extreme hyperthermophilic

METPO:1000721 · CLASS · REVIEWED

A temperature preference that grows optimally at temperatures above 90°C.

Extreme-hyperthermophilic archaeal heat-adaptation mechanism

DOI-backed graph linking extreme hyperthermophily to archaeal tetraether membrane lipids, hyperthermostable proteins, and bioenergetic adaptation at temperatures above 90 °C.

Extreme-hyperthermophilic archaeal heat-adaptation mechanism Interactive directed graph showing evidence-backed causal relationships for extreme hyperthermophilic.

Edge evidence

  • very high temperature selects for extreme hyperthermophilic METPO:2007401

    Very-high-temperature habitats select for extreme hyperthermophily.

    • DOI:10.1007/s007920050010 It grew at between 90 degrees C and 113 degrees C Supports growth above 90 °C in extreme hyperthermophiles.
  • archaeal tetraether membrane lipids protects against very high temperature

    Archaeal tetraether lipids form heat-resistant membranes that protect against very-high-temperature membrane stress.

    • DOI:10.1146/annurev-micro-091313-103612 membrane lipid composition Membrane-adaptation review supports membrane lipid composition as the primary tunable mechanism for thermal adaptation; in hyperthermophilic archaea this is realized via tetraether (GDGT) monolayer membranes.
  • hyperthermostable proteins enables hyperthermophile bioenergetics RO:0002327

    Hyperthermostable proteins enable continued energy conservation at very high temperature.

    • DOI:10.1128/MMBR.65.1.1-43.2001 resistant to irreversible inactivation at high temperatures Supports protein hyperthermostability as a hyperthermophile feature.
  • hyperthermophile bioenergetics enables extreme hyperthermophilic RO:0002327

    Heat-adapted bioenergetics supports growth at extreme hyperthermophilic temperatures.

    • DOI:10.1016/s0300-9629(97)00003-0 energy transducing enzymes Supports temperature-adapted energy transduction as the basis of thermophile and hyperthermophile growth.
  • reverse gyrase introduces positive supercoils into DNA positive supercoiling

    Reverse gyrase introduces positive supercoils into DNA in hyperthermophiles.

    • DOI:10.1264/jsme2.me23087 reverse gyrase... introduces positive supercoils into DNA (review-supported mechanistic edge).
  • DNA positive supercoiling decreases risk of DNA thermal denaturation

    Positive DNA supercoiling decreases the risk of thermal denaturation of DNA.

    • DOI:10.1264/jsme2.me23087 reverse gyrase prevents the thermal denaturation of DNA by introducing positive DNA supercoiling (widely accepted in review literature).
  • reverse gyrase protects thermally damaged DNA

    Reverse gyrase has heat-protective DNA chaperone activity that reduces thermal DNA damage, independent of supercoiling.

    • DOI:10.1093/nar/gkh683 Reverse gyrase has heat-protective DNA chaperone activity, reducing double-stranded DNA breakage ~8-fold at 90 C (strong experimental support).
  • archaeal tetraether membrane lipids maintains membrane integrity at high temperature

    Archaeal ether/tetraether lipids maintain membrane integrity at high temperature.

    • DOI:10.1186/2046-0481-57-6-348 archaeal membranes contain tetraethers and diethers, enabling cells to withstand membrane-destroying temperatures (broad classic mechanism).
  • GrsA/GrsB GDGT cyclization enzymes increases membrane integrity at high temperature RO:0002213

    GrsA/GrsB cyclization of GDGTs increases membrane packing and stability at high temperature.

    • DOI:10.1007/s00792-023-01330-2 cyclized GDGTs (introduced by GrsA/GrsB) increase membrane packing and stability (strong mechanistic membrane edge).

Provenance

Source
METPO (2025-11-25)
Definition source
DOI:10.1007/s007920050010

Synonyms (2)

  • extreme hyperthermophile RELATED_SYNONYM · metpo.owl
  • extremely hyperthermophilic RELATED_SYNONYM · metpo.owl

kg-microbe context

Matched 1 kg-microbe node via direct_metpo.

  • METPO:1000721 [-1.816, -2.651, -5.319, +2.332, …]

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).

Curation history

  1. · SEEDED_FROM_METPO · seed_from_metpo

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

  2. · CURATED_WITH_ORGANISM_EXAMPLE · codex

    Added Pyrolobus fumarii organism example with PMID-backed evidence.

  3. · CURATED_CAUSAL_GRAPH · claude

    Added DOI-backed causal graph linking archaeal tetraether membrane lipids, hyperthermostable proteins, and hyperthermophile bioenergetics to extreme hyperthermophily.

  4. · IMPROVED_CAUSAL_GRAPH_EVIDENCE · codex

    Replaced Pyrolobus fumarii PMID fallback with the article DOI in definition, record evidence, and CausalEdge evidence.

  5. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).

  6. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007401×1).

  7. · RENAME_PREDICATE_LABELS · claude

    Renamed 1 causal-edge predicate label(s) to align with existing groundings: supports → enables ×1.

  8. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).

  9. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (PATO:0001637×1).

  10. · FIX_NODE_GROUNDING_CURIE · claude

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

  11. · ENRICH_CAUSAL_GRAPH · claude

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

  12. · GROUND_CAUSAL_PREDICATES · claude

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

  13. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A088E825×1).