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dc.contributor.authorGiorgi, Victoria-
dc.contributor.authorBotto, Emiliana-
dc.contributor.authorFontana, Carolina-
dc.contributor.authorDella Mea, Luca-
dc.contributor.authorVaz, Silvio Jr.-
dc.contributor.authorMenéndez, Pilar-
dc.contributor.authorRodríguez, Paula-
dc.date.accessioned2023-11-21T11:56:51Z-
dc.date.available2023-11-21T11:56:51Z-
dc.date.issued2022-
dc.identifier.citationGiorgi, V, Botto, E, Fontana, C, y otros. "Enzymatic production of lauroyl and stearoyl monoesters of D-Xylose, L-Arabinose, and D-Glucose as potential lignocellulosic-derived products, and their evaluation as antimicrobial agents". Catalysts. [en línea] 2022, vol. 12, 15 h. DOI: https://doi.org/10.3390/catal12060610es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/41369-
dc.description.abstractForestry and agricultural industries constitute highly relevant economic activities globally. They generate large amounts of residues rich in lignocellulose that have the potential to be valorized and used in different industrial processes. Producing renewable fuels and high-value-added compounds from lignocellulosic biomass is a key aspect of sustainable strategies and is central to the biorefinery concept. In this study, the use of biomass-derived monosaccharides for the enzymatic synthesis of sugar fatty acid esters (SFAEs) with antimicrobial activity was investigated to valorize these agro-industrial residues. With the aim to evaluate if lignocellulosic monosaccharides could be substrates for the synthesis of SFAEs, D-xylose, L-arabinose, and D-glucose, lauroyl and stearoyl monoesters were synthetized by transesterification reactions catalyzed by Lipozyme RM IM as biocatalyst. The reactions were performed using commercial D-xylose, L-arabinose, and D-glucose separately as substrates, and a 74:13:13 mixture of these sugars. The proportion of monosaccharides in the latter mixture corresponds to the composition found in hemicellulose from sugarcane bagasse and switchgrass, as previously described in the literature. Products were characterized using nuclear magnetic resonance (NMR) spectroscopy and showed that only the primary hydroxyl group of these monosaccharides is involved in the esterification reaction. Antimicrobial activity assay using several microorganisms showed that 5-O-lauroyl-D-xylofuranose and 5-O-lauroyl-L-arabinofuranose have the ability to inhibit the growth of Gram-positive bacteria separately and in the products mix. Furthermore, 5-O-lauroyl-L-arabinofuranose was the only product that exhibited activity against Candida albicans yeast, and the four tested filamentous fungi. These results suggest that sugar fatty acid esters obtained from sustainable and renewable resources and produced by green methods are promising antimicrobial agents.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.publisherMDPIes
dc.relation.ispartofCatalysts v.12, 2022. -- 15 h.es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subject.otherHEMICELULOSAes
dc.subject.otherMONOSACARIDOSes
dc.subject.otherBIOCATALISISes
dc.subject.otherTRANSESTERIFICACIONes
dc.subject.otherESTERESes
dc.subject.otherANTIBACTERIANOSes
dc.subject.otherANTIFUNGICOSes
dc.subject.otherBIORREFINERIAes
dc.titleEnzymatic production of lauroyl and stearoyl monoesters of D-Xylose, L-Arabinose, and D-Glucose as potential lignocellulosic-derived products, and their evaluation as antimicrobial agentses
dc.typeArtículoes
dc.contributor.filiacionGiorgi Victoria, Universidad de la República (Uruguay). Facultad de Química, Departamento de Biociencias y Departamento de Química Orgánica, Laboratorio de Biocatálisis y Biotransformaciones-
dc.contributor.filiacionBotto Emiliana, Universidad de la República (Uruguay). Facultad de Química, Departamento de Biociencias y Departamento de Química Orgánica, Laboratorio de Biocatálisis y Biotransformaciones-
dc.contributor.filiacionFontana Carolina, Universidad de la República (Uruguay). Facultad de Química, CENUR Litoral Norte, Departamento de Química del Litoral, Laboratorio de Espectroscopía y Fisicoquímica Orgánica-
dc.contributor.filiacionDella Mea Luca, Universidad de la República (Uruguay). Facultad de Química, Departamento de Biociencias y Departamento de Química Orgánica, Laboratorio de Biocatálisis y Biotransformaciones-
dc.contributor.filiacionVaz Silvio Jr., Brazilian Agricultural Research Corporation, National Research Center for Agroenergy (Embrapa Agroenergy) Embrapa Agroenergia (Brasil)-
dc.contributor.filiacionMenéndez Pilar, Universidad de la República (Uruguay). Facultad de Química, Departamento de Biociencias y Departamento de Química Orgánica, Laboratorio de Biocatálisis y Biotransformaciones-
dc.contributor.filiacionRodríguez Paula, Universidad de la República (Uruguay). Facultad de Química, Departamento de Biociencias y Departamento de Química Orgánica, Laboratorio de Biocatálisis y Biotransformaciones-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doihttps://doi.org/10.3390/catal12060610-
Aparece en las colecciones: Publicaciones académicas y científicas - Facultad de Química

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