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| Registros recuperados : 83 | |
| 43. |  | SILVA NETO, S. P.; MARTINS, G. G.; INOUE, M. Y.; MIIKE, Y.; MATSUMOTO, K. Germinacao "in vitro" e micropropagacao de cajueiro (Anacardium occidentale L.) Revista Brasileira de Fruticultura, v.14, n.3, p.53-57, Cruz das Almas, 1992| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 46. | | FUJITA, K.; OGATA, S.; MATSUMOTO, K.; MASUDA, T.; OFOSU BUDU, G. K.; KUWATA, K. Nitrogen transfer and dry matter production in soybean and sorghum mixed cropping system at different population densities. Soil Sci. Plant Nutr., v.36, n.2, p.233-241, 1990.| Biblioteca(s): Embrapa Agrobiologia. |
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| 47. | | LU, T. C. L. A.; CARDOSO, L. D.; ALVES, R. B. N.; MATSUMOTO, K. Photomorphogenesis by LED lighting on potato and Brazilian ginseng for medium-term in vitro conservation. Acta Horticulturae, v. 1083, p. 513-518, 2015. Edição do Proceedings of the VIII International Symposium on In Vitro Culture and Horticultural Breedings, Coimbra, Portugal, May 2015 .| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 48. | | LUZ, T. C. de A.; CARDOSO, L. D.; ALVES, R. B. N.; MATSUMOTO, K. Effect of osmotic regulators on in vitro conservation of Brazilian ginseng, potato and cassava germplasms. Acta Horticulturae, v. 1083, p. 519-526, 2015. Edição do Proceedings of the VIII International Symposium on In Vitro Culture and Horticultural Breedings, Coimbra, Portugal, May 2015 .| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 49. | | SILVA NETO, S. P.; INOUE, M. Y.; MARTINS, G. G.; MLIIKE, Y.; MATSUMOTO, K. Efeito da atmosfera interna do recipiente na proliferacao de gemas e desenvolvimento vegetativo das plantulas na cultura "in vitro" de fragaria sp. Revista Brasileira de Fruticultura, v.15, n.1, p.231-234, Cruz das Almas, 1993.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 56. | | MATSUMOTO, K.; LIMA, F. A.; MORAIS, L. S.; SILVA, S. P. da; SOUZA, A. da S. Na casa de vegetacao e no campo, estudo preliminar dos hibridos somaticos de bananeira obtidos da fusao de protoplastos, em respeito ao comportamento. In: ENCONTRO LATINO-AMERICANO DE BIOTECNOLOGIA VEGETAL: REDBIO, 4., 2001, Goiania. Programa e resumos. [S.l.:s.n.], 2001. p.80. Secao resumos.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| Registros recuperados : 83 | |
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Registro Completo
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Biblioteca(s): |
Embrapa Unidades Centrais. |
|
Data corrente: |
16/10/1998 |
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Data da última atualização: |
30/07/2019 |
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Autoria: |
CONCEICAO, A. da S.; MATSUMOTO, K.; BAKRY, F.; BERND, R. B. |
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Afiliação: |
ALEXANDRE DA SILVA CONCEIÇÃO, CENARGEN; KAZUMITSU MATSUMOTO, CENARGEN; FREDERIC BAKRY, CIRAD/FLHOR; REGINA BEATRIZ BERND, Cenargen. |
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Título: |
Plant regeneration from long-term callus culture of aaa-group dessert banana. |
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Ano de publicação: |
1998 |
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Fonte/Imprenta: |
Pesquisa Agropecuária Brasileira, Brasília, DF, v. 33, n. 8, p. 1291-96, ago. 1998 |
|
Idioma: |
Inglês |
|
Notas: |
Título em português: Regeneração de plantas de bananeira do grupo AAA a partir de calos cultivados durante longo período. |
|
Conteúdo: |
The banana plant is one of the most widely cultivated crops in the world. However, banana breeding has been a slow process, due to the low seed set and low germination rates. Selection of useful somaclonal variations and genetic transformation in cells or calluses are promising techniques to accelerate the breeding process. Therefore, callus culture was carried out, aiming the establishment of one protocol for plant regeneration, to be used in banana breeding program. Leaf sheath disks of 'Nanicao' banana (Musa sp., AAA group, Cavendish subgroup) were cultured on a Murashige and Skoog (MS) basal medium supplemented with activated charcoal (0.2%), MES (2 [N-morpholino] ethanesulfonic acid) (15.3 mM) arginine (300 mM), Picloram (414 M) and 2iP (2-isopenteny adenine) (492 M). Globular calluses developed on the leaf tissue were subcultured in the same medium, acquiring a friable and translucid appearance after one and a half year of culture. The friable calluses were transferred to the medium without growth regulators and arginine, and supplemented with casein hydrolysate (0.05%), where they formed embryo-like structures after transference to light. From these structures, shoots with roots were obtained and plantlets developed. The plant regeneration protocol shown here may be useful to banana breeding via somaclonal variation. |
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Palavras-Chave: |
Cultura de tecidos. |
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Thesaurus NAL: |
Musa; tissue culture. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/45031/1/PLANT-REGENERATION-FROM.pdf
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|
Marc: |
LEADER 02051naa a2200205 a 4500
001 1095718
005 2019-07-30
008 1998 bl uuuu u00u1 u #d
100 1 $aCONCEICAO, A. da S.
245 $aPlant regeneration from long-term callus culture of aaa-group dessert banana.
260 $c1998
500 $aTítulo em português: Regeneração de plantas de bananeira do grupo AAA a partir de calos cultivados durante longo período.
520 $aThe banana plant is one of the most widely cultivated crops in the world. However, banana breeding has been a slow process, due to the low seed set and low germination rates. Selection of useful somaclonal variations and genetic transformation in cells or calluses are promising techniques to accelerate the breeding process. Therefore, callus culture was carried out, aiming the establishment of one protocol for plant regeneration, to be used in banana breeding program. Leaf sheath disks of 'Nanicao' banana (Musa sp., AAA group, Cavendish subgroup) were cultured on a Murashige and Skoog (MS) basal medium supplemented with activated charcoal (0.2%), MES (2 [N-morpholino] ethanesulfonic acid) (15.3 mM) arginine (300 mM), Picloram (414 M) and 2iP (2-isopenteny adenine) (492 M). Globular calluses developed on the leaf tissue were subcultured in the same medium, acquiring a friable and translucid appearance after one and a half year of culture. The friable calluses were transferred to the medium without growth regulators and arginine, and supplemented with casein hydrolysate (0.05%), where they formed embryo-like structures after transference to light. From these structures, shoots with roots were obtained and plantlets developed. The plant regeneration protocol shown here may be useful to banana breeding via somaclonal variation.
650 $aMusa
650 $atissue culture
653 $aCultura de tecidos
700 1 $aMATSUMOTO, K.
700 1 $aBAKRY, F.
700 1 $aBERND, R. B.
773 $tPesquisa Agropecuária Brasileira, Brasília, DF$gv. 33, n. 8, p. 1291-96, ago. 1998
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Embrapa Unidades Centrais (AI-SEDE) |
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