acidotolerant
METPO:1003008 · CLASS · REVIEWED
A pH growth preference characterized by the ability to tolerate acidic environments (typically pH below 5.5) while maintaining optimal growth near neutral pH.
Acidotolerant acid-stress pH homeostasis mechanism
Edge evidence
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acidic exposure
challenges
acidotolerant
METPO:2007406Acidotolerant organisms withstand acidic external pH that can be toxic to non-adapted cells.
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DOI:10.1038/nrmicro2549external pH values that would otherwise be toxic
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acidic exposure
increases influx pressure of
proton
Acid exposure increases proton pressure on the cytoplasmic membrane.
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DOI:10.1016/j.tim.2007.02.005rate at which protons leak inward
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proton efflux transport
removes
proton
Proton export helps prevent excessive cytoplasmic acidification.
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DOI:10.1016/j.tim.2007.02.005remove excess protons from the cytoplasm
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cytoplasmic pH homeostasis
confers
acidotolerant
METPO:2007700Acid tolerance depends on maintaining cytoplasmic pH during acid challenge.
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DOI:10.1038/nrmicro2549bacterial pH homeostasis is a cell-wide physiological process
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amino-acid decarboxylase system
maintains
cytoplasmic pH homeostasis
Amino-acid decarboxylation (e.g. GadA/B converting glutamate to GABA + CO2) consumes intracellular H+ and sustains cytoplasmic pH homeostasis under acid stress.
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DOI:10.3390/microorganisms12091774
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membrane lipid remodeling
increases
acidotolerant
RO:0002213Membrane lipid remodeling (e.g. conversion of unsaturated to cyclopropane fatty acids) reduces proton permeability and improves acid resistance.
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DOI:10.3390/microorganisms12091774
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membrane lipid remodeling
decreases
inward proton leakage
RO:0002212Changes in membrane lipids and porins minimize passive inward proton leakage, a broad cross-taxon pH-homeostasis mechanism.
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DOI:10.1038/nrmicro2549
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inward proton leakage
challenges
cytoplasmic pH homeostasis
METPO:2007406Inward proton leakage raises cytoplasmic proton load, opposing maintenance of internal pH.
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DOI:10.1038/nrmicro2549
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cation/H+ antiport
contributes to
cytoplasmic pH homeostasis
RO:0002326Na+/H+ and K+/H+ antiporters exchange cations for protons to stabilize intracellular pH, a core cross-bacterial homeostasis mechanism.
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DOI:10.1038/nrmicro2549
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Provenance
- Source
- METPO (2025-11-25)
- Author
- Jed Dongjin Kim-Ozaeta
- Definition source
- DOI:10.1038/nrmicro2549
Parent traits (1)
Synonyms (1)
- aciduric
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1003008[-2.269, -2.440, -2.363, -0.685, …]
Nearest neighbors in embedding space
- environment acidophilic 0.983
- environment facultatively acidophilic 0.981
- environment alkaphilic 0.981
- environment obligately alkaphilic 0.980
- environment neutrophilic 0.980
- environment facultatively alkaphilic 0.979
- environment obligately acidophilic 0.979
- environment alkalotolerant 0.979
Deep research
# Curation-focused research report: microbial acidotolerance ## Executive summary **Target:** `METPO:1003008` — **acidotolerant** (synonym: *aciduric*); category **ENVIRONMENT**; term kind **CLASS**; mapping **REVIEWED**; parent `METPO:1003000`. For TraitMech, the safest interpretation is: **a microorganism whose growth optimum is near neutral pH but that can maintain growth at acidic external pH, commonly below approximately 5.5**. This is a growth-preference/capacity phenotype, not merely survival after a short lethal challenge. Neutralophilic bacteria generally keep cytoplasmic pH near 7.2–7.8 over an external range near pH 5.5–9.0; acidotolerance extends function toward the acidic edge by limiting proton entry, exporting or consuming protons, producing alkali, and repairing acid damage (rebelo2023unravelingtherole pages 18-20). The strongest generic graph backbone is: **low external pH / membrane-permeant weak acid → increased cytoplasmic proton load → pH-homeostasis modules (proton extrusion, proton-consuming decarboxylation, ammonia production, membrane remodeling) → maintained intracellular pH → growth or survival under acid stress.** Weak organic acids deserve an explicit branch because their undissociated forms cross membranes and then dissociate in the cytoplasm, imposing both proton and anion stress (lund2014copingwithlow pages 1-2). Recent work emphasizes that “acid tolerance” is not one conserved pathway. A 2023 *E. coli* Ribo-seq/RNA-seq study found sharply condition-dependent responses at pH 5.8 versus 4.4 and 18 previously unannotated acid-induced small ORFs; a 2023 *Alicyclobacillus* study connected acid response to amino-acid metabolism, urea hydrolysis, energy supply and lipid remodeling; and a 2024 *Salmonella* knockout study showed that PhoP/PhoQ chiefly affected acid-induced cross-protection rather than being indispensable for acid tolerance itself (liu2023molecularmechanismof pages 12-15, gao2024theeffectof pages 13-14, schumacher2023ribosomeprofilingreveals pages 21-23, schumacher2023ribosomeprofilingreveals pages 1-2). ## 1. Trait scope and boundaries ### In scope 1. **Growth under acidic conditions:** demonstrated biomass increase, colony formation, growth rate or yield below the organism’s optimal pH. 2. **Maintenance of physiological function at low pH:** intracellular-pH regulation, ATP generation, membrane integrity and macromolecular function causally linked to growth. 3. **Acid survival as a supporting assay:** survival after a defined low-pH exposure can support a mechanism, but should not by itself establish the growth-preference trait. 4. **Constitutive or inducible mechanisms:** both may contribute, provided the terminal graph phenotype is acid growth/tolerance rather than only expression induction. ### Nearby traits that should remain distinct - **Acidophile:** optimal growth occurs at acidic pH. Acidotolerant organisms retain an optimum closer to neutral. Therefore, *Alicyclobacillus acidoterrestris*, described as strongly acidophilic, is mechanistically informative but not an ideal taxonomic exemplar of this METPO class. - **Acid resistance:** often operationally means survival of a severe, short challenge—such as pH 2–3—without requiring growth. - **Acid-tolerance response/adaptation:** increased resistance following prior exposure to a milder acidic condition. This is a regulated state transition, not identical to the baseline trait. - **Organic-acid tolerance:** overlaps with acidotolerance but adds acid-specific anion toxicity and depends on acid pKa, concentration and lipophilicity; equal extracellular pH values are not equivalent exposures (lund2014copingwithlow pages 1-2). - **Acid production:** production of lactic, acetic or other acids does not prove tolerance to the resulting pH. - **Gastric survival, biofilm formation or cross-protection:** useful application phenotypes, but not synonyms for acidotolerant. **Recommended phenotype endpoint:** `maintained microbial growth under external pH <5.5 relative to a near-neutral control`, annotated with medium, buffering capacity, acidulant, temperature, oxygen, growth phase and exposure duration. A binary acidotolerant call should not be inferred solely from gene presence. ## 2. Candidate nodes, grouped by type ### Trait and phenotype nodes - acidotolerant — `METPO:1003008` - growth under acidic conditions — label-only pending METPO alignment - acid survival — label-only; supporting phenotype, not equivalent to the trait - acid-tolerance response — label-only regulated process - intracellular-pH homeostasis — candidate process node; validate the current GO identifier before YAML insertion - acid-induced cross-protection — label-only and preferably a separate subgraph ### Environmental and experimental nodes - acidic environment / low external pH - extracellular proton activity; proton — candidate `CHEBI:15378` - weak organic acid, undissociated weak organic acid and conjugate-base anion - acetic acid — candidate `CHEBI:15366` - lactic acid — use the stereochemically appropriate ChEBI term after checking the assay - benzoic, sorbic and propionic acids as acid-specific challenge nodes - mild acid adaptation versus severe acid challenge - pH, exposure time, acidulant, buffer capacity and growth phase as experimental-factor nodes ### Compartments and structures - extracellular space - cytoplasm/cytosol — candidate `GO:0005737`
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 acidotolerant trait and added DOI-backed evidence and causal graph for acid-stress 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:2007406×1).
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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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FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 causal-node grounding(s) (obsolete/wrong GO -> corrected, verified vs OAK).
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ENRICH_CAUSAL_GRAPH · claude
Added 5 evidence-backed generic edges (4 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 4 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002213×1, METPO:2000017×1, METPO:2007406×1, RO:0002326×1).
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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 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.
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REGROUND_CAUSAL_EDGE · claude
Relabelled 1 causal edge from `reduces` to `decreases` and re-grounded it from METPO:2007802 to RO:0002212 (negatively regulates), issue 330. The corpus wrote two senses under the single label `reduces` - genuine electron donation, and a lessens/decreases sense - and METPO:2007802 is defined as donating electrons to the object and lowering its oxidation state, which this edge does not assert. The two senses could not be separated mechanically because the label was identical, so they migrated together in issue 329 and were split here by reading each edge. RO:0002212 declares no rdfs:domain or rdfs:range, so this introduces no entailment of the kind issue 301 removed.
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NORMALISE_NODE_TYPE · claude
Under the PATHWAY-vs-BIOLOGICAL_PROCESS rule, one node_id means one thing corpus-wide (issue 356): amino_acid_decarboxylation is typed BIOLOGICAL_PROCESS. PATHWAY is a named, conventionally enumerable multi-step route; BIOLOGICAL_PROCESS is everything else. A REACTION CLASS, not a route. The corpus describes it that way in neutrophilic.yaml -- 'Enzyme-catalyzed decarboxylation reaction that consumes cytoplasmic protons' -- and the wording varies by record, so read that as the family's sense rather than as this record's own text. Named systems that implement it (Gad) would be pathways; the reaction class is not. Was 4 BIOLOGICAL_PROCESS to 2 before this tranche.