4.6 Article

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

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 281, Issue 26, Pages 18033-18042

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M513174200

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Funding

  1. NIGMS NIH HHS [R01 GM 64530, R01 GM 65183] Funding Source: Medline

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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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