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Registro Completo |
Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
Data corrente: |
22/03/2017 |
Data da última atualização: |
29/03/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
BALZON, T. A.; LUIS, Z. G.; PEREIRA, J. E. S. |
Afiliação: |
Talita Aparecida Balzon; Zanderluce Gomes Luis, UnB; JONNY EVERSON SCHERWINSKI PEREIRA, Cenargen. |
Título: |
New approaches to improve the efficiency of somatic embryogenesis in oil palm (Elaeis guineensis Jacq.) from mature zygotic embryos. |
Ano de publicação: |
2013 |
Fonte/Imprenta: |
In Vitro Cellular e Developmental Biology, v. 49, p. 41-50, 2013. |
Idioma: |
Inglês |
Conteúdo: |
We developed an efficient and simple system for inducing somatic embryogenesis and regenerating plantlets from mature zygotic embryos of oil palm. Embryogenic calli were induced from mature zygotic embryos of oil palm on modified Murashige and Skoog medium with 2,4-dichlorophenoxyacetic acid or picloram, alone or in combination with activated charcoal. The greatest frequency of embryogenic callus induction (97.5%) was obtained by culturing mature zygotic embryos on callus induction medium with 450 μM picloram and 2.5 gL−1 activated charcoal. Embryogenic calli proliferated on a medium with a reduced concentration of picloram. Embryogenic calli were then subcultured on a medium supplemented with 12.3 μM 2-isopentenyladenine and 0.54 μM naphthaleneacetic acid, with subcultures at 4-wk intervals. Somatic embryos were regenerated on a medium with Murashige and Skoog macro- and micronutrients at halfstrength concentrations supplemented with 20 gL−1 sucrose, 2.5 gL−1 activated charcoal, and 2.5 gL−1 Phytagel. Detailed histological analysis revealed that somatic embryogenesis followed an indirect pathway. Primary calli were observed after 4?6 wk of culture and progressed to embryogenic calli at 12 wk. Embryogenic cells exhibited dense protoplasm, a high nucleoplasmic ratio, and small starch grains. Proembryos, which seemed to have a multicellular origin, formed after 16?20 wk of culture and successive cell divisions. Differentiated somatic embryos had a haustorium, a plumule, and the first and second foliar sheaths. In differentiated embryos, the radicular protrusion was not apparent because it generally does not appear until after the first true leaves emerge. MenosWe developed an efficient and simple system for inducing somatic embryogenesis and regenerating plantlets from mature zygotic embryos of oil palm. Embryogenic calli were induced from mature zygotic embryos of oil palm on modified Murashige and Skoog medium with 2,4-dichlorophenoxyacetic acid or picloram, alone or in combination with activated charcoal. The greatest frequency of embryogenic callus induction (97.5%) was obtained by culturing mature zygotic embryos on callus induction medium with 450 μM picloram and 2.5 gL−1 activated charcoal. Embryogenic calli proliferated on a medium with a reduced concentration of picloram. Embryogenic calli were then subcultured on a medium supplemented with 12.3 μM 2-isopentenyladenine and 0.54 μM naphthaleneacetic acid, with subcultures at 4-wk intervals. Somatic embryos were regenerated on a medium with Murashige and Skoog macro- and micronutrients at halfstrength concentrations supplemented with 20 gL−1 sucrose, 2.5 gL−1 activated charcoal, and 2.5 gL−1 Phytagel. Detailed histological analysis revealed that somatic embryogenesis followed an indirect pathway. Primary calli were observed after 4?6 wk of culture and progressed to embryogenic calli at 12 wk. Embryogenic cells exhibited dense protoplasm, a high nucleoplasmic ratio, and small starch grains. Proembryos, which seemed to have a multicellular origin, formed after 16?20 wk of culture and successive cell divisions. Differentiated somatic embr... Mostrar Tudo |
Palavras-Chave: |
Zygotic embryo. |
Thesaurus Nal: |
morphogenesis. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/180927/1/Balzon2013-Article-NewApproachesToImproveTheEffic.pdf
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Marc: |
LEADER 02287naa a2200169 a 4500 001 2067490 005 2023-03-29 008 2013 bl uuuu u00u1 u #d 100 1 $aBALZON, T. A. 245 $aNew approaches to improve the efficiency of somatic embryogenesis in oil palm (Elaeis guineensis Jacq.) from mature zygotic embryos.$h[electronic resource] 260 $c2013 520 $aWe developed an efficient and simple system for inducing somatic embryogenesis and regenerating plantlets from mature zygotic embryos of oil palm. Embryogenic calli were induced from mature zygotic embryos of oil palm on modified Murashige and Skoog medium with 2,4-dichlorophenoxyacetic acid or picloram, alone or in combination with activated charcoal. The greatest frequency of embryogenic callus induction (97.5%) was obtained by culturing mature zygotic embryos on callus induction medium with 450 μM picloram and 2.5 gL−1 activated charcoal. Embryogenic calli proliferated on a medium with a reduced concentration of picloram. Embryogenic calli were then subcultured on a medium supplemented with 12.3 μM 2-isopentenyladenine and 0.54 μM naphthaleneacetic acid, with subcultures at 4-wk intervals. Somatic embryos were regenerated on a medium with Murashige and Skoog macro- and micronutrients at halfstrength concentrations supplemented with 20 gL−1 sucrose, 2.5 gL−1 activated charcoal, and 2.5 gL−1 Phytagel. Detailed histological analysis revealed that somatic embryogenesis followed an indirect pathway. Primary calli were observed after 4?6 wk of culture and progressed to embryogenic calli at 12 wk. Embryogenic cells exhibited dense protoplasm, a high nucleoplasmic ratio, and small starch grains. Proembryos, which seemed to have a multicellular origin, formed after 16?20 wk of culture and successive cell divisions. Differentiated somatic embryos had a haustorium, a plumule, and the first and second foliar sheaths. In differentiated embryos, the radicular protrusion was not apparent because it generally does not appear until after the first true leaves emerge. 650 $amorphogenesis 653 $aZygotic embryo 700 1 $aLUIS, Z. G. 700 1 $aPEREIRA, J. E. S. 773 $tIn Vitro Cellular e Developmental Biology$gv. 49, p. 41-50, 2013.
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Registro original: |
Embrapa Recursos Genéticos e Biotecnologia (CENARGEN) |
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Registro Completo
Biblioteca(s): |
Embrapa Milho e Sorgo. |
Data corrente: |
29/10/1998 |
Data da última atualização: |
21/07/2018 |
Tipo da produção científica: |
Capítulo em Livro Técnico-Científico |
Autoria: |
MACHADO, P. L. O. de A.; FABRICIO, A. C.; PRIMAVESI, A. C.; ROSSO, C. de; FERREIRA, C. J. A.; PRATES, H. T.; FERRAZ, M. R.; ARMELIN, M. J. A.; MIYAZAWA, M.; PRIMAVESI, O.; MENDES, P. J.; FERRACINI, V. L. |
Afiliação: |
EMBRAPA-CNPMS. |
Título: |
Solos. |
Ano de publicação: |
1998 |
Fonte/Imprenta: |
In: NOGUEIRA, A. R. de A.; MACHADO, P. L. O. de A.; CARMO, C. A. F. de S. de; FERREIRA, J. R.; Manual de laboratório: solo, água, nutrição vegetal, nutrição animal e alimentos. I. Coleta, acondicionamento e preparo de amostras. Sao Carlos: EMBRAPA-CPPSE, 1998. p. 7-23. |
Idioma: |
Português |
Palavras-Chave: |
Coleta. |
Thesagro: |
Acondicionamento; Amostragem; Solo. |
Thesaurus NAL: |
sampling; soil. |
Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/53925/1/solos.pdf
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Marc: |
LEADER 01016naa a2200313 a 4500 001 1480739 005 2018-07-21 008 1998 bl uuuu u00u1 u #d 100 1 $aMACHADO, P. L. O. de A. 245 $aSolos.$h[electronic resource] 260 $c1998 650 $asampling 650 $asoil 650 $aAcondicionamento 650 $aAmostragem 650 $aSolo 653 $aColeta 700 1 $aFABRICIO, A. C. 700 1 $aPRIMAVESI, A. C. 700 1 $aROSSO, C. de 700 1 $aFERREIRA, C. J. A. 700 1 $aPRATES, H. T. 700 1 $aFERRAZ, M. R. 700 1 $aARMELIN, M. J. A. 700 1 $aMIYAZAWA, M. 700 1 $aPRIMAVESI, O. 700 1 $aMENDES, P. J. 700 1 $aFERRACINI, V. L. 773 $tIn: NOGUEIRA, A. R. de A.; MACHADO, P. L. O. de A.; CARMO, C. A. F. de S. de; FERREIRA, J. R.; Manual de laboratório: solo, água, nutrição vegetal, nutrição animal e alimentos. I. Coleta, acondicionamento e preparo de amostras. Sao Carlos: EMBRAPA-CPPSE, 1998. p. 7-23.
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