Component
Human beta-carotene oxygenase 2 / BCO2
Human beta-carotene oxygenase 2 / BCO2. Species, exposure and limitations are retained in each linked claim.
6 recorded relationships. Experimental role, claim status and evidence remain attached to each record.
How nutrients influence it
Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
How nutrients reach it in more than one step
Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.
Tracing routes…
What it does
Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.
What it acts on
Human BCO2 binding to tested macular carotenoids was 10–40-fold weaker than mouse BCO2 in the 2014 comparison.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/24982131.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0", "start_char": 0, "end_char": 1743, "text_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0"}
- experimental_model
- Recombinant enzyme expression and comparative binding
- exposure
- Zeaxanthin-producing bacteria; surface plasmon resonance
- limitations
- Historical assay result; later work demonstrates human catalytic competence with altered protein processing and expression conditions.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human and mouse proteins; bacterial expression
- plain_language
- The early protein preparations differed in pigment binding.
- primary_references
- [lutein-p24982131] Inactivity of human β,β-carotene-9',10'-dioxygenase (BCO2) underlies retinal accumulation of the human macular carotenoid pigment. (2014). https://pubmed.ncbi.nlm.nih.gov/24982131/ DOI: 10.1073/pnas.1402526111
- tissue_or_cell_type
- Recombinant BCO2 and retina
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 268–279
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Recombinant enzyme expression and comparative binding · source_derived_draft · unverified_draft
### lutein-bco2-2014-binding Human BCO2 binding to tested macular carotenoids was 10–40-fold weaker than mouse BCO2 in the 2014 comparison. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The early protein preparations differed in pigment binding. organism: Human and mouse proteins; bacterial expression tissue_or_cell_type: Recombinant BCO2 and retina experimental_model: Recombinant enzyme expression and comparative binding limitations: Historical assay result; later work demonstrates human catalytic competence with altered protein processing and expression conditions. exposure: Zeaxanthin-producing bacteria; surface plasmon resonance evidence_span: {"source_cache": "artifacts/lutein-research/24982131.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0", "start_char": 0, "end_char": 1743, "text_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0"} [lutein-p24982131] Inactivity of human β,β-carotene-9',10'-dioxygenase (BCO2) underlies retinal accumulation of the human macular carotenoid pigment. (2014). https://pubmed.ncbi.nlm.nih.gov/24982131/ DOI: 10.1073/pnas.1402526111
Complete structured claim and evidenceThe 2014 expression assay detected zeaxanthin cleavage by mouse BCO2 but not human BCO2.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/24982131.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0", "start_char": 0, "end_char": 1743, "text_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0"}
- experimental_model
- Recombinant enzyme expression and comparative binding
- exposure
- Zeaxanthin-producing bacteria; surface plasmon resonance
- limitations
- Historical assay result; later work demonstrates human catalytic competence with altered protein processing and expression conditions.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human and mouse proteins; bacterial expression
- plain_language
- One early assay found no detectable human enzyme activity.
- primary_references
- [lutein-p24982131] Inactivity of human β,β-carotene-9',10'-dioxygenase (BCO2) underlies retinal accumulation of the human macular carotenoid pigment. (2014). https://pubmed.ncbi.nlm.nih.gov/24982131/ DOI: 10.1073/pnas.1402526111
- tissue_or_cell_type
- Recombinant BCO2 and retina
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 255–266
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Recombinant enzyme expression and comparative binding · source_derived_draft · unverified_draft
### lutein-bco2-2014-inactive The 2014 expression assay detected zeaxanthin cleavage by mouse BCO2 but not human BCO2. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: One early assay found no detectable human enzyme activity. organism: Human and mouse proteins; bacterial expression tissue_or_cell_type: Recombinant BCO2 and retina experimental_model: Recombinant enzyme expression and comparative binding limitations: Historical assay result; later work demonstrates human catalytic competence with altered protein processing and expression conditions. exposure: Zeaxanthin-producing bacteria; surface plasmon resonance evidence_span: {"source_cache": "artifacts/lutein-research/24982131.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0", "start_char": 0, "end_char": 1743, "text_sha256": "975bef59c81c57ad6e18b45581b23174165732965e8d7e017275fe98ca3ab4a0"} [lutein-p24982131] Inactivity of human β,β-carotene-9',10'-dioxygenase (BCO2) underlies retinal accumulation of the human macular carotenoid pigment. (2014). https://pubmed.ncbi.nlm.nih.gov/24982131/ DOI: 10.1073/pnas.1402526111
Complete structured claim and evidenceActivity assays indicated interaction between BCO2 and intracellular carotenoid-transporting Aster proteins.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/39978586.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe", "start_char": 0, "end_char": 1561, "text_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe"}
- experimental_model
- Validated antibodies, localization, donor-retina analysis and activity assays
- exposure
- BCO2 precursor/processed protein comparison; Aster interactions
- limitations
- Protein expression and interaction evidence does not by itself quantify lutein cleavage in living human retina.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human cells/donor retina and macaque retina
- plain_language
- Transport and breakdown machinery can work together in the assay.
- primary_references
- [lutein-p39978586] Unveiling BCO2 function in macular pigment metabolism: Mitochondrial processing and expression in the primate retina. (2025). https://pubmed.ncbi.nlm.nih.gov/39978586/ DOI: 10.1016/j.bbalip.2025.159600
- tissue_or_cell_type
- Retinal regions and mitochondria
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 346–357
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Validated antibodies, localization, donor-retina analysis and activity assays · source_derived_draft · unverified_draft
### lutein-bco2-aster Activity assays indicated interaction between BCO2 and intracellular carotenoid-transporting Aster proteins. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Transport and breakdown machinery can work together in the assay. organism: Human cells/donor retina and macaque retina tissue_or_cell_type: Retinal regions and mitochondria experimental_model: Validated antibodies, localization, donor-retina analysis and activity assays limitations: Protein expression and interaction evidence does not by itself quantify lutein cleavage in living human retina. exposure: BCO2 precursor/processed protein comparison; Aster interactions evidence_span: {"source_cache": "artifacts/lutein-research/39978586.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe", "start_char": 0, "end_char": 1561, "text_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe"} [lutein-p39978586] Unveiling BCO2 function in macular pigment metabolism: Mitochondrial processing and expression in the primate retina. (2025). https://pubmed.ncbi.nlm.nih.gov/39978586/ DOI: 10.1016/j.bbalip.2025.159600
Complete structured claim and evidenceHuman BCO2 associated with the inner mitochondrial membrane in cell-line experiments.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/25002123.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "13eecc413b623871f99140525333718bec180923ca6673fab15a9dee19a0551b", "start_char": 0, "end_char": 1308, "text_sha256": "13eecc413b623871f99140525333718bec180923ca6673fab15a9dee19a0551b"}
- experimental_model
- Subcellular localization and mitochondrial fractionation
- exposure
- Cleavable N-terminal leaders and compartment analyses
- limitations
- Human cell localization and mouse organelle fractionation are separate evidence components.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human isoforms in cell lines and mouse liver
- plain_language
- Carotenoid breakdown is organized within a particular compartment.
- primary_references
- [lutein-p25002123] Evidence for compartmentalization of mammalian carotenoid metabolism. (2014). https://pubmed.ncbi.nlm.nih.gov/25002123/ DOI: 10.1096/fj.14-252411
- tissue_or_cell_type
- Inner mitochondrial membrane
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 307–318
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Subcellular localization and mitochondrial fractionation · source_derived_draft · unverified_draft
### lutein-bco2-inner-membrane Human BCO2 associated with the inner mitochondrial membrane in cell-line experiments. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Carotenoid breakdown is organized within a particular compartment. organism: Human isoforms in cell lines and mouse liver tissue_or_cell_type: Inner mitochondrial membrane experimental_model: Subcellular localization and mitochondrial fractionation limitations: Human cell localization and mouse organelle fractionation are separate evidence components. exposure: Cleavable N-terminal leaders and compartment analyses evidence_span: {"source_cache": "artifacts/lutein-research/25002123.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "13eecc413b623871f99140525333718bec180923ca6673fab15a9dee19a0551b", "start_char": 0, "end_char": 1308, "text_sha256": "13eecc413b623871f99140525333718bec180923ca6673fab15a9dee19a0551b"} [lutein-p25002123] Evidence for compartmentalization of mammalian carotenoid metabolism. (2014). https://pubmed.ncbi.nlm.nih.gov/25002123/ DOI: 10.1096/fj.14-252411
Complete structured claim and evidenceHuman donor retina had higher BCO2 protein expression peripherally than centrally.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/39978586.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe", "start_char": 0, "end_char": 1561, "text_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe"}
- experimental_model
- Validated antibodies, localization, donor-retina analysis and activity assays
- exposure
- BCO2 precursor/processed protein comparison; Aster interactions
- limitations
- Protein expression and interaction evidence does not by itself quantify lutein cleavage in living human retina.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Human cells/donor retina and macaque retina
- plain_language
- The breakdown enzyme was unevenly distributed across the retina.
- primary_references
- [lutein-p39978586] Unveiling BCO2 function in macular pigment metabolism: Mitochondrial processing and expression in the primate retina. (2025). https://pubmed.ncbi.nlm.nih.gov/39978586/ DOI: 10.1016/j.bbalip.2025.159600
- tissue_or_cell_type
- Retinal regions and mitochondria
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 333–344
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Validated antibodies, localization, donor-retina analysis and activity assays · source_derived_draft · unverified_draft
### lutein-bco2-regional Human donor retina had higher BCO2 protein expression peripherally than centrally. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The breakdown enzyme was unevenly distributed across the retina. organism: Human cells/donor retina and macaque retina tissue_or_cell_type: Retinal regions and mitochondria experimental_model: Validated antibodies, localization, donor-retina analysis and activity assays limitations: Protein expression and interaction evidence does not by itself quantify lutein cleavage in living human retina. exposure: BCO2 precursor/processed protein comparison; Aster interactions evidence_span: {"source_cache": "artifacts/lutein-research/39978586.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe", "start_char": 0, "end_char": 1561, "text_sha256": "3546acef9586e54733ec1f03797741c67643606de59f80a7762815b32c3c03fe"} [lutein-p39978586] Unveiling BCO2 function in macular pigment metabolism: Mitochondrial processing and expression in the primate retina. (2025). https://pubmed.ncbi.nlm.nih.gov/39978586/ DOI: 10.1016/j.bbalip.2025.159600
Complete structured claim and evidenceThe 2024 study reported greater BCO2 expression in the macular region than peripherally.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/zeaxanthin-research/39151780.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e43805b4445f15c3f6490ab163d908ee7a43f475538b3160fc1ea9771cff9ab4", "start_char": 0, "end_char": 1282, "text_sha256": "e43805b4445f15c3f6490ab163d908ee7a43f475538b3160fc1ea9771cff9ab4"}
- experimental_model
- Confocal Raman/fluorescence imaging and expression analysis
- exposure
- Twelve carotenoid-related proteins; Western blot and single-cell RNA database
- limitations
- Localization is not proof of transport direction or rate. Regional BCO2 result differs from the 2025 study; antibody specificity, sampling and compartment remain unresolved comparison variables.
- nutrient_topic
- Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
- organism
- Human donor retina and RPE
- plain_language
- This paper placed more BCO2 centrally.
- primary_references
- [zeaxanthin-p39151780] Imaging macular carotenoids and their related proteins in the human retina with confocal resonance Raman and fluorescence microscopy. (2024). https://pubmed.ncbi.nlm.nih.gov/39151780/ DOI: 10.1016/j.exer.2024.110043
- tissue_or_cell_type
- Central versus peripheral retinal regions
Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 561–572
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Confocal Raman/fluorescence imaging and expression analysis · source_derived_draft · unverified_draft
### zeaxanthin-bco2-central-2024 The 2024 study reported greater BCO2 expression in the macular region than peripherally. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: This paper placed more BCO2 centrally. organism: Human donor retina and RPE tissue_or_cell_type: Central versus peripheral retinal regions experimental_model: Confocal Raman/fluorescence imaging and expression analysis limitations: Localization is not proof of transport direction or rate. Regional BCO2 result differs from the 2025 study; antibody specificity, sampling and compartment remain unresolved comparison variables. exposure: Twelve carotenoid-related proteins; Western blot and single-cell RNA database evidence_span: {"source_cache": "artifacts/zeaxanthin-research/39151780.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e43805b4445f15c3f6490ab163d908ee7a43f475538b3160fc1ea9771cff9ab4", "start_char": 0, "end_char": 1282, "text_sha256": "e43805b4445f15c3f6490ab163d908ee7a43f475538b3160fc1ea9771cff9ab4"} [zeaxanthin-p39151780] Imaging macular carotenoids and their related proteins in the human retina with confocal resonance Raman and fluorescence microscopy. (2024). https://pubmed.ncbi.nlm.nih.gov/39151780/ DOI: 10.1016/j.exer.2024.110043
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.