Many drugs isolated from microorganisms have complex molecular structures, making it difficult for chemists to modify them. But it seems that enzymes can provide a short cut to drug variants.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Rent or buy this article
Get just this article for as long as you need it
$39.95
Prices may be subject to local taxes which are calculated during checkout

References
Zhang, C. et al. Science 313, 1291–1294 (2006).
Walsh, C. T., Losey, H. C. & Freel Meyers, C. L. Biochem. Soc. Trans. 31, 487–492 (2003).
Oberthur, M., Leimkuhler, C. & Kahne, D. Org. Lett. 6, 2873–2876 (2004).
Oberthur, M. et al. J. Am. Chem. Soc. 127, 10747–10752 (2005).
Fischbach, M. A. & Walsh, C. T. Chem. Rev. 106, 3468–3496 (2006).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Walsh, C. A sweet exchange. Nature 443, 285–286 (2006). https://doi.org/10.1038/443285a
Published:
Issue Date:
DOI: https://doi.org/10.1038/443285a