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Registro Completo |
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Biblioteca(s): |
Embrapa Acre; Embrapa Agroindústria Tropical; Embrapa Amazônia Ocidental; Embrapa Amazônia Oriental; Embrapa Arroz e Feijão; Embrapa Cerrados; Embrapa Clima Temperado; Embrapa Cocais; Embrapa Gado de Leite; Embrapa Meio Norte / UEP-Parnaíba; Embrapa Meio-Norte; Embrapa Recursos Genéticos e Biotecnologia; Embrapa Rondônia; Embrapa Semiárido; Embrapa Soja; Embrapa Solos / UEP-Recife; Embrapa Tabuleiros Costeiros; Embrapa Unidades Centrais; Embrapa Uva e Vinho. MenosEmbrapa Acre; Embrapa Agroindústria Tropical; Embrapa Amazônia Ocidental; Embrapa Amazônia Oriental; Embrapa Arroz e Feijão; Embrapa Cerrados; Embrapa Clima Temperado; Embrapa Cocais; Embrapa Gado de Leite; Embrapa Meio Norte / UEP-Parnaíba... Mostrar Todas |
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Data corrente: |
27/11/2001 |
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Data da última atualização: |
10/08/2021 |
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Tipo da produção científica: |
Autoria/Organização/Edição de Livros |
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Autoria: |
SOARES, J. M.; LEAO, P. C. de S. (ed.). |
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Afiliação: |
JOSÉ MONTEIRO SOARES, CPATSA; PATRICIA COELHO DE SOUZA LEAO, CPATSA. |
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Título: |
A vitivinicultura no Semiárido brasileiro. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
Brasília, DF: Embrapa Informação Tecnológica; Petrolina: Embrapa Semi-Árido, 2009. |
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Páginas: |
756 p. |
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Descrição Física: |
il. color ; 18,5 cm X 25,5 cm |
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ISBN: |
978-85-7383-460-4 ; 978-85-7405-010-2 |
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Idioma: |
Português |
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Conteúdo: |
1. Histórico e importância Socioeconômica; 2. Exigências climáticas; 3. Aspectos fisiológicos; 4. Melhoramento genético; 5. Principais cultivares; 6. Mecanização agrícola, manejo e conservação do solo; 7. Implantação do vinhedo; 8. Manejo da copa; 9. Irrigação; 10. Nutrição e adubação; 11. Fertiirrigação; 12. Pragas e alternativas de controle; 13. Doenças e alternativas de controle; 14. Fisiologia, tecnologia e manejo pós-colheita; 15. Sistema de produção integrada; 16. Vitinicultura e enologia; 17. Custos de produção e 18. Mercados de uvas de mesa e de vinho. |
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Palavras-Chave: |
Brasil; Cultivar; Cultivation; Cultivo; Diseases; Exportação de fruta; Genetic; Implantação do vinhedo; Manejo de copa; Melhoramento genético; Seedless grapes; Uva sem semente; Vale do São Francisco; Videira; Vitivinicultura. |
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Thesagro: |
Adubação; Colheita; Custo; Custo de Produção; Doença; Doença de planta; Enologia; Fertirrigação; Fisiologia vegetal; Irrigação; Manejo; Mecanização; Melhoramento Genético Vegetal; Mercado; Nutrição; Plantio; Pós-colheita; Praga; Praga de planta; Produção; Produção Integrada; Sistema de Cultivo; Uva; Variedade; Vinho; Viticultura. |
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Thesaurus Nal: |
Brazil; grapes; irrigation; nutrition; Physiology; plant breeding; Postharvest physiology; Postharvest technology; varieties; Viticulture; Vitis. |
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Categoria do assunto: |
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A Sistemas de Cultivo
E Economia e Indústria Agrícola
F Plantas e Produtos de Origem Vegetal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/224993/1/Embrapa-Vitinicultura.pdf
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Marc: |
LEADER 02524nam a2200757 a 4500
001 1513781
005 2021-08-10
008 2009 bl uuuu 00u1 u #d
100 1 $aSOARES, J. M.
245 $aA vitivinicultura no Semiárido brasileiro.
260 $aBrasília, DF: Embrapa Informação Tecnológica; Petrolina: Embrapa Semi-Árido$c2009
300 $a756 p.$cil. color ; 18,5 cm X 25,5 cm
520 $a1. Histórico e importância Socioeconômica; 2. Exigências climáticas; 3. Aspectos fisiológicos; 4. Melhoramento genético; 5. Principais cultivares; 6. Mecanização agrícola, manejo e conservação do solo; 7. Implantação do vinhedo; 8. Manejo da copa; 9. Irrigação; 10. Nutrição e adubação; 11. Fertiirrigação; 12. Pragas e alternativas de controle; 13. Doenças e alternativas de controle; 14. Fisiologia, tecnologia e manejo pós-colheita; 15. Sistema de produção integrada; 16. Vitinicultura e enologia; 17. Custos de produção e 18. Mercados de uvas de mesa e de vinho.
650 $aBrazil
650 $agrapes
650 $airrigation
650 $anutrition
650 $aPhysiology
650 $aplant breeding
650 $aPostharvest physiology
650 $aPostharvest technology
650 $avarieties
650 $aViticulture
650 $aVitis
650 $aAdubação
650 $aColheita
650 $aCusto
650 $aCusto de Produção
650 $aDoença
650 $aDoença de planta
650 $aEnologia
650 $aFertirrigação
650 $aFisiologia vegetal
650 $aIrrigação
650 $aManejo
650 $aMecanização
650 $aMelhoramento Genético Vegetal
650 $aMercado
650 $aNutrição
650 $aPlantio
650 $aPós-colheita
650 $aPraga
650 $aPraga de planta
650 $aProdução
650 $aProdução Integrada
650 $aSistema de Cultivo
650 $aUva
650 $aVariedade
650 $aVinho
650 $aViticultura
653 $aBrasil
653 $aCultivar
653 $aCultivation
653 $aCultivo
653 $aDiseases
653 $aExportação de fruta
653 $aGenetic
653 $aImplantação do vinhedo
653 $aManejo de copa
653 $aMelhoramento genético
653 $aSeedless grapes
653 $aUva sem semente
653 $aVale do São Francisco
653 $aVideira
653 $aVitivinicultura
700 1 $aLEAO, P. C. de S.
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Registro original: |
Embrapa Semiárido (CPATSA) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Café. Para informações adicionais entre em contato com biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Café. |
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Data corrente: |
14/03/2017 |
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Data da última atualização: |
14/03/2017 |
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Tipo da produção científica: |
Orientação de Tese de Pós-Graduação |
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Autoria: |
COTTA, M. G. |
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Afiliação: |
MICHELLE GUITTON COTTA. |
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Título: |
Molecular mechanisms in the first step of aba-mediated response in Coffea ssp. |
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Ano de publicação: |
2016 |
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Fonte/Imprenta: |
2016. |
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Páginas: |
169 p. |
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Idioma: |
Inglês |
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Notas: |
Tese (doutorado Biotecnologia Vegetal) - Universidade Federal de Lavras, Lavras, MG. Orientador: Alan Carvalho Andrade. Coorientador: Pierre Roger René Marraccini. |
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Conteúdo: |
Abscisic acid (ABA) pathway is a phytohormone universally conserved in land plants which coordinates several aspects of the plant response to water deficit such as root architecture, seed dormancy and regulation of stomatal closure. A mechanism of ABA signal transduction has been proposed, evolving intracellular ABA receptors (PYR/PYL/RCARs) interacting with PP2Cs phosphatases and SnRK2 protein kinases regulating this tripartite protein system. The goal of this study was to identify and characterize for the first time the orthologs genes of this tripartite system in Coffea. For this purpose, protein sequences from Arabidopsis, citrus, rice, grape, tomato and potato were chosen as query to search orthologous genes in the Coffee Genome Hub (http://coffee-genome.org/). Differential expression in tissues as leaves, seeds, roots and floral organs waschecked through in silico analyses. In vivo gene expression analyses were also performed by RT-qPCR in leaves and roots of drought-tolerant (DT 14, 73 and 120) and drought-susceptible (DS 22) C. canephora Conilon clones submitted (or not) to drought. The expression profiles of the tripartite system CcPYL-PP2C-SnRK2 genes were also analyzed in leaves of C. arabica and C. canephora plants growing under hydroponic condition and submitted to ABA exogenous treatment (500 ?M). This approach allowed the identification and characterization of 24 candidate genes (9 PYL/RCARs, 6 PP2Cs and 9 SnRK2s) in C. canephora genome. The protein motifs identified in predict coffee sequences enabled characterize these genes as family’s members of PYL/RCARs receptors, PP2Cs phosphatases or SnRK2 kinases of the ABA response pathway. These families were functionally annotated in the C. canephora genome. In vivo analyses revealed that eight genes are upregulated under drought conditions in both leaves and roots tissues. Among them, three genes coding phosphatases were expressed in all (DT and DS) clones therefore suggesting that they were activated as a general response to cope with drought stress. However, two other phosphatase coding genes were up-regulated only in the DT clones, suggesting that they constituted key-genes for drought tolerance in these clones. The DT clones also showed differential gene expression profiles for five other genes therefore reinforcing the idea that multiple biological mechanisms are involved drought tolerance in C. canephora. In response to exogenous ABA, 17 genes were expressed in leaves of C. canephora and C. arabica plants. Several genes were differentially expressed in the DT clone 14 either in control condition or after 24h ABA treatment. Under control conditions, five genes were higher expressed in the C. canephora and C. arabica DT plants. The kinase CcSnRK2.6 was highlighted as gene specifically expressed in the C. canephora plants (DT and DS) after 72h of ABA treatment. Overall, it was observed that ABA signaling pathway is delayed in the DS C. arabica Rubi. Those molecular evidences corroborated with microscopies analyses which showed that the DT clone 14 was more efficient to control stomatal closure than other coffee plants in response to ABA treatment. All these evidences will help us to identify the genetic determinism of drought tolerance through ABA pathway essential to obtain molecular markers that could be used in coffee breeding programs.. MenosAbscisic acid (ABA) pathway is a phytohormone universally conserved in land plants which coordinates several aspects of the plant response to water deficit such as root architecture, seed dormancy and regulation of stomatal closure. A mechanism of ABA signal transduction has been proposed, evolving intracellular ABA receptors (PYR/PYL/RCARs) interacting with PP2Cs phosphatases and SnRK2 protein kinases regulating this tripartite protein system. The goal of this study was to identify and characterize for the first time the orthologs genes of this tripartite system in Coffea. For this purpose, protein sequences from Arabidopsis, citrus, rice, grape, tomato and potato were chosen as query to search orthologous genes in the Coffee Genome Hub (http://coffee-genome.org/). Differential expression in tissues as leaves, seeds, roots and floral organs waschecked through in silico analyses. In vivo gene expression analyses were also performed by RT-qPCR in leaves and roots of drought-tolerant (DT 14, 73 and 120) and drought-susceptible (DS 22) C. canephora Conilon clones submitted (or not) to drought. The expression profiles of the tripartite system CcPYL-PP2C-SnRK2 genes were also analyzed in leaves of C. arabica and C. canephora plants growing under hydroponic condition and submitted to ABA exogenous treatment (500 ?M). This approach allowed the identification and characterization of 24 candidate genes (9 PYL/RCARs, 6 PP2Cs and 9 SnRK2s) in C. canephora genome. The protein motifs ide... Mostrar Tudo |
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Palavras-Chave: |
Déficit hídrico. |
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Thesagro: |
Ácido abscísico; Hormonio vegetal. |
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Thesaurus NAL: |
Abscisic acid; Coffea; Plant hormones. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 04070nam a2200205 a 4500
001 2066980
005 2017-03-14
008 2016 bl uuuu m 00u1 u #d
100 1 $aCOTTA, M. G.
245 $aMolecular mechanisms in the first step of aba-mediated response in Coffea ssp.$h[electronic resource]
260 $a2016.$c2016
300 $a169 p.
500 $aTese (doutorado Biotecnologia Vegetal) - Universidade Federal de Lavras, Lavras, MG. Orientador: Alan Carvalho Andrade. Coorientador: Pierre Roger René Marraccini.
520 $aAbscisic acid (ABA) pathway is a phytohormone universally conserved in land plants which coordinates several aspects of the plant response to water deficit such as root architecture, seed dormancy and regulation of stomatal closure. A mechanism of ABA signal transduction has been proposed, evolving intracellular ABA receptors (PYR/PYL/RCARs) interacting with PP2Cs phosphatases and SnRK2 protein kinases regulating this tripartite protein system. The goal of this study was to identify and characterize for the first time the orthologs genes of this tripartite system in Coffea. For this purpose, protein sequences from Arabidopsis, citrus, rice, grape, tomato and potato were chosen as query to search orthologous genes in the Coffee Genome Hub (http://coffee-genome.org/). Differential expression in tissues as leaves, seeds, roots and floral organs waschecked through in silico analyses. In vivo gene expression analyses were also performed by RT-qPCR in leaves and roots of drought-tolerant (DT 14, 73 and 120) and drought-susceptible (DS 22) C. canephora Conilon clones submitted (or not) to drought. The expression profiles of the tripartite system CcPYL-PP2C-SnRK2 genes were also analyzed in leaves of C. arabica and C. canephora plants growing under hydroponic condition and submitted to ABA exogenous treatment (500 ?M). This approach allowed the identification and characterization of 24 candidate genes (9 PYL/RCARs, 6 PP2Cs and 9 SnRK2s) in C. canephora genome. The protein motifs identified in predict coffee sequences enabled characterize these genes as family’s members of PYL/RCARs receptors, PP2Cs phosphatases or SnRK2 kinases of the ABA response pathway. These families were functionally annotated in the C. canephora genome. In vivo analyses revealed that eight genes are upregulated under drought conditions in both leaves and roots tissues. Among them, three genes coding phosphatases were expressed in all (DT and DS) clones therefore suggesting that they were activated as a general response to cope with drought stress. However, two other phosphatase coding genes were up-regulated only in the DT clones, suggesting that they constituted key-genes for drought tolerance in these clones. The DT clones also showed differential gene expression profiles for five other genes therefore reinforcing the idea that multiple biological mechanisms are involved drought tolerance in C. canephora. In response to exogenous ABA, 17 genes were expressed in leaves of C. canephora and C. arabica plants. Several genes were differentially expressed in the DT clone 14 either in control condition or after 24h ABA treatment. Under control conditions, five genes were higher expressed in the C. canephora and C. arabica DT plants. The kinase CcSnRK2.6 was highlighted as gene specifically expressed in the C. canephora plants (DT and DS) after 72h of ABA treatment. Overall, it was observed that ABA signaling pathway is delayed in the DS C. arabica Rubi. Those molecular evidences corroborated with microscopies analyses which showed that the DT clone 14 was more efficient to control stomatal closure than other coffee plants in response to ABA treatment. All these evidences will help us to identify the genetic determinism of drought tolerance through ABA pathway essential to obtain molecular markers that could be used in coffee breeding programs..
650 $aAbscisic acid
650 $aCoffea
650 $aPlant hormones
650 $aÁcido abscísico
650 $aHormonio vegetal
653 $aDéficit hídrico
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Embrapa Café (CNPCa) |
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