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Aspartyl-tRNA synthetase is the target of peptide nucleotide antibiotic Microcin C
Authors:Metlitskaya Anastasia  Kazakov Teymur  Kommer Aigar  Pavlova Olga  Praetorius-Ibba Mette  Ibba Michael  Krasheninnikov Igor  Kolb Vyacheslav  Khmel Inessa  Severinov Konstantin
Institution:Institute of Molecular Genetics, Russian Academy of Sciences, Moscow 123182, Russia.
Abstract: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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