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Updated: May 10, 2026

In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa
Published on: February 17, 2014
An efflux pump is required for siderophore recycling by Pseudomonas aeruginosa
Emilie Yeterian1, Lois W Martin, Iain L Lamont
1Metaux et microorganismes: Chimie, Biologie et Applications. FRE 3211, CNRS-Université de Strasbourg, ESBS, Blvd Sébastien Brant, F-67413 Illkirch, Strasbourg, France. Department of Biochemistry, University of Otago, PO Box 56, Dunedin, New Zealand.
Abstract:
Pyoverdine (PVDI) is a siderophore produced by Pseudomonas aeruginosa in order to obtain iron. This molecule is composed of a fluorescent chromophore linked to an octapeptide. Following secretion from the bacteria, PVDI chelates iron ions and the resulting Fe-PVDI complexes are taken up by the bacteria through a cell surface receptor protein. The iron is released in the periplasm and the resulting PVDI is recycled, being secreted out of the bacteria by a previously unknown mechanism. Three genes with the potential to encode an efflux system are adjacent to, and coregulated with, genes required for PVDI-mediated iron transport. Mutation of genes encoding this efflux pump (named PvdRT-OpmQ) prevented recycling of PVDI from the periplasm into the extracellular medium. Fluorescence microscopy showed that in the mutant bacteria PVDI accumulated in the periplasm. Gallium (Ga(3+) ), a metal that cannot be removed from PVDI by reduction, is taken up by P. aeruginosa when chelated by PVDI. Recycling did not occur after transport of PVDI-Ga(3+) and fluorescence accumulated in the periplasm even when the PvdRT-OpmQ efflux pump was functional. Cellular fractionation showed that PVDI-synthesizing bacteria lacking PvdRT-OpmQ secreted PVDI but had an approximately 20-fold increase in the amount of PVD present in the periplasm, consistent with an inability to recycle PVDI. Collectively, these data show that PvdRT-OpmQ is involved in recycling of PVDI from the periplasm to the extracellular medium and recycling requires release of the metal ion from PVDI.
Insights
Pyoverdine (PVDI) recycling in Pseudomonas aeruginosa is facilitated by the PvdRT-OpmQ efflux pump. This system is crucial for secreting PVDI from the periplasm, requiring metal ion release for efficient recycling.
Area of Science:
- Microbiology
- Bacterial Physiology
- Metal Ion Transport
Background:
- Pyoverdine (PVDI) is a siderophore essential for iron acquisition by Pseudomonas aeruginosa.
- PVDI chelates iron, forms complexes, and is internalized via cell surface receptors.
- The mechanism for PVDI recycling from the periplasm remained unknown.
Purpose of the Study:
- To elucidate the mechanism of pyoverdine (PVDI) recycling in Pseudomonas aeruginosa.
- To identify the molecular components responsible for PVDI efflux from the periplasm.
- To investigate the role of metal ion release in PVDI recycling.
Main Methods:
- Gene mutation analysis of potential efflux system genes (PvdRT-OpmQ).
- Fluorescence microscopy to track PVDI localization within bacterial cells.
- Cellular fractionation to quantify periplasmic PVDI levels.
- Experiments using Gallium (Ga3+) to assess metal ion influence on recycling.
Main Results:
- Mutation of PvdRT-OpmQ genes blocked PVDI recycling from the periplasm.
- PVDI accumulated in the periplasm of mutant strains, confirmed by fluorescence microscopy.
- PVDI-Gallium complexes also failed to recycle, even with a functional efflux pump.
- Bacteria lacking PvdRT-OpmQ showed a 20-fold increase in periplasmic PVDI.
Conclusions:
- The PvdRT-OpmQ efflux system is essential for PVDI recycling in P. aeruginosa.
- PVDI recycling requires the release of the chelated metal ion within the periplasm.
- This study reveals a novel mechanism for siderophore recycling in bacteria.
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