Aspartyl-tRNA synthetase is the target of peptide nucleotide antibiotic Microcin C

被引:129
作者
Metlitskaya, Anastasia
Kazakov, Teymur
Kommer, Aigar
Pavlova, Olga
Praetorius-Ibba, Mette
Ibba, Michael
Krasheninnikov, Igor
Kolb, Vyacheslav
Khmel, Inessa
Severinov, Konstantin
机构
[1] Russian Acad Sci, Inst Mol Genet, Moscow 123182, Russia
[2] Russian Acad Sci, Inst Prot Res, Pushchino 142292, Russia
[3] Moscow MV Lomonosov State Univ, Dept Virol, Moscow 119899, Russia
[4] Moscow MV Lomonosov State Univ, Dept Mol Biol, Moscow 119899, Russia
[5] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
[6] Rutgers State Univ, Waksman Inst, Dept Biochem & Mol Biol, Piscataway, NJ 08854 USA
关键词
D O I
10.1074/jbc.M513174200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microcin C is a ribosome-synthesized heptapeptide that contains a modified adenosine monophosphate covalently attached to the C-terminal aspartate. Microcin C is a potent inhibitor of bacterial cell growth. Based on the in vivo kinetics of inhibition of macromolecular synthesis, Microcin C targets translation, through a mechanism that remained undefined. Here, we show that Microcin C is a subject of specific degradation inside the sensitive cell. The product of degradation, a modified aspartyl-adenylate containing an N-acylphosphoramidate linkage, strongly inhibits translation by blocking the function of aspartyl-tRNA synthetase.
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收藏
页码:18033 / 18042
页数:10
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