Function
Locations
First committed acylation of the glycerol backbone at sn-1, initiating de novo glycerolipid assembly on the ER.
A taxon-neutral decomposition of plant seed storage-oil (triacylglycerol, TAG) assembly as a recursively decomposable module. In developing oilseeds, acyl groups (produced by plastidial fatty acid synthesis and activated as acyl-CoA) are assembled onto a glycerol backbone at the endoplasmic reticulum by the glycerol-phosphate (Kennedy) pathway and packaged into cytosolic oil bodies (lipid droplets) stabilized by oleosins. The module separates (1) acylation of glycerol-3-phosphate to lysophosphatidic acid (GPAT), (2) acylation of LPA to phosphatidic acid (LPAAT), (3) dephosphorylation of PA to diacylglycerol (PAP), (4) the final acyl transfer to DAG forming TAG by two alternative routes - acyl-CoA-dependent (DGAT1/DGAT2) and acyl-CoA-independent (PDAT, using phospholipid acyl donors) - and (5) oil-body biogenesis and oleosin stabilization. It is phrased as functions and pathway segments rather than a fixed gene list so it can represent Arabidopsis and crop oilseeds (soybean, rapeseed/canola, oil palm, camelina); concrete UniProt members are Arabidopsis exemplars, not species-restricting claims. Plastidial de novo fatty acid synthesis, acyl-chain desaturation/modification, and TAG catabolism (lipolysis/beta-oxidation) are upstream/downstream and out of scope. As a bioenergy module, total TAG flux (DGAT/PDAT capacity), the acyl-CoA pool, and oil-body number/size (oleosin dosage) are the principal engineering levers for raising seed-oil yield for biodiesel and oleochemical feedstocks.
Identifiers are grounded only where verified against the local GO term cache or UniProt; descriptors without a `term` (e.g. acyl-CoA donor, glycerolipid intermediates) are deliberate rather than oversights. The final TAG step is represented as a variant set because plants use two mechanistically distinct routes - acyl-CoA-dependent DGAT1/DGAT2 and acyl-CoA-independent PDAT1 - that are genetically redundant in Arabidopsis (dgat1 pdat1 double mutants are pollen/seed lethal for oil). Some DAG can also be recruited from the phosphatidylcholine acyl-editing pool rather than solely de novo PAP output; that acyl-editing cycle is acknowledged but not expanded here. Representative UniProt members are concrete Arabidopsis exemplars for orientation, not exhaustive or species-restricting; crop oilseeds use orthologous machinery.
All recommended fields populated.
✗ none found
No MODULE:plant_seed_triacylglycerol_biosynthesis deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
✓ every PRECEDES step chains, or its break is acknowledged via chaining_status.
1 complete review(s) · 1 with deep research · 8 missing review · 0 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| DGAT1 Q9SLD2 | ✓ | ✓ | ✓ |
| Soybean DGAT1B (GmDGAT1B) I1MSF2 | ✗ | — | — |
| Soybean DGAT2D (GmDGAT2D) K7K424 | ✗ | — | — |
| Arabidopsis OLEO2 (oleosin 21.2 kDa) Q39165 | ✗ | — | — |
| Arabidopsis GPAT9 Q8GWG0 | ✗ | — | — |
| Arabidopsis LPAT2 Q8LG50 | ✗ | — | — |
| Arabidopsis DGAT2 Q9ASU1 | ✗ | — | — |
| Arabidopsis PDAT1 Q9FNA9 | ✗ | — | — |
| Arabidopsis PAH1 Q9SF47 | ✗ | — | — |
First committed acylation of the glycerol backbone at sn-1, initiating de novo glycerolipid assembly on the ER.
sn-2 acylation completing phosphatidic acid, the branch point to both storage (TAG) and membrane (phospholipid) glycerolipids.
Generates the diacylglycerol acceptor consumed by the final TAG- forming acyltransferases.
The committed, oil-defining step. Plants use two mechanistically distinct and genetically redundant routes to acylate DAG at sn-3.
Uses acyl-CoA as the sn-3 acyl donor; DGAT1 carries most bulk TAG flux and is the primary seed-oil-yield engineering target.
Transfers an acyl group from the sn-2 of a phospholipid to DAG without acyl-CoA; redundant with DGAT1 and jointly essential for seed/pollen oil.
TAG accumulates between the ER bilayer leaflets and buds into cytosolic oil bodies bounded by a phospholipid monolayer studded with oleosins, which set droplet size and prevent coalescence - critical for desiccation tolerance and for oil recovery from the seed.
Coats the oil body, controlling droplet size and stability; oleosin dosage tunes oil-body number and total oil packaging capacity.