Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases
- Autores
- Cimino, Cecilia Verónica; Vairo Cavalli, Sandra Elizabeth; Spina, Francisco; Natalucci, Claudia Luisa; Priolo de Lufrano, Nora Silvia
- Año de publicación
- 2006
- Idioma
- español castellano
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The objective of this work was the optimization of the conditions of in vitro culture for callus production of Silybum marianum (L.) Gaertn. (Asteraceae). Sections of cotyledons, previously disinfected by washing successively with ethanol 70º, NaClO (10% w/v) and Tween 20 (0.05% v/v) and rinsing with sterile distilled water, were used as explants. For its initial culture, B5 medium supplemented with BA and 2,4-D solidified with phytagel was used, and a 63% survival was achieved. To obtain callus, two solid media were assayed (S1 and S2) using B5 medium supplemented with growth regulators (BA and 2,4-D or NAA and BA, respectively). The calli were grown at 25ºC during 45 days in darkness. Growth kinetics was studied using S1 medium obtaining a typical growth curve with an exponential phase after 14 days of incubation (rate of growth 0.005 g dry weight/ day) and stationary phase after 35 days. The rate of growth in S2 medium was slower, and rhizogenesis was observed starting on the fifth week of incubation. From these results, the best culture medium for callus production of Silybum marianum was S1 medium.
Facultad de Ciencias Exactas - Materia
-
Ciencias Exactas
Asteraceae, callus, rhizogenesis, Silybum marianum
Asteraceae
peptidasas - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-nd/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/67027
Ver los metadatos del registro completo
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Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidasesCimino, Cecilia VerónicaVairo Cavalli, Sandra ElizabethSpina, FranciscoNatalucci, Claudia LuisaPriolo de Lufrano, Nora SilviaCiencias ExactasAsteraceae, callus, rhizogenesis, Silybum marianumAsteraceaepeptidasasThe objective of this work was the optimization of the conditions of in vitro culture for callus production of Silybum marianum (L.) Gaertn. (Asteraceae). Sections of cotyledons, previously disinfected by washing successively with ethanol 70º, NaClO (10% w/v) and Tween 20 (0.05% v/v) and rinsing with sterile distilled water, were used as explants. For its initial culture, B5 medium supplemented with BA and 2,4-D solidified with phytagel was used, and a 63% survival was achieved. To obtain callus, two solid media were assayed (S1 and S2) using B5 medium supplemented with growth regulators (BA and 2,4-D or NAA and BA, respectively). The calli were grown at 25ºC during 45 days in darkness. Growth kinetics was studied using S1 medium obtaining a typical growth curve with an exponential phase after 14 days of incubation (rate of growth 0.005 g dry weight/ day) and stationary phase after 35 days. The rate of growth in S2 medium was slower, and rhizogenesis was observed starting on the fifth week of incubation. From these results, the best culture medium for callus production of Silybum marianum was S1 medium.Facultad de Ciencias Exactas2006info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf237-240http://sedici.unlp.edu.ar/handle/10915/67027spainfo:eu-repo/semantics/altIdentifier/url/http://www.ejbiotechnology.info/index.php/ejbiotechnology/article/view/v9n3-14/280info:eu-repo/semantics/altIdentifier/issn/0717-3458info:eu-repo/semantics/altIdentifier/doi/10.2225/vol9-issue3-fulltext-14info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:02:08Zoai:sedici.unlp.edu.ar:10915/67027Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:02:09.088SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
title |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
spellingShingle |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases Cimino, Cecilia Verónica Ciencias Exactas Asteraceae, callus, rhizogenesis, Silybum marianum Asteraceae peptidasas |
title_short |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
title_full |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
title_fullStr |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
title_full_unstemmed |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
title_sort |
Callus culture for biomass production of milk thistle as a potential source of milk clotting peptidases |
dc.creator.none.fl_str_mv |
Cimino, Cecilia Verónica Vairo Cavalli, Sandra Elizabeth Spina, Francisco Natalucci, Claudia Luisa Priolo de Lufrano, Nora Silvia |
author |
Cimino, Cecilia Verónica |
author_facet |
Cimino, Cecilia Verónica Vairo Cavalli, Sandra Elizabeth Spina, Francisco Natalucci, Claudia Luisa Priolo de Lufrano, Nora Silvia |
author_role |
author |
author2 |
Vairo Cavalli, Sandra Elizabeth Spina, Francisco Natalucci, Claudia Luisa Priolo de Lufrano, Nora Silvia |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Asteraceae, callus, rhizogenesis, Silybum marianum Asteraceae peptidasas |
topic |
Ciencias Exactas Asteraceae, callus, rhizogenesis, Silybum marianum Asteraceae peptidasas |
dc.description.none.fl_txt_mv |
The objective of this work was the optimization of the conditions of in vitro culture for callus production of Silybum marianum (L.) Gaertn. (Asteraceae). Sections of cotyledons, previously disinfected by washing successively with ethanol 70º, NaClO (10% w/v) and Tween 20 (0.05% v/v) and rinsing with sterile distilled water, were used as explants. For its initial culture, B5 medium supplemented with BA and 2,4-D solidified with phytagel was used, and a 63% survival was achieved. To obtain callus, two solid media were assayed (S1 and S2) using B5 medium supplemented with growth regulators (BA and 2,4-D or NAA and BA, respectively). The calli were grown at 25ºC during 45 days in darkness. Growth kinetics was studied using S1 medium obtaining a typical growth curve with an exponential phase after 14 days of incubation (rate of growth 0.005 g dry weight/ day) and stationary phase after 35 days. The rate of growth in S2 medium was slower, and rhizogenesis was observed starting on the fifth week of incubation. From these results, the best culture medium for callus production of Silybum marianum was S1 medium. Facultad de Ciencias Exactas |
description |
The objective of this work was the optimization of the conditions of in vitro culture for callus production of Silybum marianum (L.) Gaertn. (Asteraceae). Sections of cotyledons, previously disinfected by washing successively with ethanol 70º, NaClO (10% w/v) and Tween 20 (0.05% v/v) and rinsing with sterile distilled water, were used as explants. For its initial culture, B5 medium supplemented with BA and 2,4-D solidified with phytagel was used, and a 63% survival was achieved. To obtain callus, two solid media were assayed (S1 and S2) using B5 medium supplemented with growth regulators (BA and 2,4-D or NAA and BA, respectively). The calli were grown at 25ºC during 45 days in darkness. Growth kinetics was studied using S1 medium obtaining a typical growth curve with an exponential phase after 14 days of incubation (rate of growth 0.005 g dry weight/ day) and stationary phase after 35 days. The rate of growth in S2 medium was slower, and rhizogenesis was observed starting on the fifth week of incubation. From these results, the best culture medium for callus production of Silybum marianum was S1 medium. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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http://sedici.unlp.edu.ar/handle/10915/67027 |
url |
http://sedici.unlp.edu.ar/handle/10915/67027 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) |
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openAccess |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) |
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