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| Registros recuperados : 41 | |
| 4. |  | CARVALHO, L. J. C. B.; CASCARDO, J. C. M.; FERREIRA, M. A.; LOUREIRO, M. E. Studies on proteins and enzymes related to tuverization and starch biosynthesis in cassava roots. Cali, Colombia: CIAT, 1993 234-238p CIAT, Working Document,123 International scientific meeting Cassava Biotechnology Network, 1, 1992, Cartajena, Colombia. Proceedinjs... Cali, Colombia: CIAT, 1993.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 6. | | VALLE, A. M. A.; CARVALHO, L. J. C. B.; CASCARDO, J. C. M.; SOUZA, C. B. Diversidade bioquímica e genética de síntese de carotenóides em raiz de reserva de mandioca (Manihot esculenta Crantz). In: CONGRESSO BRASILEIRO DE GENÉTICA, 52., 2006, Foz do Iguaçu, PR. Resumos... Ribeirão Preto, SP: Sociedade Brasileira de Genética, 2006. p. 947.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 9. | | FALCAO, L. L.; RAMOS, A.; GESTEIRA, A.; ARGOUT, X.; CASCARDO, J. C.; MICHELI, F.; MARCELLINO, L. H. Gene expression variation in cocoa inolulcate with endophyte. In: INTERNATIONAL CONGRESS OF PLANT MOLECULAR BIOLOGY, 9., 2009, St. Louis, Missouri. Proceedings... [S.l.]: The International Society for Plant Molecular Biology, 2009.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 11. | | SILVA, T. E. R. da; CIDADE, L. C.; ALVIM, F. C.; CASCARDO, J. C. de M.; COSTA, M. G. C. Somatic embryogenesis and plant regeneration in elite clones of Theobroma cacao. Pesquisa Agropecuária Brasileira, Brasília, DF, v. 43, n. 10, p. 1433-1436, out. 2008 Notas Científicas.
Título em português: Embriogênese somática e regeneração in vitro de clones elite de Theobroma cacao.| Biblioteca(s): Embrapa Unidades Centrais. |
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| 13. | | GONCALVES, R. C.; LAU, D.; OLIVEIRA, J. R.; MAFFIA, L. A.; CASCARDO, J. C. M.; ALFENAS, A. C. Etiology of bacterial leaf blight of eucalyptus in Brazil. Tropical Plant Pathology, Brasília, DF, v. 33, n. 3, p. 180-188, May/Jun. 2008.| Biblioteca(s): Embrapa Acre; Embrapa Trigo. |
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| 14. | | FIGUEIREDO, J. E. F.; CASCARDO, J. C. M.; CAROLINO, S. M. B.; ALVIM, F. C.; FONTES, E. P. B. Water-stress regulation and molecular analysis of the soybean BIP gene family. Revista Brasileira de Fisiologia Vegetal, Londrina, v. 9, n. 2, p. 103-110, 1997.| Biblioteca(s): Embrapa Milho e Sorgo. |
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| 16. | | JESUS, J, de; CASCARDO, J. C. de M.; FIGUEIRA, A.; SOUZA JUNIOR, M. T.; CORDEIRO, Z. J. M. Uso de mercadores RAPD no estudo de isolados dd Fusarium oxysporum f. sp. cubense Magistra, v.7, n.7, p.127-149, 1995| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 17. | | PUNGARTNIK, C.; SILVA, A. C. da; MELO, S. A. de; GRAMACHO, K. P.; CASCARDO, J. C. de M.; BRENDEL, M.; MICHELI, F.; GESTEIRA, A. da S. High-affinity copper transport and Snq2 export permease of Saccharomyces cerevisiae modulate cytotoxicity of PR-10 from Theobroma cacao. Molecular Plant-Microbe Interactions, St. Paul, v. 22, n. 1, p. 39-51, jan. 2009. DOI: 10.1094/MPMI - 22 - 1 - 0039| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 18. | | BRITO, D. S.; DUARTE, E. A. A.; GONZALEZ, E. R.; SILVA, J. F.; GESTEIRA, A. da S.; CASCARDO, J. M. C. Gene expression analysis by SSH on xylems of Eucalyptus genotypes segregating for components of wood quality. In: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 3, 2011, Ilhéus. Resumos. [S. l.]: Sociedade Brasileira de Genética, 2011. 1 CD-ROM. pdf 35221. Julio Cézar Matos Cascardo, UESC, in memorium.| Biblioteca(s): Embrapa Mandioca e Fruticultura. |
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| 19. | | NASCIMENTO, S. B.; CASCARDO, J. C. de M.; MENEZES, I. C. de; DUARTE, M. de L. R.; DARNET, S.; HARADA, M. L.; SOUZA, C. R. B. de. Identifying sequences potentially related to resistance response of Piper tuberculatum to Fusarium solani f. sp. piperis by suppression subtractive hybridization. Protein & Peptide Letters, v. 16, n. 12, p. 1429-1434, 2009.| Biblioteca(s): Embrapa Amazônia Oriental. |
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| Registros recuperados : 41 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Mandioca e Fruticultura. Para informações adicionais entre em contato com cnpmf.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
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Data corrente: |
11/01/2013 |
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Data da última atualização: |
19/05/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 2 |
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Autoria: |
BRITTO, D. S.; PIROVANI, C. P.; GONZALEZ, E. R.; SILVA, J. F.; GESTEIRA, A. da S.; CASCARDO, J. C. de M. |
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Afiliação: |
DAHYANA SANTOS BRITTO, UESC; CARLOS PRIMINHO PIROVANI, UESC; ESTEBAN ROBERTO GONZALEZ, Suzano Papel e Celulose; JOÃO FLAVIO da SILVA, Suzano Papel e Celulose; ABELMON DA SILVA GESTEIRA, CNPMF; JÚLIO CÉSAR DE MATTOS CASCARDO. |
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Título: |
Oxidative stress proteins as an indicator of a low quality of eucalyptus clones for the pulp and paper industry. |
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Ano de publicação: |
2012 |
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Fonte/Imprenta: |
Genetics and Molecular Research, v. 11, n. 4, p. 3798-3813, 2012. |
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ISSN: |
1676-5680 |
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Idioma: |
Inglês |
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Conteúdo: |
Eucalyptus is a genus widely cultivated in many tropical and subtropical regions of the world as one of the main sources of raw materials for the pulp and paper industry. Identification of clones and selection of genotypes with desirable agronomic characteristics would be useful. We assessed eucalyptus full-sibs that varied in wood quality, using a combination of two-dimensional gel electrophoresis and mass spectrometry to identify differentially expressed proteins as candidates for quality markers. Thirty-one differently expressed proteins were identified, including three proteins of clone X1, four of clone X2, and 12 each of clones X3 and X4. These proteins are involved in various biological processes, including polyphosphate biosynthesis, catalytic activity, nucleotide excision repair, cellular metabolic processes, cell redox homeostasis, response to salt stress, response to temperature, oxidation and reduction processes, cellular water homeostasis, and protein phosphorylation. In the cambial region of each clone, the proteins ketol-acid reductoisomerase, uncharacterized protein MG428, receptor-like serine/threonine-protein kinase and a heat shock protein were found in larger quantities in clone X4 than in clone X1. These proteins are known to be related to protection against oxidative stress and biosynthesis of lignin. A high buildup of proteins involved in response to stress in the cambial region of eucalyptus would indicate clones with undesirable characteristics for use in the pulp and paper industry. MenosEucalyptus is a genus widely cultivated in many tropical and subtropical regions of the world as one of the main sources of raw materials for the pulp and paper industry. Identification of clones and selection of genotypes with desirable agronomic characteristics would be useful. We assessed eucalyptus full-sibs that varied in wood quality, using a combination of two-dimensional gel electrophoresis and mass spectrometry to identify differentially expressed proteins as candidates for quality markers. Thirty-one differently expressed proteins were identified, including three proteins of clone X1, four of clone X2, and 12 each of clones X3 and X4. These proteins are involved in various biological processes, including polyphosphate biosynthesis, catalytic activity, nucleotide excision repair, cellular metabolic processes, cell redox homeostasis, response to salt stress, response to temperature, oxidation and reduction processes, cellular water homeostasis, and protein phosphorylation. In the cambial region of each clone, the proteins ketol-acid reductoisomerase, uncharacterized protein MG428, receptor-like serine/threonine-protein kinase and a heat shock protein were found in larger quantities in clone X4 than in clone X1. These proteins are known to be related to protection against oxidative stress and biosynthesis of lignin. A high buildup of proteins involved in response to stress in the cambial region of eucalyptus would indicate clones with undesirable characteristics for u... Mostrar Tudo |
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Palavras-Chave: |
Differential proteins. |
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Thesaurus NAL: |
Eucalyptus; Heat shock proteins. |
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Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
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Marc: |
LEADER 02250naa a2200229 a 4500
001 1944868
005 2023-05-19
008 2012 bl uuuu u00u1 u #d
022 $a1676-5680
100 1 $aBRITTO, D. S.
245 $aOxidative stress proteins as an indicator of a low quality of eucalyptus clones for the pulp and paper industry.$h[electronic resource]
260 $c2012
520 $aEucalyptus is a genus widely cultivated in many tropical and subtropical regions of the world as one of the main sources of raw materials for the pulp and paper industry. Identification of clones and selection of genotypes with desirable agronomic characteristics would be useful. We assessed eucalyptus full-sibs that varied in wood quality, using a combination of two-dimensional gel electrophoresis and mass spectrometry to identify differentially expressed proteins as candidates for quality markers. Thirty-one differently expressed proteins were identified, including three proteins of clone X1, four of clone X2, and 12 each of clones X3 and X4. These proteins are involved in various biological processes, including polyphosphate biosynthesis, catalytic activity, nucleotide excision repair, cellular metabolic processes, cell redox homeostasis, response to salt stress, response to temperature, oxidation and reduction processes, cellular water homeostasis, and protein phosphorylation. In the cambial region of each clone, the proteins ketol-acid reductoisomerase, uncharacterized protein MG428, receptor-like serine/threonine-protein kinase and a heat shock protein were found in larger quantities in clone X4 than in clone X1. These proteins are known to be related to protection against oxidative stress and biosynthesis of lignin. A high buildup of proteins involved in response to stress in the cambial region of eucalyptus would indicate clones with undesirable characteristics for use in the pulp and paper industry.
650 $aEucalyptus
650 $aHeat shock proteins
653 $aDifferential proteins
700 1 $aPIROVANI, C. P.
700 1 $aGONZALEZ, E. R.
700 1 $aSILVA, J. F.
700 1 $aGESTEIRA, A. da S.
700 1 $aCASCARDO, J. C. de M.
773 $tGenetics and Molecular Research$gv. 11, n. 4, p. 3798-3813, 2012.
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