@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.}
}
