Khare Garima, Nangpal Prachi, Tyagi Anil K
Department of Biochemistry, University of Delhi South Campus, Benito Juarez Road, New Delhi, India.
Vice Chancellor, Guru Gobind Singh Indraprastha University, Sector 16-C, Dwarka New Delhi, India.
PLoS One. 2017 Jan 6;12(1):e0169545. doi: 10.1371/journal.pone.0169545. eCollection 2017.
Ferritins and bacterioferritins are iron storage proteins that represent key players in iron homeostasis. Several organisms possess both forms of ferritins, however, their relative physiological roles are less understood. Mycobacterium tuberculosis possesses both ferritin (BfrB) and bacterioferritin (BfrA), playing an essential role in its pathogenesis as reported by us earlier. This study provides insights into the role of these two proteins in iron homeostasis by employing M. tuberculosis bfr mutants. Our data suggests that BfrA is required for efficient utilization of stored iron under low iron conditions while BfrB plays a crucial role as the major defense protein under excessive iron conditions. We show that these two proteins provide protection against oxidative stress and hypoxia. Iron incorporation study showed that BfrB has higher capacity for storing iron than BfrA, which augurs well for efficient iron quenching under iron excess conditions. Moreover, iron release assay demonstrated that BfrA has 3 times superior ability to release stored iron emphasizing its requirement for efficient iron release under low iron conditions, facilitated by the presence of heme. Thus, for the first time, our observations suggest that the importance of BfrA or BfrB separately might vary depending upon the iron situation faced by the cell.
铁蛋白和细菌铁蛋白是铁储存蛋白,是铁稳态的关键参与者。几种生物体都拥有这两种形式的铁蛋白,然而,它们相对的生理作用却鲜为人知。结核分枝杆菌同时拥有铁蛋白(BfrB)和细菌铁蛋白(BfrA),正如我们之前报道的,它们在其发病机制中起着至关重要的作用。本研究通过使用结核分枝杆菌bfr突变体,深入探讨了这两种蛋白质在铁稳态中的作用。我们的数据表明,在低铁条件下,BfrA是有效利用储存铁所必需的,而BfrB在高铁条件下作为主要防御蛋白发挥关键作用。我们表明,这两种蛋白质可提供针对氧化应激和缺氧的保护。铁掺入研究表明,BfrB储存铁的能力高于BfrA,这对于在铁过量条件下有效淬灭铁是个好兆头。此外,铁释放试验表明,BfrA释放储存铁的能力高出3倍,强调了在低铁条件下其对有效释放铁的需求,血红素的存在促进了这一过程。因此,我们的观察首次表明,BfrA或BfrB各自的重要性可能因细胞面临的铁状况而异。