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| 27. |  | CENTEC Processamento de pescado. 2. ed. rev. Fortaleza : D. Rocha ; Brasília : Ministério da Ciência e Tecnologia, 2004 . 32 p. il. color. ; 28 cm (Cadernos Tecnológicos). Inclui bibliografia| Biblioteca(s): Biblioteca Rui Tendinha; São Gabriel da Palha; Sooretama. |
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| 30. | | LISBOA, A.; BRAGA, C. P. M. de C.; CARDOSO, I. dos S.; FREIRE, M. A.; SOUZA, M. C. de.; DIAS, M. J. C.; RIOS, R. R.; CIABOTTI, S.; MOREANO, T. B. Queijo Mussarela : Queijo Provolone fresco defumado. Brasília (DF) : SENAR , 1998. 2 52 p. il. ; 21cm - Coleção SENAR. (Trabalhador na produção de derivados do leite).| Biblioteca(s): Biblioteca Rui Tendinha. |
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Registro Completo |
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Biblioteca(s): |
Biblioteca Rui Tendinha. |
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Data corrente: |
03/10/2016 |
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Data da última atualização: |
03/10/2016 |
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Tipo da produção científica: |
Publicação em Anais de Congresso |
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Autoria: |
MARRACCINI, P.; RAMOS, H.; VIEIRA, L. G. E.; FERRÃO, M. A. G.; SILVA, F. R. da; TAQUITA, J. A.; BLOCH JÚNIOR, C.; ANDRADE, A. C. |
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Afiliação: |
Maria Amélia Gava Ferrão, Incaper/Embrapa Café. |
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Título: |
Study of drought-tolerance mechanisms in coffee plants by an integrated analysis. |
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Ano de publicação: |
2008 |
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Fonte/Imprenta: |
In: INTERNATIONAL CONFERENCE ON COFFEE SCIENCE, 22., 2008, Campinas, Brazil. Programme abstracts. Montpellier, France: Association for Science and Information on Coffee, 2008. |
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Idioma: |
Inglês |
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Notas: |
Também publicado como resumo. |
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Conteúdo: |
The principal aim of this study was to investigate the molecular mechanisms underlying the response to drought stress in coffee plants by different approaches. In order to indentify candidate genes involved in controlling drought tolerance in coffee plants, different strategies were followed in our laboratories. The first used the nucleic data generated by the Brazilian Coffee EST project to identify candidate genes (CG) by in silico analysis (electronic Northern-blot). Differential expression of these CG was verified in leaves and roots from drought-tolerant and susceptible clones of C. canephora var. Conilon by Northern-blot and quantitative PCR experiments. The second was based on the screening of macroarray membranes spotted with coffee ESTs which were hybridized separately with leaf cDNA probes of the same clones. Finally, 2D gel electrophoresis was also performed to selected proteins presenting differential accumulation in leaves of the same clones. These proteins were analyzed by MALDI-TOF-MS/MS leading to the identification of a new set of CG. Results concerning the identification of CG by these different approaches are presented and discussed. |
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Palavras-Chave: |
Coffee; Drought tolerance; Seca; Tolerância à seca. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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URL: |
http://biblioteca.incaper.es.gov.br/digital/bitstream/item/2352/1/BRT-studyofdrought-tolerance-andrade.pdf
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Marc: |
LEADER 02034nam a2200253 a 4500
001 1012510
005 2016-10-03
008 2008 bl uuuu u01u1 u #d
100 1 $aMARRACCINI, P.
245 $aStudy of drought-tolerance mechanisms in coffee plants by an integrated analysis.$h[electronic resource]
260 $aIn: INTERNATIONAL CONFERENCE ON COFFEE SCIENCE, 22., 2008, Campinas, Brazil. Programme abstracts. Montpellier, France: Association for Science and Information on Coffee$c2008
500 $aTambém publicado como resumo.
520 $aThe principal aim of this study was to investigate the molecular mechanisms underlying the response to drought stress in coffee plants by different approaches. In order to indentify candidate genes involved in controlling drought tolerance in coffee plants, different strategies were followed in our laboratories. The first used the nucleic data generated by the Brazilian Coffee EST project to identify candidate genes (CG) by in silico analysis (electronic Northern-blot). Differential expression of these CG was verified in leaves and roots from drought-tolerant and susceptible clones of C. canephora var. Conilon by Northern-blot and quantitative PCR experiments. The second was based on the screening of macroarray membranes spotted with coffee ESTs which were hybridized separately with leaf cDNA probes of the same clones. Finally, 2D gel electrophoresis was also performed to selected proteins presenting differential accumulation in leaves of the same clones. These proteins were analyzed by MALDI-TOF-MS/MS leading to the identification of a new set of CG. Results concerning the identification of CG by these different approaches are presented and discussed.
653 $aCoffee
653 $aDrought tolerance
653 $aSeca
653 $aTolerância à seca
700 1 $aRAMOS, H.
700 1 $aVIEIRA, L. G. E.
700 1 $aFERRÃO, M. A. G.
700 1 $aSILVA, F. R. da
700 1 $aTAQUITA, J. A.
700 1 $aBLOCH JÚNIOR, C.
700 1 $aANDRADE, A. C.
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Biblioteca Rui Tendinha (BRT) |
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