Identification and characterization of a new intermediate in the ribosylative inactivation pathway of rifampin by Mycobacterium smegmatis

被引:9
作者
Imai, T
Watanabe, K
Mikami, Y
Yazawa, K
Ando, A
Nagata, Y
Morisaki, N
Hashimoto, Y
Furihata, K
Dabbs, ER
机构
[1] Chiba Univ, Pathogen Fungi & Microbial Toxicoses Res Ctr, Chuo Ku, Chiba 2608673, Japan
[2] Chiba Univ, Dept Biotechnol, Grad Sch Sci & Technol, Inage Ku, Chiba 2718510, Japan
[3] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[4] Univ Tokyo, Div Agr & Agr Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
[5] Univ Witwatersrand, Dept Genet, ZA-2050 Johannesburg, South Africa
来源
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE | 1999年 / 5卷 / 04期
关键词
D O I
10.1089/mdr.1999.5.259
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Mycobacterium smegmatis DSM 43756 inactivates rifampin by ribosylation. To study this process of rifampicin, all possible inactivated forms of the antibiotic were extracted and purified. Structural studies showed the presence of a new inactivation product, designated RIP-TAp(23-phosphoribosyl-rifampin), Formation of 23(O-ADP-ribosyl)rifampin (RIP-TAs) is the first step, followed by removal of AMP to give rise to the newly identified compound. Lastly, dephosphorylation leads to formation of 23-ribosyl-rifampin (RIP-Mb), Feeding experiments with the ADP-ribosylated antibiotic obtained from the cell homogenates of an Escherichia coli strain carrying the cloned M. smegmatis gene confirmed this rifampin inactivation process.
引用
收藏
页码:259 / 264
页数:6
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