pigmentation
METPO:1003021 · CLASS · REVIEWED
A phenotype characterized by the color of pigments produced by a microorganism.
Microbial pigmentation biosynthetic mechanism
Edge evidence
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pigment biosynthesis
has output
chromophore-containing metabolites
RO:0002234Pigment biosynthetic pathways produce colored metabolites.
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DOI:10.1016/j.procbio.2013.06.006bacterial pigments and their applications
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chromophore-containing metabolites
causes
visible colony color
biolink:causesChromophore-containing metabolites cause visible microbial color.
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DOI:10.1177/1934578X1801301240such as melanin, carotenoids, pyocyanin, bacteriochlorophylls, violacein, prodigiosin
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environmental regulation
modulates
pigment biosynthesis
RO:0002211Growth and environmental conditions can modulate pigment biosynthesis.
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DOI:10.3389/fsufs.2020.00100bacterial pigments ... production ... genetic engineering
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visible colony color
manifests as
pigmentation
METPO:2007400Visible colony color manifests the pigmentation phenotype.
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DOI:10.1016/j.procbio.2013.06.006focus on applications of bacterial pigments
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mevalonate pathway
provides precursor for
carotenoid biosynthesis
The mevalonate pathway supplies C5 isoprenoid precursors (IPP/DMAPP) for carotenoid biosynthesis.
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DOI:10.3390/microorganisms11122920
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MEP pathway
provides precursor for
carotenoid biosynthesis
The MEP pathway supplies C5 isoprenoid precursors (IPP/DMAPP) for carotenoid biosynthesis.
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DOI:10.3390/microorganisms11122920
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crtE/crtB/crtI/crtY gene set
enables
beta-carotene biosynthesis
RO:0002327The crtE/crtB/crtI/crtY gene set encodes enzymes enabling beta-carotene biosynthesis.
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DOI:10.3390/microorganisms11030614
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beta-carotene biosynthesis
is a
carotenoid biosynthesis
rdfs:subClassOfBeta-carotene biosynthesis is a specific carotenoid biosynthetic route.
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DOI:10.3390/microorganisms11030614
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shikimate pathway
precursor of
phenazine biosynthesis
The shikimate pathway provides aromatic precursors for phenazine biosynthesis.
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DOI:10.3390/microorganisms11122920
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hppD 4-hydroxyphenylpyruvate dioxygenase
produces
homogentisate
METPO:2007800HppD converts 4-hydroxyphenylpyruvate to homogentisate in the pyomelanin pathway.
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DOI:10.1128/spectrum.00410-24
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homogentisate
polymerizes to form
pyomelanin
Homogentisate auto-oxidizes and polymerizes to form the pigment pyomelanin.
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DOI:10.1128/spectrum.00410-24
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hmgA homogentisate 1,2-dioxygenase
prevents accumulation of
pyomelanin
HmgA converts homogentisate to maleylacetoacetate, preventing pyomelanin accumulation.
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DOI:10.1128/spectrum.00410-24
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1016/j.procbio.2013.06.006
Parent traits (1)
Children (10)
- black pigmented
METPO:1003022 - brown pigmented
METPO:1003023 - carotenoid pigmentation
METPO:1003031 - cream pigmented
METPO:1003024 - green pigmented
METPO:1003025 - orange pigmented
METPO:1003026 - pink pigmented
METPO:1003027 - red pigmented
METPO:1003028 - white pigmented
METPO:1003029 - yellow pigmented
METPO:1003030
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1003021[-2.062, -1.921, -1.630, -0.024, …]
Nearest neighbors in embedding space
- morphology carotenoid pigmentation 0.913
- morphology green pigmented 0.899
- morphology black pigmented 0.866
- morphology pink pigmented 0.839
- morphology white pigmented 0.834
- morphology red pigmented 0.829
- morphology cream pigmented 0.798
- morphology brown pigmented 0.795
Deep research
# Curation report: microbial pigmentation ## Executive summary **Target trait:** `METPO:1003021` (quoted verbatim) **Label:** pigmentation **Category:** morphology **Definition supplied:** “A phenotype characterized by the color of pigments produced by a microorganism.” **Parent:** `METPO:1000059` For TraitMech, pigmentation should be modeled as an **observable cell, colony, biomass, or culture color resulting from production, accumulation, localization, or secretion of one or more microbial pigments**. Pigment biosynthesis is the causal process; the pigment molecule is the proximate color-bearing entity; and `METPO:1003021` is the phenotype endpoint. Pigments absorb and reflect visible wavelengths, whereas dyes are generally distinguished by solubility and mode of dispersion. A recent review places the relevant visible range at approximately 400–800 nm. (barreto2023microbialpigmentsmajor pages 1-2) The best-supported initial graph consists of taxon-specific modules rather than a single universal linear pathway. Priority modules are: (1) prodigiosin in *Serratia*, (2) violacein in *Chromobacterium* or a heterologous host, and (3) pyomelanin through homogentisate. Broader carotenoid, bacteriochlorophyll, DOPA-melanin, and DHN-melanin branches should be separate modules sharing only the terminal relation “pigment accumulation causes pigmentation.” | module | strongest direct causal chain | exemplar taxon | evidence strength | curation recommendation | |---|---|---|---|---| | prodigiosin | cpxR ⟶ represses pig gene cluster transcription ⟶ decreased prodigiosin production/red pigmentation; parallel direct support for metR ⟶ represses PigP ⟶ represses pig operon, and χ phage infection ⟶ increases pig operon transcription ⟶ increased prodigiosin | *Serratia marcescens* JNB 5-1 / ATCC 274 | high | Curate as a priority core bacterial pigmentation module with regulator-to-operon-to-pigment edges; annotate regulator and phage effects as strain-specific where applicable. | | violacein | L-tryptophan ⟶ VioA/VioB/VioE/VioD/VioC pathway ⟶ violacein; CviIR quorum sensing at high cell density ⟶ activates violacein production | *Chromobacterium violaceum* | high | Curate as a priority pathway module with precursor-to-enzyme-set-to-pigment edges; add quorum-sensing activation as a separate regulatory branch. | | pyomelanin/melanin | tyrosine degradation ⟶ homogentisate ⟶ pyomelanin; 4-hydroxyphenylpyruvate dioxygenase supports homogentisate production and homogentisate 1,2-dioxygenase supports homogentisate oxidation | *Shewanella oneidensis* MR-1 | high for pyomelanin, moderate/review-only for broader melanin classes | Curate pyomelanin first using direct enzyme/metabolite evidence; defer broader DOPA-, DHN-, tyrosinase-, laccase-, and PKS-based melanin graph expansion until primary species-specific causal papers are added. | | carotenoids/photopigments | light/oxygen regulatory context ⟶ photosynthesis gene expression and pigment synthesis; excess membrane-bound carotenoids ⟶ scavenging capacity that safeguards bacteriochlorophyll synthesis/photosystem assembly | *Sediminicoccus* sp. KRV36 | moderate | Curate a limited photopigment submodule for light/oxygen-linked pigment maintenance and membrane localization; defer generic carotenoid biosynthesis edges unless supported by direct primary pathway papers in target taxa. | *Table: This matrix ranks the main microbial pigmentation modules by directness of causal evidence and immediate suitability for TraitMech curation. It helps prioritize robust pathway/regulatory branches before adding broader review-derived pigment biology.* ## 1. Scope and boundary cases ### Included * Visible color of microbial cells, colonies, aggregates, spores, biomass, or culture supernatant caused by endogenous pigment production. * Intracellular, membrane-associated, cell-wall-associated, or extracellular pigments. For example, *Rhodotorula* carotenoids accumulate intracellularly and yield orange, salmon, pink, or red colonies; fungal melanin may be localized in the cell wall or secreted. (qin2024melanininfungi pages 1-2, ochoavinals2024currentadvancesin pages 1-2) * Loss, gain, or quantitative change in color following mutation, pathway transfer, altered gene expression, precursor supply, environmental treatment, or infection. * Pigment mixtures where the assay measures a composite color, provided the chemical ambiguity is recorded. “Crude violacein,” for example, includes violacein and deoxyviolacein. (fang2015highcrudeviolacein pages 1-2) ### Excluded or separately modeled * Color imparted only by medium pH indicators, exogenous dyes, blood products, host pigments, or stained substrates. * Fluorescence or bioluminescence without corresponding visible pigment coloration. * Structural color or iridescence not caused by a pigment molecule. * Biological functions such as antioxidant activity, virulence, UV protection, or electron transfer unless linked through a distinct causal edge to pigment production or accumulation. * Pigment-production capacity inferred only from genomic annotation. A biosynthetic gene cluster is not sufficient evidence that a strain is visibly pigmented. * Taxonomic identification based on colony color alone. Pigmentation can vary with strain, growth phase, medium, temperature, light, oxygen, and spontaneous regulatory state. ## 2. Candidate graph nodes Identifiers below are deliberately conservative. Label-only nodes are preferable to unverified CURIEs. ### Trait and phenotype nodes | Node | Grounding | Comment | |---|---|---| | microbial pigmentation | `METPO:1003021` | Required phenotype endpoint. | | morphology parent | `METPO:1000059` | Supplied parent. | | red pigmentation | label only | Prodigiosin-associated assay phenotype. | | violet/purple pigmentation | label only | Violacein-associated phenotype. | | brown/black pigmentation | label only | Melanin-associated phenotype. | | orange/pink/red yeast pigmentation | label only | Carotenoid-associated phenotype. | ### Pigments, precursors, and metabolites * Prodigiosin; 2-methyl-3-*n*-amyl-pyrrole (MAP); 4-methoxy-2,2′-bipyrrole-5-carbaldehyde (MBC); trans-2-octenal; L-proline; pyruvate; malonyl-CoA; S-adenosyl-L-methionine.
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_WITH_LITERATURE · codex
Reviewed pigmentation and added DOI-backed causal graph for pigment biosynthesis, chromophore metabolites, environmental regulation, and visible colony color.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:causes×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007400×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0046148×1).
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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, rdfs:subClassOf×1, METPO:2000202×1).
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GROUND_CAUSAL_NODES · claude
Grounded 4 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0016117×1, GO:0009423×1, GO:1901812×1, CHEBI:16169×1).
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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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MIGRATE_MICROBE_DOMAIN_EDGES_PART2 · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (1 to produces), issue 301 part 2. 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. Each replacement is a 1:1 mirror of its source predicate that changes only the domain, so the claim each edge makes is unchanged and directions are unchanged. The replacements are proposed in proposals/metpo_traitmech_v9 and are placeholder ids until METPO mints them.
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NORMALISE_NODE_TYPE · claude
Under the PATHWAY-vs-BIOLOGICAL_PROCESS rule, one node_id means one thing corpus-wide (issue 356): carotenoid_biosynthesis is typed PATHWAY, phenazine_biosynthesis is typed PATHWAY. PATHWAY is a named, conventionally enumerable multi-step route; BIOLOGICAL_PROCESS is everything else. A named biosynthetic route. Most descriptions call it one outright, including BIOLOGICAL_PROCESS-typed ones ('Enzymatic pathway producing carotenoid pigments'); red_pigmented.yaml instead ENUMERATES the steps -- 'Phytoene synthase condenses two GGPP to phytoene, then desaturation/isomerization yields lycopene' -- which is the rule's own test for PATHWAY met explicitly rather than by naming. Applied AGAINST the majority, which was 5 BIOLOGICAL_PROCESS to 1 before this tranche. A named biosynthetic route; both typings say 'Biosynthetic pathway producing phenazine pigments'. The rule breaks the 1-1 tie.