temperature delta high
METPO:1000487 · CLASS · REVIEWED
A temperature delta phenotype with a growth-supporting temperature breadth above approximately 30 °C, characteristic of extreme-eurythermal physiology.
Temperature-delta-high eurythermal breadth
Edge evidence
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maximal thermal-adaptation flexibility
confers
temperature delta high
METPO:2007700Maximal thermal-adaptation flexibility yields an extreme temperature-delta breadth.
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DOI:10.1128/MMBR.65.1.1-43.2001resistant to irreversible inactivation at high temperatures
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temperature delta high
is a
temperature delta
rdfs:subClassOfTemperature delta high is a quantitative bin of the temperature-delta phenotype.
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DOI:10.1146/annurev-micro-091313-103612more unsaturated fatty acids
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decreased growth temperature
increases
unsaturated fatty acid biosynthesis
RO:0002213Lower growth temperature increases incorporation of unsaturated fatty acids (homoviscous adaptation).
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DOI:10.1146/annurev-micro-091313-103612
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homoviscous adaptation
maintains
membrane fluidity homeostasis
Homoviscous adaptation maintains membrane fluidity/permeability homeostasis across thermal shifts.
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DOI:10.1146/annurev-micro-091313-103612
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decreased membrane fluidity
upregulates
unsaturated fatty acid biosynthesis
Reduced membrane fluidity is sensed and upregulates unsaturated fatty acid biosynthesis.
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DOI:10.1146/annurev-micro-091313-103612
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lipid desaturase activity
increases
membrane fluidity
RO:0002213Lipid desaturases introduce cis double bonds (~30 deg kink) creating packing defects that increase fluidity.
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DOI:10.3390/cells12101353
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cis-trans isomerase activity
increases
membrane viscosity at higher temperature
RO:0002213Cis-trans isomerization of existing UFAs yields trans-UFAs resembling SFAs, raising membrane viscosity during warming.
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DOI:10.3390/cells12101353
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increased short-/branched-/unsaturated fatty acids
increases
membrane fluidity
RO:0002213Shifts in acyl chain length/branching and unsaturation jointly increase membrane fluidity at lower temperatures.
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DOI:10.3390/cells12101353
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hyperthermophilic enzyme thermostability
resists
irreversible inactivation at high temperatures
Intrinsic enzyme thermostability resists irreversible inactivation, extending upper growth limits.
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DOI:10.1128/MMBR.65.1.1-43.2001
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1146/annurev-micro-091313-103612
Parent traits (1)
Synonyms (1)
- Td_>30
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000487[-0.692, +0.274, -0.785, +3.229, …]
Nearest neighbors in embedding space
- environment temperature range very low 0.813
- environment pH range low 0.712
- environment pH range mid2 0.711
- environment pH range mid3 0.709
- environment pH range mid1 0.700
- environment temperature range low 0.697
- environment temperature range high 0.690
- environment temperature range mid1 0.665
Deep research
# Curation report: microbial “temperature delta high”
## Executive assessment
**Trait:** “temperature delta high”
**Identifier:** `METPO:1000487`
**Parent:** `METPO:1000303`
**Category:** ENVIRONMENT; **term kind:** CLASS; **mapping:** REVIEWED
**Operational definition:** a microbial phenotype in which reproducible growth is supported across a temperature interval, \(T_{max}-T_{min}\), greater than approximately 30°C.
The strongest exemplar recovered is *Exiguobacterium chiriqhucha* RW2, which grew from **4–50°C**, a 46°C breadth and the broadest reported range among the examined *Exiguobacterium* isolates. Its membrane phospholipid composition was measured at 4, 18, 30, and 50°C; iso-C17:1Δ5 declined from **17.0 ± 0.5 mol% at 4°C to 1.1 ± 0.3 mol% at 50°C**, a reduction exceeding 93%. This directly anchors the phenotype and strongly associates temperature-dependent membrane remodeling with it, although it does not prove that the lipid change is sufficient or necessary for the full breadth. (white2019thecompletegenome pages 17-18, white2019thecompletegenome pages 10-11, white2019thecompletegenome pages 7-9)
The best-supported mechanistic architecture is therefore **modular rather than a single pathway**:
1. low-temperature membrane sensing and homoviscous lipid remodeling;
2. RNA remodeling and maintenance of translation at the cold end;
3. chaperone/protease-mediated proteostasis and protein thermostability at the warm end;
4. possibly compatible-solute and antioxidant systems that protect membranes and macromolecules.
Only the first three have evidence strong enough to contribute selected graph edges, and even these differ substantially in evidential strength. Recent 2023 literature consolidates bacterial temperature-response mechanisms, but the search found little 2023–2024 work that directly perturbs a mechanism and demonstrates a **greater-than-30°C growth breadth**. Most recent studies address one thermal endpoint or acute survival rather than eurythermal growth. (moon2023temperaturemattersbacterial pages 7-9)
## 1. Trait scope and boundaries
### Included phenotype
A positive annotation should require:
- measured microbial growth—not merely viability—at multiple temperatures;
- documented lower and upper growth limits, or sufficient tested points to establish a breadth above approximately 30°C;
- comparable medium, pH, salinity, oxygenation, inoculum, and incubation criteria across temperatures;
- preferably serial propagation or quantitative growth curves near both endpoints.
RW2 is a strong positive example because growth was reported over 4–50°C and lipid analyses used cultures grown at 4, 18, 30, and 50°C. The strain also tolerates pH 5–11 and varying salinity, emphasizing that assay covariates must be represented separately rather than folded into the temperature trait. (white2019thecompletegenome pages 17-18, white2019thecompletegenome pages 7-9, white2019thecompletegenome pages 3-4)
### Excluded or adjacent phenotypes
- **Thermophily/hyperthermophily:** describes a high optimum or high growth range, not necessarily a range wider than 30°C. Hyperthermophilic enzymes can remain active and resist irreversible inactivation at high temperature, but that does not establish low-temperature growth.
- **Psychrophily/psychrotolerance:** establishes low-temperature growth, not a high upper limit.
- **Heat-shock or cold-shock survival:** survival after an acute exposure is not equivalent to sustained growth.
- **Thermotolerance of spores or resting states:** should not be transferred automatically to vegetative growth.
- **Broad enzyme activity range:** an isolated enzyme is not an organism-level growth phenotype.
- **Temperature optimum:** one optimum value cannot determine \(T_{max}-T_{min}\).
For example, recombinant CspL substantially improves growth at elevated temperature, but the tested spans do not establish a >30°C breadth. It is evidence for a component mechanism, not direct evidence of `METPO:1000487`. (zhou2021acoldshock pages 5-6, zhou2021acoldshock pages 1-2)
## 2. Candidate nodes and ontology grounding
Identifiers below are included only where grounding is sufficiently clear. Gene symbols, strain-specific lipids, and complexes should remain label-only until reconciled against the exact TraitMech ontology import and taxon-specific database records.
### Trait, taxa, and environmental/experimental nodes
- `METPO:1000487` — temperature delta high.
- `METPO:1000303` — supplied parent trait.
- *Exiguobacterium chiriqhucha* RW2 — exemplar taxon/strain; **label-only pending NCBITaxon verification**.
- *Bacillus subtilis* — DesK/DesR/des model organism; use a verified NCBITaxon CURIE during implementation.
- *Bacillus coagulans* 2-6 — CspL source strain; label-only pending strain-level verification.
- low temperature; high temperature; temperature downshift; heat shock; cold shock — environmental or experimental nodes; map to ENVO or assay ontology terms only after exact term verification.
- growth-supporting temperature minimum, maximum, and breadth — assay-derived quantities; preserve the temperatures, medium, atmosphere, duration, and growth criterion as evidence metadata.
### Genes, proteins, and complexes
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 definition and causal graph linking maximal thermal-adaptation flexibility to the eurythermal temperature-delta-high bin.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×1, rdfs:subClassOf×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 7 evidence-backed generic edges (12 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:0002213×4).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (METPO:1007505×1).
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0006636×1, GO:0016859×1).
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MIGRATE_MICROBE_DOMAIN_EDGES · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates (1 to confers), issue 301. 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. Edge directions are unchanged - this pass only relabels and re-grounds. RO:0002234 (has output) is used where the subject is an activity, since biolink gives it the domain 'biological process or activity'; the METPO replacements are proposed in proposals/metpo_traitmech_v8 and v9 and are placeholder ids until METPO mints them.
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NORMALISE_NODE_TYPE · claude
Normalised causal-node type(s) so one node_id means one thing corpus-wide (issue 356): membrane_fluidity_homeostasis: STATE -> BIOLOGICAL_PROCESS. The counterpart of the above, and the reason the rename was not needed: this id already exists for the process sense. Both occurrences describe 'Maintenance of membrane fluidity ...', and the schema's STATE definition excludes exactly this -- 'the state is the gradient / steady-value, NOT ITS ESTABLISHMENT'. Maintenance is establishment. So the STATE-typed one (temperature_delta_high.yaml) is retyped to match the process it describes.