Bacterial inactivation of the anticancer drug doxorubicin.

Chem Biol

M.G. DeGroote Institute for Infectious Disease Research, Department of Biochemistry and Biomedical Sciences, DeGroote School of Medicine, McMaster University, 1280 Main Street W, Hamilton, ON L8N 4K1, Canada.

Published: October 2012

Microbes are exposed to compounds produced by members of their ecological niche, including molecules with antibiotic or antineoplastic activities. As a result, even bacteria that do not produce such compounds can harbor the genetic machinery to inactivate or degrade these molecules. Here, we investigated environmental actinomycetes for their ability to inactivate doxorubicin, an aminoglycosylated anthracycline anticancer drug. One strain, Streptomyces WAC04685, inactivates doxorubicin via a deglycosylation mechanism. Activity-based purification of the enzymes responsible for drug inactivation identified the NADH dehydrogenase component of respiratory electron transport complex I, which was confirmed by gene inactivation studies. A mechanism where reduction of the quinone ring of the anthracycline by NADH dehydrogenase leads to deglycosylation is proposed. This work adds anticancer drug inactivation to the enzymatic inactivation portfolio of actinomycetes and offers possibilities for novel applications in drug detoxification.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.chembiol.2012.08.011DOI Listing

Publication Analysis

Top Keywords

anticancer drug
12
drug inactivation
8
nadh dehydrogenase
8
drug
5
bacterial inactivation
4
inactivation anticancer
4
drug doxorubicin
4
doxorubicin microbes
4
microbes exposed
4
exposed compounds
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!