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Registro Completo |
Biblioteca(s): |
Embrapa Clima Temperado; Embrapa Meio-Norte; Embrapa Pecuária Sul; Embrapa Suínos e Aves; Embrapa Trigo. |
Data corrente: |
07/01/1991 |
Data da última atualização: |
31/03/1999 |
Autoria: |
BRESOLIN, M.; VIOLA, E. A. |
Título: |
O milho no contexto mundial, nacional e do Rio Grande do Sul. |
Ano de publicação: |
1995 |
Fonte/Imprenta: |
Porto Alegre: EMATER-RS, 1995. |
Páginas: |
100p. |
Série: |
(Serie Realidade Rural, 18) |
Idioma: |
Português |
Conteúdo: |
Situacao mundial; Producao nacional; A producao dos estados que compoem o Codesul; O milho no Rio Grande do Sul; Zoneamento agroclimatico e epocas de semeadura; Adubacao praticada; Armazenagem; Fluxo de comercializacao e destino da producao; Resposta a tecnologia; Problemas da cultura; Precos; Pesquisa; Assistencia tecnica e extensao rural; O milho e o Mercosul. |
Palavras-Chave: |
Brasil; Producao mundial; Producao nacional; Production; Rio Grande do Sul. |
Thesagro: |
Milho; Produção; Zea Mays. |
Thesaurus Nal: |
corn. |
Categoria do assunto: |
-- |
Marc: |
LEADER 00997nam a2200253 a 4500 001 1055074 005 1999-03-31 008 1995 bl uuuu 00u1 u #d 100 1 $aBRESOLIN, M. 245 $aO milho no contexto mundial, nacional e do Rio Grande do Sul. 260 $aPorto Alegre: EMATER-RS$c1995 300 $a100p. 490 $a(Serie Realidade Rural, 18) 520 $aSituacao mundial; Producao nacional; A producao dos estados que compoem o Codesul; O milho no Rio Grande do Sul; Zoneamento agroclimatico e epocas de semeadura; Adubacao praticada; Armazenagem; Fluxo de comercializacao e destino da producao; Resposta a tecnologia; Problemas da cultura; Precos; Pesquisa; Assistencia tecnica e extensao rural; O milho e o Mercosul. 650 $acorn 650 $aMilho 650 $aProdução 650 $aZea Mays 653 $aBrasil 653 $aProducao mundial 653 $aProducao nacional 653 $aProduction 653 $aRio Grande do Sul 700 1 $aVIOLA, E. A.
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Embrapa Meio-Norte (CPAMN) |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Recursos Genéticos e Biotecnologia. Para informações adicionais entre em contato com cenargen.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
Data corrente: |
10/02/2012 |
Data da última atualização: |
27/02/2023 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
ABREU, E. F. M.; ANDRADE, E. C. de; ARAGAO, F. J. L. |
Afiliação: |
Emanuel Felipe Medereiros Abreu, UnB; EDUARDO CHUMBINHO DE ANDRADE, CNPMF; FRANCISCO JOSE LIMA ARAGAO, CENARGEN. |
Título: |
Molecular comparison between isolates of Cowpea severe mosaic virus and Cowpea aphid borne mosaic virus from Northeast Brazil. |
Ano de publicação: |
2011 |
Fonte/Imprenta: |
In: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 3, 2011, Ilhéus. Resumos. [S. l.]: Sociedade Brasileira de Genética, 2011. pdf 34699 |
Páginas: |
p. 6 |
Idioma: |
Inglês |
Conteúdo: |
Cowpea (Vigna unguiculata) is an important plant crop in Northeast Brazil being traditionally cultivated by small farmers. Virus diseases are considered to be the main factor limiting cowpea yield in the region. The severe mosaic disease caused by the Cowpea severe mosaic virus (CpSMV), family Comoviridae, genus Comovirus, seems to be one of the most prevalent diseases leading to high yield losses in this crop. The CABMV belongs to the genus Potyvirus in the Potyviridae family, and infects cowpea worldwide. In the northeastern Region of Brazil, both viruses can be found in cowpea planted areas. The aim of the present study was to access the degree of homology among a 2500 and 1500bp region of different isolates of CpSMV and CABMV, respectively; obtained in different northeastern regions in Brazil, and to compare it to isolates throughout the world. Plants with CPSMV and CABMV symptoms from the states of Piauí, Ceará, Rio Grande do Norte, Paraiba, Pernambuco, Alagoas, Sergipe and Bahia were collected, and the isolates were identified by RT-PCR analysis. Total RNA was extracted from infected tissue with Trizol Reagent (Invitrogen) according to manufacturer's recommendations, and afterwards used for synthesis of cDNA fragments by RT-PCR using the Superscript® III Reverse Polymerase and Taq DNA Polymerase (Invitrogen), according to manufacturer?s recommendations. The synthesized primers were able to amplify fragments of 2500 and 1500bp of the CpSMV and CABMV virus, respectively, by RT-PCR. Amplification products were directly cloned into the pGEMT-Easy plasmid vector (Promega), according to the manufacturer?s instructions. Cloned fragments were sequenced in both orientations. Deduced amino acid sequences of the virus were compared to sequences available from GenBank. Multiple sequence alignments were obtained with Clustal W. Phylogenetic trees using the MEGA version 4.1 software package and the neighbour-joining method with Poisson correction. Tree branches were bootstrapped with 1000 permutations. CpSMV and CABMV diseases remain as limiting factors in this crop in Brazil, and breeding programs, either by conventional or engineered approaches, should be targeted at establishing resistance of cowpeas to CpSMV and CABMV. MenosCowpea (Vigna unguiculata) is an important plant crop in Northeast Brazil being traditionally cultivated by small farmers. Virus diseases are considered to be the main factor limiting cowpea yield in the region. The severe mosaic disease caused by the Cowpea severe mosaic virus (CpSMV), family Comoviridae, genus Comovirus, seems to be one of the most prevalent diseases leading to high yield losses in this crop. The CABMV belongs to the genus Potyvirus in the Potyviridae family, and infects cowpea worldwide. In the northeastern Region of Brazil, both viruses can be found in cowpea planted areas. The aim of the present study was to access the degree of homology among a 2500 and 1500bp region of different isolates of CpSMV and CABMV, respectively; obtained in different northeastern regions in Brazil, and to compare it to isolates throughout the world. Plants with CPSMV and CABMV symptoms from the states of Piauí, Ceará, Rio Grande do Norte, Paraiba, Pernambuco, Alagoas, Sergipe and Bahia were collected, and the isolates were identified by RT-PCR analysis. Total RNA was extracted from infected tissue with Trizol Reagent (Invitrogen) according to manufacturer's recommendations, and afterwards used for synthesis of cDNA fragments by RT-PCR using the Superscript® III Reverse Polymerase and Taq DNA Polymerase (Invitrogen), according to manufacturer?s recommendations. The synthesized primers were able to amplify fragments of 2500 and 1500bp of the CpSMV and CABMV virus, respectively,... Mostrar Tudo |
Palavras-Chave: |
CABMV; Cowpea; CpSMV; Molecular and RT-PCR analysis; Virus diseases. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
Marc: |
LEADER 02995nam a2200205 a 4500 001 1915005 005 2023-02-27 008 2011 bl uuuu u01u1 u #d 100 1 $aABREU, E. F. M. 245 $aMolecular comparison between isolates of Cowpea severe mosaic virus and Cowpea aphid borne mosaic virus from Northeast Brazil.$h[electronic resource] 260 $aIn: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 3, 2011, Ilhéus. Resumos. [S. l.]: Sociedade Brasileira de Genética, 2011. pdf 34699$c2011 300 $ap. 6 520 $aCowpea (Vigna unguiculata) is an important plant crop in Northeast Brazil being traditionally cultivated by small farmers. Virus diseases are considered to be the main factor limiting cowpea yield in the region. The severe mosaic disease caused by the Cowpea severe mosaic virus (CpSMV), family Comoviridae, genus Comovirus, seems to be one of the most prevalent diseases leading to high yield losses in this crop. The CABMV belongs to the genus Potyvirus in the Potyviridae family, and infects cowpea worldwide. In the northeastern Region of Brazil, both viruses can be found in cowpea planted areas. The aim of the present study was to access the degree of homology among a 2500 and 1500bp region of different isolates of CpSMV and CABMV, respectively; obtained in different northeastern regions in Brazil, and to compare it to isolates throughout the world. Plants with CPSMV and CABMV symptoms from the states of Piauí, Ceará, Rio Grande do Norte, Paraiba, Pernambuco, Alagoas, Sergipe and Bahia were collected, and the isolates were identified by RT-PCR analysis. Total RNA was extracted from infected tissue with Trizol Reagent (Invitrogen) according to manufacturer's recommendations, and afterwards used for synthesis of cDNA fragments by RT-PCR using the Superscript® III Reverse Polymerase and Taq DNA Polymerase (Invitrogen), according to manufacturer?s recommendations. The synthesized primers were able to amplify fragments of 2500 and 1500bp of the CpSMV and CABMV virus, respectively, by RT-PCR. Amplification products were directly cloned into the pGEMT-Easy plasmid vector (Promega), according to the manufacturer?s instructions. Cloned fragments were sequenced in both orientations. Deduced amino acid sequences of the virus were compared to sequences available from GenBank. Multiple sequence alignments were obtained with Clustal W. Phylogenetic trees using the MEGA version 4.1 software package and the neighbour-joining method with Poisson correction. Tree branches were bootstrapped with 1000 permutations. CpSMV and CABMV diseases remain as limiting factors in this crop in Brazil, and breeding programs, either by conventional or engineered approaches, should be targeted at establishing resistance of cowpeas to CpSMV and CABMV. 653 $aCABMV 653 $aCowpea 653 $aCpSMV 653 $aMolecular and RT-PCR analysis 653 $aVirus diseases 700 1 $aANDRADE, E. C. de 700 1 $aARAGAO, F. J. L.
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