Mogi Tatsushi, Matsushita Kazunobu, Murase Yoshiro, Kawahara Kenji, Miyoshi Hideto, Ui Hideaki, Shiomi Kazuro, Omura Satoshi, Kita Kiyoshi
Department of Biomedical Chemistry, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
FEMS Microbiol Lett. 2009 Feb;291(2):157-61. doi: 10.1111/j.1574-6968.2008.01451.x. Epub 2008 Dec 5.
In bacterial membranes and plant, fungus and protist mitochondria, NADH dehydrogenase (NDH-II) serves as an alternative NADH : quinone reductase, a non-proton-pumping single-subunit enzyme bound to the membrane surface. Because NDH-II is absent in mammalian mitochondria, it is a promising target for new antibiotics. However, inhibitors for NDH-II are rare and unspecific. Taking advantage of the simple organization of the respiratory chain in Gluconobacter oxydans, we carried out screening of natural compounds and identified scopafungin and gramicidin S as inhibitors for G. oxydans NDH-II. Further, we examined their effects on Mycobacterium smegmatis and Plasmodium yoelii NDH-II as model pathogen enzymes.
在细菌膜以及植物、真菌和原生生物的线粒体中,NADH脱氢酶(NDH-II)作为一种替代的NADH:醌还原酶,是一种结合在膜表面的非质子泵单亚基酶。由于哺乳动物线粒体中不存在NDH-II,它是新型抗生素的一个有前景的靶点。然而,针对NDH-II的抑制剂很少且不具有特异性。利用氧化葡萄糖酸杆菌呼吸链结构简单的特点,我们对天然化合物进行了筛选,并鉴定出scopafungin和短杆菌肽S是氧化葡萄糖酸杆菌NDH-II的抑制剂。此外,我们还研究了它们对耻垢分枝杆菌和约氏疟原虫NDH-II这两种模式病原酶的影响。