Handling culture medium composition for optimizing plant cell suspension culture in shake flasks
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s11240-017-1368-3 http://hdl.handle.net/11449/179430 |
Resumo: | This work aimed to optimize statistically the culture medium composition for cell plant suspension culture using as a model Capsicum baccatum L. var. pendulum cells. The cell growth was maximized as well as the secondary metabolite yields with antioxidant activity, which could find applications in pharmaceutical and food industries. A Box–Behnken statistical design was utilized to optimize the basal Murashige and Skoog medium, which is widely used in plant cell culture. Three relevant ingredients, saccharose (A, 15–45 g L−1), KH2PO4 (B, 0.085–0.255 g L−1) and KNO3 (C, 0.95–2.85 g L−1) were considered. The cell growth index as well as antioxidant activity, total phenolic compounds and flavonoids from dry extracts (DE) derived of cell cultures, were determined. Growth index (GI) and flavonoids content (F) were sensitive to the changes in nutrient composition in culture medium, and they were modeled statistically according to modified quadratic (GI = 1.76 + 0.59 A - 0.32 B - 0.42 AC) and two-factor interaction (F (mg of rutin / g DE) = 0.88 + 0.35 AC - 0.29 BC) models, respectively. Antioxidant activity and total polyphenols were independent of the nutrient concentrations within the range under study. The optimized culture medium composition was defined for two approaches: maximization of the cell growth (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 0.95 g L−1 KNO3) and maximization of flavonoids production (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 2.85 g L−1 KNO3). According to the current results, other elicitation strategies should be assessed to make this bioprocess more efficient for manufacturing secondary metabolites with antioxidant activity from suspension culture of Capsicum baccatum L. var. pendulum cells. |
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Handling culture medium composition for optimizing plant cell suspension culture in shake flasksBioprocess optimizationCapsicum baccatum L. var. pendulumPlant cell culturePolyphenolic compoundsSuspension cultureThis work aimed to optimize statistically the culture medium composition for cell plant suspension culture using as a model Capsicum baccatum L. var. pendulum cells. The cell growth was maximized as well as the secondary metabolite yields with antioxidant activity, which could find applications in pharmaceutical and food industries. A Box–Behnken statistical design was utilized to optimize the basal Murashige and Skoog medium, which is widely used in plant cell culture. Three relevant ingredients, saccharose (A, 15–45 g L−1), KH2PO4 (B, 0.085–0.255 g L−1) and KNO3 (C, 0.95–2.85 g L−1) were considered. The cell growth index as well as antioxidant activity, total phenolic compounds and flavonoids from dry extracts (DE) derived of cell cultures, were determined. Growth index (GI) and flavonoids content (F) were sensitive to the changes in nutrient composition in culture medium, and they were modeled statistically according to modified quadratic (GI = 1.76 + 0.59 A - 0.32 B - 0.42 AC) and two-factor interaction (F (mg of rutin / g DE) = 0.88 + 0.35 AC - 0.29 BC) models, respectively. Antioxidant activity and total polyphenols were independent of the nutrient concentrations within the range under study. The optimized culture medium composition was defined for two approaches: maximization of the cell growth (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 0.95 g L−1 KNO3) and maximization of flavonoids production (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 2.85 g L−1 KNO3). According to the current results, other elicitation strategies should be assessed to make this bioprocess more efficient for manufacturing secondary metabolites with antioxidant activity from suspension culture of Capsicum baccatum L. var. pendulum cells.Laboratório de Biotecnologia Vegetal Departamento de Biotecnologia Universidade Estadual Paulista – UNESP, Campus-Assis, Avenida Dom Antônio, 2100Laboratório de Fitoterápicos e Produtos Naturais (FITOLAB) Departamento de Biotecnologia Universidade Estadual Paulista – UNESP, Campus-Assis, Avenida Dom Antônio, 2100Centro de Ciências Naturais e Humanas (CCNH) Universidade Federal do ABC, Avenida dos Estados, 5001Laboratório de Biotecnologia Vegetal Departamento de Biotecnologia Universidade Estadual Paulista – UNESP, Campus-Assis, Avenida Dom Antônio, 2100Laboratório de Fitoterápicos e Produtos Naturais (FITOLAB) Departamento de Biotecnologia Universidade Estadual Paulista – UNESP, Campus-Assis, Avenida Dom Antônio, 2100Universidade Estadual Paulista (Unesp)Universidade Federal do ABC (UFABC)Fidemann, Tiago [UNESP]de Araujo Pereira, Gabriela Aparecida [UNESP]Heluy, Tárik Reis [UNESP]Gallego, Rodrigo Boccoli [UNESP]Bertão, Mônica Rosa [UNESP]da Silva, Regildo Márcio Gonçalves [UNESP]Fernández Núñez, Eutimio Gustavo2018-12-11T17:35:09Z2018-12-11T17:35:09Z2018-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article137-146application/pdfhttp://dx.doi.org/10.1007/s11240-017-1368-3Plant Cell, Tissue and Organ Culture, v. 133, n. 1, p. 137-146, 2018.1573-50440167-6857http://hdl.handle.net/11449/17943010.1007/s11240-017-1368-32-s2.0-850377234792-s2.0-85037723479.pdf4478021043584581Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPlant Cell, Tissue and Organ Culture0,8550,855info:eu-repo/semantics/openAccess2024-06-13T17:38:18Zoai:repositorio.unesp.br:11449/179430Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-06-13T17:38:18Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
title |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
spellingShingle |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks Fidemann, Tiago [UNESP] Bioprocess optimization Capsicum baccatum L. var. pendulum Plant cell culture Polyphenolic compounds Suspension culture |
title_short |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
title_full |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
title_fullStr |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
title_full_unstemmed |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
title_sort |
Handling culture medium composition for optimizing plant cell suspension culture in shake flasks |
author |
Fidemann, Tiago [UNESP] |
author_facet |
Fidemann, Tiago [UNESP] de Araujo Pereira, Gabriela Aparecida [UNESP] Heluy, Tárik Reis [UNESP] Gallego, Rodrigo Boccoli [UNESP] Bertão, Mônica Rosa [UNESP] da Silva, Regildo Márcio Gonçalves [UNESP] Fernández Núñez, Eutimio Gustavo |
author_role |
author |
author2 |
de Araujo Pereira, Gabriela Aparecida [UNESP] Heluy, Tárik Reis [UNESP] Gallego, Rodrigo Boccoli [UNESP] Bertão, Mônica Rosa [UNESP] da Silva, Regildo Márcio Gonçalves [UNESP] Fernández Núñez, Eutimio Gustavo |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade Federal do ABC (UFABC) |
dc.contributor.author.fl_str_mv |
Fidemann, Tiago [UNESP] de Araujo Pereira, Gabriela Aparecida [UNESP] Heluy, Tárik Reis [UNESP] Gallego, Rodrigo Boccoli [UNESP] Bertão, Mônica Rosa [UNESP] da Silva, Regildo Márcio Gonçalves [UNESP] Fernández Núñez, Eutimio Gustavo |
dc.subject.por.fl_str_mv |
Bioprocess optimization Capsicum baccatum L. var. pendulum Plant cell culture Polyphenolic compounds Suspension culture |
topic |
Bioprocess optimization Capsicum baccatum L. var. pendulum Plant cell culture Polyphenolic compounds Suspension culture |
description |
This work aimed to optimize statistically the culture medium composition for cell plant suspension culture using as a model Capsicum baccatum L. var. pendulum cells. The cell growth was maximized as well as the secondary metabolite yields with antioxidant activity, which could find applications in pharmaceutical and food industries. A Box–Behnken statistical design was utilized to optimize the basal Murashige and Skoog medium, which is widely used in plant cell culture. Three relevant ingredients, saccharose (A, 15–45 g L−1), KH2PO4 (B, 0.085–0.255 g L−1) and KNO3 (C, 0.95–2.85 g L−1) were considered. The cell growth index as well as antioxidant activity, total phenolic compounds and flavonoids from dry extracts (DE) derived of cell cultures, were determined. Growth index (GI) and flavonoids content (F) were sensitive to the changes in nutrient composition in culture medium, and they were modeled statistically according to modified quadratic (GI = 1.76 + 0.59 A - 0.32 B - 0.42 AC) and two-factor interaction (F (mg of rutin / g DE) = 0.88 + 0.35 AC - 0.29 BC) models, respectively. Antioxidant activity and total polyphenols were independent of the nutrient concentrations within the range under study. The optimized culture medium composition was defined for two approaches: maximization of the cell growth (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 0.95 g L−1 KNO3) and maximization of flavonoids production (45 g L−1 saccharose, 0.09 g L−1 KH2PO4, 2.85 g L−1 KNO3). According to the current results, other elicitation strategies should be assessed to make this bioprocess more efficient for manufacturing secondary metabolites with antioxidant activity from suspension culture of Capsicum baccatum L. var. pendulum cells. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:35:09Z 2018-12-11T17:35:09Z 2018-04-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1007/s11240-017-1368-3 Plant Cell, Tissue and Organ Culture, v. 133, n. 1, p. 137-146, 2018. 1573-5044 0167-6857 http://hdl.handle.net/11449/179430 10.1007/s11240-017-1368-3 2-s2.0-85037723479 2-s2.0-85037723479.pdf 4478021043584581 |
url |
http://dx.doi.org/10.1007/s11240-017-1368-3 http://hdl.handle.net/11449/179430 |
identifier_str_mv |
Plant Cell, Tissue and Organ Culture, v. 133, n. 1, p. 137-146, 2018. 1573-5044 0167-6857 10.1007/s11240-017-1368-3 2-s2.0-85037723479 2-s2.0-85037723479.pdf 4478021043584581 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Plant Cell, Tissue and Organ Culture 0,855 0,855 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
137-146 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1826303778135998464 |