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Resumen
The study involves the use of commercial cellulase Cellic CTec2 in combination with two in-house xylanases, PxXyn10A (XynA), a recombinant purified enzyme from Paenibacillus xylanivorans A59, and a xylanase enzymatic extract from native Moesziomyces aphidis PYCC 5535T (MaPYCC 5535T), for the enzymatic hydrolysis of pretreated blue agave bagasse (BAB) at the high solids load of 20% (w/v). Three different combinations of cellulase and xylanases were [ver mas...]
dc.contributor.authorMontiel, Carmina
dc.contributor.authorHernández-Meléndez, Oscar
dc.contributor.authorMarques, Susana
dc.contributor.authorGírio, Francisco
dc.contributor.authorTavares, João
dc.contributor.authorOntañon, Ornella Mailen
dc.contributor.authorCampos, Eleonora
dc.contributor.authorBárzana, Eduardo
dc.date.accessioned2024-08-22T09:58:05Z
dc.date.available2024-08-22T09:58:05Z
dc.date.issued2024-08
dc.identifier.issn2071-1050
dc.identifier.otherhttps://doi.org/10.3390/su16166722
dc.identifier.urihttp://hdl.handle.net/20.500.12123/19057
dc.identifier.urihttps://www.mdpi.com/2071-1050/16/16/6722
dc.description.abstractThe study involves the use of commercial cellulase Cellic CTec2 in combination with two in-house xylanases, PxXyn10A (XynA), a recombinant purified enzyme from Paenibacillus xylanivorans A59, and a xylanase enzymatic extract from native Moesziomyces aphidis PYCC 5535T (MaPYCC 5535T), for the enzymatic hydrolysis of pretreated blue agave bagasse (BAB) at the high solids load of 20% (w/v). Three different combinations of cellulase and xylanases were evaluated. When Cellic® CTec2 was used at a dosage of 10 FPU/g oven-dried solids (ODS) supplemented with XynA or MaPYCC 5535T at an endo-xylanase dosage of 100 U/g ODS, increases in the xylose yield of 30% and 33%, respectively, were obtained. When applying in-house xylanases alone (at an endo-xylanase dosage of 100 U/g ODS), xylan in BAB was selectively hydrolyzed into xylose with 5% yield with MaPYCC 5535T, while no xylose was detected with XynA. Interestingly, a synergic effect of Cellic® CTec 2 with both xylanases was observed when using a low dosage of 1 FPU/g ODS (allowing for some liquefaction of the reaction mixture), promoting xylose and glucose release by either xylanase. A higher concentration of monomeric sugars was obtained with 10 FPU/g ODS of Cellic® Ctec 2 supplemented with 100 U/g ODS of MaPYCC 5535T, followed by XynA. The improvement in saccharification through the synergistic combination of in-house xylanases and commercial cellulases allows for the obtention of sugar-rich hydrolysates, which enhances the technical sustainability of the process. Hydrolysates were then fermented using recombinant Cellux 4TM yeast to yield 45 g/L ethanol, representing an increase of about 30% with respect to the control obtained with only the commercial cellulase cocktail. The surface modification of agave biomass with the different combinations of enzymes was evidenced by scanning electron microscopy (SEM).eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherMDPIes_AR
dc.rightsinfo:eu-repo/semantics/openAccesses_AR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/es_AR
dc.sourceSustainability 16 (16) : 6722 (Agosto 2024)es_AR
dc.subjectAgavees_AR
dc.subjectEnzymatic Hydrolysiseng
dc.subjectHidrólisis Enzimáticaes_AR
dc.subjectFermentationeng
dc.subjectFermentaciónes_AR
dc.subjectCellulaseeng
dc.subjectCelulasaes_AR
dc.subjectBioethanoleng
dc.subjectBioetanoles_AR
dc.subject.otherXylanase Enzymaticeng
dc.subject.otherXilanasa Enzimáticaes_AR
dc.titleApplication of In-house xylanases as an addition to a commercial cellulase cocktail for the sustainable saccharification of pretreated blue agave bagasse used for bioethanol productiones_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)es_AR
dc.description.origenInstituto de Biotecnologíaes_AR
dc.description.filFil: Montiel, Carmina. Universidad Nacional Autónoma de México. Facultad de Química. Departamento de Alimentos y Biotecnología; Méxicoes_AR
dc.description.filFil: Hernández-Meléndez, Oscar. Universidad Nacional Autónoma de México. Facultad de Química. Departamento de Ingeniería Química; Méxicoes_AR
dc.description.filFil: Marques, Susana. Laboratório Nacional de Energia e Geologia. Unidade de Bioenergia e Biorrefinarias; Portugales_AR
dc.description.filFil: Gírio, Francisco. Laboratório Nacional de Energia e Geologia. Unidade de Bioenergia e Biorrefinarias; Portugales_AR
dc.description.filFil: Tavares, João. Laboratório Nacional de Energia e Geologia. Unidade de Bioenergia e Biorrefinarias; Portugales_AR
dc.description.filFil: Ontañon, Ornella Mailen. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Agrobiotecnología y Biología Molecular; Argentinaes_AR
dc.description.filFil: Ontañon, Ornella Mailen. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Campos, Eleonora. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Agrobiotecnología y Biología Molecular; Argentinaes_AR
dc.description.filFil: Campos, Eleonora. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Bárzana, Eduardo. Universidad Nacional Autónoma de México. Facultad de Química. Departamento de Alimentos y Biotecnología; Méxicoes_AR
dc.subtypecientifico


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