Abstract
The Bacillus subtilis multidrug efflux transporter Bmr demonstrates 44% amino acid sequence identity with a product of the Staphylococcus aureus gene norA, which is responsible for clinically relevant resistance to fluoroquinolones. We show here that overexpression of bmr in B. subtilis provides strong resistance to fluoroquinolones that can be reversed by reserpine, an inhibitor of Bmr.
MeSH Terms
Amino Acid Sequence
Bacillus subtilis/genetics,metabolism
Bacterial Proteins/analysis,metabolism
Carrier Proteins
Membrane Transport Proteins
Molecular Sequence Data
Multidrug Resistance-Associated Proteins
Reserpine/pharmacology
Sequence Homology, Nucleic Acid
Staphylococcus aureus/genetics,metabolism
Chemicals
Bacterial Proteins
Carrier Proteins
Membrane Transport Proteins
Multidrug Resistance-Associated Proteins
NorA protein, Staphylococcus
Bmr protein, Bacillus subtilis
Reserpine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Neyfakh A A
Department of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago 60680.
References (5)
5 references, click to expand
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