# Genome-centric metagenomics reveals electroactive syntrophs in a conductive particle-dependent consortium from coastal sediments

## TL;DR

The study reveals a methane-producing microbial community in coastal sediments that relies on conductive particles to transfer electrons.

## Contribution

The discovery of a new electroactive genus, Ca. Geosyntrophus acetoxidans, and its role in a particle-dependent electron transfer pathway.

## Key findings

- Ca. Geosyntrophus acetoxidans has a complete acetate oxidation pathway and extracellular electron transfer machinery.
- Electrons from electrogenic syntrophs transfer via granular activated carbon to a Methanosarcina methanogen.
- A secondary syntroph, Lentimicrobium sp., provides an alternative electron transfer route for acetate oxidation.

## Abstract

Conductive particles are common in coastal sediments, yet their role in shaping methane-producing communities and pathways remains unclear. We applied genome-resolved metagenomics to a sediment-derived consortium serially transferred for a decade and obligately dependent on granular activated carbon (GAC). We discovered a particle-obligate food web composed of electrogenic syntrophic acetate oxidizers (SAO), an electrotrophic methanogen, and necromass recyclers. The primary SAO electrogen, Candidatus Geosyntrophus acetoxidans, represents a new genus and possesses a complete acetate oxidation pathway and extracellular electron-transfer (EET) machinery, including two porin-cytochrome conduits, 43 additional multiheme cytochromes and conductive pili. A secondary SAO, a Lentimicrobium sp. with a giant PCC-cluster, supplies an alternative EET-linked acetate-oxidation route. Electrons from electrogens transfer via GAC to a Methanosarcina equipped with the heptaheme cytochrome MmcA and flagellin for electron uptake. These results provide a genomic blueprint of this particle-obligate environmental consortium and suggest an overlooked acetate-to-methane electron-transfer route in geoconductor-rich anoxic sediments.

In this study, the authors provide a genomic blueprint for a conductive particle-dependent environmental consortium from coastal sediments and use long-read metagenomics to show how syntrophic partners can exchange electrons via conductive matrices.