temperature preference

METPO:1000613 · CLASS · REVIEWED

A phenotype that describes characteristic growth with respect to environmental temperature.

Environmental temperature control of growth preference

Evidence-backed causal sketch linking environmental temperature to membrane fluidity, protein stability, and growth-rate phenotypes.

Environmental temperature control of growth preference Interactive directed graph showing evidence-backed causal relationships for temperature preference.

Edge evidence

  • environmental temperature regulates microbial growth rate RO:0002211

    Microbial growth rate varies with growth temperature.

    • DOI:10.1038/sj.jim.2900572 growth rate vs temperature Study analyzes temperature dependence of microbial growth rates across psychrotrophs, mesophiles, and thermophiles.
  • low temperature decreases membrane fluidity RO:0002212

    Cold temperature reduces membrane fluidity and transport efficiency.

    • DOI:10.1038/sj.embor.7400662 decreased membrane fluidity Review identifies membrane fluidity loss as a core cold challenge.
  • high temperature challenges protein stability METPO:2007406

    Elevated temperature challenges protein folding and functional stability.

    • DOI:10.1128/MMBR.65.1.1-43.2001 resistant to irreversible inactivation at high temperatures Review supports thermostable enzymes as a high-temperature adaptation.
  • high temperature increases membrane fluidity RO:0002213

    High temperature increases membrane permeability and fluidity, creating a limit on growth.

    • DOI:10.1016/s0300-9629(97)00003-0 proton permeability ... increase with the temperature Review links increased membrane permeability to upper temperature growth limits.
  • membrane fluidity regulates temperature preference RO:0002211

    Temperature preference reflects the range in which membrane function remains compatible with growth.

    • DOI:10.1146/annurev-micro-091313-103612 optimizes the performance of cellular physiological processes Review supports membrane fluidity adaptation as a temperature-sensing and response mechanism.
  • protein stability regulates temperature preference RO:0002211

    Growth at preferred temperatures requires proteins to remain active and stable.

    • DOI:10.1128/MMBR.65.1.1-43.2001 molecular mechanisms involved in protein thermostabilization Supports protein stability as a determinant of high-temperature growth.
  • fatty acid desaturase increases unsaturated membrane fatty acids RO:0002213

    Desaturase expression increases double bonds in membrane fatty acids (homeoviscous adaptation).

    • DOI:10.1007/s42770-023-01057-4 Activation of des (desaturase) transcription increases double bonds in membrane fatty acids; generic UFA-biosynthesis module.
  • unsaturated membrane fatty acids increases membrane fluidity RO:0002213

    Increased unsaturated membrane fatty acids restore/raise membrane fluidity.

    • DOI:10.1007/s42770-023-01057-4 Increasing double bonds in membrane fatty acids restores membrane fluidity; core homeoviscous-adaptation edge broadly curatable across microbes.
  • high temperature melts RNA thermometer

    Elevated temperature melts RNA thermometer hairpins, relieving translational repression.

    • DOI:10.1007/s12275-023-00031-x RNA thermometers (ROSE/FourU) control translation by occluding Shine-Dalgarno/start codons and melt with temperature; bacterial heat-sensing mechanism.
  • RNA thermometer permits translation of heat-shock gene translation

    RNA thermometer melting permits translation of heat-shock genes.

    • DOI:10.1007/s12275-023-00031-x Post-transcriptional RNA thermometers in 5-UTRs mediate rapid temperature-dependent control of translation; strong generic edge.
  • low temperature induces cold-shock RNA chaperone activity

    Cold shock induces CspA-mediated RNA chaperone activity that maintains translatable RNA.

    • DOI:10.1007/s12275-023-00031-x Cold shock induces cold-shock proteins (CspA) that help maintain single-stranded RNA for translation at low temperature.
  • temperature downshift induces fatty acid desaturase

    Cold downshift induces fatty-acid desaturase activity to maintain membrane fluidity.

    • DOI:10.1038/sj.jim.2900572 Connecting edge wiring the enrichment node into the graph.

Provenance

Source
METPO (2025-11-25)
Definition source
DOI:10.1038/sj.jim.2900572

Parent traits (1)

Synonyms (2)

  • Physiology and metabolism.culture temp.temperature RELATED_SYNONYM · metpo.owl
  • range_tmp RELATED_SYNONYM · metpo.owl

kg-microbe context

Matched 1 kg-microbe node via direct_metpo.

  • METPO:1000613 [-1.543, -2.658, -5.268, +1.287, …]

512-dim DeepWalkSkipGramEnsmallen embedding from kg-microbe (2026-04-25).

Nearest neighbors in embedding space

Top-8 cosine-similar METPO traits from the 2026-04-25 deepwalk (512-D).

Deep research

Generated by just research-trait; source: research/traits/environment/temperature_preference-deep-research-falcon.md

Unreviewed literature output — not curated TraitMech content Ontology identifiers suggested below have not been resolved against their ontologies, and some are known to be wrong. Check any CURIE against the source before using it.
# Curation report: microbial temperature preference

## Trait record and recommended interpretation

- **Trait label:** temperature preference
- **Trait identifier:** **`METPO:1000613`**
- **Category / kind / status:** ENVIRONMENT / CLASS / REVIEWED
- **Given definition:** “A phenotype that describes characteristic growth with respect to environmental temperature.”
- **Parent:** `METPO:1000059`
- **Synonyms:** *Physiology and metabolism.culture temp.temperature*; *range_tmp*

### Scope summary

For TraitMech, **temperature preference should be represented as an assay-conditioned microbial growth phenotype**, not as a single intrinsic temperature value. Its core observable is a thermal performance curve relating temperature to a growth endpoint—preferably maximum specific growth rate, μ—and its cardinal parameters:

- **TMIN:** lower boundary permitting detectable growth;
- **TOPT:** temperature giving the maximum specific growth rate, μopt;
- **TMAX:** upper boundary permitting growth.

Thermal growth curves are typically asymmetric or “hump-shaped”; TOPT is therefore not equivalent to the midpoint of TMIN and TMAX. It can also differ from the temperature maximizing biomass yield, product formation, survival, or enzyme activity. Cardinal temperatures are the standard parameters used to delimit the growth niche and its optimum. (noll2020modelingandexploiting pages 6-8, noll2020modelingandexploiting pages 19-20)

The phenotype is **conditional on the assay**. The record should preserve strain, medium and carbon source, pH, oxygen/redox condition, salinity, pressure, inoculum history, acclimation time, temperature-shift versus steady-state design, incubation duration, and measurement endpoint. For example, *Thermoanaerobacter kivui* was assayed in defined or complex medium under strict anoxia, at pH 7.5, with specified carbon sources and growth measured by OD600; its experimentally observed TMIN under those conditions was 39°C. (lehmann2023adaptivelaboratoryevolution pages 2-3, lehmann2023adaptivelaboratoryevolution pages 1-2)

### Boundary cases

1. **Acute thermal survival is not temperature preference.** Heat-shock killing, freeze–thaw survival, or transient stress tolerance measures viability after an insult, whereas temperature preference concerns sustained growth across temperatures. In 2024, *Salmonella* `dnaJ` loss increased acute heat resistance by 10³–10⁵-fold but impaired growth at 37°C and above, directly demonstrating that these phenotypes can oppose one another. (berdejo2024evolutionarytradeoffbetween pages 8-10)
2. **Cold/heat-shock response is not necessarily adaptation of TOPT.** A transient transcriptional or metabolic response may restore homeostasis without shifting the strain’s cardinal temperatures.
3. **Environmental occurrence is not proof of preference.** Detection in ice, hot springs, or hydrothermal sediment does not establish active growth or TOPT.
4. **Enzyme temperature optimum is not organismal TOPT.** Mean enzyme optima correlate with growth temperature, but individual enzymes and genome annotations do not determine organismal preference by themselves. (engqvist2018correlatingenzymeannotations pages 4-6, engqvist2018correlatingenzymeannotations pages 9-10)
5. **Thermotolerance, psychrotolerance, and cardinal-temperature classes should remain separate annotations.** A commonly used scheme defines psychrophiles by TOPT <15°C, mesophiles by approximately 20–45°C, thermophiles by >45°C, extreme thermophiles by >65–70°C, and hyperthermophiles by >80°C. These thresholds are conventions rather than mechanisms. (lehmann2023adaptivelaboratoryevolution pages 1-2)
6. **Growth rate, lag, yield, and product formation are different endpoints.** Evolution at low temperature may shorten lag or improve yield without increasing μ or changing TOPT. (lehmann2023adaptivelaboratoryevolution pages 8-9)

## Current mechanistic model

Temperature simultaneously changes reaction kinetics, protein and nucleic-acid stability, membrane viscosity, diffusion, transport, ribosome function, energy demand, and oxidative damage. Consequently, no universal “temperature-preference gene” is expected. The phenotype emerges from the temperature dependence of multiple cellular subsystems.

The strongest experimentally resolved module is **homeoviscous adaptation**. Cooling packs membrane lipids more tightly and lowers fluidity; cells compensate by increasing unsaturated, branched, or shorter acyl chains. Heating generally favors more saturated or longer chains. In *Escherichia coli*, recent work resolved this response into a temperature-sensitive fatty-acid flux valve plus transcriptional feedback, rather than merely a generic stress response. (hoogerland2024atemperaturesensitivemetabolic pages 1-2)

Other modules include protein folding and degradation, RNA structure and translation, DNA topology and repair, compatible-solute accumulation, ice management, oxidative-stress defense, and central-metabolic buffering. These systems often support growth within a thermal range but do not individually establish TOPT.

## Candidate nodes grouped by type

Identifiers below are supplied only where the grounding is unambiguous. **Label-only nodes are preferable to uncertain or invented CURIEs.** Gene symbols should additionally carry organism-specific locus or UniProt identifiers during implementation.

### Trait and assay nodes

| Candidate node | Suggested grounding or treatment | Curation note |
|---|---|---|
| temperature preference | `METPO:1000613` | Target trait; quote CURIE verbatim |
| minimum growth temperature, TMIN | Label-only or verified METPO term | Assay-derived cardinal parameter |
| optimal growth temperature, TOPT | Label-only or verified METPO term | Temperature maximizing a stated growth endpoint |
| maximum growth temperature, TMAX | Label-only or verified METPO term | Assay-derived upper growth boundary |
| specific growth rate | Label plus verified ontology term if available | Prefer μ from exponential growth |
| growth thermal performance curve | Label-only | Relation among temperature, μ, and cardinal parameters |
| growth medium, pH, oxygen availability, salinity, hydrostatic pressure, substrate, incubation time | ENVO/CHEBI terms after record-level verification | Experimental modifiers, not components of the organism |
| acute heat-shock survival; freeze–thaw survival | Separate phenotype nodes | Must not be merged into `METPO:1000613` |

### Environmental and physical nodes

- Environmental temperature and temperature shift.

Showing the first 60 of 284 lines of findings; the linked file also carries the run's front matter and the prompt it was given — read the full report.

Curation history

  1. · SEEDED_FROM_METPO · seed_from_metpo

    imported from data/raw/metpo.owl (CLASS)

  2. · CURATED_WITH_LITERATURE · codex

    Reviewed temperature preference trait and added DOI-backed causal graph for temperature effects on membrane fluidity, protein stability, and growth.

  3. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007406×1).

  4. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0000383×1).

  5. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (METPO:1007505×1).

  6. · RETYPE_CAUSAL_NODES · claude

    Re-typed 1 causal-node node_type field(s) to align with CausalNodeTypeEnum semantics: membrane fluidity: BIOLOGICAL_PROCESS → QUALITY ×1.

  7. · RENAME_PREDICATE_LABELS · claude

    Renamed 3 causal-edge predicate label(s) to align with existing groundings: constrains → regulates ×2; influences → regulates ×1.

  8. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×3).

  9. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1, RO:0002213×1).

  10. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0001305×1).

  11. · FIX_NODE_GROUNDING_CURIE · claude

    Overwrote 1 causal-node grounding(s) to corrected CURIEs (phase-2 id-label fix; verified vs OAK).

  12. · ENRICH_CAUSAL_GRAPH · claude

    Added 5 evidence-backed generic edges (6 new nodes) from the deep-research report.

  13. · FIX_ORPHAN_NODE · claude

    Connected orphaned node 'fatty_acid_desaturase' via temperature_downshift -[induces]-> fatty_acid_desaturase.

  14. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002213×2).

  15. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A031GJU0×1).

  16. · 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)

  17. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (InterPro:IPR012171×1).