4.7 Review

Limitations of microbial iron reduction under extreme conditions

Journal

FEMS MICROBIOLOGY REVIEWS
Volume 46, Issue 6, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/femsre/fuac033

Keywords

extremophiles; microbial iron reduction; thermodynamics; biochemistry; limits to life

Categories

Funding

  1. Science and Technology Facilities (STFC) [ST/V000586/1]
  2. Natural Environmental Research Council (NERC) Fellowship [NE/R013462/1]

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Microbial iron reduction is a widespread and ancient metabolism that could potentially support microbial life on other planets. However, the exact limits of this metabolism are still not well understood. In this study, the authors investigated the limits of microbial iron reduction in different pH and temperature conditions. They found that microbial iron reduction is often observed at extremes of pH or temperature alone, but not when these extremes are combined. The results provide insights into the limits of microbial iron reduction and have implications for our understanding of the range of conditions that can support life.
Microbial iron reduction is a widespread and ancient metabolism on Earth, and may plausibly support microbial life on Mars and beyond. Yet, the extreme limits of this metabolism are yet to be defined. To investigate this, we surveyed the recorded limits to microbial iron reduction in a wide range of characterized iron-reducing microorganisms (n = 141), with a focus on pH and temperature. We then calculated Gibbs free energy of common microbially mediated iron reduction reactions across the pH-temperature habitability space to identify thermodynamic limits. Comparing predicted and observed limits, we show that microbial iron reduction is generally reported at extremes of pH or temperature alone, but not when these extremes are combined (with the exception of a small number of acidophilic hyperthermophiles). These patterns leave thermodynamically favourable combinations of pH and temperature apparently unoccupied. The empty spaces could be explained by experimental bias, but they could also be explained by energetic and biochemical limits to iron reduction at combined extremes. Our data allow for a review of our current understanding of the limits to microbial iron reduction at extremes and provide a basis to test more general hypotheses about the extent to which biochemistry establishes the limits to life. The authors present a comprehensive review of the observed limits of growth by iron-reducing microorganisms characterized to date, alongside predictions of energetic limits using thermodynamic calculations, and discuss the unexplored regions of the habitability space for this widespread and ancient metabolism, with implications for our understanding of life in the most extreme environments on Earth and the search for life elsewhere.

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