temperature range mid2
METPO:1000451 · CLASS · REVIEWED
A temperature range phenotype in which the growth-supporting ambient temperature range spans approximately 27–30 °C, characteristic of mesophilic physiology.
Temperature-range-mid2 baseline-mesophile range
Edge evidence
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baseline mesophile adaptation
confers
temperature range mid2
METPO:2007700Baseline mesophile adaptation enables growth across 27–30 °C.
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DOI:10.1146/annurev-micro-091313-103612more unsaturated fatty acids
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temperature range mid2
is a
temperature range
rdfs:subClassOfTemperature range mid2 is a quantitative bin of the temperature-range phenotype.
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DOI:10.1016/s0300-9629(97)00003-0adapted to environments of high temperature
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homeoviscous adaptation
maintains
membrane fluidity
Homeoviscous adaptation maintains membrane lipid viscosity/fluidity.
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DOI:10.1007/s42770-023-01057-4
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unsaturated fatty acid fraction
increases
membrane fluidity
RO:0002213Increased unsaturated fatty acid fraction increases membrane fluidity.
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DOI:10.1007/s12275-023-00031-x
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hopanoids / sterol-like molecules
regulates
membrane fluidity
RO:0002211Hopanoids / sterol-like molecules regulate membrane fluidity.
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DOI:10.1007/s42770-023-01057-4
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membrane fluidity
confers
temperature range mid2
METPO:2007700Maintained membrane fluidity enables growth across the mid2 temperature range.
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DOI:10.1146/annurev-micro-091313-103612
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elevated temperature
opens
RNA thermometer 5′-UTR structure
Elevated temperature melts/opens RNA thermometer 5′-UTR secondary structure.
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DOI:10.1007/s12551-025-01290-1
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temperature shift / heat shock
induces
heat-shock proteins / chaperones
Temperature shift / heat shock induces heat-shock proteins and chaperones.
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DOI:10.1007/s12275-023-00031-x
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heat-shock proteins / chaperones
counteracts
protein denaturation / aggregation
Heat-shock proteins / chaperones counteract protein denaturation and aggregation.
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DOI:10.1007/s12275-023-00031-x
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baseline mesophile adaptation
characterizes
mesophilic organisms
Mesophilic organisms grow between ~20 °C and ~45 °C, bracketing the mid2 range.
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DOI:10.1007/s42770-023-01057-4
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1146/annurev-micro-091313-103612
Parent traits (1)
Synonyms (2)
- Mesophilie
- TR_27_to_30
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000451[-1.548, -0.208, -2.721, +3.019, …]
Nearest neighbors in embedding space
- environment temperature range mid3 0.921
- environment temperature range mid4 0.917
- environment temperature range mid1 0.881
- environment temperature range low 0.837
- environment pH range mid2 0.766
- environment pH range mid1 0.762
- environment pH range low 0.759
- environment pH optimum mid1 0.723
Deep research
# Curation report: microbial **temperature range mid2** ## Executive assessment **Target:** `METPO:1000451` (quoted verbatim) **Label:** temperature range mid2 **Category:** ENVIRONMENT; **term kind:** CLASS; **status:** REVIEWED **Parent:** `METPO:1000306` **Synonyms:** *Mesophilie*; `TR_27_to_30` This trait should be interpreted as an **assay-observed capacity for growth across an ambient-temperature interval whose width is approximately 27–30 °C**. It should **not** be interpreted as an optimum temperature of 27–30 °C, nor as growth exclusively between 27 and 30 °C. It is also distinct from survival after heat/cold shock, transient stress tolerance, growth rate at one temperature, or the broad informal category “mesophile.” The strongest mechanistic graph supported by the literature is a **generic thermoadaptation module**—temperature changes membrane order, membrane sensing activates lipid remodeling, and remodeling restores physiologically useful membrane properties. However, the available evidence does **not** demonstrate that any one gene or module causes an organism’s growth-supporting interval specifically to span 27–30 °C. Consequently, mechanistic edges within the module can be curated, but the terminal edge to `METPO:1000451` should remain **uncertain/inferred** pending direct growth-range perturbation experiments. ## 1. Trait scope and boundary cases ### Positive scope A defensible phenotype call requires growth measurements at multiple temperatures under otherwise controlled conditions. Ideally, growth-supporting lower and upper limits should be estimated using a standardized medium, atmosphere, pH, salinity, inoculum, incubation duration, and growth threshold. The approximately 27–30 °C quantity describes the **span**: `upper growth-supporting temperature − lower growth-supporting temperature ≈ 27–30 °C`. The exact endpoints may differ among taxa. Thus, an organism growing from 10 to 38 °C and another growing from 15 to 43 °C could both fall in this range-width class, although their optima and ecological niches differ. ### Exclusions and neighboring phenotypes * **Temperature optimum:** a peak in growth rate or yield is not the same as the breadth of the supported interval. * **Cardinal temperatures:** minimum, optimum, and maximum temperatures are related measurements but should be represented separately. * **Cold/heat survival:** viability after acute exposure does not prove sustained growth. * **Lag-phase acclimation:** recovery after a shift can reflect stress-response kinetics without changing cardinal growth limits. * **Generic mesophily:** literature often uses “mesophilic” for optima around ordinary environmental or host temperatures; this does not establish a 27–30 °C range width. * **Community/process temperature:** reactor performance at a “mesophilic” set point measures a community and operating regime, not necessarily a strain-level phenotype. ## 2. Current mechanistic understanding Temperature affects membrane phase behavior, RNA structure, translation, protein folding, enzyme kinetics, and macromolecular damage. In bacteria lacking cholesterol-based thermal buffering, lower temperature promotes lipid ordering and can drive a liquid-crystalline-to-gel transition. Cis-unsaturated and anteiso-branched fatty acids disrupt tight acyl-chain packing, lower the phase-transition temperature, and support fluidity; saturated straight-chain fatty acids have the opposite tendency. This regulated remodeling is conventionally termed **homeoviscous adaptation**. (The source uses “homoviscous,” but “homeoviscous” is standard usage.) (mendoza2014temperaturesensingby pages 4-5, mendoza2014temperaturesensingby pages 2-4) The best-resolved bacterial circuit is the *Bacillus subtilis* Des pathway. Increased membrane order changes DesK activity; DesK autophosphorylates at His-188 and transfers phosphate to DesR Asp-54; DesR-P activates `des`; and membrane-bound Δ5-desaturase introduces cis double bonds into membrane fatty acids. Importantly, membrane physical state—not temperature alone—is the proximal signal: isoleucine limitation can reduce anteiso-branched fatty acids and induce `des` at 37 °C. (mendoza2014temperaturesensingby pages 5-6) Cold also stabilizes inhibitory RNA secondary structures and impairs ribosome biogenesis and translation. CspA acts as an RNA chaperone, while the ATP-dependent helicase CsdA supports ribosomal function. Heat causes protein unfolding and aggregation, inducing DnaK/DnaJ/GrpE, ClpB, and proteases such as Lon and FtsH. These systems plausibly help maintain growth near temperature limits, but current sources primarily establish **stress acclimation**, not causation of an exact growth-range width. (moon2023temperaturemattersbacterial pages 7-9, moon2023temperaturemattersbacterial pages 10-11, moon2023temperaturemattersbacterial pages 11-12, moon2023temperaturemattersbacterial pages 13-14) ## 3. Candidate nodes Identifiers below are included only where confidence is high. Taxon-specific genes/proteins should ultimately be grounded to the exact strain’s UniProt or locus identifier rather than assigned a generic protein CURIE. ### Trait and environmental nodes | Node | Suggested grounding | Role | |---|---|---| | temperature range mid2 | `METPO:1000451` | Target phenotype | | parent temperature-range phenotype | `METPO:1000306` | Parent class | | ambient temperature | label-only pending project ontology convention | Experimental/environmental variable | | low-temperature shift | label-only | Perturbation that increases membrane order and cold responses | | high-temperature/heat shift | label-only | Perturbation causing excess fluidity and proteotoxic stress | | growth-supporting temperature interval | label-only | Assay-derived interval; terminal graph measurement | | growth rate, yield, lag, viability | label-only assay nodes | Measurements needed to distinguish growth from survival | ### Cellular structures and physical states | Node | Suggested grounding | Role |
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 baseline mesophile adaptation to the temperature-range-mid2 bin.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1, rdfs:subClassOf×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 8 evidence-backed generic edges (10 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 (RO:0002213×1, RO:0002211×1, RO:0002327×1).
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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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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.