@article {338,
	title = {De Novo terpenoid biosynthesis by the dendronotid nudibranch Melibe leonina},
	journal = {Chemoecology},
	volume = {12},
	number = {4},
	year = {2002},
	note = {ISI Document Delivery No.: 635GATimes Cited: 6Cited Reference Count: 23},
	pages = {199-202},
	type = {Article},
	abstract = {Stable isotope feeding studies using [1,2-C-13(2)]-sodium acetate have demonstrated that 2,6-dimetbyl-5-heptenal (1), a putative defensive allomone, is made by the Dendronotid nudibranch Melibe leonina via de novo biosynthesis.},
	keywords = {biosynthesis, CADLINA-LUTEOMARGINATA, chemical, CHEMICAL DEFENSE, defense nudibranch, DORID-NUDIBRANCHS, ECOLOGY, ISOTOPE INCORPORATION EVIDENCE, OPISTHOBRANCH MOLLUSK, ORIGIN, terpenoid, TRIOPHAMINE},
	isbn = {0937-7409},
	url = {<Go to ISI>://000180389600006},
	author = {Barsby, T. and Linington, R. G. and Andersen, R. J.}
}
@article {4589,
	title = {Evidence for de novo biosynthesis of the polyketide fragment of diaulusterol a by the northeastern Pacific Dorid nudibranch Diaulula sandiegensis},
	journal = {Journal of Natural Products},
	volume = {62},
	number = {5},
	year = {1999},
	note = {ISI Document Delivery No.: 201YPTimes Cited: 2Cited Reference Count: 16},
	month = {May},
	pages = {777-779},
	type = {Article},
	abstract = {Stable isotope incorporation experiments using sodium [1,2-C-13(2)]acetate have demonstrated that the 3-hydroxybutyrate substituent of diaulusterol A (1) is biosynthesized de novo by the dorid nudibranch Diaulula sandiegensis. There was no evidence for acetate incorporation into the steroid portion of 1, nor were radiolabeled mevalonate or cholesterol incorporated.},
	keywords = {DEFENSE, ISOTOPE INCORPORATION EVIDENCE, MARINE MOLLUSKS, TRIOPHAMINE},
	isbn = {0163-3864},
	url = {<Go to ISI>://000080625100030},
	author = {Kubanek, J. and Andersen, R. J.}
}
