temperature preference
METPO:1000613 · CLASS · REVIEWED
A phenotype that describes characteristic growth with respect to environmental temperature.
Environmental temperature control of growth preference
Edge evidence
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environmental temperature
regulates
microbial growth rate
RO:0002211Microbial growth rate varies with growth temperature.
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DOI:10.1038/sj.jim.2900572growth rate vs temperature
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low temperature
decreases
membrane fluidity
RO:0002212Cold temperature reduces membrane fluidity and transport efficiency.
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DOI:10.1038/sj.embor.7400662decreased membrane fluidity
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high temperature
challenges
protein stability
METPO:2007406Elevated temperature challenges protein folding and functional stability.
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DOI:10.1128/MMBR.65.1.1-43.2001resistant to irreversible inactivation at high temperatures
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high temperature
increases
membrane fluidity
RO:0002213High temperature increases membrane permeability and fluidity, creating a limit on growth.
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DOI:10.1016/s0300-9629(97)00003-0proton permeability ... increase with the temperature
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membrane fluidity
regulates
temperature preference
RO:0002211Temperature preference reflects the range in which membrane function remains compatible with growth.
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DOI:10.1146/annurev-micro-091313-103612optimizes the performance of cellular physiological processes
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protein stability
regulates
temperature preference
RO:0002211Growth at preferred temperatures requires proteins to remain active and stable.
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DOI:10.1128/MMBR.65.1.1-43.2001molecular mechanisms involved in protein thermostabilization
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fatty acid desaturase
increases
unsaturated membrane fatty acids
RO:0002213Desaturase expression increases double bonds in membrane fatty acids (homeoviscous adaptation).
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DOI:10.1007/s42770-023-01057-4
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unsaturated membrane fatty acids
increases
membrane fluidity
RO:0002213Increased unsaturated membrane fatty acids restore/raise membrane fluidity.
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DOI:10.1007/s42770-023-01057-4
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high temperature
melts
RNA thermometer
Elevated temperature melts RNA thermometer hairpins, relieving translational repression.
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DOI:10.1007/s12275-023-00031-x
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RNA thermometer
permits translation of
heat-shock gene translation
RNA thermometer melting permits translation of heat-shock genes.
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DOI:10.1007/s12275-023-00031-x
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low temperature
induces
cold-shock RNA chaperone activity
Cold shock induces CspA-mediated RNA chaperone activity that maintains translatable RNA.
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DOI:10.1007/s12275-023-00031-x
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temperature downshift
induces
fatty acid desaturase
Cold downshift induces fatty-acid desaturase activity to maintain membrane fluidity.
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DOI:10.1038/sj.jim.2900572
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1038/sj.jim.2900572
Parent traits (1)
Children (8)
Synonyms (2)
- Physiology and metabolism.culture temp.temperature
- range_tmp
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000613[-1.543, -2.658, -5.268, +1.287, …]
Nearest neighbors in embedding space
- environment extreme hyperthermophilic 0.979
- environment facultative psychrophilic 0.900
- environment thermotolerant 0.846
- environment psychrotolerant 0.833
- environment piezophilic 0.558
- physiology chemotaxis 0.558
- physiology catalase activity 0.558
- environment piezotolerant 0.558
Deep research
# 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.
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 temperature preference trait and added DOI-backed causal graph for temperature effects on membrane fluidity, protein stability, and growth.
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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 (PATO:0000383×1).
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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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RETYPE_CAUSAL_NODES · claude
Re-typed 1 causal-node node_type field(s) to align with CausalNodeTypeEnum semantics: membrane fluidity: BIOLOGICAL_PROCESS → QUALITY ×1.
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RENAME_PREDICATE_LABELS · claude
Renamed 3 causal-edge predicate label(s) to align with existing groundings: constrains → regulates ×2; influences → regulates ×1.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×3).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1, RO:0002213×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0001305×1).
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FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 causal-node grounding(s) to corrected CURIEs (phase-2 id-label fix; verified vs OAK).
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ENRICH_CAUSAL_GRAPH · claude
Added 5 evidence-backed generic edges (6 new nodes) from the deep-research report.
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FIX_ORPHAN_NODE · claude
Connected orphaned node 'fatty_acid_desaturase' via temperature_downshift -[induces]-> fatty_acid_desaturase.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002213×2).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A031GJU0×1).
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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)
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (InterPro:IPR012171×1).