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Genetic regulation of fluxes: iron homeostasis escherichia coli

    Research output: Contribution to journal › Journal article › Research › peer-review

    Abstract

    Iron is an essential trace-element for most organisms. However, because high concentration of free intracellular iron is cytotoxic, cells have developed complex regulatory networks that keep free intracellular iron concentration at optimal range, allowing the incorporation of the metal into iron-using enzymes and minimizing damage to the cell. We built a mathematical model of the network that controls iron uptake and usage in the bacterium Escherichia coli to explore the dynamics of iron flow. We simulate the effect of sudden decrease or increase in the extracellular iron level on intracellular iron distribution. Based on the results of simulations we discuss the possible roles of the small RNA RyhB and the Fe-S cluster assembly systems in the optimal redistribution of iron flows. We suggest that Fe-S cluster assembly is crucial to prevent the accumulation of toxic levels of free intracellular iron when the environment suddenly becomes iron rich.

    Original languageEnglish
    JournalNucleic Acids Research
    Volume34
    Issue number17
    Pages (from-to)4960-4967
    Number of pages8
    ISSN0305-1048
    DOIs
    Publication statusPublished - 2006

    Keywords

    • Biological Transport
    • Escherichia coli
    • Escherichia coli Proteins
    • Gene Expression Regulation, Bacterial
    • Homeostasis
    • Iron
    • Iron-Sulfur Proteins
    • Kinetics
    • Models, Biological
    • Systems Biology
    • Journal Article
    • Research Support, Non-U.S. Gov't

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