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Registro Completo |
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Biblioteca(s): |
Embrapa Meio-Norte. |
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Data corrente: |
20/05/2022 |
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Data da última atualização: |
12/12/2023 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
RAUPP, S. V.; KIMPARA, J. M. |
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Afiliação: |
STELA VALENTI RAUPP, Bolsista pós-doutorado em Aquavitae-Horizon 2020, UE.; JANAINA MITSUE KIMPARA, CPAMN. |
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Título: |
Cultivo multitrófico integrado de camarões e macroalgas no Nordeste brasileiro. |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
In: JORNADA CIENTIFICA DA EMBRAPA MEIO-NORTE, 6., 2020,Teresina, PI. Anais... Teresina: Embrapa Meio-Norte, 2021. p. 35 (Embrapa Meio-Norte. Documentos, 284). |
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Idioma: |
Português |
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Conteúdo: |
Portanto o objetivo deste trabalho foi integrar macroalgas na carcinicultura, delineando um sistema IMTA para o Nordeste brasileiro. Avaliou-se a introdução de duas espécies de macroalgas nativas (Hypnea pseudomusciformis e Gracilaria spp.) e dois tipos de estrutura de cultivo em viveiros de camarão marinho (Litopenaeus vannamei) em fazenda localizada em Caiçara do Norte, RN. |
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Palavras-Chave: |
Maricultura; Sustentabilidade. |
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Thesagro: |
Alga Marinha. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1143335/1/CultivoMultitroficoIntegradoCamaroesMacroalgasVIJCCPAMN2021.pdf
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Marc: |
LEADER 00974nam a2200157 a 4500
001 2143335
005 2023-12-12
008 2021 bl uuuu u00u1 u #d
100 1 $aRAUPP, S. V.
245 $aCultivo multitrófico integrado de camarões e macroalgas no Nordeste brasileiro.$h[electronic resource]
260 $aIn: JORNADA CIENTIFICA DA EMBRAPA MEIO-NORTE, 6., 2020,Teresina, PI. Anais... Teresina: Embrapa Meio-Norte, 2021. p. 35 (Embrapa Meio-Norte. Documentos, 284).$c2021
520 $aPortanto o objetivo deste trabalho foi integrar macroalgas na carcinicultura, delineando um sistema IMTA para o Nordeste brasileiro. Avaliou-se a introdução de duas espécies de macroalgas nativas (Hypnea pseudomusciformis e Gracilaria spp.) e dois tipos de estrutura de cultivo em viveiros de camarão marinho (Litopenaeus vannamei) em fazenda localizada em Caiçara do Norte, RN.
650 $aAlga Marinha
653 $aMaricultura
653 $aSustentabilidade
700 1 $aKIMPARA, J. M.
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Registro original: |
Embrapa Meio-Norte (CPAMN) |
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Registro Completo
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
26/11/2012 |
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Data da última atualização: |
16/04/2018 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
MORALES, A.; O'ROURKE, J. A.; BORÉM, A.; ABDELNOOR, R. V.; PEDLEY, K. F.; WHITHAM, S. A.; GRAHAM, M. A. |
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Afiliação: |
AGUIDA MORALES; JAMIE A.O'ROURKE, USDA-ARS; ALUÍZIO BORÉM, UFV; RICARDO VILELA ABDELNOOR, CNPSO; KERRY F. PEDLEY, USDA-ARS; STEVEN A. WHITHAM, IOWA STATE UNIVERSITY; MICHELLE A. GRAHAM, USDA-ARS. |
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Título: |
Combining transcriptome analyses and virus induced gene silencing to identify genes in the Rpp4-mediated asian soybean rust resistance Pathway. |
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Ano de publicação: |
2012 |
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Fonte/Imprenta: |
In: MOLECULAR & CELLULAR BIOLOGY OF TE SOYBEAN, 14., Des Moines, 2012. [Proceedings...]. Des Moines: Iowa State University, 2012. |
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Páginas: |
p. 137. |
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Idioma: |
Inglês |
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Conteúdo: |
Six Asian Soybean Rust (ASR) resistance loci have been identified and mapped in soybean genome: Rpp1 (Resistance to Phakopsora pachyrhizi 1), Rpp2, Rpp3, Rpp4, Rpp5 and Rpp6. Of particular interest is Rpp4, which has remained stable and confers resistance against Phakopsora pachyrhizi isolates from around the world. Sequencing of the region harboring Rpp4 in the susceptible cultivar Williams 82 (Wm82) and the resistant cultivar (PI459025B) genotype identified a cluster of CC-NBS-LRR resistance genes. Meyers et al. (2009) developed Virus Induced Gene Silencing constructs from the LRR regions of the Wm82 Rpp4 candidate genes to confirm that orthologous genes were responsible for resistance in the resistant parent (PI459025B). In this study, RNA samples extracted from the same Rpp4 LRR silenced and empty vector treated plants, also infected with P. pachyrhizi (described by Meyer et al., 2009) were compared using the GeneChip® Soybean Genome Array (Affymetrix®). Since the plant samples differed only in the expression of Rpp4, comparisons of these samples would identify genes downstream of Rpp4 in the signaling pathway. In total, 383 differentially expressed probes were identified, many with functions related to defense. While the time point analyzed was late in defense signaling, bioinformatic approaches were useful in characterizing the defense response and identify transcription factors regulating the response. |
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Thesagro: |
Doença de planta; Ferrugem; Phakopsora Pachyrhizi; Soja. |
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Thesaurus NAL: |
Plant diseases and disorders; Rust diseases; Soybeans. |
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Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/70834/1/ID-33817.pdf
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Marc: |
LEADER 02354nam a2200277 a 4500
001 1940523
005 2018-04-16
008 2012 bl uuuu u00u1 u #d
100 1 $aMORALES, A.
245 $aCombining transcriptome analyses and virus induced gene silencing to identify genes in the Rpp4-mediated asian soybean rust resistance Pathway.$h[electronic resource]
260 $aIn: MOLECULAR & CELLULAR BIOLOGY OF TE SOYBEAN, 14., Des Moines, 2012. [Proceedings...]. Des Moines: Iowa State University$c2012
300 $ap. 137.
520 $aSix Asian Soybean Rust (ASR) resistance loci have been identified and mapped in soybean genome: Rpp1 (Resistance to Phakopsora pachyrhizi 1), Rpp2, Rpp3, Rpp4, Rpp5 and Rpp6. Of particular interest is Rpp4, which has remained stable and confers resistance against Phakopsora pachyrhizi isolates from around the world. Sequencing of the region harboring Rpp4 in the susceptible cultivar Williams 82 (Wm82) and the resistant cultivar (PI459025B) genotype identified a cluster of CC-NBS-LRR resistance genes. Meyers et al. (2009) developed Virus Induced Gene Silencing constructs from the LRR regions of the Wm82 Rpp4 candidate genes to confirm that orthologous genes were responsible for resistance in the resistant parent (PI459025B). In this study, RNA samples extracted from the same Rpp4 LRR silenced and empty vector treated plants, also infected with P. pachyrhizi (described by Meyer et al., 2009) were compared using the GeneChip® Soybean Genome Array (Affymetrix®). Since the plant samples differed only in the expression of Rpp4, comparisons of these samples would identify genes downstream of Rpp4 in the signaling pathway. In total, 383 differentially expressed probes were identified, many with functions related to defense. While the time point analyzed was late in defense signaling, bioinformatic approaches were useful in characterizing the defense response and identify transcription factors regulating the response.
650 $aPlant diseases and disorders
650 $aRust diseases
650 $aSoybeans
650 $aDoença de planta
650 $aFerrugem
650 $aPhakopsora Pachyrhizi
650 $aSoja
700 1 $aO'ROURKE, J. A.
700 1 $aBORÉM, A.
700 1 $aABDELNOOR, R. V.
700 1 $aPEDLEY, K. F.
700 1 $aWHITHAM, S. A.
700 1 $aGRAHAM, M. A.
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Embrapa Soja (CNPSO) |
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