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Authordc.contributor.authorCórdova, Pamela 
Authordc.contributor.authorGonzález, Ana María 
Authordc.contributor.authorNelson, David R. 
Authordc.contributor.authorGutiérrez, María Soledad 
Authordc.contributor.authorBaeza Cancino, Marcelo 
Authordc.contributor.authorCifuentes Guzmán, Víctor 
Authordc.contributor.authorAlcaíno Gorman, Jennifer 
Admission datedc.date.accessioned2018-05-14T17:34:29Z
Available datedc.date.available2018-05-14T17:34:29Z
Publication datedc.date.issued2017
Cita de ítemdc.identifier.citationBMC Genomics (2017) 18:540es_ES
Identifierdc.identifier.other10.1186/s12864-017-3942-9
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/147726
Abstractdc.description.abstractBackground: The cytochromes P450 (P450s) are a large superfamily of heme-containing monooxygenases involved in the oxidative metabolism of an enormous diversity of substrates. These enzymes require electrons for their activity, and the electrons are supplied by NAD(P) H through a P450 electron donor system, which is generally a cytochrome P450 reductase (CPR). The yeast Xanthophyllomyces dendrorhous has evolved an exclusive P450-CPR system that specializes in the synthesis of astaxanthin, a carotenoid with commercial potential. For this reason, the aim of this work was to identify and characterize other potential P450 genes in the genome of this yeast using a bioinformatic approach. Results: Thirteen potential P450-encoding genes were identified, and the analysis of their deduced proteins allowed them to be classified in ten different families: CYP51, CYP61, CYP5139 (with three members), CYP549A, CYP5491, CYP5492 (with two members), CYP5493, CYP53, CYP5494 and CYP5495. Structural analyses of the X. dendrorhous P450 proteins showed that all of them have a predicted transmembrane region at their N-terminus and have the conserved domains characteristic of the P450s, including the heme-binding region (FxxGxRxCxG); the PER domain, with the characteristic signature for fungi (PxRW); the ExxR motif in the K-helix region and the oxygenbinding domain (OBD) (AGxDTT); also, the characteristic secondary structure elements of all the P450 proteins were identified. The possible functions of these P450s include primary, secondary and xenobiotic metabolism reactions such as sterol biosynthesis, carotenoid synthesis and aromatic compound degradation. Conclusions: The carotenogenic yeast X. dendrorhous has thirteen P450-encoding genes having potential functions in primary, secondary and xenobiotic metabolism reactions, including some genes of great interest for fatty acid hydroxylation and aromatic compound degradation. These findings established a basis for future studies about the role of P450s in the carotenogenic yeast X. dendrorhous and their potential biotechnological applications.es_ES
Patrocinadordc.description.sponsorshipFONDECYT, 1160202es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherBIOMED Central Ltd.es_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceBMC Genomicses_ES
Keywordsdc.subjectCytochrome P450es_ES
Keywordsdc.subjectXanthophyllomyces dendrorhouses_ES
Keywordsdc.subjectAstaxanthin synthasees_ES
Títulodc.titleCharacterization of the cytochrome P450 monooxygenase genes (P450ome) from the carotenogenic yeast Xanthophyllomyces dendrorhouses_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadortjnes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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