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嗜热嗜酸古菌硫化叶菌属菌株7需氧呼吸系统的解析。I. 古菌末端氧化酶超复合物是呼吸复合物III和IV的功能性融合体,不含c型细胞色素。

Resolution of the aerobic respiratory system of the thermoacidophilic archaeon, Sulfolobus sp. strain 7. I. The archaeal terminal oxidase supercomplex is a functional fusion of respiratory complexes III and IV with no c-type cytochromes.

作者信息

Iwasaki T, Matsuura K, Oshima T

机构信息

Department of Life Science, Tokyo Institute of Technology, Yokohama, Japan.

出版信息

J Biol Chem. 1995 Dec 29;270(52):30881-92. doi: 10.1074/jbc.270.52.30881.

Abstract

The aerobic respiratory system of the thermoacidophilic archaeon, Sulfolobus sp. strain 7, is unusual in that it consists of only a- and b-type cytochromes but no c-type cytochromes. In previous studies, a novel cytochrome oxidase a583-aa3 subcomplex has been purified, which showed a ferrocytochrome c oxidase but no caldariellaquinol oxidase activity (Wakagi, T., Yamauchi, T., Oshima, T., Müller, M., Azzi, A., and Sone, N. (1989) Biochem. Biophys. Res. Commun. 165, 1110-1114). We show here that the cytochrome subcomplex could be copurified with a non-CO-reactive cytochrome b562 as a novel terminal oxidase "supercomplex," which also contained a Rieske-type FeS cluster at gy = 1.89. It contained one copper and all four heme centers detectable in the archaeal membranes by the low temperature spectrophotometry and the potentiometric titration: cytochromes b562 (+146 mV), a583 (+270 mV), and aa3 (+117 and +325 mV). The presence of one copper atom indicates that it contains the conventional heme a3-CuB binuclear center for reducing molecular oxygen. In conjunction with the presence of a Rieske-type FeS center, inhibitor studies suggest that the terminal oxidase segment of the respiratory chain of Sulfolobus sp. strain 7 is a functional fusion of respiratory complexes III and IV, where cytochrome b562 and the Rieske-type FeS center probably play a central role in the oxidation of caldariellaquinol. This archaeal terminal oxidase supercomplex reconstitutes the in vitro succinate oxidase respiratory chain for the first time together with caldariellaquinone and the purified cognate succinate:caldariellaquinone oxidoreductase complex. The reconstitution system requires caldariellaquinone for the activity, and is highly sensitive to cyanide and 2-heptyl-4-hydroxy-quinoline-N-oxide. These results are also discussed in terms of the evolutionary considerations.

摘要

嗜热嗜酸古菌硫化叶菌属菌株7的有氧呼吸系统不同寻常,因为它仅由a型和b型细胞色素组成,不含c型细胞色素。在先前的研究中,一种新型的细胞色素氧化酶a583 - aa3亚复合物已被纯化,它表现出亚铁细胞色素c氧化酶活性,但没有嗜热栖热菌醌氧化酶活性(若木彻、山内敏、大岛彻、米勒、阿齐、索尼,(1989年)《生物化学与生物物理研究通讯》165卷,1110 - 1114页)。我们在此表明,细胞色素亚复合物可与一种非CO反应性细胞色素b562共纯化,形成一种新型的末端氧化酶“超级复合物”,该复合物在g = 1.89处还含有一个 Rieske 型铁硫簇。通过低温分光光度法和电位滴定法,它含有一个铜原子以及在古菌膜中可检测到的所有四个血红素中心:细胞色素b562(+146 mV)、a583(+270 mV)和aa3(+117和+325 mV)。一个铜原子的存在表明它含有用于还原分子氧的传统血红素a3 - CuB双核中心。结合Rieske型铁硫中心的存在,抑制剂研究表明硫化叶菌属菌株7呼吸链的末端氧化酶部分是呼吸复合物III和IV的功能性融合,其中细胞色素b562和Rieske型铁硫中心可能在嗜热栖热菌醌的氧化中起核心作用。这种古菌末端氧化酶超级复合物首次与嗜热栖热菌醌和纯化的同源琥珀酸:嗜热栖热菌醌氧化还原酶复合物一起在体外重建了琥珀酸氧化酶呼吸链。重建系统需要嗜热栖热菌醌来发挥活性,并且对氰化物和2 - 庚基 - 4 - 羟基喹啉 - N - 氧化物高度敏感。这些结果也从进化的角度进行了讨论。

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