Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 3-Buten-1-ol | HCID 69389 | — |
| Reactant | acetyl CoA | HCID 444493 | — |
| Reactant | Malonyl CoA | HCID 644066 | — |
| Reactant | Penta-2,4-dienoate | HCID 73155734 | — |
| Product | HCID 86661434 | HCID 86661434 | — |
Reaction Steps
Pathways to 3-butene-1-ol, butadiene and 2,4-pentadienoate from malonyl-CoA and acetyl-CoA are shown in FIG. 21. In these pathways, malonyl-CoA and acetyl-CoA are joined by a thiolase to form 3-oxoglutaryl-CoA. This intermediate can then be converted to 3,5-dihydroxypentanoate by several alternate routes (Steps B/C/D, Steps B/G, Steps H/I/J, Steps H/L/D, K/J). Once formed, 3,5-dihydroxypentanoate can be decarboxylated by a 3-hydroxyacid decarboxylase to form 3-butene-1-ol (Step M). Subsequent dehydration by a 3-butene-1-ol dehydrogenase or a chemical catalyst yields butadiene (Step O). Alternately, 3,5-dihydroxypentanoate can be dehydrated to 5-hydroxypent-2-enoate as shown in Step E. This intermediate can then be decarboxylated to 3-butene-1-ol (Step N) or further dehydrated to 2,4-pentadienoate (Step F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08715957B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-6c55b5697992423b96a698721edb17eb |
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| Source note | uspto-grants-2014_05 |
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