| EC |
1.14.19.14 |
| Accepted name: |
linoleoyl-lipid Δ9 conjugase |
| Reaction: |
a linoleoyl-[glycerolipid] + reduced acceptor + O2 = an (8E,10E,12Z)-octadeca-8,10,12-trienoyl-[glycerolipid] + acceptor + 2 H2O |
| Glossary: |
calendate = (8E,10E,12Z)-octadeca-8,10,12-trienoate |
| Systematic name: |
linoleoyl-lipid,reduced acceptor:oxygen 8,11-allylic oxidase (8E,10E-forming) |
| Comments: |
The enzyme, characterized from the plant Calendula officinalis, converts a single cis double bond at position 9 of fatty acids incorporated into glycerolipids into two conjugated trans double bonds at positions 8 and 10. |
| Links to other databases: |
BRENDA, EXPASY, KEGG, MetaCyc |
| References: |
| 1. |
Qiu, X., Reed, D.W., Hong, H., MacKenzie, S.L. and Covello, P.S. Identification and analysis of a gene from Calendula officinalis encoding a fatty acid conjugase. Plant Physiol. 125 (2001) 847–855. [PMID: 11161042] |
| 2. |
Cahoon, E.B., Ripp, K.G., Hall, S.E. and Kinney, A.J. Formation of conjugated Δ8,Δ10-double bonds by Δ12-oleic-acid desaturase-related enzymes: biosynthetic origin of calendic acid. J. Biol. Chem. 276 (2001) 2637–2643. [DOI] [PMID: 11067856] |
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| [EC 1.14.19.14 created 2015] |
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