima, indicating cytoplasmic origin. Characterization of the NADH-specific reductases indicated that NADH-FeCN reductase may be a soluble form of the microsomal membrane NADH dehydrogenase but that NADH-cytochrome-c reductase may be normally soluble and possibly involved in cyanide-sensitive NADH oxidation.The induced development of all three reductases was inhibited by 6-methylpurine, ethionine and cycloheximide, indicating dependence on both RNA and protein synthesis. The inhibition by cycloheximide could be reversed but this reversion required a 20-h washing-out period to be complete.
芜菁的可溶(上清)部分能催化 FeCN 和 DCPIP 的还原,但在 NADH 或 NADPH 存在的条件下通常不能还原细胞色素 c。芜菁组织的切片和老化会诱导这些活性的增加以及 NADH-细胞色素 c 还原酶活性的发展。(NH4)2SO4 和 Sephadex 分级分离表明,至少有三种酶参与其中:NADH-细胞色素 c 还原酶、NADH-FeCN 还原酶以及 NAD(P)H-DCPIP 和 FeCN 还原酶。虽然后一种还原酶具有酸性 pH 最佳值,表明其起源于液泡,但 NADH-细胞色素 c 和 FeCN 还原酶均具有中性 pH 最佳值,表明其起源于细胞质。对 NADH 特异性还原酶的特性分析表明,NADH-FeCN 还原酶可能是微粒体膜 NADH 脱氢酶的可溶性形式,而 NADH-细胞色素 c 还原酶可能通常是可溶性的,并且可能参与氰化物敏感的 NADH 氧化。所有三种还原酶的诱导发展均被 6-甲基嘌呤、乙硫氨酸和环己酰亚胺抑制,表明其依赖于 RNA 和蛋白质合成。环己酰亚胺的抑制作用可以逆转,但这种逆转需要 20 小时的洗涤期才能完全逆转。