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MMAR_2770,一种新的参与生物素生物合成的酶,对于分枝杆菌在巨噬细胞和斑马鱼中的生长是必需的。

MMAR_2770, a new enzyme involved in biotin biosynthesis, is essential for the growth of Mycobacterium marinum in macrophages and zebrafish.

机构信息

Key Laboratory of Medical Molecular Virology, Institute of Biomedical Sciences and Medical Microbiology, Fudan University, 138 Yi Xue Yuan Road, Shanghai, China.

出版信息

Microbes Infect. 2011 Jan;13(1):33-41. doi: 10.1016/j.micinf.2010.08.010. Epub 2010 Oct 23.

Abstract

Biotin, which functions as an essential cofactor for certain carboxylases and decarboxylases, is synthesized by a multistep pathway in microorganisms and plants. Biotin biosynthesis has not been studied in detail in mycobacteria. In this study, we isolated a mutant of Mycobacterium marinum in which MMAR_2770, a previously uncharacterized gene encoding a predicted short-chain dehydrogenase/reductase, was inactivated. We found that this mutant is a biotin auxotroph that cannot grow in a minimal medium (Sauton) unless biotin is supplemented. Complementation of the mutant with an intact MMAR_2770 or its homolog Rv1882c of Mycobacterium tuberculosis restored the growth of the mutant, suggesting that MMAR_2770 is involved in biotin biosynthesis. We further showed that the mutant was unable to grow in cultured macrophages and was attenuated in zebrafish. Taken together, our results demonstrate that biotin biosynthesis is essential for the growth of mycobacteria in vitro and in vivo and have provided validation for targeting biotin biosynthetic enzymes for antimycobacterial drug development. The potential role of MMAR_2770 in mycobacterial biotin biosynthesis is discussed.

摘要

生物素作为某些羧化酶和脱羧酶的必需辅酶,在微生物和植物中通过多步途径合成。分枝杆菌中的生物素生物合成尚未得到详细研究。在本研究中,我们分离到一株耻垢分枝杆菌突变体,其中以前未被表征的基因 MMAR_2770 失活,该基因编码一个预测的短链脱氢酶/还原酶。我们发现该突变体是生物素营养缺陷型,除非添加生物素,否则无法在最小培养基(Sauton)中生长。用完整的 MMAR_2770 或其结核分枝杆菌的同源物 Rv1882c 对突变体进行互补恢复了突变体的生长,表明 MMAR_2770 参与生物素生物合成。我们进一步表明,突变体在培养的巨噬细胞中无法生长,在斑马鱼中减毒。总之,我们的结果表明生物素生物合成对于分枝杆菌在体外和体内的生长是必不可少的,并为针对生物素生物合成酶开发抗分枝杆菌药物提供了验证。讨论了 MMAR_2770 在分枝杆菌生物素生物合成中的潜在作用。

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