Matsumoto S, Furugen M, Yukitake H, Yamada T
Oral Bacteriology, Nagasaki University, School of Dentistry, Sakamoto 1-7-1, Nagasaki, Japan.
FEMS Microbiol Lett. 2000 Jan 15;182(2):297-301. doi: 10.1111/j.1574-6968.2000.tb08911.x.
Pathogenic species of Mycobacterium are slowly growing intracellular bacteria. Slow growth is important for the parasitism of these organisms and chronicity of the disease, but its precise mechanism has not been elucidated. Recently, we found that a novel DNA-binding protein (MDPI) was expressed (7-10% in total protein) in mycobacteria, such as Mycobacterium bovis bacillus Calmette-Guérin, Mycobacterium tuberculosis, and Mycobacterium leprae. In this study, we observed that MDPI interfered with replication, transcription, and translation in the analysis in in vitro E. coli cell-free macromolecular biosynthesizing systems. Furthermore, MDPI inhibited the rapid growth of both Escherichia coli and Mycobacterium smegmatis, and NH(2)-terminal second amino acid, asparagine, was observed to be important in terms of this function. These data suggest an important role of MDPI for suppression of growth rates of mycobacteria.
分枝杆菌的致病菌种是生长缓慢的胞内细菌。生长缓慢对于这些微生物的寄生以及疾病的慢性化很重要,但其确切机制尚未阐明。最近,我们发现一种新型DNA结合蛋白(MDPI)在分枝杆菌中表达(占总蛋白的7 - 10%),如卡介苗、结核分枝杆菌和麻风分枝杆菌。在本研究中,我们观察到在体外大肠杆菌无细胞大分子生物合成系统分析中,MDPI干扰了复制、转录和翻译。此外,MDPI抑制了大肠杆菌和耻垢分枝杆菌的快速生长,并且观察到NH(2)-末端的第二个氨基酸天冬酰胺在该功能方面很重要。这些数据表明MDPI在抑制分枝杆菌生长速率方面具有重要作用。