Anaerobic respiration
METPO:1000802 · CLASS · REVIEWED
A respiration in which an organism uses electron acceptors other than oxygen for energy production.
Anaerobic respiration with nitrogen oxide acceptors
Edge evidence
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denitrification
occurs in
anaerobic or microaerophilic condition
biolink:occurs_inDenitrification can occur under anaerobic and microaerophilic conditions.
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DOI:10.1128/mmbr.61.4.533-616.1997under anaerobic, microaerophilic, and occasionally aerobic conditions
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nitrogen oxides
acts as
terminal electron acceptor
Nitrogen oxides serve as terminal electron acceptors.
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DOI:10.1128/mmbr.61.4.533-616.1997N oxides as terminal electron acceptors
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denitrification
uses
nitrogen oxides
Denitrification uses nitrogen oxides in respiratory bioenergetics.
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DOI:10.1128/mmbr.61.4.533-616.1997making use of N oxides
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denitrification
conserves
cellular energy conservation
Denitrification is a respiratory route for energy conservation.
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DOI:10.1128/mmbr.61.4.533-616.1997distinct means of energy conservation
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Anaerobic respiration
exemplified by
denitrification
Denitrification is a representative anaerobic respiratory process.
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DOI:10.1128/mmbr.61.4.533-616.1997terminal electron acceptors for cellular bioenergetics
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oxygen limitation / anoxic transition
increases activity of
denitrification reductases
Onset of anoxia drives early transcription and activity of denitrification reductases.
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DOI:10.1038/s41467-024-51688-w
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respiratory nitrate reductase (NarGHI)
catalyzes reduction of
nitrate
Respiratory nitrate reductase NarGHI catalyzes the reduction of nitrate to nitrite.
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DOI:10.1128/msystems.00967-23
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respiratory nitrate reductase (NarGHI)
produces
nitrite
METPO:2007800Reduction of nitrate by NarGHI yields nitrite.
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DOI:10.1128/msystems.00967-23
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nitrous oxide reductase (NosZ)
reduces
nitrous oxide
METPO:2007802NosZ reduces nitrous oxide to dinitrogen, the terminal step of complete denitrification.
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DOI:10.1128/msystems.00967-23
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nitrous oxide reductase (NosZ)
produces
dinitrogen
METPO:2007800NosZ-catalyzed reduction of nitrous oxide produces dinitrogen.
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DOI:10.1128/msystems.00967-23
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1128/mmbr.61.4.533-616.1997
Parent traits (1)
Children (5)
Synonyms (2)
- Anoxic respiration
- Dissimilatory respiration (non-O₂)
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000802[-0.426, -1.069, -1.023, +1.207, …]
Nearest neighbors in embedding space
- metabolism anaerobic oxidation of methane 1.000
- metabolism dissimilatory sulfate reduction 1.000
- metabolism dissimilatory nitrate reduction to ammonium 1.000
- metabolism denitrification 1.000
- metabolism dissimilatory metal reduction 1.000
- metabolism dissimilatory iron reduction 1.000
- metabolism dissimilatory manganese reduction 1.000
- metabolism respiration 0.968
Deep research
# TraitMech Curation Report: Anaerobic Respiration ## 1. Trait record and scope - **Trait label:** Anaerobic respiration - **Trait identifier:** **METPO:1000802** - **Category / kind / status:** METABOLISM / CLASS / REVIEWED - **Parent:** METPO:1000800 - **Synonyms:** anoxic respiration; dissimilatory respiration (non-O₂) ### Operational definition Anaerobic respiration is an energy-conserving respiratory process in which electrons from an organic or inorganic donor pass through an electron-transport chain to a terminal electron acceptor other than molecular oxygen. Electron transfer generates a transmembrane electrochemical gradient that drives ATP synthesis. This mechanistic criterion—not merely growth without oxygen—is the recommended defining feature for TraitMech (little2024dietaryandhostderived pages 1-3, bueno2012bacterialadaptationof pages 1-2). ### Boundaries 1. **Versus aerobic respiration:** aerobic respiration terminates electron flow at O₂; anaerobic respiration uses a non-O₂ acceptor. Low oxygen commonly induces anaerobic systems in facultative bacteria, but strict anaerobes need not possess the FNR/Arc regulatory architecture of *Escherichia coli* (price2021bacterialapproachesto pages 11-12, price2021bacterialapproachesto pages 6-8). 2. **Versus fermentation:** fermentation does not require an external terminal acceptor or a respiratory electron-transport chain. In *Desulfovibrio vulgaris*, a recent analysis estimated approximately **1 mol ATP per mol lactate** from fermentation versus **2.5 mol ATP per mol lactate** during sulfate respiration, illustrating the energetic distinction; these yields are organism- and model-specific, not universal constants (marbehan2024combiningmetabolicflux pages 1-2). 3. **Versus anaerobic growth:** anaerobic growth is broader and includes fermentation, disproportionation, acetogenesis and methanogenesis. Do not infer this trait solely from growth under N₂ or low O₂. 4. **Versus denitrification:** denitrification is one subtype, normally reducing nitrate/nitrite through NO and N₂O toward N₂. Nitrate respiration can instead end in nitrite or ammonium (DNRA), so nitrate reduction alone does not establish denitrification (bueno2012bacterialadaptationof pages 1-2). 5. **Assimilatory versus dissimilatory reduction:** assimilatory nitrate or sulfate reduction supplies biomass precursors; respiratory/dissimilatory reduction supports energy conservation. The trait should represent the latter. 6. **Detoxification boundary:** cytosolic detoxification reductases such as ArsC should not automatically be equated with respiratory arsenate reductase Arr. Evidence of growth, membrane electron transport, ATP production or an established respiratory complex is needed. ## 2. Candidate nodes grouped by type ### Trait, processes and pathways - Anaerobic respiration — **METPO:1000802**; GO candidate **GO:0009061** - Anaerobic electron-transport chain — GO candidate **GO:0019646**; verify against the project’s GO release - Ion-motive force/proton gradient; oxidative phosphorylation; ATP synthesis - Nitrate respiration; denitrification; DNRA - Fumarate, TMAO and DMSO respiration - Dissimilatory sulfate/sulfite reduction - Extracellular Fe(III)/Mn(IV) reduction - Arsenate, selenate, chlorate/perchlorate and organohalide respiration - Organic-metabolite respiration in the gut ### Environmental and experimental factors - Oxygen limitation/anoxia; nitrate, nitrite or other acceptor availability - Electron-donor availability and donor:acceptor ratio - Redox potential; pH; salinity; temperature - Anoxic culture or microcosm; acceptor-dependent growth; ATP assay - Mutant/complementation assay; reductase activity assay - Transcriptomics/proteomics; isotope tracing; electrochemical current - Anaerobic/anoxic reactor stage; poised electrode ### Electron donors and intermediates - NADH, formate, H₂, lactate, pyruvate, acetate, ethanol, sulfide and reduced organic carbon - Quinone/quinol pools, including menaquinone and ubiquinone - Periplasmic or membrane-associated formate dehydrogenases and hydrogenases Sulfate-reducing microorganisms couple sulfate reduction to oxidation of lactate, pyruvate, formate, ethanol or H₂; in the absence of sulfate, some can instead ferment organic substrates (marbehan2024combiningmetabolicflux pages 1-2). ### Terminal acceptors and products - Nitrate (**CHEBI:17632**) → nitrite → NO → N₂O → N₂, or nitrite → ammonium - Fumarate → succinate - TMAO → trimethylamine; DMSO → dimethyl sulfide
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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ADDED_CAUSAL_GRAPH · codex
Added DOI-backed causal graph for anaerobic respiration using denitrification and nitrogen oxide terminal electron acceptors.
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (METPO:1007504×1).
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RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: occurs under → occurs in ×1.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:occurs_in×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:35196×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 5 evidence-backed generic edges (8 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×2, METPO:2000017×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:17632×1).
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GROUND_CAUSAL_NODES · claude
Grounded 3 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:16301×1, CHEBI:17045×1, CHEBI:17997×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0050304×1).
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MIGRATE_MICROBE_DOMAIN_EDGES_PART2 · claude
Re-grounded 3 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (2 to produces, 1 to reduces), issue 301 part 2. The previous predicates are transitively rdfs:subPropertyOf METPO:2000001, whose rdfs:domain is METPO:1000525 (microbe), so a causal-graph subject entailed that the subject IS a microbe; CausalNodeTypeEnum has no organism member, so no such edge could ever satisfy the domain. Each replacement is a 1:1 mirror of its source predicate that changes only the domain, so the claim each edge makes is unchanged and directions are unchanged. The replacements are proposed in proposals/metpo_traitmech_v9 and are placeholder ids until METPO mints them.