Loading 3D model…
Illustration rendered from curated morphology (shape, size, pili, motility) — not a micrograph. Drag to rotate, scroll to zoom.

Methanogen hydrogenotrophic · Electrotroph · N₂ fixer

Methanococcus maripaludis S2

Methanobacteriota · Methanococci · Methanococcaceae

ElectroactiveEET inwardBSL-1Partial record
  • Methanogen
  • Marine
  • Halotolerant
  • Tier 2
  • Contested EET
Inward
Electron transfer
electroactive
37°C
Optimal temperature
grows 20–45 °C
6.9
Optimal pH
grows pH 6.5–7.5

01 · Identity

Identity

Where this organism sits in the tree of life, how to obtain it, and what a cell looks like.

Lineage

  1. domainArchaea
  2. ›phylumMethanobacteriota
  3. ›classMethanococci
  4. ›orderMethanococcales
  5. ›familyMethanococcaceae
  6. ›genusMethanococcus
  7. ›speciesMethanococcus maripaludis S2

Culture collections & accessions

NCBI taxon
267377

Cell morphology

Coccus · Archaeal s layer only

  • Motile: yes

02 · Electron transfer

Electron transfer

How electrons cross the cell envelope — the property that makes a microbe useful in an electrochemical system.

ElectroactiveEET inward

No extracellular electron-transfer route is curated for this organism yet.

Mechanisms

Direct transfer — detail

Notes
Lohner et al. (2014) reported H2-independent cathodic methane production via Hdr-related pathways; later work (Deutzmann et al. 2015) showed much of the current under those conditions is mediated by extracellularly released hydrogenases / formate dehydrogenases that catalyze H2/formate generation at the cathode. Practical implication for kinetic priors: treat as 'mediated' by default.
Completeness
Contested

Other

Cathode electron uptake mechanism
Contested

03 · Growth envelope

Growth envelope

The conditions this organism tolerates and what it eats and breathes — the operating window for a reactor.

Obligate anaerobeChemolithoautotroph
Temperature37 (20–45) °C
0100 °C
pH6.9 (6.5–7.5)
014
Salinity25 (10–40) g/L
050 g/L

Energy metabolism

Electron donors

  • H2
  • Formate
  • Cathode

Electron acceptors

  • CO2

Carbon sources

  • CO2
  • Formate

Metabolism — detail

N₂ fixation
Yes
Carbon fixation pathway
Wood ljungdahl

04 · Growth & electron-transfer kinetics

Growth & electron-transfer kinetics

How fast this organism grows and how hard it pushes electrons into an anode, as the corpus reports it, and what those constants imply when you run them.

Kinetic evidence

ParameterMedian10–90 %nSource
Max. specific growth rate μmax0.1 h⁻¹0.05–0.183genus prior · 2 refs
Half-saturation constant Ks8 mg/L1–301genus prior · 2 refs
Biomass yield Y0.04 g/g0.01–0.072genus prior · 2 refs
Decay coefficient kdNot in the corpus yet
Exchange current density i₀Not in the corpus yet
Transfer coefficient αNot in the corpus yet
Tafel slopeNot in the corpus yet

Median of the extracted values, the 10–90 % spread behind it and how many values it pools.

Evidence rows (0)

Genus-level prior: Methanococcus maripaludis

A genus-level prior is a summary for the whole genus, not a measurement on this strain.

Constants that drive the simulation

Scenario — values you set, not evidence

Initial substrate1000 mg/L
Anode potential vs SHE0 V
Duration72 h
Initial attached biomass0.1 g/m²
Anode area per liquid volume100 m²/m³
Reactor mode

Growth simulation

Scenario: Initial substrate 1000 mg/L · Initial attached biomass 0.1 g/m² · Anode area per liquid volume 100 m²/m³ · Duration 72 h · Batch. Values you set, not evidence.

0.5g/m²
Peak biomass
15.6h
Time to 90 % substrate removal
Attached biomassg/m²
00.250.50204060h
Bulk substratemg/L
050010000204060h

No current model

The current needs Max. current density jmax, Half-saturation potential E_KA, which this source does not have.

  • Substrate-saturated growth
  • Slowing
  • Stationary

Monod growth has no lag phase; the bands mark where the net growth rate is near its maximum, falling, near zero or negative.

Simulator notes
  • decayPerH absent: no endogenous decay term, so growth is an upper bound
  • biofilmDensityKgPerM3 absent: thickness not computed (thicknessUm = null)
  • no anodePotentialVvsShe / overpotentialV given: current not computed (currentDensityAPerM2 = null)
  • substrate floored at 0 on 1 step(s): reduce dtH for a finer exhaustion front

These curves are a Monod and Nernst-Monod idealisation (after Marcus et al. 2007 and Torres et al. 2008), parameterised only by the constants listed above: each one carries its n and its 10–90 % range, and a constant with n = 1 has no spread at all. No diffusion inside the biofilm, no detachment, no coulombic-efficiency split. The scenario values are yours, not evidence.

05 · Performance

Performance

Reported electrochemical output, the role it plays in a reactor, and what it produces.

Role in a reactor

Cathode chamberCathode: primary product producer

Products (1)

ProductMax titerg/LMax rateCoulombic efficiency
methane———

06 · Ecology & biofilm

Ecology & biofilm

How it lives on an electrode, who it partners with, and where it is found in nature.

Ecosystems

  • Marine
  • Sediment marine

07 · Applications, engineering & safety

Applications, engineering & safety

Where it has been put to work, how tractable it is to engineer, and what handling it requires.

Applications (1)

  • Microbial electrosynthesis methane
    TRL 3/9

Biosafety

BSL-1
  • Pathogen: no

08 · Sources & data quality

Sources & data quality

Every value above traces to a citation. This is how complete and how confident the record is.

Record quality

PartialMedium confidenceCurated: manual

Literature reviewed 2026-05-13 · schema v1.3.0 · updated 2026-05-13 · imported 2026-05-13

Open data gaps (2)

  • 'Direct' vs hydrogenase-mediated cathode uptake debate unresolved.
  • Genetic tractability is excellent but biochemical mapping of EET path incomplete.

References (2)

  1. Lohner ST, et al. (2014). Hydrogenase-independent uptake and metabolism of electrons by the archaeon Methanococcus maripaludis. ISME J 8:1673-1681.doi:10.1038/ismej.2014.82
  2. Deutzmann JS, Sahin M, Spormann AM (2015). Extracellular enzymes facilitate electron uptake in biocorrosion and bioelectrosynthesis. mBio 6:e00496-15.doi:10.1128/mBio.00496-15