Light-Independent Fe<sub>3</sub>O<sub>4</sub>–Methanosarcina acetivorans Biohybrid Enhances NitrogenFixation and Methanogenesis

Biohybrid systems that integrate microorganisms with nanomaterials have emerged as promising solutions for sustainable nitrogen fixation. However, key challenges, such as the dependence on light and the vulnerability of nitrogenase to oxidative damage, have limited their application. Here, we report a novel, light-independent biohybrid system integrating Fe<sub>3</sub>O<sub>4</sub> nanoparticles with Methanosarcina acetivorans C2A, resulting in a significant enhancement of both nitrogen fixation activity and methane production. Fe<sub>3</sub>O<sub>4</sub> nanoparticles facilitate directional electron transfer, thereby enhancing methanogenesis and nitrogenase function. Furthermore, the biohybrid system enhances adenosine triphosphate (ATP) synthesis through improved electron flow along membrane-bound electron chains, further supporting nitrogenase activity. Our findings provide a new strategy for advancing nitrogen fixation in archaea, offering an efficient and sustainable approach for biological nitrogen fixation without reliance on solar energy.

Publication Details

Journal
Figshare
Published
2025-02-22
DOI
https://doi.org/10.1021/jacs.4c17259.s001
Primary Topic
Metalloenzymes and iron-sulfur proteins
Type
article
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article

Light-Independent Fe3O4–Methanosarcina acetivorans Biohybrid Enhances NitrogenFixation and Methanogenesis

Figshare
Metalloenzymes and iron-sulfur proteins
article

Light-Independent Fe3O4–Methanosarcina acetivorans Biohybrid Enhances NitrogenFixation and Methanogenesis

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Abstract

Biohybrid systems that integrate microorganisms with nanomaterials have emerged as promising solutions for sustainable nitrogen fixation. However, key challenges, such as the dependence on light and the vulnerability of nitrogenase to oxidative damage, have limited their application. Here, we report a novel, light-independent biohybrid system integrating Fe<sub>3</sub>O<sub>4</sub> nanoparticles with Methanosarcina acetivorans C2A, resulting in a significant enhancement of both nitrogen fixation activity and methane production. Fe<sub>3</sub>O<sub>4</sub> nanoparticles facilitate directional electron transfer, thereby enhancing methanogenesis and nitrogenase function. Furthermore, the biohybrid system enhances adenosine triphosphate (ATP) synthesis through improved electron flow along membrane-bound electron chains, further supporting nitrogenase activity. Our findings provide a new strategy for advancing nitrogen fixation in archaea, offering an efficient and sustainable approach for biological nitrogen fixation without reliance on solar energy.

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Metalloenzymes and iron-sulfur proteins
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Light-Independent Fe<sub>3</sub>O<sub>4</sub>–Methanosarcina acetivorans Biohybrid Enhances NitrogenFixation and Methanogenesis · Figshare (2025) | TGRS Research Map | TGRS