chemolithotrophic
METPO:1000639 · CLASS · REVIEWED
A trophic type characterized by the use of inorganic chemical compounds as electron donors and carbon dioxide as the primary carbon source for energy generation and biosynthesis.
Chemolithotrophic inorganic chemical oxidation
Edge evidence
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chemolithotrophic
has electron donor
inorganic chemical electron donor
METPO:2007701Inorganic chemicals serve as the electron donors for chemolithotrophy.
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DOI:10.1016/B978-0-12-378630-2.00219-Xoxidize inorganic atoms or molecules
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ammonia monooxygenase
oxidizes
ammonia
METPO:2007803Ammonia monooxygenase initiates ammonia oxidation.
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DOI:10.1146/annurev.micro.55.1.485ammonia-oxidizing bacteria
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ammonia
oxidized to
hydroxylamine
METPO:2007405Ammonia oxidation proceeds through hydroxylamine.
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DOI:10.1007/s00775-020-01820-0convert ammonia to hydroxylamine
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hydroxylamine
oxidized to
nitrite
METPO:2007405Hydroxylamine oxidation yields nitrite in ammonia oxidizers.
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DOI:10.3389/fmicb.2012.00210oxidation of hydroxylamine to nitrite
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Sox enzyme system
oxidizes
thiosulfate
METPO:2007803Sox proteins mediate oxidation of reduced sulfur compounds such as thiosulfate.
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DOI:10.1111/j.1574-6976.2009.00187.xoxidation of thiosulfate
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inorganic chemical electron donor
feeds electrons into
respiratory chain
METPO:2007402Oxidation of inorganic donors feeds electrons into respiratory chains.
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DOI:10.1016/j.bbabio.2008.09.008membrane-bound electron transport chain
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respiratory chain
has output
ATP
RO:0002234Respiratory energy conservation produces ATP.
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DOI:10.1016/j.bbabio.2008.09.008drives ATP synthesis
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Calvin-Benson-Bassham cycle
mediates fixation of
carbon dioxide
Chemolithoautotrophs fix CO2 via the Calvin-Benson-Bassham cycle.
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DOI:10.3390/microorganisms12030590
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acidification
decreases
nitrification rate
RO:0002212Environmental acidification reduces nitrification rates.
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DOI:10.1038/s41467-023-37104-9
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acidification
stimulates generation of
nitrous oxide
Acidification stimulates N2O byproduct generation during nitrification.
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DOI:10.1038/s41467-023-37104-9
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Provenance
- Source
- METPO (2025-11-25)
- Author
- Anthea Guo
- Definition source
- DOI:10.1016/B978-0-12-378630-2.00219-X
Parent traits (1)
Synonyms (1)
- chemolithotroph
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000639[-0.145, -1.567, -3.045, -0.245, …]
Nearest neighbors in embedding space
- physiology trophic type 0.677
- physiology hydrogenotrophic 0.657
- physiology carboxydotrophic 0.653
- physiology photolithoautotrophic 0.646
- physiology photoorganoheterotrophic 0.635
- physiology lithoautotrophic 0.625
- physiology chemoautotrophic 0.618
- physiology mixotrophic 0.617
Deep research
# Curation report: chemolithotrophic ## 1. Executive scope **Trait:** chemolithotrophic **Identifier:** `METPO:1000639` **Category:** PHYSIOLOGY; **term kind:** CLASS; **mapping:** REVIEWED **Parent:** `METPO:1000631` **Synonym:** chemolithotroph For this term, the defensible scope is **chemolithoautotrophy**: a cell oxidizes one or more inorganic chemical electron donors, conserves the released energy as ATP and reducing power, and uses CO2/dissolved inorganic carbon as its primary biomass-carbon source. The phenotype therefore requires both an **energy module** and an **autotrophic carbon-assimilation module**. Oxidation of an inorganic compound alone is insufficient. This interpretation agrees with contemporary descriptions of chemolithoautotrophs as organisms that use energy released by oxidation of reduced compounds to drive inorganic-carbon fixation. It also matches the supplied definition more narrowly than the broader usage of “chemolithotroph,” which can include organisms using inorganic donors but organic carbon. (laufermeiser2024oxidationofsulfur pages 1-2, bayer2024contributionofammonia pages 1-4) ### Recommended inclusion criteria Curate the trait when evidence establishes: 1. Growth or energy conservation supported by an inorganic donor such as NH3, NO2−, H2, Fe2+, H2S/HS−, S0, thiosulfate, CO, or another reduced inorganic compound. 2. CO2/HCO3−/DIC as the primary carbon source, preferably demonstrated by growth in mineral medium, isotope incorporation, or a complete and expressed fixation pathway. 3. A compatible electron acceptor and respiratory or energy-conserving mechanism. 4. Biomass production or sustained growth—not merely oxidation, detoxification, or transient maintenance. ### Boundary cases - **Chemolithoheterotrophy:** inorganic donor oxidation with organic carbon as the biomass source is outside this term. *Arcobacter peruensis* oxidizes sulfide and reduces nitrate but assimilates acetate and does not substantially fix CO2; it is therefore a strong negative-control example. (callbeck2019arcobacterperuensissp. pages 1-2) - **Mixotrophy:** simultaneous CO2 fixation and organic-carbon uptake should be represented separately or qualified as facultative/mixotrophic. In sulfur-stimulated groundwater microcosms, mixotrophs rather than strict autotrophs dominated and balanced CO2 fixation with organic-carbon uptake. (taubert2022bolsteringfitnessvia pages 1-2) - **Electroautotrophy:** direct uptake of electrode-derived electrons can support CO2 fixation, but it is mechanistically distinct because the energy input is an electrode rather than oxidation of an inorganic chemical donor. *Acidithiobacillus ferrooxidans* changes pilin, porin, EPS, and electron-transfer expression under electrode growth. (wang2024characterizethegrowth pages 22-23) - **Photolithoautotrophy:** light, rather than chemical oxidation, is the principal energy source and should be excluded. - **Methanotrophy/methylotrophy:** methane and reduced one-carbon organics are generally treated as organic substrates, not lithotrophic donors. H2-supported growth by a methanotroph may represent mixotrophic flexibility rather than the defining trait. - **Sulfur detoxification:** possession or activity of Sqr alone does not establish energy-conserving sulfur chemolithotrophy. Donor disappearance must be linked to respiration, ATP/reductant formation, CO2 fixation, and growth. - **Genomic potential alone:** donor-oxidation genes plus carbon-fixation genes are suggestive but do not prove that the modules are simultaneously functional. ## 2. Candidate nodes Only identifiers that can be used with high confidence are given below. Nodes whose exact database accession depends on protonation state, species, enzyme family, or taxonomic context should remain **label-only pending ontology lookup** rather than receive a guessed CURIE. ### Trait and biological-process nodes - chemolithotrophic — `METPO:1000639` - Calvin–Benson–Bassham cycle — `GO:0019253` - proton transmembrane transport — `GO:0015992` - ATP synthesis coupled to proton transport — use the appropriate GO child after confirming cellular context - reductive TCA cycle — label only pending exact pathway grounding - 3-hydroxypropionate/4-hydroxybutyrate cycle — label only pending exact pathway grounding - Wood–Ljungdahl pathway, 3-hydroxypropionate bicycle, dicarboxylate/4-hydroxybutyrate cycle — optional taxon-specific alternatives; do not imply that every chemolithotroph uses the CBB cycle - phosphoglycolate salvage; glycerate pathway; malate cycle — label-only maintenance modules ### Chemicals and environmental factors **Electron donors:** ammonia, nitrite, molecular hydrogen, ferrous iron, hydrogen sulfide/sulfide, elemental sulfur, thiosulfate, carbon monoxide, and potentially other reduced inorganic species. Preserve chemical state explicitly—for example, NH3 rather than NH4+ for AMO substrate and Fe2+ rather than generic “iron.” The 2023 AOA review states that NH3, not NH4+, is the AMO substrate. (wright2023nitrificationandbeyond pages 1-2) **Carbon source:** carbon dioxide — `CHEBI:16526`; bicarbonate/DIC may be included as experimentally supplied inorganic-carbon forms. **Electron acceptors:** oxygen, nitrate, and—in taxon-specific anaerobic systems—Fe3+. Hydrogen-grown *A. ferrooxidans* can transfer electrons to O2 aerobically or Fe3+ anaerobically. (kucera2020amodelof pages 1-2, kucera2020amodelof pages 4-8) **Energy/redox products:** ATP — `CHEBI:15422`; NADH — `CHEBI:57540`; NADPH; proton motive force; quinone/quinol pools. **Environmental nodes:** oxic, microoxic, and anoxic conditions; low pH; hydrothermal vent mixing zone; aphotic/dark ocean; groundwater; sulfide–nitrate redoxcline; bioleaching reactor; donor concentration; CO2 availability; temperature and salinity.
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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ADDED_CAUSAL_GRAPH · codex
Added DOI-backed causal graph for inorganic chemical electron donors, ammonia oxidation, sulfur oxidation, respiratory energy conservation, and ATP synthesis.
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ADDED_ORGANISM_EXAMPLE · claude
Added Nitrosomonas europaea organism example with PMID-backed evidence.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 4 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000016×2, METPO:2000009×1, METPO:2000202×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007405×2, METPO:2007402×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0022904×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A059V4Z9×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:33542×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:15429×1).
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FIX_NODE_GROUNDING_CURIE · claude
Overwrote 1 causal-node grounding(s) to corrected CURIEs (phase-2 id-label fix; verified vs OAK).
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ENRICH_CAUSAL_GRAPH · claude
Added 3 evidence-backed generic edges (5 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:17045×1).
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RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 1 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0018597×1).
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REVERSE_CAUSAL_EDGE_DIRECTION · claude
Reversed 1 causal edge from <trait> uses electron donor <chemical> to <chemical> enables <trait> (predicate_id METPO:2000009 -> RO:0002327), issue 295. METPO:2000009 is rdfs:subPropertyOf METPO:2000001, whose rdfs:domain is METPO:1000525 (microbe), so the trait-subject form entailed that this TRAIT node is a microbe; CausalNodeTypeEnum has no organism member, so no causal-graph edge can satisfy that domain. Evidence unchanged; only subject/predicate/object/predicate_id and the edge description moved. Note RO:0002327 has range 'biological process or activity', so the new form is not fully range-correct either - tracked in issue 302.
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MIGRATE_ENABLES_TRAIT_EDGES · claude
Migrated 1 causal edge(s) off enables/RO:0002327 with a TRAIT object (1 to has electron donor), 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. 1 electron edge(s) were also reversed back to trait -> chemical, restoring the donor/acceptor role that PR 300 collapsed onto enables (issue 303); the organism-subject problem that forced that collapse does not arise here because these predicates take a causal-node domain rather than METPO:2000001's microbe domain (issue 301).
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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 2 causal edge(s) off microbe-domain METPO predicates onto their causal-graph counterparts (2 to oxidizes), 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.