EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
4.2.3.18 | Picea abies | - |
bifunctional levopimaradiene/abietadiene synthase | - |
4.2.3.32 | Picea abies | Q675L4 | - |
- |
EC Number | Reaction | Comment | Organism | Reaction ID |
---|---|---|---|---|
4.2.3.18 | (+)-copalyl diphosphate = abieta-7,13-diene + diphosphate | reaction mechanism proceeds via water quenching of the abieta-8(14)-en-13-yl carbocation, resulting in 13-hydroxy-8(14)-abietene | Picea abies |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
4.2.3.18 | (+)-copalyl diphosphate | - |
Picea abies | (+-)-13-hydroxy-8(14)-abietene + diphosphate | initial product of the reaction, thermally unstable. Dehydration of the alcohol products of (+)-copalyl diphosphate, yielding the well established diterpene products levopimaradiene, abietadiene, neoabietadiene, and palustradiene, may occurr due to three conditions of the GC-MS analysis typically used for identification of diterpene synthase products: a hot injector, a hot oven temperature necessary for eluting the compounds, and the high temperature and high energy of the MS and its interface | ? | |
4.2.3.32 | (+)-copalyl-diphosphate | - |
Picea abies | 13-hydroxy-8(14)-abietene + diphosphate | the initial products formed and released in vitro are unstable alcohols identified as epimeric thermally unstable allylic tertiary alcohols, 13-hydroxy-8(14)-abietene. The dehydration of the alcohol products, yielding the well established diterpene products levopimaradiene, abietadiene, neoabietadiene, and palustradiene, occurs due to the conditions of the GC-MS analysis typically used | ? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
4.2.3.18 | PaLAS | - |
Picea abies |
4.2.3.32 | levopimaradiene/abietadiene synthase | - |
Picea abies |
4.2.3.32 | PaLAS | - |
Picea abies |