Department of Molecular Cell Biology, Faculty of Earth and Life Sciences, VU University Amsterdam, Amsterdam, The Netherlands.
FEMS Microbiol Lett. 2010 Jul 1;308(1):1-7. doi: 10.1111/j.1574-6968.2010.01959.x. Epub 2010 Mar 20.
Mycobacterium tuberculosis, the causative agent of tuberculosis, poses a global health challenge due to the emergence of drug-resistant strains. Recently, bacterial energy metabolism has come into focus as a promising new target pathway for the development of antimycobacterial drugs. This review summarizes our current knowledge on mycobacterial respiratory energy conversion, in particular, during the physiologically dormant state that is associated with latent or persistent tuberculosis infections. Targeting components of respiratory ATP production, such as type-2 NADH dehydrogenase or ATP synthase, is illustrated as an emerging strategy in the development of novel drugs.
结核分枝杆菌是结核病的病原体,由于耐药菌株的出现,对全球健康构成了挑战。最近,细菌能量代谢已成为开发抗分枝杆菌药物的一个有前途的新靶点途径。本综述总结了我们目前对分枝杆菌呼吸能量转换的认识,特别是在与潜伏性或持续性结核病感染相关的生理休眠状态下。以靶向呼吸 ATP 产生的组件(如 2 型 NADH 脱氢酶或 ATP 合酶)为例,说明了在新型药物开发中这是一种新兴策略。