magnetosome
traitmech:000071 · CLASS · REVIEWED
A membrane-bounded intracellular organelle containing a magnetic iron-mineral crystal (magnetite or greigite); chains of magnetosomes allow magnetotactic bacteria to align with and navigate along geomagnetic field lines.
Trait evidence
Magnetosome chains enable magnetotactic navigation
MECHANISTIC · The taxon-matched protein example anchors one experimentally supported causal branch; it is not presented as a universal mechanism for every taxon or every contextual branch in this graph.
Edge evidence
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magnetic iron-mineral crystal
located in
magnetosome
biolink:located_inThe magnetic mineral crystal sits inside the magnetosome membrane.
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magnetosome
enables
magnetotaxis
RO:0002327Chains of magnetosomes act as a cellular compass, aligning the organism with geomagnetic field lines.
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MamK
organizes
magnetosome chain assembly
The actin-like protein MamK organizes magnetosomes into chains.
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MamK
polymerizes into
actin-like MamK filaments
MamK polymerizes into long actin-like filaments that scaffold the magnetosome chain.
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magnetosome chain assembly
enables
magnetotaxis
RO:0002327Chain assembly of magnetosomes underlies the cellular compass enabling magnetotaxis.
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MamAB magnetosome protein module
sufficient for
magnetosome biomineralization
The mamAB operon is sufficient for rudimentary magnetosome biomineralization.
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magnetosome biomineralization
has output
magnetic iron-mineral crystal
RO:0002234Biomineralization forms the magnetic iron-mineral crystal within the magnetosome.
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MamB
promotes
magnetosome membrane invagination
RO:0002213MamB promotes invagination of the cytoplasmic membrane to form the magnetosome vesicle.
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oxygen-poor, low-sulfide environment
favors
magnetite crystal
Oxygen-poor, low-sulfide environments favor magnetite magnetosomes.
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sulfide-rich habitat
favors
greigite crystal
Sulfide-rich habitats favor greigite magnetosomes.
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magnetosome membrane invagination
precedes
magnetosome biomineralization
Magnetosome-membrane invagination forms the vesicle before mineral biomineralization begins.
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DOI:10.1111/mmi.15330Biomineralization of magnetite crystals occurs after the formation of magnetosome vesicles
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magnetite crystal
located in
magnetosome
biolink:located_inMagnetite is one mineral-crystal form contained by magnetosomes.
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DOI:10.1111/mmi.15330The structure and morphology of magnetosomes differ across all MTB species, with some producing iron oxide magnetite (Fe3O4)
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greigite crystal
located in
magnetosome
biolink:located_inGreigite is one mineral-crystal form contained by magnetosomes.
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DOI:10.1111/mmi.15330others synthesizing iron sulfide greigite (Fe3S4), and some capable of producing both, depending on their environmental conditions
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Protein and taxon examples
| Graph node | Protein | Taxon | UniProt status | Role and evidence |
|---|---|---|---|---|
| MamK |
UniProtKB:Q6NE59
Actin-like protein MamK |
Magnetospirillum gryphiswaldense MSR-1
NCBITaxon:431944
|
REVIEWED |
MamK polymerizes into an actin-like scaffold that organizes magnetosomes into chains.
|
Provenance
- Identifier source
- TraitMech local identifier
- Definition source
DOI:10.1038/nrmicro.2016.99
Parent traits (1)
Cross-references
GO:0110143
kg-microbe context
Matched 1 kg-microbe node via parent_proxy.
METPO:1000059[-2.682, -2.070, -3.656, -0.652, …]
Nearest neighbors in embedding space
- morphology polyhydroxyalkanoate granule 1.000
- environment cadmium tolerant 1.000
- environment cobalt tolerant 1.000
- environment copper tolerant 1.000
- environment desiccation tolerant 1.000
- environment piezotolerant 1.000
- morphology gas vesicle 1.000
- environment UV radiation tolerant 1.000
Deep research
# Magnetosome TraitMech Curation Report **Target:** `traitmech:000071` **Label:** magnetosome **Category:** MORPHOLOGY | **Term kind:** CLASS | **Status:** REVIEWED **Parent:** `traitmech:000066` ## 1. Scope and current definition A **magnetosome** is the combined membrane-plus-mineral bacterial organelle: a cytoplasmic-membrane-derived lipid-bilayer compartment containing a biomineralized magnetic crystal, usually magnetite (Fe₃O₄) or greigite (Fe₃S₄). Chains of these organelles generate a cellular magnetic dipole. **Magnetotaxis** or **magnetoaerotaxis** is the resulting behavior—not the organelle itself—where magnetic alignment assists swimming toward favorable oxygen/redox zones. This distinction should be explicit in the graph: `magnetosome chain enables magnetotaxis`, rather than treating “magnetosome” and “magnetotactic” as exact biological equivalents. (ferrara2024bacterialorganellesin pages 2-4, awal2023experimentalanalysisof pages 1-2, mccausland2022globalanalysisof pages 1-2) ### Boundary cases - **Include:** mature magnetite- or greigite-containing membrane compartments; chains and alternative intracellular arrangements; and empty or immature magnetosome vesicles when discussing the organelle-biogenesis process. - **Do not equate with:** free intracellular iron particles, synthetic magnetic nanoparticles, ferrosomes, ferritin-like storage compartments, sulfur globules, or generic iron biomineralization. Ferrosomes and encapsulated ferritin-like structures are separate iron-related organelles. (ferrara2024bacterialorganellesin pages 2-4) - **Do not require magnetotactic behavior as the defining assay:** defective chain organization or undersized/superparamagnetic crystals can yield structurally recognizable magnetosomes but weak or absent magnetic alignment. The Δ`mamP` phenotype is an example. (amor2024magnetochromecatalyzedoxidationof pages 7-8, amor2024magnetochromecatalyzedoxidationof pages 1-2) - **Mineral identity is variable:** magnetite is associated mainly with oxygen-poor, low-sulfide settings; greigite predominates in sulfide-rich habitats; some organisms can produce both depending on conditions. This ecological association is not a universal deterministic rule. (ferrara2024bacterialorganellesin pages 2-4) - **Taxonomic caution:** most causal mechanisms were established in *Magnetospirillum magneticum* AMB-1 and *M. gryphiswaldense* MSR-1. Deep-branching MTB can use additional lineage-specific proteins and architectures. (ferrara2024bacterialorganellesin pages 2-4, awal2023experimentalanalysisof pages 1-2) ## 2. Candidate graph nodes and ontology grounding Only identifiers that can be stated confidently are supplied. Protein accessions and exact GO terms should be added after organism-specific validation; gene symbols alone are preferable to invented or cross-species UniProt identifiers. ### Trait, structures, and locations | Candidate node | Type | Grounding recommendation | |---|---|---| | magnetosome | morphology/organelle | `traitmech:000071` | | magnetosome membrane | cellular structure | Label-only pending exact ontology review | | magnetosome lumen | cellular location | Label-only | | magnetosome vesicle | cellular structure/developmental state | Label-only | | magnetosome chain | supramolecular cellular structure | Label-only | | cytoplasmic membrane | cellular component | Ground to an appropriate GO cellular-component term after validation | | MamK filament / magnetoskeleton | cytoskeletal structure | Label-only; do not equate automatically with generic actin cytoskeleton | | magnetic single-domain crystal | material state | Label-only | ### Genes, proteins, transporters, and complexes - **Conserved/core MAPs:** `mamA`, `mamB`, `mamE`, `mamK`, `mamM`, `mamO`, `mamP`, `mamQ`, `mamI`. A 2024 synthesis reports nine core genes, `mamABEKMOPQI`, conserved across known MTB, while noting that not all functions are fully resolved. (ferrara2024bacterialorganellesin pages 2-4) - **Membrane formation:** MamI, MamL, MamQ, MamB; MamA scaffold. - **Iron acquisition/transport:** FeoB1, FeoB2, MamB, MamM, MamH, MamZ. - **Biomineralization/redox and crystal control:** MamE, MamO, MamP, MamT, MamX, Mms6, MamC, MamD, MamF. - **Chain organization:** MamK, MamJ, LimJ, MamY, McaA, McaB; lineage-specific Mad28 and other MamK interactors. - **Environment-linked metabolism:** CysC; nitrate/denitrification modules and `nap` operon as condition-dependent candidates. MamB and MamM are CDF-family transporters; MamK is an actin-like ATP-dependent filament protein; MamJ is an adaptor connecting magnetosome membranes to MamK; and MamP contains c-type-cytochrome-like magnetochrome domains. These molecular-function descriptions can guide later GO/InterPro grounding but should not be converted into unverified CURIEs. (amor2024magnetochromecatalyzedoxidationof pages 1-2, ferrara2024bacterialorganellesin pages 4-6, awal2023experimentalanalysisof pages 1-2) ### Chemicals and minerals | Node | Suggested grounding | |---|---| | iron atom | `CHEBI:18248` | | ferrous iron / Fe(II) | `CHEBI:29033` | | ferric iron / Fe(III) | `CHEBI:29034` | | magnetite | `CHEBI:46726` | | oxygen | `CHEBI:15379` | | reactive oxygen species | `CHEBI:26523` | | greigite | Label-only pending ChEBI verification | | sulfide, sulfate, nitrate, nitrite | Use exact ChEBI species only after protonation-state and assay context are checked |
Canonical examples
-
Magnetospirillum gryphiswaldense MSR-1
NCBITaxon:431944DOI:10.1038/s41579-025-01234-2
Curation history
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·
PROPOSED_FROM_RESEARCH · claude
Proposed candidate MORPHOLOGY trait (magnetosome); organelle sub-variant of intracellular inclusion.
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CURATED_CAUSAL_GRAPH · claude
Added evidence-backed causal graph (magnetosome / magnetotaxis) with RO/biolink predicate groundings; promoted PROPOSED to REVIEWED.
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ENRICH_CAUSAL_GRAPH · claude
Added 8 evidence-backed generic edges (11 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:0002327×1, METPO:2000202×1, RO:0002213×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A6J4ZQS8×1).
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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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MIGRATE_MICROBE_DOMAIN_EDGES · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates (1 to has output), 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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CURATE_PROTEIN_TAXON_EXAMPLE · claude
Backfilled provenance (review issue 517) for the codex protein-taxon review tranche of 2026-08-24/25, which shipped without a per-record event. In this record the tranche: set graph scope magnetosome_magnetotaxis=MECHANISTIC with scope_notes; marked 3 GENE_OR_PROTEIN node(s) REVIEWED_LABEL_ONLY with grounding_notes (mamk_protein, mamab_operon, mamb_protein); added taxon-paired protein example(s) UniProtKB:Q6NE59 on mamk_protein (NCBITaxon:431944).
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ADD_EXACT_ONTOLOGY_MATCH · codex
Ontology exact-match review (2026-08-25): approved exact xref(s): GO:0110143. Evidence is predicate-scoped in the versioned ontology snapshots; OAK cross-checked direct data, and OLS4 spot-checked release deltas and disputed hits.
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CONNECT_CAUSAL_GRAPH_COMPONENTS · codex
Resolved issue #183 graph fragmentation (4 components to 1) using 3 source- and verbatim-snippet-backed connector(s). Clarified the magnetite and greigite nodes as mineral crystals contained within magnetosomes. No paid research service was called.
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GROUND_CAUSAL_NODES · codex
Grounded the magnetotaxis causal-graph process node to newly minted traitmech:000176 and moved the adjectival magnetotactic related synonym to the magnetotaxis trait; resolves issue 851.