oxygen preference
METPO:1000601 · CLASS · REVIEWED
A phenotype that is relating to an organism's oxygen requirements or tolerance for growth.
Oxygen-preference O2-availability axis
Edge evidence
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ambient molecular oxygen
defines
oxygen preference
METPO:2007500Ambient molecular-oxygen concentration is the quantitative axis defining oxygen-preference phenotypes.
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DOI:10.3389/fmicb.2014.00674various capacities in their utilization of molecular oxygen
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aerobic
is a
oxygen preference
rdfs:subClassOfAerobic is a child oxygen-preference phenotype.
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DOI:10.3389/fmicb.2014.00674aerobic ... respiration capacities
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anaerobic
is a
oxygen preference
rdfs:subClassOfAnaerobic is a child oxygen-preference phenotype.
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DOI:10.3389/fmicb.2014.00674aerobic, microaerobic, and anaerobic reductases
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microaerophilic
is a
oxygen preference
rdfs:subClassOfMicroaerophilic is a child oxygen-preference phenotype.
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DOI:10.3389/fmicb.2014.00674aerophilic, microaerophilic, or anaerobic
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facultative oxygen preference
is a
oxygen preference
rdfs:subClassOfFacultative oxygen preference is a child oxygen-preference phenotype.
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DOI:10.1111/cmi.13338cope with changing oxygen levels
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O2 as terminal electron acceptor
confers
aerobic
METPO:2007700Obligate aerobic growth depends on molecular oxygen as terminal electron acceptor.
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DOI:10.1371/journal.ppat.1012084
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molecular oxygen
serves as
O2 as terminal electron acceptor
Molecular oxygen functions as the terminal electron acceptor in aerobic respiration.
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DOI:10.1371/journal.ppat.1012084
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oxygen / reactive oxygen species stress
upregulates
detoxifying-enzyme gene expression
O2 or H2O2 stress upregulates detoxifying-enzyme genes.
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DOI:10.1128/aem.00606-23
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detoxifying-enzyme gene expression
increases
oxygen preference
RO:0002213A larger detoxifying-enzyme repertoire increases survival under oxygen exposure.
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DOI:10.1128/aem.00606-23
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catalase
degrades
hydrogen peroxide
METPO:2007809Catalase rapidly degrades hydrogen peroxide, a reactive oxygen species.
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DOI:10.1038/s43705-023-00251-7
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superoxide dismutase
increases
oxygen preference
RO:0002213Higher superoxide dismutase activity is associated with higher oxygen tolerance.
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DOI:10.1038/s43705-023-00251-7
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- PMID:21413255
Parent traits (1)
Children (10)
- aerobic
METPO:1000602 - aerotolerant
METPO:1000609 - anaerobic
METPO:1000603 - facultative oxygen preference
METPO:1000612 - facultatively aerobic
METPO:1000608 - facultatively anaerobic
METPO:1000605 - microaerophilic
METPO:1000604 - microaerotolerant
METPO:1000610 - obligately aerobic
METPO:1000606 - obligately anaerobic
METPO:1000607
Synonyms (2)
- Physiology and metabolism.oxygen tolerance.oxygen tolerance
- metabolism
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000601[-1.145, -2.522, -2.827, -0.321, …]
Nearest neighbors in embedding space
- environment microaerotolerant 0.912
- environment aerotolerant 0.766
- environment pressure optimum 0.531
- environment copper tolerant 0.531
- environment desiccation tolerant 0.531
- morphology heterocyst 0.531
- morphology intracellular inclusion 0.531
- morphology magnetosome 0.531
Deep research
# Curation-focused research report: microbial oxygen preference ## 1. Scope and recommended interpretation **Target trait:** oxygen preference **Identifier:** **METPO:1000601** **Category/kind:** ENVIRONMENT / CLASS **Reviewed definition:** “A phenotype that is relating to an organism's oxygen requirements or tolerance for growth.” For TraitMech, oxygen preference should be modeled primarily as an **observed growth phenotype along an environmental O2-availability/concentration axis**, rather than as the mere presence of an O2-reactive enzyme. Operational states include obligate aerobic, microaerophilic, facultatively anaerobic, aerotolerant anaerobic, and obligately anaerobic growth. The phenotype is conditional on O2 concentration, exposure duration, medium, electron donors and alternative acceptors, redox state, temperature, pressure, and growth phase. The central mechanistic balance is: 1. **Benefit:** O2 serves as a high-potential terminal electron acceptor, enabling respiratory energy conservation. 2. **Cost:** O2 directly damages oxygen-labile enzymes and indirectly produces reactive oxygen species (ROS). 3. **Adaptation:** terminal oxidases, oxygen sensors, metabolic switching, O2-reducing enzymes, and ROS-defense systems alter the O2 range over which growth remains possible. This framing is preferable to a strict aerobic/anaerobic binary. Microorganisms can respire O2 at nanomolar concentrations, and aerobic and anaerobic respiration can coexist up to at least 25 µM O2. The estimated theoretical lower limit for aerobic respiration ranges from approximately 0.1 nM to several hundred nanomolar depending on cell size and growth efficiency. High-affinity oxidases are preferentially expressed below roughly 1–10 µM O2. (berg2022howlowcan pages 5-7) ### Boundary cases - **Oxygen utilization is not automatically oxygen preference.** Anaerobes may express O2-reducing enzymes solely for detoxification. - **Oxygen tolerance is not aerobic growth.** Survival after air exposure, ROS resistance, or reversible inhibition should not be curated as growth in O2 unless biomass increase or cell division was measured. - **Microaerophily is not simply possession of cytochrome bd or cbb3 oxidase.** High-affinity oxidases support low-O2 respiration, but their genes also occur in facultative organisms and may serve stress-defense functions. - **Aerotolerance differs from facultative anaerobiosis.** Aerotolerant organisms survive or grow fermentatively in O2 without using it as the terminal acceptor; facultative anaerobes can switch between aerobic and anaerobic energy metabolism. - **Obligate anaerobiosis is graded.** Some nominal obligate anaerobes grow at low O2 or endure substantial transient exposure. Reported examples range from a 0.02–0.04% O2 preference in *Desulfovibrio vulgaris* to microoxic growth or tolerance at considerably higher concentrations in selected clostridia and archaea. (lu2021whenanaerobesencounter pages 3-4) - **Assay atmosphere is not dissolved O2.** Headspace percentage, dissolved concentration, redox potential, and diffusion geometry must be stored separately. ## 2. Candidate causal-graph nodes ### A. Trait and phenotype nodes - oxygen preference — **METPO:1000601** - obligate aerobic growth — label-only pending verified phenotype CURIE - microaerophilic growth — label-only - facultative anaerobic growth — label-only - aerotolerant anaerobic growth — label-only - obligate anaerobic growth — label-only - oxygen tolerance/survival — label-only; keep separate from growth preference - oxygen-inhibited metabolic activity — label-only ### B. Environmental and experimental factors - dioxygen — **CHEBI:15379** - O2 availability; dissolved O2 concentration; O2 partial pressure — label-only measurement/context nodes - oxic, microoxic/hypoxic, and anoxic environment — use ENVO terms only after identifier verification - duration and periodicity of O2 exposure - medium redox potential - electron-donor availability - alternative electron acceptors: nitrate, fumarate, sulfate and related compounds; ground individual chemicals only after validation - temperature, pH, hydrostatic pressure, agitation, gas-transfer rate, biofilm diffusion, cell density, and growth phase - inhibitors: cyanide, carbon monoxide, sulfide, nitric oxide; context modifiers rather than universal determinants ### C. Chemicals and metabolites - water — **CHEBI:15377** - superoxide — **CHEBI:18421** - hydrogen peroxide — **CHEBI:16240** - hydroxyl radical — label/CHEBI grounding to verify - quinol/quinone pool — label-only unless the specific ubiquinone or menaquinone species is known
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_CAUSAL_GRAPH · claude
Added DOI-backed causal graph framing oxygen preference as the O2-availability axis with child aerobic, anaerobic, microaerophilic, and facultative phenotypes.
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IMPROVED_CAUSAL_GRAPH_EVIDENCE · codex
Replaced PMID fallback CausalEdge references with DOI-backed oxygen-utilization and facultative oxygen-response citations.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 4 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (rdfs:subClassOf×4).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007500×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 6 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 (RO:0002213×2, RO:0002327×1).
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GROUND_CAUSAL_NODES · claude
Grounded 3 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:15379×1, UniProtKB:A0A071MK53×1, UniProtKB:A0A009QPW9×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:16240×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000007×1).
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RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 2 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0004096×1, GO:0004784×1).
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MIGRATE_ENABLES_TRAIT_EDGES · claude
Migrated 1 causal edge(s) off enables/RO:0002327 with a TRAIT object (1 to confers), issue 302. RO:0002327 has range 'biological process or activity', which a trait (a disposition) cannot satisfy, so the previous form entailed trait is-a BiologicalProcessOrActivity. The replacements are proposed in proposals/metpo_traitmech_v8 and are placeholder ids until METPO mints them.
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MIGRATE_MICROBE_DOMAIN_EDGES_PART2 · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (1 to degrades), 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.
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MERGE_CAUSAL_NODE · claude
Merged node oxygen_tolerance into oxygen_preference_trait and repointed its edges. Issue 352. A SIXTH restatement (#360). METPO:1000601's own definition is 'an organism's oxygen requirements OR TOLERANCE for growth', so 'capacity of a cell to survive exposure to molecular oxygen' is part of what the anchor already says. I had grounded it METPO:1000609 (aerotolerant), which METPO defines as 'does NOT USE O2 for growth but tolerates its presence' -- the aerotolerant-anaerobe phenotype, false of the obligate aerobes this node also covers -- and which is itself sub METPO:1000601, making it a sixth child phenotype in a graph that wires the other four in with `is a` and left this one unlinked. aerotolerant.yaml, the record FOR 1000609, has no such node at all: it models the same biology as detoxification processes. Merging attaches the ROS-defence island to the trait, which unlike a retype is a real connectivity gain.
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NORMALISE_NODE_SENSE · claude
One node_id per SENSE (issues 356, 384): ambient_oxygen is the chemical sense here. Already the ambient sense. Listed so a re-run still normalises the label and still retracts ENVO:01001495 if it has been re-applied — the grounder keys on (label, node_type), so an un-normalised label is what lets the retracted CURIE come back.