| Literature DB >> 23907010 |
Jennifer Shepherd1, Michael Ibba.
Abstract
Prokaryotic aminoacylated-transfer RNAs often need to be efficiently segregated between translation and other cellular biosynthetic pathways. Many clinically relevant bacteria, including Streptococcus pneumoniae, Staphylococcus aureus, Enterococcus faecalis and Pseudomonas aeruginosa direct some aminoacylated-tRNA species into peptidoglycan biosynthesis and/or membrane phospholipid modification. Subsequent indirect peptidoglycan cross-linkage or change in membrane permeability is often a prerequisite for high-level antibiotic resistance. In Streptomycetes, aminoacylated-tRNA species are used for antibiotic synthesis as well as antibiotic resistance. The direction of coding aminoacylated-tRNA molecules away from translation and into antibiotic resistance and synthesis pathways are discussed in this review.Entities:
Keywords: Antibiotic; Antibiotic resistance; Pathogenesis; Peptidoglycan; Protein synthesis; Translation; tRNA
Mesh:
Substances:
Year: 2013 PMID: 23907010 PMCID: PMC3786784 DOI: 10.1016/j.febslet.2013.07.036
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124