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Operational assay
TEM-EDS localization assay for intracellular Bi in Fusarium sp. BI
AssayMech:fusarium-intracellular-bi-tem-eds
Bioaccumulation
Use thin-section TEM with energy-dispersive X-ray spectroscopy to assess intracellular Bi localization in Fusarium sp. BI exposed to bismuth subsalicylate.
Download source YAML · View source at this revision
Scoped operational assay. Consult the sourced method, controls and limitations; missing protocol details remain explicit research gaps.
Record evidence
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — Primary methods prepare washed 96-hour biomass from bismuth-subsalicylate and salicylate cultures for TEM-EDS of 60 nm sections.
Source reference · html:#sec7 · Source licence: Not recorded for this source
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — The localization analysis compares intracellular granules with the salicylate control and warns that the EDS beam samples surrounding material.
Source reference · html:#sec15 · Source licence: Not recorded for this source
Interpretation and limitations
- This is qualitative spatial localization, not bulk biomass uptake capacity, uptake rate, or whole-feed recovery.
- The EDS beam is larger than the granules; the spectrum includes adjacent cellular material.
- Element co-localization does not establish a unique Bi-polyphosphate molecular structure, crystalline phase, oxidation state or transport route.
- The experiment concerns the unresolved Fusarium sp. BI isolate and defined laboratory feed; no other strain, ore or industrial process is implied.
Ontology groundings
Assay identity, measured phenotype and tested predicate are distinct relations. A property grounding does not turn that property into an assay identity.
accumulates · METPO:2000210
Tests predicate · Entity type: Object property
Ontology source: metpo.json
Exact source revision: 800c9d27913158efdf466edf2cd710dbf1ce893f
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METPO ontology at commit 800c9d27913158efdf466edf2cd710dbf1ce893f — METPO accumulates is an object property; intracellular localization provides scoped evidence relevant to accumulation, not an ontology assay identity.
Source reference · /graphs/0/nodes/1530 · Source licence: CC-BY-4.0
Method summary
Wash and prepare 96-hour biomass grown with 1.5 mM bismuth subsalicylate or 1.5 mM salicylate; examine approximately 60 nm sections by TEM and obtain EDS spectra from selected intracellular regions.
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — Primary methods prepare washed 96-hour biomass from bismuth-subsalicylate and salicylate cultures for TEM-EDS of 60 nm sections.
Source reference · html:#sec7 · Source licence: Not recorded for this source
Measurement and interpretation
- Target
- Bi signal associated with intracellular phosphorus-rich granules.
- Readout
- Spatially targeted elemental EDS signal interpreted alongside TEM morphology and the salicylate-grown control.
- Unit
- No unit recorded
- Interpretation
- Supports localization when Bi is detected in the intracellular regions; does not quantify total uptake or uniquely identify the Bi-containing chemical species.
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — Primary methods prepare washed 96-hour biomass from bismuth-subsalicylate and salicylate cultures for TEM-EDS of 60 nm sections.
Source reference · html:#sec7 · Source licence: Not recorded for this source
-
Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — The localization analysis compares intracellular granules with the salicylate control and warns that the EDS beam samples surrounding material.
Source reference · html:#sec15 · Source licence: Not recorded for this source
Controls
Salicylate-grown biomass processed for the same microscopy/elemental comparison; its granules lacked detected Bi in the reported comparison.
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — Primary methods prepare washed 96-hour biomass from bismuth-subsalicylate and salicylate cultures for TEM-EDS of 60 nm sections.
Source reference · html:#sec7 · Source licence: Not recorded for this source
-
Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — The localization analysis compares intracellular granules with the salicylate control and warns that the EDS beam samples surrounding material.
Source reference · html:#sec15 · Source licence: Not recorded for this source
Scoped CMM relationships
Measures process · cmmmech:bismuth
Corpus: cmmmech
The target mechanism explicitly cites Dodge 2005 intracellular TEM-EDS localization; this assay scopes the link to that component of accumulation evidence.
Scope: Fusarium sp. BI; intracellular Bi localization by thin-section TEM-EDS, not the paper's separate soluble-Bi time course.
Target locator: /mechanisms/0
Linked source record: data/records/bismuth.yaml
Source revision: df061de720fb9884dcc6e41369a3049cef52a059
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CMMMech bismuth mechanism at df061de720fb9884dcc6e41369a3049cef52a059 — The target mechanism explicitly cites Dodge 2005 intracellular TEM-EDS localization; this assay scopes the link to that component of accumulation evidence.
Source reference · /mechanisms/0 · Source licence: CC-BY-4.0
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Metabolism of Bismuth Subsalicylate and Intracellular Accumulation of Bismuth by Fusarium sp. Strain BI — The localization analysis compares intracellular granules with the salicylate control and warns that the EDS beam samples surrounding material.
Source reference · html:#sec15 · Source licence: Not recorded for this source
Research gaps
- protocol_parameters: This summary does not establish a quantitative detection limit, independent culture replicate count or calibrated mass-uptake conversion for TEM-EDS.