支原体
生物
分枝杆菌
微生物学
结核分枝杆菌
麻风分枝杆菌
质粒
细菌
病毒学
肺结核
遗传学
基因
麻风病
免疫学
医学
病理
作者
Ian L. Sparks,Keith M. Derbyshire,William R. Jacobs,Yasu S. Morita
出处
期刊:Journal of Bacteriology
[American Society for Microbiology]
日期:2023-01-04
卷期号:205 (1): e0033722-e0033722
被引量:146
摘要
155 have since provided previously unattainable insights on these same features in its slow-growing relatives. Notably, tuberculosis (TB) drugs, including the first-line drugs isoniazid and ethambutol, are active against M. smegmatis, but not against E. coli, allowing the identification of their physiological targets. Furthermore, Bedaquiline, the first new TB drug in 40 years, was discovered through an M. smegmatis screen. M. smegmatis has become a model bacterium, not only for M. tuberculosis, but for all other Mycobacterium species and related genera. With a repertoire of bioinformatic and physical resources, including the recently established Mycobacterial Systems Resource, M. smegmatis will continue to accelerate mycobacterial research and advance the field of microbiology.
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