This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McNicholas, P. M.
Right arrow Articles by Black, T. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McNicholas, P. M.
Right arrow Articles by Black, T. A.

Next Article 

Antimicrobial Agents and Chemotherapy, May 2000, p. 1121-1126, Vol. 44, No. 5
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Evernimicin Binds Exclusively to the 50S Ribosomal Subunit and Inhibits Translation in Cell-Free Systems Derived from both Gram-Positive and Gram-Negative Bacteria

Paul M. McNicholas,* David J. Najarian, Paul A. Mann, David Hesk, Roberta S. Hare, Karen J. Shaw, and Todd A. Black

Schering-Plough Research Institute, Kenilworth, New Jersey 07033

Received 3 August 1999/Returned for modification 26 November 1999/Accepted 18 January 2000

Evernimicin (SCH 27899) is a new antibiotic with activity against a wide spectrum of gram-positive bacteria and activity against some gram-negative bacteria. Previous metabolic labeling studies indicated that evernimicin specifically inhibited protein synthesis in Staphylococcus aureus. Using a susceptible Escherichia coli strain, we demonstrated that evernimicin also inhibited protein synthesis in E. coli. In cell-free translation assays with extracts from either E. coli or S. aureus, evernimicin had a 50% inhibitory concentration of approximately 125 nM. In contrast, cell-free systems derived from wheat germ and rabbit reticulocytes were inhibited only by very high levels of evernimicin. Evernimicin did not promote transcript misreading. [14C]evernimicin specifically bound to the 50S subunit from E. coli. Nonlinear regression analysis of binding data generated with 70S ribosomes from E. coli and S. aureus and 50S subunits from E. coli returned dissociation constants of 84, 86, and 160 nM, respectively. In binding experiments, performed in the presence of excess quantities of a selection of antibiotics known to bind to the 50S subunit, only the structurally similar drug avilamycin blocked binding of [14C]evernimicin to ribosomes.


* Corresponding author. Mailing address: Schering-Plough Research Institute, Bldg. K15-4-4700, 2015 Galloping Hill Rd., Kenilworth NJ 07033. Phone: (908) 740-7644. Fax: (908) 740-3918. E-mail: paul.mcnicholas{at}spcorp.com.


Antimicrobial Agents and Chemotherapy, May 2000, p. 1121-1126, Vol. 44, No. 5
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Llano-Sotelo, B., Hickerson, R. P., Lancaster, L., Noller, H. F., Mankin, A. S. (2009). Fluorescently labeled ribosomes as a tool for analyzing antibiotic binding. RNA 15: 1597-1604 [Abstract] [Full Text]  
  • Boll, R., Hofmann, C., Heitmann, B., Hauser, G., Glaser, S., Koslowski, T., Friedrich, T., Bechthold, A. (2006). The Active Conformation of Avilamycin A Is Conferred by AviX12, a Radical AdoMet Enzyme. J. Biol. Chem. 281: 14756-14763 [Abstract] [Full Text]  
  • Xiong, L., Korkhin, Y., Mankin, A. S. (2005). Binding Site of the Bridged Macrolides in the Escherichia coli Ribosome. Antimicrob. Agents Chemother. 49: 281-288 [Abstract] [Full Text]  
  • Treede, I., Hauser, G., Muhlenweg, A., Hofmann, C., Schmidt, M., Weitnauer, G., Glaser, S., Bechthold, A. (2005). Genes Involved in Formation and Attachment of a Two-Carbon Chain as a Component of Eurekanate, a Branched-Chain Sugar Moiety of Avilamycin A. Appl. Environ. Microbiol. 71: 400-406 [Abstract] [Full Text]  
  • Butaye, P., Devriese, L. A., Haesebrouck, F. (2003). Antimicrobial Growth Promoters Used in Animal Feed: Effects of Less Well Known Antibiotics on Gram-Positive Bacteria. Clin. Microbiol. Rev. 16: 175-188 [Abstract] [Full Text]  
  • Zarazaga, M., Tenorio, C., Del Campo, R., Ruiz-Larrea, F., Torres, C. (2002). Mutations in Ribosomal Protein L16 and in 23S rRNA in Enterococcus Strains for Which Evernimicin MICs Differ. Antimicrob. Agents Chemother. 46: 3657-3659 [Abstract] [Full Text]  
  • Aarestrup, F. M., McNicholas, P. M. (2002). Incidence of High-Level Evernimicin Resistance in Enterococcus faecium among Food Animals and Humans. Antimicrob. Agents Chemother. 46: 3088-3090 [Abstract] [Full Text]  
  • Belova, L., Tenson, T., Xiong, L., McNicholas, P. M., Mankin, A. S. (2001). A novel site of antibiotic action in the ribosome: Interaction of evernimicin with the large ribosomal subunit. Proc. Natl. Acad. Sci. USA 10.1073/pnas.071527498v1 [Abstract] [Full Text]  
  • Weitnauer, G., Gaisser, S., Trefzer, A., Stockert, S., Westrich, L., Quiros, L. M., Mendez, C., Salas, J. A., Bechthold, A. (2001). An ATP-Binding Cassette Transporter and Two rRNA Methyltransferases Are Involved in Resistance to Avilamycin in the Producer Organism Streptomyces viridochromogenes Tu57. Antimicrob. Agents Chemother. 45: 690-695 [Abstract] [Full Text]  
  • McNicholas, P. M., Mann, P. A., Najarian, D. J., Miesel, L., Hare, R. S., Black, T. A. (2001). Effects of Mutations in Ribosomal Protein L16 on Susceptibility and Accumulation of Evernimicin. Antimicrob. Agents Chemother. 45: 79-83 [Abstract] [Full Text]  
  • Aarestrup, F. M., Jensen, L. B. (2000). Presence of Variations in Ribosomal Protein L16 Corresponding to Susceptibility of Enterococci to Oligosaccharides (Avilamycin and Evernimicin). Antimicrob. Agents Chemother. 44: 3425-3427 [Abstract] [Full Text]  
  • Adrian, P. V., Mendrick, C., Loebenberg, D., McNicholas, P., Shaw, K. J., Klugman, K. P., Hare, R. S., Black, T. A. (2000). Evernimicin (SCH27899) Inhibits a Novel Ribosome Target Site: Analysis of 23S Ribosomal DNA Mutants. Antimicrob. Agents Chemother. 44: 3101-3106 [Abstract] [Full Text]  
  • Belova, L., Tenson, T., Xiong, L., McNicholas, P. M., Mankin, A. S. (2001). A novel site of antibiotic action in the ribosome: Interaction of evernimicin with the large ribosomal subunit. Proc. Natl. Acad. Sci. USA 98: 3726-3731 [Abstract] [Full Text]