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Biotransformation of Rosamicin Antibiotic into 10,11-Dihydrorosamicin with Enhanced In Vitro Antibacterial Activity Against MRSA

  • Nguyen, Lan Huong (Department of Pharmaceutical Engineering, SunMoon University) ;
  • Nguyen, Huu Hoang (Department of Pharmaceutical Engineering, SunMoon University) ;
  • Shrestha, Anil (Department of Pharmaceutical Engineering, SunMoon University) ;
  • Sohng, Jae Kyung (Department of Pharmaceutical Engineering, SunMoon University) ;
  • Yoon, Yeo Joon (Department of Chemistry and Nano Science, Ewha Womans University) ;
  • Park, Je Won (Department of Pharmaceutical Engineering, SunMoon University)
  • Received : 2013.06.24
  • Accepted : 2013.09.23
  • Published : 2014.01.28

Abstract

A biotransformation approach using microbes as biocatalysts can be an efficient tool for the targeted modification of existing antibiotic chemical scaffolds to create previously uncharacterized therapeutic agents. By employing a recombinant Streptomyces venezuelae strain as a microbial catalyst, a reduced macrolide, 10,11-dihydrorosamicin, was created from rosamicin macrolide. Its chemical structure was spectroscopically elucidated, and the new rosamicin analog showed 2-4-fold higher antibacterial activity against two strains of methicillin-resistant Staphylococcus aureus compared with its parent rosamicin. This kind of biocatalytic approach is able to expand existing antibiotic entities and can also provide more diverse therapeutic resources.

Keywords

References

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