facultatively alkaphilic
METPO:1003005 · CLASS · REVIEWED
A pH growth preference in which an organism can grow at alkaline pH but does not require it.
Facultative alkaliphily sodium-cycle pH homeostasis mechanism
Edge evidence
-
alkaline external pH
confers
facultatively alkaphilic
METPO:2007700Facultative alkaliphiles grow well under alkaline pH conditions.
-
DOI:10.3389/fbioe.2015.00075grow well at pH values exceeding pH 9
-
-
near-neutral external pH
is compatible with
facultatively alkaphilic
Facultative alkaliphiles retain growth capacity near neutral pH.
-
DOI:10.3389/fbioe.2015.00075capable of growing near neutral pH
-
-
alkaline external pH
challenges
cytoplasmic pH homeostasis
METPO:2007406Alkaline external pH requires cytoplasmic proton accumulation or retention.
-
DOI:10.1038/nrmicro2549active proton accumulation or generation in the cytoplasm
-
-
Na+/H+ antiporter
exports
sodium ion
METPO:2007804Sodium efflux is one limb of the alkaliphile Na+ cycle.
-
DOI:10.1016/S0005-2728(00)00285-1Na+ efflux
-
-
Na+/H+ antiporter
accumulates
proton
METPO:2007810Na+/H+ antiport contributes to net proton accumulation during alkaline pH homeostasis.
-
DOI:10.1016/S0005-2728(00)00285-1net H+ accumulation
-
-
cytoplasmic pH homeostasis
confers
facultatively alkaphilic
METPO:2007700Growth across alkaline and near-neutral pH requires pH homeostasis.
-
DOI:10.1016/S0005-2728(00)00285-1pH homeostasis ... appears to set the upper pH limit for growth
-
-
alkaline external pH
selects for
Na+/H+ antiport activity
METPO:2007401Alkaline external pH selects for electrogenic Na+/H+ antiport that acidifies the cytoplasm.
-
DOI:10.3389/fbioe.2015.00075
-
-
Na+/H+ antiport activity
maintains
cytoplasmic pH homeostasis
Na+/H+ antiport keeps the cytoplasm 2-2.3 units below external pH under alkaline conditions.
-
DOI:10.1007/978-981-19-1573-4_3
-
-
acidic secondary cell-wall components
attracts
proton
Surface acidity enriches protons and repels hydroxide, supporting alkaline adaptation.
-
DOI:10.3389/fmicb.2018.02331
-
-
F1Fo-ATP synthase
supports
ATP production at alkaline pH
Proton-coupled ATP synthase sustains ATP production despite low bulk PMF at alkaline pH.
-
DOI:10.3389/fbioe.2015.00075
-
Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.3389/fbioe.2015.00075
Parent traits (1)
Synonyms (3)
- facultative alkaliphile
- facultative alkaphilic
- facultatively alkaliphilic
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1003005[-2.320, -2.077, -2.647, -0.697, …]
Nearest neighbors in embedding space
- environment acidophilic 0.982
- environment obligately acidophilic 0.981
- environment obligately alkaphilic 0.981
- environment alkalotolerant 0.980
- environment facultatively acidophilic 0.979
- environment acidotolerant 0.979
- environment neutrophilic 0.979
- environment alkaphilic 0.978
Deep research
# Curation report: facultatively alkaphilic ## Trait record and scope - **Trait label:** facultatively alkaphilic - **Trait identifier:** **METPO:1003005** - **Category / kind / status:** ENVIRONMENT / CLASS / REVIEWED - **Definition:** a pH-growth preference in which an organism grows under alkaline conditions but does not require alkaline pH. - **Parent:** METPO:1003000 - **Synonyms:** facultative alkaliphile; facultative alkaphilic; facultatively alkaliphilic. The clearest operational interpretation is **an alkaline growth optimum together with reproducible growth near neutral pH**. Preiss et al. define facultative alkaliphiles as strains that “grow optimally under stringent alkaline conditions but are also capable of growing near neutral pH.” Their review places alkaliphile growth generally above pH 9 and often within pH 10–13. (preiss2015alkaliphilicbacteriawith pages 1-2) A 2024 study uses a more explicit scheme: alkali-tolerant organisms have an optimum at pH 7–9 and do not grow above approximately pH 9.5; facultative alkaliphiles grow well near neutral pH but have an optimum at pH 10 or above; obligate alkaliphiles grow optimally above pH 10 but not below pH 9. These numerical cutoffs are useful assay conventions, not universal biological constants. (maksimova2024metabolicandmorphological pages 1-2) ### Boundary cases 1. **Obligately alkaliphilic:** requires alkaline conditions and fails to grow near neutral pH. This is outside **METPO:1003005** even if its alkaline-homeostasis machinery resembles that of facultative strains. (preiss2015alkaliphilicbacteriawith pages 1-2) 2. **Alkali-tolerant:** survives or grows at elevated pH but retains a neutral or mildly alkaline optimum. High-pH survival alone is insufficient to infer facultative alkaliphily. (maksimova2024metabolicandmorphological pages 1-2) 3. **Haloalkaliphilic:** combines alkaline preference with a salt requirement or strong salt adaptation. Salinity should be represented separately; it is not entailed by this trait. Horikoshi distinguished alkaliphiles from haloalkaliphiles requiring both pH above 9 and high salinity. (horikoshi1999alkaliphilessomeapplications pages 1-3) 4. **Assay-dependent classifications:** nutrient composition, sodium concentration, temperature, aeration, buffer, growth phase, and the distinction between growth and short-term metabolic activity can alter the apparent pH optimum. Horikoshi explicitly noted that some organisms exhibit multiple optima depending on nutrients, metals, and temperature. (horikoshi1999alkaliphilessomeapplications pages 1-3) 5. **Mechanism versus phenotype:** possession of an Mrp antiporter, sodium motor, or alkaliphile-like ATP synthase motif does not by itself establish the trait. The phenotype requires a pH-resolved growth curve demonstrating both alkaline preference and near-neutral growth. ## Current mechanistic model The best-supported model is a coupled **proton–sodium cycle**. Respiratory complexes export protons and establish membrane potential. Electrogenic Mrp and related cation/proton antiporters then export Na+ while importing more H+, acidifying the cytoplasm relative to the alkaline exterior. Na+/solute symport, MotPS, and voltage-gated sodium channels replenish intracellular sodium, sustaining antiport. Proton entry through the F-type ATP synthase simultaneously supports ATP production and cytoplasmic pH homeostasis. (preiss2015alkaliphilicbacteriawith pages 4-5, krulwich2011molecularaspectsof pages 12-14, lebre2019genomicsofalkaliphiles. pages 13-17) This creates an inverted ΔpH—inside more acidic than outside—which opposes the productive electrical component of proton motive force. Facultative alkaliphiles therefore depend heavily on ΔΨ, carefully controlled ion cycling, and adapted energy-transducing proteins. In *Bacillus* sp. TA2.A1, PMF reportedly changed from −164 mV at pH 7.5 to −78 mV at pH 10, illustrating the energetic penalty of alkaline growth. (lebre2019genomicsofalkaliphiles. pages 13-17) For the model strain *Bacillus pseudofirmus* OF4, continuous cultures maintained pHin near 7.5 between external pH 7.5 and 9.5; at the approximate optimum pHout 10.5, pHin was 8.3. Growth continued more slowly at pHout at least 11 despite pHin at least 9.5, and the reported upper growth limit was approximately pH 11.4. (preiss2015alkaliphilicbacteriawith pages 4-5, krulwich2011molecularaspectsof pages 12-14) ## Candidate nodes grouped by type ### Trait, environment, and assay nodes - **facultatively alkaphilic** — **METPO:1003005** - **alkaline environmental pH** — label-only pending verification of the appropriate ENVO/PATO representation - **near-neutral environmental pH** — label-only - **external pH / pHout** — assay variable - **intracellular pH / pHin** — assay variable - **inverted transmembrane pH gradient** — label-only - **membrane potential, ΔΨ** — label-only - **proton motive force** — label-only; GO grounding should be verified before curation - **sodium motive force** — label-only - **oxygen availability / aeration** — label-only environmental factor - **sodium concentration and salinity** — CHEBI:29101 for sodium(1+) may be used where the node is the ion; do not use it for salinity itself - **malate-containing growth medium**, **growth rate**, and **growth at pH 7.5/10.5** — assay-context nodes ### Chemicals and metabolites - **proton** — CHEBI:15378 - **sodium(1+)** — CHEBI:29101 - **potassium(1+)** — CHEBI:29103 - **oxygen** — CHEBI:15379 - **ATP** — CHEBI:15422 - **ADP** — CHEBI:16761 - **phosphate** — use a protonation-state-appropriate CHEBI identifier after checking assay context - **menaquinone / reduced menaquinone pool** — specific CHEBI identifier depends on quinone species - **acetate** — CHEBI:30089 - **magnesium ion** — CHEBI:18420
Curation history
-
·
SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
-
·
CURATED_WITH_LITERATURE · codex
Reviewed facultatively alkaphilic trait and added DOI-backed evidence and causal graph for alkaline and near-neutral pH growth capacity.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007406×1).
-
·
RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: supports → enables ×1.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0030641×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A068T423×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0001429×1, PATO:0001432×1).
-
·
FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 causal-node grounding(s) (obsolete/wrong GO -> corrected, verified vs OAK).
-
·
FIX_NODE_GROUNDING_CURIE · claude
Overwrote 2 pH causal-node grounding(s) to corrected PATO CURIEs (phase-2; verified vs OAK).
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000209×1, METPO:2000210×1).
-
·
ENRICH_CAUSAL_GRAPH · claude
Added 4 evidence-backed generic edges (4 new nodes) from the deep-research report.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007401×1).
-
·
RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 1 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
-
·
MIGRATE_ENABLES_TRAIT_EDGES · claude
Migrated 2 causal edge(s) off enables/RO:0002327 with a TRAIT object (2 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.
-
·
MIGRATE_MICROBE_DOMAIN_EDGES_PART2 · claude
Re-grounded 2 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (1 to accumulates, 1 to exports), 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.