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Studies on the biosynthesis of cordycepin
dc.contributor.authorKredich, Nicholas M.en_US
dc.contributor.authorGuarino, Armand J.en_US
dc.date.accessioned2006-04-13T14:58:10Z
dc.date.available2006-04-13T14:58:10Z
dc.date.issued1961-03-04en_US
dc.identifier.citationKredich, Nicholas M., Guarino, Armand J. (1961/03/04)."Studies on the biosynthesis of cordycepin." Biochimica et Biophysica Acta 47(3): 529-534. <http://hdl.handle.net/2027.42/32376>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B73G9-47FWDH2-88/2/15425d798efdff9f9f1f4d6b83424047en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32376
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=13754189&dopt=citationen_US
dc.description.abstractThe carboxyl carbons of acetate and isovalerate do not serve to any appreciable extent as precursors of cordycepin, thus arguing against the origin of cordycepose from pathways of isoprenoid biosynthesis. Exogenously added [8-14C]adenine, [I-14C]-glucose, and [6-14C]glucose serve as excellent precursors, the latter two compounds labeling both the base and sugar of the nucleoside. [6-14C]glucose labels cordycepose better than [I-14C]glucose, thereby indicating a loss of carbon atom number one of the glucose molecule in cordycepose synthesis.en_US
dc.format.extent368401 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleStudies on the biosynthesis of cordycepinen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich., U.S.A.en_US
dc.contributor.affiliationumThe Department of Biological Chemistry, The University of Michigan, Ann Arbor, Mich., U.S.A.en_US
dc.identifier.pmid13754189en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32376/1/0000451.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-3002(61)90546-7en_US
dc.identifier.sourceBiochimica et Biophysica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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