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dc.contributor.authorJaramillo, David-
dc.contributor.authorMéndez, María-
dc.contributor.authorVargas, Gabriela-
dc.contributor.authorStashenko, Elena-
dc.contributor.authorVasco Palacios, Aída Marcela-
dc.contributor.authorCeballos, Andrés-
dc.contributor.authorCaicedo, Nelson-
dc.date.accessioned2022-06-29T01:10:08Z-
dc.date.available2022-06-29T01:10:08Z-
dc.date.issued2020-
dc.identifier.citationJaramillo DA, Méndez MJ, Vargas G, Stashenko EE, Vasco-Palacios AM, Ceballos A, Caicedo NH. Biocatalytic Potential of Native Basidiomycetes from Colombia for Flavour/Aroma Production. Molecules. 2020 Sep 22;25(18):4344. doi: 10.3390/molecules25184344.spa
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/10495/29453-
dc.description.abstractABSTRACT : Aromas and flavours can be produced from fungi by either de novo synthesis or biotransformation processes. Herein, the biocatalytic potential of seven basidiomycete species from Colombia fungal strains isolated as endophytes or basidioma was evaluated. Ganoderma webenarium, Ganoderma chocoense, and Ganoderma stipitatum were the most potent strains capable of decolourizing β,β-carotene as evidence of their potential as biocatalysts for de novo aroma synthesis. Since a species’ biocatalytic potential cannot solely be determined via qualitative screening using β,β-carotene biotransformation processes, we focused on using α-pinene biotransformation with mycelium as a measure of catalytic potential. Here, two strains of Trametes elegans—namely, the endophytic (ET-06) and basidioma (EBB-046) strains—were screened. Herein, T. elegans is reported for the first time as a novel biocatalyst for the oxidation of α-pinene, with a product yield of 2.9 mg of cis-Verbenol per gram of dry weight mycelia used. The EBB-046 strain generated flavour compounds via the biotransformation of a Cape gooseberry medium and de novo synthesis in submerged cultures. Three aroma-producing compounds were identified via GC–MS—namely, methyl-3-methoxy-4H-pyran-4-one, hexahydro-3-(methylpropyl)-pyrrolo[1,2-a]pyrazine-1,4-dione, and hexahydro-3-(methylphenyl)-pyrrolo[1,2-a]pyrazine-1,4-dione.spa
dc.format.extent18spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherMDPI (Multidisciplinary Digital Publishing Institute)spa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleBiocatalytic Potential of Native Basidiomycetes from Colombia for Flavour/Aroma Productionspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupBIOMICROspa
dc.publisher.groupMicrobiología Ambientalspa
dc.identifier.doi10.3390/molecules25184344-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.citationtitleMoleculesspa
oaire.citationstartpage1spa
oaire.citationendpage18spa
oaire.citationvolume25spa
oaire.citationissue18spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeBasilea, Suizaspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsOdorantes-
dc.subject.decsOdorants-
dc.subject.decsBasidiomycota-
dc.subject.decsBioprospección-
dc.subject.decsBioprospecting-
dc.subject.proposalα-Pinenespa
dc.description.researchgroupidCOL0111863spa
dc.description.researchgroupidCOL0040189spa
dc.relation.ispartofjournalabbrevMoleculesspa
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