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Colneleic acid is an ester product. | [Definition]
ChEBI: A long-chain, divinyl ether fatty acid composed of 8-nonenoic acid having the E- hydrogen at position 9 substituted by a (1E,3Z)-nona-1,3,-dien-1-yloxy group. | [References]
[1] T GALLIARD D R P. The enzymic conversion of linoleic acid into 9-(nona-1’,3’-dienoxy)non-8-enoic acid, a novel unsaturated ether derivative isolated from homogenates of Solanum tuberosum tubers.[J]. Biochemical Journal, 1972, 129 3: 743-753. DOI: 10.1042/bj1290743
[2] P. FAHLSTADIUS M H. Stereospecific removal of the pro-R hydrogen at C-8 of (9S)-hydroperoxyoctadecadienoic acid in the biosynthesis of colneleic acid[J]. Journal of The Chemical Society-perkin Transactions 1, 1990, 883 1: 2027-2030. DOI: 10.1039/p19900002027
[3] H WEBER. Divinyl ether fatty acid synthesis in late blight-diseased potato leaves.[J]. Plant Cell, 1999, 11 3: 485-494. DOI: 10.1105/tpc.11.3.485
[4] REN WANG. A novel lipoxygenase gene from developing rice seeds confers dual position specificity and responds to wounding and insect attack.[J]. Plant Molecular Biology, 2008, 66 4: 401-414. DOI: 10.1007/s11103-007-9278-0 |
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