Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/46012
Campo DC Valoridioma
dc.contributor.authorMioso, R.en_US
dc.contributor.authorToledo Marante, F. J.en_US
dc.contributor.authorHerrera Bravo de Laguna, I.en_US
dc.date.accessioned2018-11-23T00:37:33Z-
dc.date.available2018-11-23T00:37:33Z-
dc.date.issued2015en_US
dc.identifier.issn1364-5072en_US
dc.identifier.urihttp://hdl.handle.net/10553/46012-
dc.description.abstractThis is a comprehensive review, with 114 references, of the chemical diversity found in the fungus Penicillium roqueforti. Secondary metabolites of an alkaloidal nature are described, for example, ergot alkaloids such as festuclavine, isofumigaclavines A and B, and diketopiperazine alkaloids such as roquefortines A–D, which are derived from imidazole. Other metabolites are marcfortines A–C, PR‐toxin, eremofortines A–E, mycophenolic and penicillic acids, and some γ‐lactones. Also, recent developments related to the structural characteristics of botryodiplodin and andrastin are studied—the latter has anticancer properties. Finally, we discuss the enzymes of P. roqueforti, which can participate in the biotechnological production of high value‐added molecules, as well as the use of secondary metabolite profiles for taxonomic purposes.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Applied Microbiologyen_US
dc.sourceJournal of Applied Microbiology [ISSN 1364-5072], v. 118 (4), p. 781-791en_US
dc.subject23 Químicaen_US
dc.subject.otherBiotechnologyen_US
dc.subject.otherCell-factoryen_US
dc.subject.otherEnzymesen_US
dc.subject.otherMetabolitesen_US
dc.subject.otherPenicillium roquefortien_US
dc.titlePenicillium roqueforti: a multifunctional cell factory of high value-added moleculesen_US
dc.typeinfo:eu-repo/semantics/reviewes
dc.typeArticlees
dc.identifier.doi10.1111/jam.12706
dc.identifier.scopus84924787194
dc.identifier.scopus84924787194-
dc.identifier.isi000351392200001
dc.contributor.authorscopusid55535031500-
dc.contributor.authorscopusid6508338024-
dc.contributor.authorscopusid56442634600-
dc.description.lastpage791-
dc.identifier.issue4-
dc.description.firstpage781-
dc.relation.volume118-
dc.investigacionCienciasen_US
dc.type2Reseñaen_US
dc.contributor.daisngid2546418
dc.contributor.daisngid17875752
dc.contributor.daisngid3019866
dc.contributor.wosstandardWOS:Mioso, R
dc.contributor.wosstandardWOS:Marante, FT
dc.contributor.wosstandardWOS:de Laguna, IHB
dc.date.coverdateEnero 2015
dc.identifier.ulpgces
dc.description.sjr0,928
dc.description.jcr2,156
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0003-1369-2037-
crisitem.author.orcid0000-0002-7842-591X-
crisitem.author.fullNameMioso, Roberto-
crisitem.author.fullNameToledo Marante, Francisco Javier-
crisitem.author.fullNameHerrera Bravo De Laguna, Irma Esther-
Colección:Reseña
Vista resumida

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.