acidophilic
METPO:1003003 · CLASS · REVIEWED
A pH growth preference in which an organism grows optimally at pH values below 5.
Acidophilic pH homeostasis mechanism
Edge evidence
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acidic external pH
selects for
acidophilic
METPO:2007401Acidic environments select for organisms whose optimal growth is below neutral pH.
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DOI:10.1038/nrmicro2549growing at pH 1.0-3.0
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acidic external pH
increases gradient of
proton
METPO:2007601Acidic external pH imposes a proton gradient across the membrane.
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DOI:10.1016/j.tim.2007.02.005major contributor to the proton motive force
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low proton permeability membrane
limits influx of
proton
Low proton permeability helps acidophiles avoid cytoplasmic acidification.
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DOI:10.1016/j.tim.2007.02.005highly impermeable cell membranes
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reversed membrane potential
mitigates influx of
proton
A reversed membrane potential can reduce inward proton movement.
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DOI:10.1016/j.tim.2007.02.005reversed membrane potential
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cytoplasmic pH homeostasis
confers
acidophilic
METPO:2007700Acidophilic growth requires maintaining cytoplasmic pH compatible with biomolecular function.
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DOI:10.1038/nrmicro2549maintain a cytoplasmic pH of approximately 6.0
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primary proton pumps
catalyzes active transport of
proton
Primary proton pumps such as respiratory-chain complexes actively export protons, contributing to pH homeostasis.
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DOI:10.1038/nrmicro2549
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proton-coupled ATPases
catalyzes active transport of
proton
Proton-coupled ATPases actively transport protons across the membrane.
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DOI:10.1038/nrmicro2549
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acidic external pH
selects for
cytoplasmic pH homeostasis
METPO:2007401Low external pH / acid challenge imposes the demands of cytoplasmic pH homeostasis, a unifying principle of bacterial pH homeostasis.
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DOI:10.1038/nrmicro2549
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pumping K+ and Na+ into cytoplasm
reduces influx of
proton
Pumping K+ and Na+ into the cytoplasm reduces proton influx by electrostatic repulsion.
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DOI:10.1111/1758-2229.70019
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hopanoid lipids and membrane proteins (Omp40, PspA)
enables
proton exclusion
RO:0002327Hopanoid lipids and membrane proteins (Omp40, PspA) are structural adaptations used for proton exclusion.
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DOI:10.1111/1758-2229.70019
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bipolar tetraether lipids (GDNT/GDGT)
maintains
low passive proton permeability
Bipolar tetraether lipids maintain a low passive proton permeability, enabling a near-neutral intracellular pH.
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DOI:10.3389/frbis.2023.1338019
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1038/nrmicro2549
Parent traits (1)
Synonyms (2)
- acidophil
- acidophile
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1003003[-2.194, -1.869, -2.537, -0.747, …]
Nearest neighbors in embedding space
- environment acidotolerant 0.983
- environment facultatively alkaphilic 0.982
- environment alkalotolerant 0.981
- environment obligately alkaphilic 0.981
- environment neutrophilic 0.980
- environment obligately acidophilic 0.979
- environment facultatively acidophilic 0.978
- environment alkaphilic 0.978
Deep research
# Curation report: microbial acidophily ## Executive assessment **Target trait:** acidophilic **Identifier:** **METPO:1003003** **Category:** ENVIRONMENT; **term kind:** CLASS; **mapping:** REVIEWED **Definition:** optimal growth at pH values below 5 **Parent:** METPO:1003000 **Synonyms:** acidophil; acidophile The trait should represent a **stable growth preference**, established from a growth-rate or biomass-versus-pH assay, rather than survival after a short acid shock. Extreme acidophiles are a nested boundary class commonly growing at pH 1–3. Their pH-homeostasis systems are often constitutively expressed, unlike inducible acid-stress systems in neutralophiles. Constitutive preparedness may reduce fitness near neutral pH because of energetic costs and proteins specialized for extreme conditions. (krulwich2011molecularaspectsof pages 3-5) The best-supported causal architecture has two layers: **(i) restriction of proton entry**, principally through unusually impermeable membranes and an inside-positive electrical potential, and **(ii) removal, neutralization, or buffering of protons that enter**. The endpoint is maintenance of an intracellular pH compatible with macromolecular function despite a large transmembrane proton gradient. In thermoacidophilic archaea growing at pH ≤4, intracellular pH is generally 5.4–6.5; *Picrophilus* is exceptional at approximately 4.6. (gonzalezrosales2022integrativegenomicssheds pages 1-2, chong2024archaeamembranesin pages 2-3) The strongest graph-ready module is the archaeal bipolar-tetraether-membrane chain. Bacterial potassium-potential, hopanoid, porin, and proton-consuming modules are biologically plausible but are more often supported by comparative genomics, expression data, or experiments in only a few taxa. They should therefore carry taxon and evidence qualifiers. ## 1. Trait scope and boundary cases ### Include 1. An organism whose **measured optimum growth pH is <5**, including moderate and extreme acidophiles. 2. The environmental condition of low extracellular pH and mechanisms that causally enable growth under it. 3. Constitutive or environmentally regulated processes that maintain membrane integrity, limit proton influx, sustain intracellular pH, or repair secondary acid damage. 4. Taxon-specific modules when the organism and evidence type are recorded explicitly. ### Exclude or annotate separately - **Acid resistance/tolerance:** survival at low pH by a neutralophile does not establish optimal growth below pH 5. - **Acid shock response:** transient induction after abrupt exposure is not equivalent to acidophily. - **Acid production:** production of lactate, acetate, sulfuric acid, or another acid is a metabolic output, not proof of an acidophilic optimum. - **Occurrence in an acidic habitat:** metagenomic detection in acid mine drainage does not establish the isolate’s optimum pH. - **Aciduric phenotype:** persistence over a broad pH range should remain distinct unless the optimum itself is below 5. - **Extreme acidophily:** useful as a narrower annotation. A major review describes extreme acidophilic bacteria as growing at pH 1–3, but this should not replace the supplied METPO threshold. (krulwich2011molecularaspectsof pages 3-5) - **Organic-acid resistance:** weak organic acids cross membranes in uncharged form and impose additional anion toxicity; this is not mechanistically identical to adaptation to high extracellular proton activity. ### Recommended assay representation Record optimum pH, tested pH range, medium and acidulant, temperature, oxygen regime, growth measure, growth phase, and whether pH was controlled. Temperature is especially important for thermoacidophilic membrane phenotypes: *Sulfolobus acidocaldarius* maintains an approximately pH 2.5 outside/pH 6.5 inside gradient over 65–90°C. (chong2024archaeamembranesin pages 3-4) ## 2. Candidate nodes grouped by type ### Trait, environmental, and experimental nodes - acidophilic — **METPO:1003003** - parent environmental growth-preference trait — **METPO:1003000** - acidic environment — candidate **ENVO** grounding should be verified before YAML insertion - extracellular pH below 5 — label-only assay node - extreme acidic condition, pH 1–3 — label-only boundary node - optimum growth pH — label-only experimental factor - transmembrane pH gradient — label-only process/state - chloride stress / NaCl exposure — chloride **CHEBI:17996**; sodium chloride **CHEBI:26710** - elevated temperature — label-only environmental factor ### Chemicals and physicochemical states - proton — **CHEBI:15378** - potassium ion — **CHEBI:29103** - sodium ion — **CHEBI:29101** - spermidine — **CHEBI:16610**
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_WITH_LITERATURE · codex
Reviewed acidophilic trait and added DOI-backed evidence and causal graph for acidic pH homeostasis.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007401×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0030641×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0001428×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007601×1).
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FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 causal-node grounding(s) (obsolete/wrong GO -> corrected, verified vs OAK).
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FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 pH causal-node grounding(s) to corrected PATO CURIEs (phase-2; verified vs OAK).
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ENRICH_CAUSAL_GRAPH · claude
Added 6 evidence-backed generic edges (7 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007401×1, RO:0002327×1).
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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.