Ahmed Wareed, Menon Shruti, Godbole Adwait Anand, Karthik Pullela V D N B, Nagaraja Valakunja
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.
FEMS Microbiol Lett. 2014 Apr;353(2):116-23. doi: 10.1111/1574-6968.12412. Epub 2014 Apr 3.
Topoisomerases are an important class of enzymes for regulating the DNA transaction processes. Mycobacterium tuberculosis (Mtb) is one of the most formidable pathogens also posing serious challenges for therapeutic interventions. The organism contains only one type IA topoisomerase (Rv3646c), offering an opportunity to test its potential as a candidate drug target. To validate the essentiality of M. tuberculosis topoisomerase I (TopoI(Mt) ) for bacterial growth and survival, we have generated a conditionally regulated strain of topoI in Mtb. The conditional knockdown mutant exhibited delayed growth on agar plate. In liquid culture, the growth was drastically impaired when TopoI expression was suppressed. Additionally, novobiocin and isoniazid showed enhanced inhibitory potential against the conditional mutant. Analysis of the nucleoid revealed its altered architecture upon TopoI depletion. These studies establish the essentiality of TopoI for the M. tuberculosis growth and open up new avenues for targeting the enzyme.
拓扑异构酶是调节DNA交易过程的一类重要酶。结核分枝杆菌(Mtb)是最具威胁性的病原体之一,也给治疗干预带来了严峻挑战。该生物体仅含有一种IA型拓扑异构酶(Rv3646c),这为测试其作为候选药物靶点的潜力提供了机会。为了验证结核分枝杆菌拓扑异构酶I(TopoI(Mt))对细菌生长和存活的必要性,我们构建了一株Mtb中topoI条件性调控菌株。条件性敲低突变体在琼脂平板上生长延迟。在液体培养中,当TopoI表达被抑制时,生长受到严重损害。此外,新生霉素和异烟肼对条件性突变体显示出增强的抑制潜力。对类核的分析表明,TopoI缺失后其结构发生了改变。这些研究证实了TopoI对结核分枝杆菌生长的必要性,并为靶向该酶开辟了新途径。