moderately halophilic
METPO:1000623 · CLASS · REVIEWED
A halophily preference where growth and proliferation requires high levels of sodium chloride, usually above or about 0.2 M.
Moderate halophile compatible-solute mechanism
Edge evidence
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elevated NaCl
causes
osmotic stress
biolink:causesModerate NaCl elevation imposes osmotic stress that must be balanced for growth.
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DOI:10.1371/journal.pone.0168818cope with high salinities
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ectoine
mitigates
osmotic stress
METPO:2007407Ectoine accumulation helps cells maintain osmotic balance at moderate salinity.
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DOI:10.1371/journal.pone.0168818synthesizes ectoine as its major compatible solute
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glycine betaine
mitigates
osmotic stress
METPO:2007407Glycine betaine uptake can contribute to bacterial osmoprotection.
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DOI:10.1093/femsre/fuy009glycine betaine uptake
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ectoine
confers
moderately halophilic
METPO:2007700Compatible-solute accumulation supports growth at elevated NaCl.
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DOI:10.1371/journal.pone.0168818allows microorganisms to cope with high salinities
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elevated NaCl
selects for
moderately halophilic
METPO:2007401Moderate halophiles grow best under elevated salinity.
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DOI:10.1093/femsre/fuy009Moderately halophilic bacteria
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osmotic stress
induces
compatible solute accumulation
Osmotic stress under elevated NaCl induces accumulation of organic compatible solutes.
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DOI:10.1128/mmbr.62.2.504-544.1998
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EctD (ectoine hydroxylase)
converts
hydroxyectoine
Ectoine hydroxylase EctD converts ectoine to hydroxyectoine, a generic ectoine-pathway step across halophiles.
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DOI:10.1186/s12934-021-01567-6
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BCCT transporters
imports
glycine betaine
METPO:2007805BCCT-family carriers (BetT, BetP, OpuD) import compatible solutes such as glycine betaine.
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DOI:10.58088/07hg-r941
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TeaABC TRAP transporter
imports
hydroxyectoine
METPO:2007805TeaABC TRAP transporter imports ectoine and hydroxyectoine for osmoadaptation.
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DOI:10.58088/07hg-r941
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TeaABC TRAP transporter
imports
ectoine
METPO:2007805TeaABC TRAP transporter imports ectoine for osmoadaptation.
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DOI:10.58088/07hg-r941
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salt-out (compatible-solute) strategy
predominates in
moderately halophilic
The salt-out / compatible-solute strategy predominates among moderate halophiles.
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DOI:10.3389/frmbi.2023.1329925
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Provenance
- Source
- METPO (2025-11-25)
- Author
- Anthea Guo
- Definition source
- PMID:9758852
Parent traits (1)
Synonyms (1)
- moderate-halophilic
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000623[-94.883, -13.167, +11.221, +70.341, …]
Nearest neighbors in embedding space
- morphology square shaped 0.300
- environment halophily preference 0.288
- morphology vibrio shaped 0.281
- environment euryhaline 0.262
- environment haloalkaliphilic 0.260
- morphology swarming motility 0.251
- morphology twitching motility 0.251
- morphology motile 0.251
Deep research
# Curation report: moderately halophilic **Target trait:** `METPO:1000623` (“moderately halophilic”) **Category:** ENVIRONMENT · **Term kind:** CLASS · **Mapping:** REVIEWED **Parent:** `METPO:1000629` · **Synonym:** moderate-halophilic ## 1. Scope and current interpretation Moderate halophily is best represented as an **assay-observed requirement or preference for elevated environmental salinity that supports growth and proliferation**, rather than simply survival after salt exposure. The supplied METPO definition sets the lower boundary at “above or about 0.2 M” NaCl. Classical microbiological schemes are narrower, commonly placing moderate halophiles around **3–15% NaCl (approximately 0.5–2.5 M)**, although published boundaries vary. Consequently, the graph should record the actual NaCl concentration, medium, temperature, carbon source, growth endpoint, and whether the value is a minimum, optimum, or maximum rather than encoding one universal numerical cutoff. *Halomonas elongata* is a strong organism-level exemplar. It thrives above 10% NaCl (about 1.7 M), while experiments have compared low, near-optimal, and high salinity at 0.17, 1.0, and 2.0 M NaCl, respectively. Its phenotype is supported by compatible-solute metabolism, ectoine recycling, ion handling, and salinity-dependent respiratory and behavioral responses—not ectoine alone. (hobmeier2022adaptationtovarying pages 2-3, hobmeier2022adaptationtovarying pages 1-2) ### Boundary cases - **Halotolerant versus halophilic:** growth at high salt is insufficient by itself. A halotolerant organism may grow optimally without added salt; a halophile has an elevated-salinity optimum or requirement. - **Slight versus moderate halophily:** strains near the lower cutoff require a measured growth curve. The METPO threshold near 0.2 M overlaps ranges that some traditional schemes call slight halophily. - **Moderate versus extreme halophily:** organisms whose optimum lies at near-saturated salt should not inherit this trait merely because they also grow at intermediate NaCl. - **Broad-range/euryhaline strains:** the trait should follow the optimum or requirement, not maximum tolerated NaCl alone. - **Haloalkaliphiles and other polyextremophiles:** high pH, MgCl₂, temperature, or desiccation adaptations should be represented separately; they can confound attribution of growth to NaCl. - **Osmotic stress versus ionic stress:** sucrose-induced osmolarity and NaCl exposure are not mechanistically equivalent. Na⁺/Cl⁻ homeostasis should remain distinct from generic hyperosmotic stress. ## 2. Candidate nodes ### Trait, taxon, and environmental nodes - **moderately halophilic** — `METPO:1000623` - **parent trait** — `METPO:1000629` - ***Halomonas elongata*** — label plus verified NCBITaxon identifier during implementation; do not infer the identifier from memory - ***Aquibacillus salsiterrae*, *A. albus*, *A. halophilus*** — comparative/taxon-restricted branches - **sodium chloride** — ChEBI grounding should be registry-verified before YAML entry - **high-NaCl environment**, **hyperosmotic stress**, **hypoosmotic shock**, **salinity-dependent growth** — label-only until exact ENVO/GO terms are verified - **cytoplasm**, **cytoplasmic membrane**, **extracellular medium** — cellular-location nodes; use verified GO cellular-component CURIEs ### Chemicals and metabolites - **L-aspartate** - **L-aspartyl phosphate** - **L-aspartate-semialdehyde** - **L-2,4-diaminobutyrate (DABA)** - **Nγ-acetyl-L-2,4-diaminobutyrate** - **ectoine** - **5-hydroxyectoine** - **L-glutamate** - **γ-aminobutyric acid (GABA)** - **Na⁺, K⁺, H⁺, Cl⁻** - **water/turgor** All chemical CURIEs should be resolved against ChEBI in the curation environment. This report intentionally does not supply unverified numeric identifiers. ### Genes, proteins, transporters, and complexes - **lysC** — aspartate kinase - **asd** — aspartate-semialdehyde dehydrogenase - **ectB** — DABA transaminase - **ectA** — DABA acetyltransferase - **ectC** — ectoine synthase - **ectD** — ectoine hydroxylase; taxon-limited in the 2023 comparative study - **TeaABC** — osmoregulated tripartite ATP-independent periplasmic/TRAP ectoine transporter - **teaA, teaB, teaC** subunits - **TeaD** regulatory/context node
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_ORGANISM_EXAMPLE · codex
Added Halomonas elongata organism example with PMID-backed evidence.
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ADDED_CAUSAL_GRAPH · codex
Added DOI-backed causal graph for moderate halophile compatible-solute osmoadaptation.
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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 (biolink:causes×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007407×2, METPO:2007401×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0006970×1).
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REMOVE_REDUNDANT_SYNONYM · claude
Removed 1 synonym(s) whose text duplicated the label (seeder redundancy; no information lost).
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ENRICH_CAUSAL_GRAPH · claude
Added 6 evidence-backed generic edges (6 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:2000208×3).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:49432×1).
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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 3 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (3 to imports), 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.