New insight into marine alkaloid metabolic pathways: revisiting oroidin biosynthesis.

DSpace/Manakin Repository

Search OPUS


Advanced Search

Browse

My Account

Show simple item record

dc.contributor.author Genta-Jouve, G
dc.contributor.author Cachet, N
dc.contributor.author Holderith, S
dc.contributor.author Oberhänsli, F
dc.contributor.author Teyssié, JL
dc.contributor.author Jeffree, R
dc.contributor.author Al Mourabit, A
dc.contributor.author Thomas, OP
dc.date.accessioned 2012-10-12T03:33:03Z
dc.date.issued 2011-10
dc.identifier.citation Chembiochem : a European journal of chemical biology, 2011, 12 (15), pp. 2298 - 2301
dc.identifier.issn 1439-4227
dc.identifier.other C1UNSUBMIT en_US
dc.identifier.uri http://hdl.handle.net/10453/18024
dc.description.abstract Sponge natural product biosynthesis: A highly sensitive in vivo protocol based on (14)C radiolabeled precursors and beta-imager autoradiography allowed the unraveling of the origin of the pyrrole 2-aminoimidazole-containing key biosynthetic intermediate oroidin. Proline and lysine are now proposed as the early precursors of the pyrrole and the 2-aminoimidazole moieties of oroidin respectively.
dc.format Print-Electronic
dc.language eng
dc.relation.isbasedon 10.1002/cbic.201100449
dc.title New insight into marine alkaloid metabolic pathways: revisiting oroidin biosynthesis.
dc.type Journal Article
dc.parent Chembiochem : a European journal of chemical biology
dc.journal.volume 15
dc.journal.volume 12
dc.journal.number 15 en_US
dc.publocation United Kingdom en_US
dc.identifier.startpage 2298 en_US
dc.identifier.endpage 2301 en_US
dc.cauo.name SCI.Faculty of Science en_US
dc.conference Verified OK en_US
dc.for 0601 Biochemistry and Cell Biology
dc.for 0304 Medicinal and Biomolecular Chemistry
dc.personcode 110409
dc.percentage 50 en_US
dc.classification.name Medicinal and Biomolecular Chemistry en_US
dc.classification.type FOR-08 en_US
dc.edition en_US
dc.custom en_US
dc.date.activity en_US
dc.location.activity en_US
dc.description.keywords alkaloids;autoradiography;biosynthesis;feeding experiments;marine sponges en_US
dc.description.keywords Network reliability, Multi-state node acyclic network (AMIN), Hybrid quasi monte carlo method, Minimal tree/cut
dc.description.keywords Animals
dc.description.keywords Axinella
dc.description.keywords Alkaloids
dc.description.keywords Imidazoles
dc.description.keywords Pyrroles
dc.description.keywords Lysine
dc.description.keywords Proline
dc.description.keywords Metabolic Networks and Pathways
dc.description.keywords Animals
dc.description.keywords Axinella
dc.description.keywords Imidazoles
dc.description.keywords Pyrroles
dc.description.keywords Alkaloids
dc.description.keywords Lysine
dc.description.keywords Proline
dc.description.keywords Metabolic Networks and Pathways
dc.description.keywords Animals
dc.description.keywords Axinella
dc.description.keywords Imidazoles
dc.description.keywords Pyrroles
dc.description.keywords Alkaloids
dc.description.keywords Lysine
dc.description.keywords Proline
dc.description.keywords Metabolic Networks and Pathways
pubs.embargo.period Not known
pubs.organisational-group /University of Technology Sydney
pubs.organisational-group /University of Technology Sydney/Faculty of Science


Files in this item

This item appears in the following Collection(s)

Show simple item record