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Methanogens rapidly transition from methane production to iron reduction
O Sivan1, S S Shusta2, D L Valentine2
1Department of Geological and Environmental Sciences, Ben Gurion University of the Negev, Beer-Sheva, Israel.
Methanogenic archaea can rapidly switch from methane production to iron oxide reduction, even with limited resources. This metabolic flexibility impacts deep sediment ecosystems and early Earth environments.
Area of Science:
- Microbiology
- Geochemistry
- Environmental Science
Background:
- Methanogenesis is the primary process for organic matter mineralization in deep sediments.
- Archaea, responsible for methanogenesis, can also reduce iron under certain conditions.
- The interplay between methanogenesis and iron reduction in natural settings remains incompletely understood.
Purpose of the Study:
- To investigate the metabolic flexibility of methanogenic archaea, specifically their transition from methanogenesis to iron reduction.
- To determine the conditions under which this metabolic switch occurs and its rate-limiting factors.
- To explore the implications of this transition for microbial metabolism in subsurface environments.
Main Methods:
- Pure culture study using Methanosarcina barkeri under nitrogen atmosphere.
- Addition of ferrihydrite and complex organic matter to simulate sediment conditions.
- Monitoring of methane production and ferrous iron generation.
- Assessment of electron shuttle compounds (AQDS and PCA) effects.
Main Results:
- Methanogenic archaea rapidly shifted from methanogenesis to iron oxide reduction when exposed to ferrihydrite and organic matter.
- Methane production was inhibited during iron reduction.
- The iron reduction rate was first-order and dependent on initial iron concentration.
- Phenazine-1-carboxylate (PCA) enhanced ferrous iron production, suggesting a role for methanophenazines.
Conclusions:
- Methanogenic archaea exhibit significant metabolic plasticity, readily switching to iron reduction.
- This transition can explain increased ferrous iron concentrations in deep 'methanogenic' sediment zones.
- Findings have implications for understanding microbial metabolic networks in modern and ancient subsurface environments.
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