photosynthesis
traitmech:000038 · CLASS · REVIEWED
A phototrophic metabolism that uses light energy and chlorophyll- or bacteriochlorophyll-based photochemical reaction centers to drive electron flow, fixing CO2 and/or generating reducing power. Subdivided into oxygenic and anoxygenic photosynthesis.
Chlorophyll-based photosynthesis drives electron flow and CO2 fixation
Edge evidence
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photosynthesis
confers
photosynthesis
METPO:2007700Reaction-center photochemistry underlies the photosynthetic trait.
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DOI:10.1016/j.tim.2006.09.001
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photosynthesis
contributes to
carbon fixation
RO:0002326Photosynthetic electron flow powers autotrophic CO2 fixation.
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DOI:10.1146/annurev-earth-060313-054810
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light energy
enables
light harvesting / excitation transfer
RO:0002327Light energy drives pigment absorption and excitation transfer to reaction-center antennae.
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DOI:10.1111/1751-7915.14519
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light harvesting / excitation transfer
initiates
reaction-center charge separation
Transferred excitation energy drives primary charge separation at the reaction-center special pair.
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DOI:10.3390/biom14030311
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reaction-center charge separation
powers
photosynthetic electron transport
Reaction-center charge separation drives photosynthetic electron transport (linear or cyclic).
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DOI:10.3390/biom14030311
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photosynthetic electron transport
generates
transmembrane electrochemical proton gradient
biolink:producesPhotosynthetic electron transport establishes a transmembrane electrochemical proton gradient.
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DOI:10.3390/biom14030311
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transmembrane electrochemical proton gradient
drives
ATP synthesis
The proton motive force is used to drive chemiosmotic ATP synthesis.
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DOI:10.3390/biom14030311
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photosynthesis
has output
reducing power (NAD(P)H)
RO:0002234Light-dependent reactions generate ATP and NAD(P)H reducing power.
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DOI:10.5287/ora-8jgz2nrvd
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reducing power (NAD(P)H)
used in
carbon fixation
NADPH reducing power supplies electrons for autotrophic CO2 fixation.
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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)
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 phototrophy 1.000
- metabolism oxygenic photosynthesis 1.000
Deep research
# Curation report: microbial photosynthesis (`traitmech:000038`) ## Executive scope **Recommended interpretation.** `traitmech:000038` should represent the cellular capacity for **chlorophyll- or bacteriochlorophyll-based reaction-center photochemistry**: antenna pigments absorb light, excitation reaches a type I or type II reaction center, charge separation initiates electron transport, and membrane bioenergetics produces reducing power and/or ATP. It encompasses **oxygenic photosynthesis** and **anoxygenic photosynthesis**, including photoautotrophic and photoheterotrophic implementations. Type I and type II reaction centers occur in multiple bacterial lineages, whereas cyanobacteria couple heterodimeric PSI and PSII for oxygenic photosynthesis. (martin2018aphysiologicalperspective pages 2-3) **Important separation of modules.** Photosynthesis supplies photochemical energy and electrons, but it does not necessarily imply CO2 fixation. Aerobic anoxygenic phototrophs can be photoheterotrophs, while carbon-fixing phototrophs use lineage-dependent pathways, including the Calvin–Benson–Bassham (CBB) or reverse TCA cycles. Green sulfur bacteria, for example, assimilate CO2 through reverse TCA, whereas oxygenic phototrophs commonly use CBB. (tomasch2024aphotoheterotrophicbacterium pages 1-2, kushkevych2024anoxygenicphotosynthesiswith pages 1-2, li2021exogenouselectricityflowing pages 1-6) ### Boundary cases Include: - Cyanobacterial oxygenic photosynthesis using PSII and PSI. - Anoxygenic reaction-center phototrophy driven by bacteriochlorophyll. - Cyclic anoxygenic electron transport that generates proton motive force and ATP even when carbon fixation is absent. - Photoheterotrophic reaction-center activity. Exclude or model separately: - **Rhodopsin-based phototrophy**, because it uses retinal proton/ion pumps rather than chlorophyll reaction centers and charge-separated electron-transfer chains. - Chlorophyll or bacteriochlorophyll biosynthesis alone; pigment production is neither sufficient evidence of an assembled functional reaction center nor of photosynthetic growth. - CO2 fixation alone, which can be chemolithoautotrophic. - Phototaxis, fluorescence, light sensing, or photoprotection without reaction-center electron transport. - Artificial illumination and exogenous-electron inputs as defining components of the natural trait; these are experimental modifiers. A practical positive assay should demonstrate at least one of: light-dependent reaction-center charge separation/electron transport, oxygen evolution, photophosphorylation, light-dependent growth dependent on a reaction center, or a functional reaction-center spectroscopic signature. Genomic photosynthesis-gene clusters are useful predictions but should remain genotype-level evidence until function is shown. ## Candidate graph architecture A single linear graph would incorrectly imply that all phototrophs use PSII, water, oxygen evolution, PSI, and CBB. The YAML should therefore have a conserved upstream core followed by explicit **oxygenic** and **anoxygenic** branches: 1. light → antenna excitation → reaction-center excitation → charge separation; 2. oxygenic branch: PSII/water → quinone → cytochrome b6f → PSI → ferredoxin/NADPH, coupled to proton motive force and ATP synthesis; 3. anoxygenic branch: external donor and/or cyclic flow → type I or II reaction center → quinone/cytochrome or ferredoxin pathways → proton motive force/reducing power; 4. optional downstream carbon-fixation modules, linked conditionally rather than made definitional. ## Candidate nodes ### Trait and processes - photosynthesis — `traitmech:000038` - parent trait — `traitmech:000037` - photosynthesis — `GO:0015979` - light reaction of photosynthesis — `GO:0019684` - photosynthetic electron transport chain — label candidate; verify the desired GO child term for each branch - photosynthetic electron transport in photosystem II — `GO:0009772` - photosynthetic electron transport in photosystem I — `GO:0009773` - carbon fixation — `GO:0015977` - Calvin–Benson–Bassham cycle — label candidate - reverse tricarboxylic-acid cycle — label candidate - cyclic photosynthetic electron transport — label candidate - oxygenic photosynthesis; anoxygenic photosynthesis — retain as branch labels unless project-approved ontology terms are confirmed ### Complexes, proteins, and cofactors - photosystem II; photosystem I - PSII oxygen-evolving complex / Mn4CaO5 cluster - P680; D1 protein/PsbA; D2/PsbD; redox-active TyrZ (D1-Y161) - QA and QB plastoquinone sites - cytochrome b6f complex
Curation history
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PROPOSED_FROM_RESEARCH · claude
Minted intermediate axis class (photosynthesis) under phototrophy to parent the oxygenic- and anoxygenic-photosynthesis traits.
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CURATED_CAUSAL_GRAPH · claude
Added evidence-backed causal graph (reaction-center photosynthesis / CO2 fixation) with GO node groundings and RO predicate groundings; promoted PROPOSED to REVIEWED.
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ENRICH_CAUSAL_GRAPH · claude
Added 7 evidence-backed generic edges (7 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, biolink:produces×1, METPO:2000202×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0006754×1).
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MIGRATE_ENABLES_TRAIT_EDGES · claude
Migrated 1 causal edge(s) off enables/RO:0002327 with a TRAIT object (1 to confers), issue 302. RO:0002327 has range 'biological process or activity', which a trait (a disposition) cannot satisfy, so the previous form entailed trait is-a BiologicalProcessOrActivity. The replacements are proposed in proposals/metpo_traitmech_v8 and are placeholder ids until METPO mints them.
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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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NORMALISE_NODE_TYPE · claude
Normalised causal-node type(s) so one node_id means one thing corpus-wide (issue 356): reducing_power: CHEMICAL -> CAPACITY. The schema's OWN example of CAPACITY: 'an electron-donating pool, ATP charge, or other reservoir-of-X notion ... Examples include reducing power (NADH/NADPH pool)'. The lone CHEMICAL occurrence (metabolism/photosynthesis.yaml) describes 'NADPH/NAD(P)H reducing equivalents', i.e. the pool, not a single species -- which is the very distinction CAPACITY exists to draw, and the one docs/CURATION_PLAYBOOK.md records as the reservoir sense that must NOT be retyped to TRAIT (#352).