Abstract
Direct interspecies electron transfer (DIET) stands as a cornerstone in
anoxic ecosystems, facilitating electron exchange between partners
without intermediates. However, a considerable gap persists in
comprehensively elucidating how various materials promote DIET and
interact with electroactive microbial species. To uncover the influence
of different conductive materials on DIET-based anaerobic digestion
systems, three carbon sources were used to simplify the microbial
community and focus on exploring electroactive methanogens. Cyclic
voltammetry results showed unique peaks in acetate-fed cultures with
polyaniline-coated materials, highlighting the presence of DIET-active
microbial species. CO2-fed cultures with polyaniline-coated
materials exhibited robust electrotrophic methanogenic activity in
electrochemical cells. Additionally, cyclic voltammetry provided
insights into electroactive biofilm stratification on conductive
materials, allowing for a nuanced interpretation of microbiome
responses. Comparative genomics showcased Desulfobulbaceae sp.
DTU28 involvement in DIET through the identification of e-pilin.
Furthermore, a putative e-pilin protein sequence with high aromatic
amino acidic content was detected in Aminobacterium sp. DTU61. Co-occurrence analysis revealed potential syntrophic interactions between Methanosarcina sp. DTU142 and other species like Firmicutes sp. DTU111 and Bacteria
sp. DTU118, indicating potential DIET-based cooperations. By analyzing
electrochemical data and microbial genomic information, this study
elucidated the impact of each material on DIET activity and
characterized electroactive species, providing a deeper understanding of
DIET-based microbial community interactions.
| Original language | English |
|---|---|
| Article number | 158716 |
| Journal | Chemical Engineering Journal |
| Volume | 503 |
| Number of pages | 12 |
| ISSN | 1385-8947 |
| DOIs | |
| Publication status | Published - 2025 |
Keywords
- Anaerobic digestion
- Cyclic voltammetry
- DIET
- E-pilins
- Genome-centric metagenomics
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