phototrophy
traitmech:000037 · CLASS · REVIEWED
A metabolism in which an organism captures light as its energy source. It encompasses chlorophyll-based photosynthesis (with photochemical reaction centers) and retinal-based (rhodopsin) light-driven ion pumping.
Phototrophy captures light as cellular energy
Edge evidence
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light
causes
phototrophy
biolink:causesLight availability is the input the phototrophic trait realizes.
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DOI:10.1016/j.tim.2006.09.001
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phototrophy
contributes to
proton motive force
RO:0002326Chlorophyll- and retinal-based phototrophy generate proton motive force from absorbed light.
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DOI:10.1126/science.289.5486.1902
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light
activates
rhodopsin photocycle
RO:0002213Visible light activates the microbial rhodopsin photocycle across taxa.
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DOI:10.1093/ismejo/wrae175
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microbial rhodopsin
enables
rhodopsin photocycle
RO:0002327During the photocycle, microbial rhodopsins exhibit ion-transport function.
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DOI:10.1093/ismejo/wrae175
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proton motive force
drives
ATP synthesis
The proton gradient drives ATP synthesis, conserving light-derived energy.
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DOI:10.1128/spectrum.02177-23
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photosystem II
supplies electrons to
photosynthetic electron transport chain
PSII water oxidation supplies electrons to the photosynthetic electron transport chain.
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DOI:10.1111/1751-7915.14519
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photosynthetic electron transport chain
has output
NADPH
RO:0002234Electron flow through cytochrome b6f and PSI reduces ferredoxin/NADP+ to NADPH.
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DOI:10.1111/1751-7915.14519
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photosynthetic electron transport chain
has output
ATP
RO:0002234Photosynthetic electron transfer establishes a proton gradient that produces ATP.
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DOI:10.1111/1751-7915.14519
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high light intensity
damages
photosystem II
High light intensity and resulting free radicals damage PSII (photoinhibition).
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DOI:10.1111/1751-7915.14519
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1016/j.tim.2006.09.001
Parent traits (1)
Synonyms (1)
- phototrophic metabolism
kg-microbe context
Matched 1 kg-microbe node via parent_proxy.
METPO:1000060[-1.052, -1.766, -1.194, +0.291, …]
Nearest neighbors in embedding space
- metabolism lignin degradation 1.000
- metabolism sulfur oxidation 1.000
- metabolism starch degradation 1.000
- metabolism reductive tricarboxylic acid cycle 1.000
- metabolism proteorhodopsin phototrophy 1.000
- metabolism proteolysis 1.000
- metabolism photosynthesis 1.000
- metabolism oxygenic photosynthesis 1.000
Deep research
# Curation-focused research report: microbial phototrophy ## Trait record and scope - **Trait label:** phototrophy - **Trait identifier:** `traitmech:000037` - **Category / kind / status:** METABOLISM / CLASS / REVIEWED - **Parent:** `METPO:1000060` - **Recommended operational definition:** the capacity to capture photon energy and convert it into metabolically available chemical or electrochemical energy that supports cellular maintenance, growth, or biosynthesis. Phototrophy is broader than photosynthesis. Photosynthesis uses light-derived energy and reducing power to reduce CO₂ into biomass, whereas phototrophy only requires light-to-chemical-energy conversion supporting growth. Thus, every photosynthetic microorganism is phototrophic, but a rhodopsin-powered photoheterotroph that does not fix CO₂ is still phototrophic. The two independently evolved core implementations are **chlorophototrophy**, based on chlorophyll/bacteriochlorophyll photochemical reaction centers, and **retinalophototrophy**, based on retinal-bound microbial rhodopsins. (bryant2006prokaryoticphotosynthesisand pages 2-3, peterson2023usinglightfor pages 1-5, bryant2006prokaryoticphotosynthesisand pages 1-2) ### Boundaries **Include:** 1. Oxygenic chlorophototrophy in cyanobacteria and microbial eukaryotic phototrophs. 2. Anoxygenic chlorophototrophy, including cyclic photoheterotrophy and photoautotrophy using donors such as sulfide, sulfur, thiosulfate, H₂, or Fe²⁺. 3. Energy-conserving retinal phototrophy mediated by outward proton- or other ion-pumping rhodopsins. 4. Facultative phototrophy in organisms that principally use organic substrates but supplement their energy budget with light. **Do not equate with:** - **Photoautotrophy:** requires light plus autotrophic carbon fixation; it is a narrower composite phenotype. - **Photosynthesis:** in the strict definition used by Bryant and Frigaard, it includes light-powered CO₂ reduction; phototrophy need not. - **Pigmentation:** pigment presence alone does not establish energy conservation. - **Photoreception/phototaxis:** sensory rhodopsins or other photoreceptors that alter behavior without conserving photon energy should not establish this trait. - **Fluorescence or photoprotection:** light absorption without productive energy transduction is insufficient. - **Genomic potential alone:** a rhodopsin gene or photosynthesis gene cluster is evidence of candidate capacity, not necessarily an expressed phenotype. ## Candidate graph architecture The graph should have `traitmech:000037` as the phenotype endpoint and two parallel mechanistic branches. Both converge on an electrochemical gradient and/or reducing equivalents that support ATP production and growth. Oxygenic, anoxygenic, and carbon-fixing processes should be represented as conditional subgraphs rather than universal requirements. | Module | Minimal causal chain | Evidence strength | Curation status | |---|---|---|---| | Chlorophyll reaction-center phototrophy | light -> (bacterio)chlorophyll reaction center -> charge separation/electron transfer -> proton motive force -> ATP synthesis -> phototrophic energy conservation (bryant2006prokaryoticphotosynthesisand pages 2-3, bryant2006prokaryoticphotosynthesisand pages 1-2, kacar2406foundationsforreconstructing pages 15-18) | Strong review-supported core mechanism | Curate as core generalized module | | Oxygenic branch | light -> PSII/PSI-type oxygenic photosystems -> H2O oxidation -> O2 production -> electron transport -> proton motive force -> ATP/NADPH -> carbon fixation or growth support (bryant2006prokaryoticphotosynthesisand pages 1-2, kacar2406foundationsforreconstructing pages 15-18) | Strong for cyanobacterial oxygenic phototrophy; some steps review-level here | Curate as child branch; taxon-specific to oxygenic phototrophs | | Anoxygenic sulfur branch | light -> anoxygenic reaction center -> cyclic/linked electron transport -> sulfur compound oxidation (H2S/S0/thiosulfate) -> proton motive force/reducing power -> ATP + CO2 fixation or photoheterotrophic support (bryant2006prokaryoticphotosynthesisand pages 1-2, kushkevych2024anoxygenicphotosynthesiswith pages 18-18) | Strong review support; donor usage varies by lineage | Curate with uncertainty tags on donor specificity and lineage scope | | Retinal/rhodopsin branch | light -> retinal-bound microbial rhodopsin -> retinal isomerization -> proton/ion pumping -> proton motive force -> ATP synthesis -> phototrophic energy gain (bryant2006prokaryoticphotosynthesisand pages 2-3, peterson2023usinglightfor pages 1-5, davison2022engineeringarhodopsinbased pages 1-2) | Strong for proton-pumping phototrophy; direct engineering evidence for ATP-linked outcomes | Curate as core generalized module; ion specificity may need subtype nodes | | Ecological fitness branch | diurnal light-dark cycles + nutrient limitation -> facultative phototrophy deployment -> rhythmic physiology/survival advantage in stationary phase (tinguely2023diurnalcyclesdrive pages 9-10) | Moderate; direct experiment but taxon/condition specific | Curate as conditional ecology branch; mark assay- and taxon-specific | | Engineered application branch | heterologous rhodopsin + retinal + electron donor/electrode -> light-driven proton motive force -> ATP-supported CO2 fixation -> enhanced growth / photo-electrosynthesis (davison2022engineeringarhodopsinbased pages 1-2, tu2024engineeringrhodopsinbasedartificial pages 102-105) | Moderate to strong for engineered systems; not native trait evidence | Do not use as native core edge; curate separately as engineered implementation | *Table: This table summarizes the main candidate modules for a phototrophy causal graph, with minimal mechanism chains, evidence strength, and curation recommendations. It helps separate core native mechanisms from lineage-specific ecology and engineered applications.* ## Candidate nodes grouped by type ### Environmental and experimental factors - incident light / photon - wavelength or spectral quality - green light and blue light - light intensity - light–dark or diurnal cycle - nutrient limitation - anoxic or sulfidic environment - availability of H₂S, sulfur, thiosulfate, H₂, or Fe²⁺ - availability of retinal or retinal precursors - exogenous trans-retinal — assay-specific
Curation history
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PROPOSED_FROM_RESEARCH · claude
Minted intermediate axis class (phototrophy) to parent the photosynthesis and proteorhodopsin-phototrophy traits, replacing their direct attachment to METPO:1000060 (metabolism).
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CURATED_CAUSAL_GRAPH · claude
Added evidence-backed causal graph (phototrophy / light → PMF) with PATO/METPO node groundings and RO/biolink predicate groundings; promoted PROPOSED to REVIEWED.
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ENRICH_CAUSAL_GRAPH · claude
Added 7 evidence-backed generic edges (8 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 4 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×2, RO:0002213×1, RO:0002327×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:16474×1).
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0006754×1, GO:0009767×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0009523×1).
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MIGRATE_MICROBE_DOMAIN_EDGES · claude
Re-grounded 2 causal edge(s) off microbe-domain METPO predicates (2 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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REGROUND_CAUSAL_EDGE · claude
Re-grounded the edge from enables/RO:0002327 to RO:0002326 (contributes to), issue 334. biolink declares enables range 'biological process or activity' and the object is a STATE, which does not satisfy it. Unlike the tolerance/capacity nodes in this same pass, this object is a genuine state rather than a mis-typed disposition - a gradient, a community composition, an internal environment - so retyping it to TRAIT would be wrong. contributes to fits because the subject genuinely contributes to the OCCURRENCE OR GENERATION of the object, which is biolink's definition; that is the same test the motive-force edges FAILED in issue 341, where the subject powers a machine it does not generate. RO:0002326 declares no rdfs:domain or rdfs:range.
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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): photosynthetic_electron_transport is typed PATHWAY. PATHWAY is a named, conventionally enumerable multi-step route; BIOLOGICAL_PROCESS is everything else. A named route in every record that carries it, though NOT THE SAME ROUTE, which is why no single step list belongs in this rationale. metabolism/phototrophy.yaml enumerates the oxygenic form ('Electron flow from water through PSII, cytochrome b6f and PSI'); photoheterotrophic.yaml and photoorganoheterotrophic.yaml cover ANOXYGENIC phototrophy -- one reaction centre, cyclic flow, no water oxidation -- and say the neutral thing on purpose. Quoting the oxygenic steps at them would assert biology they specifically do not claim (#400 review). Both forms are named routes whose steps a curator could list, which is the test. Was 5 PATHWAY to 1 before this tranche.