Abstract
SIGNIFICANCE: Iron is required for growth and is often redox active under cytosolic conditions. As a result of its facile redox chemistry, iron homeostasis is intricately involved with oxidative stress. Bacterial adaptation to iron limitation and oxidative stress often involves ferric uptake regulator (Fur) proteins: a diverse set of divalent cation-dependent, DNA-binding proteins that vary widely in both metal selectivity and sensitivity to metal-catalyzed oxidation. Recent Advances: Bacteria contain two Fur family metalloregulators that use ferrous iron (Fe(2+)) as their cofactor, Fur and PerR. Fur functions to regulate iron homeostasis in response to changes in intracellular levels of Fe(2+). PerR also binds Fe(2+), which enables metal-catalyzed protein oxidation as a mechanism for sensing hydrogen peroxide (H(2)O(2)). CRITICAL ISSUES: To effectively regulate iron homeostasis, Fur has an Fe(2+) affinity tuned to monitor the labile iron pool of the cell and may be under selective pressure to minimize iron oxidation, which would otherwise lead to an inappropriate increase in iron uptake under oxidative stress conditions. Conversely, Fe(2+) is bound more tightly to PerR but exhibits high H(2)O(2) reactivity, which enables a rapid induction of peroxide stress genes. FUTURE DIRECTIONS: The features that determine the disparate reactivity of these proteins with oxidants are still poorly understood. A controlled, comparative analysis of the affinities of Fur/PerR proteins for their metal cofactors and their rate of reactivity with H(2)O(2), combined with structure/function analyses, will be needed to define the molecular mechanisms that have facilitated this divergence of function between these two paralogous regulators.