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Updated: May 28, 2026

Essential Metal Uptake in Gram-negative Bacteria: X-ray Fluorescence, Radioisotopes, and Cell Fractionation
Published on: February 1, 2018
Magnesium Transporters as Crucial Regulators of Bacterial Survival and Pathogenicity
Seungjun Hur1, Youngki Yoo2, Jeong Min Chung1
1Department of Biotechnology, The Catholic University of Korea, Bucheon-si 14662, Republic of Korea.
Abstract:
Magnesium is an essential divalent cation required for adenosine triphosphate (ATP)-dependent reactions, nucleic acid metabolism, and ribosomal stability. Bacteria depend on specialized transport systems to maintain intracellular Mg2+ homeostasis as it cannot freely cross the phospholipid bilayer. During infection, host nutritional immunity restricts metal availability, and magnesium limitation within the phagosome compromises bacterial metabolism and stability. This review summarizes the major bacterial magnesium transport systems and their roles in survival and pathogenicity, with an emphasis on Salmonella and extension to clinically relevant ESKAPE pathogens. We focus on the PhoPQ-regulated MgtA, MgtB, and MgtC system, in which low magnesium, acidic pH, and other host-derived signals activate PhoPQ to induce mgt gene expression. MgtA and MgtB act as high-affinity P-type ATPases, whereas MgtC promotes bacterial survival within the intramacrophage environment by inhibiting bacterial F-type ATP synthase through specific interactions with subunit a. We also discuss CorA as a conserved channel for basal Mg2+ uptake and MgtE as a Mg2+-selective channel whose gating responds to intracellular Mg2+ and ATP. Finally, we consider the conservation and variation in these systems across pathogenic bacteria and their potential as therapeutic targets for antimicrobial development.
Insights
Bacteria need magnesium (Mg2+) to survive. This review details bacterial magnesium transport systems, crucial for pathogen survival during infection and potential antimicrobial targets.
Area of Science:
- Microbiology
- Molecular Biology
- Pathogenesis
Background:
- Magnesium (Mg2+) is vital for bacterial functions like ATP-dependent reactions and nucleic acid metabolism.
- Bacteria require specialized transport systems to regulate intracellular Mg2+ homeostasis due to membrane impermeability.
- Host nutritional immunity during infection limits Mg2+ availability, impacting bacterial survival and virulence.
Purpose of the Study:
- To review major bacterial magnesium transport systems.
- To highlight their roles in bacterial survival and pathogenicity, focusing on *Salmonella* and ESKAPE pathogens.
- To explore potential therapeutic targets for antimicrobial development.
Main Methods:
- Literature review of bacterial magnesium transport systems.
- Focus on PhoPQ-regulated systems (MgtA, MgtB, MgtC) and their mechanisms.
- Discussion of conserved channels (CorA) and selective channels (MgtE).
Main Results:
- The PhoPQ-Mgt system regulates Mg2+ uptake in response to host signals.
- MgtA and MgtB are high-affinity Mg2+ ATPases; MgtC inhibits ATP synthase for intramacrophage survival.
- CorA and MgtE are key Mg2+ uptake channels with distinct regulatory mechanisms.
Conclusions:
- Bacterial Mg2+ transport systems are essential for pathogen survival and virulence.
- These systems, particularly in *Salmonella* and ESKAPE pathogens, represent promising targets for novel antimicrobial strategies.
- Understanding Mg2+ homeostasis is critical for combating bacterial infections.
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