Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1.
- Autores
- Conde Molina, Debora; Sanchez Hulmedilla, Betiana; Bogao, Guillermina; Tubio, Gisela; Corbino, Graciela
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión borrador
- Descripción
- The development of bioprocesses using agro-industrial waste is one of the most interesting challenges in biotechnology today, as it leads to the reuse of waste in an environmentally responsible way and the development of high value-added products. In the San Pedro region, sweet potato production generates considerable volumes of waste, as approximately 40% of the total production is discarded because it does not meet the requirements for commercialisation. In this study, the ability of the strain Cellulosimicrobium sp. CO1A1 to produce xylanases in a medium formulated with sweet potato root residues was evaluated; xylanase being an enzyme of great industrial application. Cellulosimicrobium sp. CO1A1 was grown in minimal saline medium containing 5 % (w/v) sweet potato root extract, at 135 rpm and 25 °C. Xylanase activity was determined using beech xylan (1%) as substrate at 50 ºC, reducing sugars released were determined by the Nelson-Somogyi method. Several assays were performed in order to evaluate xylanase activity, such as the analysis of cell fractions (supernatant -extracellular activity-, cell pellet -cell-associated activity- and cell homogenate -intracellular activity-); culture samples taken at 2, 5 and 7 days of incubation; and media formulated with different sweet potato varieties (Arapey, Beauregard, Covington, Selecta, Morada, Boni). In addition, the xylanase reaction was carried out in two buffer conditions, sodium citrate (50 mM, pH 5.2) and sodium phosphate (50 mM, pH 6.8). The results showed that although Cellulosimicrobium sp. CO1A1 showed growth in the medium formulated with sweet potato root, thus proving that it has the ability to use sweet potato root as a carbon source, it did not show the ability to produce xylanases under the conditions tested, unlike other strains of the genus Cellulosimicrobium reported.
Fil: Conde Molina, Debora. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.
Fil: Sanchez Hulmedilla, Betiana.Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.
Fil: Bogao, Guillermina. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.
Fil: Tubio, Gisela. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina.
Fil: Corbino, Graciela. Instituto Nacional de Tecnología Agropecuaria. Estación Experimental Agropecuaria San Pedro; Argentina. - Materia
-
Facultad Regional Delta
UTN
Sweet potato residues
Xylanases
Cellulosimicrobium sp. - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- 2022-12-29T20:36:02Z
- Repositorio
.jpg)
- Institución
- Universidad Tecnológica Nacional
- OAI Identificador
- oai:ria.utn.edu.ar:20.500.12272/7470
Ver los metadatos del registro completo
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Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1.Conde Molina, DeboraSanchez Hulmedilla, BetianaBogao, GuillerminaTubio, GiselaCorbino, GracielaFacultad Regional DeltaUTNSweet potato residuesXylanasesCellulosimicrobium sp.The development of bioprocesses using agro-industrial waste is one of the most interesting challenges in biotechnology today, as it leads to the reuse of waste in an environmentally responsible way and the development of high value-added products. In the San Pedro region, sweet potato production generates considerable volumes of waste, as approximately 40% of the total production is discarded because it does not meet the requirements for commercialisation. In this study, the ability of the strain Cellulosimicrobium sp. CO1A1 to produce xylanases in a medium formulated with sweet potato root residues was evaluated; xylanase being an enzyme of great industrial application. Cellulosimicrobium sp. CO1A1 was grown in minimal saline medium containing 5 % (w/v) sweet potato root extract, at 135 rpm and 25 °C. Xylanase activity was determined using beech xylan (1%) as substrate at 50 ºC, reducing sugars released were determined by the Nelson-Somogyi method. Several assays were performed in order to evaluate xylanase activity, such as the analysis of cell fractions (supernatant -extracellular activity-, cell pellet -cell-associated activity- and cell homogenate -intracellular activity-); culture samples taken at 2, 5 and 7 days of incubation; and media formulated with different sweet potato varieties (Arapey, Beauregard, Covington, Selecta, Morada, Boni). In addition, the xylanase reaction was carried out in two buffer conditions, sodium citrate (50 mM, pH 5.2) and sodium phosphate (50 mM, pH 6.8). The results showed that although Cellulosimicrobium sp. CO1A1 showed growth in the medium formulated with sweet potato root, thus proving that it has the ability to use sweet potato root as a carbon source, it did not show the ability to produce xylanases under the conditions tested, unlike other strains of the genus Cellulosimicrobium reported.Fil: Conde Molina, Debora. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.Fil: Sanchez Hulmedilla, Betiana.Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.Fil: Bogao, Guillermina. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina.Fil: Tubio, Gisela. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina.Fil: Corbino, Graciela. Instituto Nacional de Tecnología Agropecuaria. Estación Experimental Agropecuaria San Pedro; Argentina.UTN Facultad Regional San Francisco2022-12-29T20:36:02Z2022-12-29T20:36:02Z2022-08info:eu-repo/semantics/conferenceObjectinfo:eu-repo/semantics/drafthttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciapdfapplication/pdfSánchez Holmedilla B., Bogao G., Tubio G., Corbino G., Conde Molina D. Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. Jornadas de Ciencia y Tecnología. Córdoba, Argentina.http://hdl.handle.net/20.500.12272/7470enginfo:eu-repo/semantics/openAccess2022-12-29T20:36:02Zhttp://creativecommons.org/licenses/by-nc-nd/4.0/Attribution-NonCommercial-NoDerivatives 4.0 InternacionalLos autoresAtribución – No Comercial – Sin Obra Derivada (by-nc-nd)reponame:Repositorio Institucional Abierto (UTN)instname:Universidad Tecnológica Nacional2026-09-24T12:46:43Zoai:ria.utn.edu.ar:20.500.12272/7470instacron:UTNInstitucionalhttp://ria.utn.edu.ar/Universidad públicaNo correspondehttp://ria.utn.edu.ar/oaigestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2026-09-24 12:46:44.061Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacionalfalse |
| dc.title.none.fl_str_mv |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| title |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| spellingShingle |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. Conde Molina, Debora Facultad Regional Delta UTN Sweet potato residues Xylanases Cellulosimicrobium sp. |
| title_short |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| title_full |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| title_fullStr |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| title_full_unstemmed |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| title_sort |
Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. |
| dc.creator.none.fl_str_mv |
Conde Molina, Debora Sanchez Hulmedilla, Betiana Bogao, Guillermina Tubio, Gisela Corbino, Graciela |
| author |
Conde Molina, Debora |
| author_facet |
Conde Molina, Debora Sanchez Hulmedilla, Betiana Bogao, Guillermina Tubio, Gisela Corbino, Graciela |
| author_role |
author |
| author2 |
Sanchez Hulmedilla, Betiana Bogao, Guillermina Tubio, Gisela Corbino, Graciela |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Facultad Regional Delta UTN Sweet potato residues Xylanases Cellulosimicrobium sp. |
| topic |
Facultad Regional Delta UTN Sweet potato residues Xylanases Cellulosimicrobium sp. |
| dc.description.none.fl_txt_mv |
The development of bioprocesses using agro-industrial waste is one of the most interesting challenges in biotechnology today, as it leads to the reuse of waste in an environmentally responsible way and the development of high value-added products. In the San Pedro region, sweet potato production generates considerable volumes of waste, as approximately 40% of the total production is discarded because it does not meet the requirements for commercialisation. In this study, the ability of the strain Cellulosimicrobium sp. CO1A1 to produce xylanases in a medium formulated with sweet potato root residues was evaluated; xylanase being an enzyme of great industrial application. Cellulosimicrobium sp. CO1A1 was grown in minimal saline medium containing 5 % (w/v) sweet potato root extract, at 135 rpm and 25 °C. Xylanase activity was determined using beech xylan (1%) as substrate at 50 ºC, reducing sugars released were determined by the Nelson-Somogyi method. Several assays were performed in order to evaluate xylanase activity, such as the analysis of cell fractions (supernatant -extracellular activity-, cell pellet -cell-associated activity- and cell homogenate -intracellular activity-); culture samples taken at 2, 5 and 7 days of incubation; and media formulated with different sweet potato varieties (Arapey, Beauregard, Covington, Selecta, Morada, Boni). In addition, the xylanase reaction was carried out in two buffer conditions, sodium citrate (50 mM, pH 5.2) and sodium phosphate (50 mM, pH 6.8). The results showed that although Cellulosimicrobium sp. CO1A1 showed growth in the medium formulated with sweet potato root, thus proving that it has the ability to use sweet potato root as a carbon source, it did not show the ability to produce xylanases under the conditions tested, unlike other strains of the genus Cellulosimicrobium reported. Fil: Conde Molina, Debora. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina. Fil: Sanchez Hulmedilla, Betiana.Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina. Fil: Bogao, Guillermina. Universidad Tecnológica Nacional. Facultad Regional Delta. Grupo de Biotecnología y Nanotecnología Aplicada; Argentina. Fil: Tubio, Gisela. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina. Fil: Corbino, Graciela. Instituto Nacional de Tecnología Agropecuaria. Estación Experimental Agropecuaria San Pedro; Argentina. |
| description |
The development of bioprocesses using agro-industrial waste is one of the most interesting challenges in biotechnology today, as it leads to the reuse of waste in an environmentally responsible way and the development of high value-added products. In the San Pedro region, sweet potato production generates considerable volumes of waste, as approximately 40% of the total production is discarded because it does not meet the requirements for commercialisation. In this study, the ability of the strain Cellulosimicrobium sp. CO1A1 to produce xylanases in a medium formulated with sweet potato root residues was evaluated; xylanase being an enzyme of great industrial application. Cellulosimicrobium sp. CO1A1 was grown in minimal saline medium containing 5 % (w/v) sweet potato root extract, at 135 rpm and 25 °C. Xylanase activity was determined using beech xylan (1%) as substrate at 50 ºC, reducing sugars released were determined by the Nelson-Somogyi method. Several assays were performed in order to evaluate xylanase activity, such as the analysis of cell fractions (supernatant -extracellular activity-, cell pellet -cell-associated activity- and cell homogenate -intracellular activity-); culture samples taken at 2, 5 and 7 days of incubation; and media formulated with different sweet potato varieties (Arapey, Beauregard, Covington, Selecta, Morada, Boni). In addition, the xylanase reaction was carried out in two buffer conditions, sodium citrate (50 mM, pH 5.2) and sodium phosphate (50 mM, pH 6.8). The results showed that although Cellulosimicrobium sp. CO1A1 showed growth in the medium formulated with sweet potato root, thus proving that it has the ability to use sweet potato root as a carbon source, it did not show the ability to produce xylanases under the conditions tested, unlike other strains of the genus Cellulosimicrobium reported. |
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2022 |
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2022-12-29T20:36:02Z 2022-12-29T20:36:02Z 2022-08 |
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info:eu-repo/semantics/conferenceObject info:eu-repo/semantics/draft http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
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conferenceObject |
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Sánchez Holmedilla B., Bogao G., Tubio G., Corbino G., Conde Molina D. Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. Jornadas de Ciencia y Tecnología. Córdoba, Argentina. http://hdl.handle.net/20.500.12272/7470 |
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Sánchez Holmedilla B., Bogao G., Tubio G., Corbino G., Conde Molina D. Sweet potato root waste: evaluation of a culture medium to produce xylanases from Cellulosimicrobium sp. CO1A1. Jornadas de Ciencia y Tecnología. Córdoba, Argentina. |
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eng |
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eng |
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info:eu-repo/semantics/openAccess 2022-12-29T20:36:02Z http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 Internacional Los autores Atribución – No Comercial – Sin Obra Derivada (by-nc-nd) |
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2022-12-29T20:36:02Z http://creativecommons.org/licenses/by-nc-nd/4.0/ Attribution-NonCommercial-NoDerivatives 4.0 Internacional Los autores Atribución – No Comercial – Sin Obra Derivada (by-nc-nd) |
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UTN Facultad Regional San Francisco |
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UTN Facultad Regional San Francisco |
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