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Registro Completo |
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Biblioteca(s): |
Embrapa Rondônia. |
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Data corrente: |
22/09/2016 |
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Data da última atualização: |
06/10/2016 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
SANTOS, M. R. A. dos; SOUZA, C. A. de. |
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Afiliação: |
MAURICIO REGINALDO ALVES DOS SANTOS, CPAF-Rondonia; Carolina Augusto de Souza. |
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Título: |
Dedifferentiation of Leaf Cells and Growth Pattern of Calluses of Capsicum annuumcv. Etna. |
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Ano de publicação: |
2016 |
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Fonte/Imprenta: |
Australian Journal of Basic and Applied Sciences, v. 10, n. 12, p. 362-368, 2016. |
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Idioma: |
Inglês |
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Conteúdo: |
Background:In vitrocell suspension cultivation systems have been largely reported assafe and standardized methods for production of secondary metabolites with medicinaland agricultural interest.Capsicum annuumis one of the most widely grown vegetablein the world and its biological activities have been demonstrated against insects, fungi,bacteria and other groups of organisms. The determination of procedures for thededifferentiation of cells into callus cells and the subsequent study of the callus growthpattern are necessary for the establishment of cellsuspensions and also to subsidizestudies regarding the bioactivity of its secondarymetabolites. To date, no study hasdescribed the development of protocols for callus induction inC. annuumL. cv. Etna. Objective:The objective of this study was to establish a protocol for dedifferentiationof leaf cells of the cultivarC. annuumcv. Etna and to determine the growth pattern ofthe calluses with a focus on the deceleration phase, when the callus cells must besubcultured into a liquid medium in order to establish cell suspension cultivationsaiming at the production of secondary metabolites.Results:The treatment that resultedin the highest %CI, ACCC and callus weight was thecombination of 4.52 μ M 2,4-D +0.44 μ M BA. The calluses produced were friable andwhitish and their growth patternfollowed a sigmoid shape. The deceleration phase started on the 23rdday of cultivation.Conclusion:Callus induction in leaf explants ofC. annuumcv. Etnacan be achieved inMS medium supplemented with 4.52 μ M 2,4-D + 0.44 μ MBA, which results in highcellular proliferation; in order to start a cell suspension culture, callus cells on the 23rdday of culture should be used. MenosBackground:In vitrocell suspension cultivation systems have been largely reported assafe and standardized methods for production of secondary metabolites with medicinaland agricultural interest.Capsicum annuumis one of the most widely grown vegetablein the world and its biological activities have been demonstrated against insects, fungi,bacteria and other groups of organisms. The determination of procedures for thededifferentiation of cells into callus cells and the subsequent study of the callus growthpattern are necessary for the establishment of cellsuspensions and also to subsidizestudies regarding the bioactivity of its secondarymetabolites. To date, no study hasdescribed the development of protocols for callus induction inC. annuumL. cv. Etna. Objective:The objective of this study was to establish a protocol for dedifferentiationof leaf cells of the cultivarC. annuumcv. Etna and to determine the growth pattern ofthe calluses with a focus on the deceleration phase, when the callus cells must besubcultured into a liquid medium in order to establish cell suspension cultivationsaiming at the production of secondary metabolites.Results:The treatment that resultedin the highest %CI, ACCC and callus weight was thecombination of 4.52 μ M 2,4-D +0.44 μ M BA. The calluses produced were friable andwhitish and their growth patternfollowed a sigmoid shape. The deceleration phase started on the 23rdday of cultivation.Conclusion:Callus induction in leaf explants ofC. annuum... Mostrar Tudo |
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Palavras-Chave: |
Callogenesis; Calogêneses; Growth curve; Metabolismo secundário. |
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Thesagro: |
Curva de Crescimento; Pimenta. |
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Thesaurus Nal: |
secondary metabolites. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/147697/1/Differentiation-SANTOS-2016.pdf
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Marc: |
LEADER 02419naa a2200217 a 4500
001 2053310
005 2016-10-06
008 2016 bl uuuu u00u1 u #d
100 1 $aSANTOS, M. R. A. dos
245 $aDedifferentiation of Leaf Cells and Growth Pattern of Calluses of Capsicum annuumcv. Etna.$h[electronic resource]
260 $c2016
520 $aBackground:In vitrocell suspension cultivation systems have been largely reported assafe and standardized methods for production of secondary metabolites with medicinaland agricultural interest.Capsicum annuumis one of the most widely grown vegetablein the world and its biological activities have been demonstrated against insects, fungi,bacteria and other groups of organisms. The determination of procedures for thededifferentiation of cells into callus cells and the subsequent study of the callus growthpattern are necessary for the establishment of cellsuspensions and also to subsidizestudies regarding the bioactivity of its secondarymetabolites. To date, no study hasdescribed the development of protocols for callus induction inC. annuumL. cv. Etna. Objective:The objective of this study was to establish a protocol for dedifferentiationof leaf cells of the cultivarC. annuumcv. Etna and to determine the growth pattern ofthe calluses with a focus on the deceleration phase, when the callus cells must besubcultured into a liquid medium in order to establish cell suspension cultivationsaiming at the production of secondary metabolites.Results:The treatment that resultedin the highest %CI, ACCC and callus weight was thecombination of 4.52 μ M 2,4-D +0.44 μ M BA. The calluses produced were friable andwhitish and their growth patternfollowed a sigmoid shape. The deceleration phase started on the 23rdday of cultivation.Conclusion:Callus induction in leaf explants ofC. annuumcv. Etnacan be achieved inMS medium supplemented with 4.52 μ M 2,4-D + 0.44 μ MBA, which results in highcellular proliferation; in order to start a cell suspension culture, callus cells on the 23rdday of culture should be used.
650 $asecondary metabolites
650 $aCurva de Crescimento
650 $aPimenta
653 $aCallogenesis
653 $aCalogêneses
653 $aGrowth curve
653 $aMetabolismo secundário
700 1 $aSOUZA, C. A. de
773 $tAustralian Journal of Basic and Applied Sciences$gv. 10, n. 12, p. 362-368, 2016.
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Registro original: |
Embrapa Rondônia (CPAF-RO) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Trigo. Para informações adicionais entre em contato com cnpt.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Trigo. |
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Data corrente: |
15/10/2010 |
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Data da última atualização: |
15/10/2010 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
COSTAMILAN, L. M.; SCHEEREN, P. L.; FELÍCIO, J. C.; MELO, M. S. de; CAMPOS, L. A. C.; DALLA NORA, T. |
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Afiliação: |
LEILA MARIA COSTAMILAN, CNPT; PEDRO LUIZ SCHEEREN, CNPT. |
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Título: |
Efetividade de genes Pm de trigo a oídio (Blumeria graminis f. sp. tritici), em 2007. |
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Ano de publicação: |
2008 |
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Fonte/Imprenta: |
Tropical Plant Pathology, Brasília, DF, v. 33, p. S201, ago. 2008. Suplemento, ref MEL-009. Edição dos Resumos do XLI Congresso Brasileiro de Fitopatologia, Belo Horizonte, ago. 2008. |
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Idioma: |
Português |
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Thesagro: |
Doença; Trigo. |
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Categoria do assunto: |
H Saúde e Patologia |
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Marc: |
LEADER 00688naa a2200193 a 4500
001 1864365
005 2010-10-15
008 2008 bl uuuu u00u1 u #d
100 1 $aCOSTAMILAN, L. M.
245 $aEfetividade de genes Pm de trigo a oídio (Blumeria graminis f. sp. tritici), em 2007.
260 $c2008
650 $aDoença
650 $aTrigo
700 1 $aSCHEEREN, P. L.
700 1 $aFELÍCIO, J. C.
700 1 $aMELO, M. S. de
700 1 $aCAMPOS, L. A. C.
700 1 $aDALLA NORA, T.
773 $tTropical Plant Pathology, Brasília, DF$gv. 33, p. S201, ago. 2008. Suplemento, ref MEL-009. Edição dos Resumos do XLI Congresso Brasileiro de Fitopatologia, Belo Horizonte, ago. 2008.
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Embrapa Trigo (CNPT) |
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