Awasthi Divya, Freundlich Joel S
Department of Pharmacology, Physiology and Neuroscience, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Department of Pharmacology, Physiology and Neuroscience, Rutgers University - New Jersey Medical School, Newark, NJ, USA; Division of Infectious Disease, Department of Medicine, and the Ruy V. Lourenco Center for the Study of Emerging and Reemerging Pathogens, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Trends Microbiol. 2017 Sep;25(9):756-767. doi: 10.1016/j.tim.2017.05.007. Epub 2017 Jun 13.
Bacteria are capable of performing a number of biotransformations that may activate or deactivate xenobiotics. Recent efforts have utilized metabolomics techniques to study the fate of small-molecule antibacterials within the targeted organism. Examples involving Mycobacterium tuberculosis are reviewed and analyzed with regard to the insights they provide as to both activation and deactivation of the antibacterial. The studies, in particular, shed light on biosynthetic transformations performed by M. tuberculosis while suggesting avenues for the evolution of chemical tools, highlighting potential areas for drug discovery, and mechanisms of approved drugs. A two-pronged approach investigating the metabolism of antibacterials within both the host and bacterium is outlined and will be of value to both the chemical biology and drug discovery fields.
细菌能够进行多种生物转化,这些转化可能会激活或使异生物素失活。最近的研究利用代谢组学技术来研究小分子抗菌药物在目标生物体中的命运。本文综述并分析了涉及结核分枝杆菌的实例,以了解它们在抗菌药物的激活和失活方面所提供的见解。这些研究特别揭示了结核分枝杆菌进行的生物合成转化,同时为化学工具的发展指明了方向,突出了药物发现的潜在领域以及已批准药物的作用机制。本文概述了一种双管齐下的方法,用于研究抗菌药物在宿主和细菌体内的代谢情况,这将对化学生物学和药物发现领域都具有价值。