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Updated: Jun 8, 2026

Expression, Detergent Solubilization, and Purification of a Membrane Transporter, the MexB Multidrug Resistance Protein
Published on: December 3, 2010
LmrS is a multidrug efflux pump of the major facilitator superfamily from Staphylococcus aureus
Jody L Floyd1, Kenneth P Smith, Sanath H Kumar
1Eastern New Mexico University, Department of Biology, Station 33, Portales, NM 88130, USA.
Abstract:
A multidrug efflux pump designated LmrS (lincomycin resistance protein of Staphylococcus aureus), belonging to the major facilitator superfamily (MFS) of transporters, was cloned, and the role of LmrS in antimicrobial efflux was evaluated. The highest relative increase in MIC, 16-fold, was observed for linezolid and tetraphenylphosphonium chloride (TPCL), followed by an 8-fold increase for sodium dodecyl sulfate (SDS), trimethoprim, and chloramphenicol. LmrS has 14 predicted membrane-spanning domains and is homologous to putative lincomycin resistance proteins of Bacillus spp., Lactobacillus spp., and Listeria spp.
Insights
A novel multidrug efflux pump, LmrS, was identified in Staphylococcus aureus. This transporter confers resistance to critical antibiotics like linezolid and trimethoprim.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- Multidrug efflux pumps are crucial in antimicrobial resistance.
- The major facilitator superfamily (MFS) includes many clinically relevant transporters.
- Staphylococcus aureus possesses various resistance mechanisms, including efflux pumps.
Purpose of the Study:
- To clone and characterize a novel multidrug efflux pump, LmrS, from Staphylococcus aureus.
- To evaluate the role of LmrS in the efflux of various antimicrobial agents.
- To determine the substrate specificity of the LmrS transporter.
Main Methods:
- Cloning of the LmrS gene from Staphylococcus aureus.
- Determination of minimum inhibitory concentrations (MICs) for various compounds in the presence and absence of LmrS.
- Bioinformatic analysis to predict the structure and homology of LmrS.
Main Results:
- The LmrS efflux pump was successfully cloned and expressed.
- LmrS conferred a significant increase in MIC values for linezolid (16-fold) and tetraphenylphosphonium chloride (TPCL) (16-fold).
- Increased resistance was also observed for sodium dodecyl sulfate (SDS), trimethoprim, and chloramphenicol (8-fold).
Conclusions:
- LmrS is a functional multidrug efflux pump belonging to the MFS transporter family.
- LmrS contributes to Staphylococcus aureus resistance against clinically important antibiotics and biocides.
- LmrS exhibits homology to lincomycin resistance proteins in other bacterial species, suggesting conserved resistance mechanisms.
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