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Registro Completo |
Biblioteca(s): |
Embrapa Trigo. |
Data corrente: |
21/03/2017 |
Data da última atualização: |
21/03/2017 |
Tipo da produção científica: |
Artigo em Anais de Congresso |
Autoria: |
BAZZO, J. H. B.; MARINHO, J. de L.; SOUZA, D. N. de; SILVA, S. R.; CARDOSO, C. P.; CESCO, V. J. S.; FAVORETTO, V. R.; ZUCARELI, C. |
Afiliação: |
JOSÉ HENRIQUE BIZZARRI BAZZO, UNIVERSIDADE ESTADUAL DE LONDRINA; JÉSSICA DE LUCENA MARINHO, UNIVERSIDADE ESTADUAL DE LONDRINA; DIOGO NASCIMENTO DE SOUZA, UNIVERSIDADE ESTADUAL DE LONDRINA; SERGIO RICARDO SILVA, CNPT; CAROLINA PEREIRA CARDOSO, UNIVERSIDADE ESTADUAL DE LONDRINA; VICTOR JOSÉ SALOMÃO CESCO, UNIVERSIDADE ESTADUAL DE LONDRINA; VITOR RAMPAZZO FAVORETTO, UNIVERSIDADE ESTADUAL DE LONDRINA; CLAUDEMIR ZUCARELI, UNIVERSIDADE ESTADUAL DE LONDRINA. |
Título: |
Adubação nitrogenada na qualidade fisiológica de sementes de genótipos trigo. |
Ano de publicação: |
2016 |
Fonte/Imprenta: |
In: REUNIÃO DA COMISSÃO BRASILEIRA DE PESQUISA DE TRIGO E TRITICALE, 10., 2016, Londrina. Anais... Londrina: Comissão Brasileira de Pesquisa de Trigo e Triticale, 2016. |
Páginas: |
5 p. |
Descrição Física: |
1 CD-ROM. |
Idioma: |
Português |
Thesagro: |
Fertilizante nitrogenado; Fisiologia vegetal; Nitrogênio; Trigo. |
Thesaurus Nal: |
Nitrogen; Nitrogen fertilizers; Plant physiology; Wheat. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/157940/1/ID43991-2016RCBPTT10BASSO103.pdf
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Marc: |
LEADER 00957nam a2200289 a 4500 001 2067424 005 2017-03-21 008 2016 bl uuuu u00u1 u #d 100 1 $aBAZZO, J. H. B. 245 $aAdubação nitrogenada na qualidade fisiológica de sementes de genótipos trigo.$h[electronic resource] 260 $aIn: REUNIÃO DA COMISSÃO BRASILEIRA DE PESQUISA DE TRIGO E TRITICALE, 10., 2016, Londrina. Anais... Londrina: Comissão Brasileira de Pesquisa de Trigo e Triticale$c2016 300 $a5 p.$c1 CD-ROM. 650 $aNitrogen 650 $aNitrogen fertilizers 650 $aPlant physiology 650 $aWheat 650 $aFertilizante nitrogenado 650 $aFisiologia vegetal 650 $aNitrogênio 650 $aTrigo 700 1 $aMARINHO, J. de L. 700 1 $aSOUZA, D. N. de 700 1 $aSILVA, S. R. 700 1 $aCARDOSO, C. P. 700 1 $aCESCO, V. J. S. 700 1 $aFAVORETTO, V. R. 700 1 $aZUCARELI, C.
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Registro original: |
Embrapa Trigo (CNPT) |
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Registro Completo
Biblioteca(s): |
Embrapa Arroz e Feijão. |
Data corrente: |
13/04/2021 |
Data da última atualização: |
13/04/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
SOUSA, T. P. de; CHAIBUB, A. A.; CORTES, M. V. de C. B.; BATISTA, T. F. C.; BEZERRA, G. de A.; SILVA, G. B. da; FILIPPI, M. C. C. de. |
Afiliação: |
THATYANE PEREIRA DE SOUSA, UFG; AMANDA ABDALLAH CHAIBUB, UFG; MARCIO VINICIUS DE C BARROS CORTES, CNPAF; TELMA FATIMA COELHO BATISTA, UNIVERSIDADE FEDERAL RURAL DA AMAZONIA; GUSTAVO DE ANDRADE BEZERRA, UFG; GISELE BARATA DA SILVA, UNIVERSIDADE FEDERAL RURAL DA AMAZONIA; MARTA CRISTINA CORSI DE FILIPPI, CNPAF. |
Título: |
Molecular identification of Trichoderma sp. isolates and biochemical characterization of antagonistic interaction against rice blast. |
Ano de publicação: |
2021 |
Fonte/Imprenta: |
Archives of Microbiology, 2021. |
ISSN: |
0302-8933 |
DOI: |
https://doi.org/10.1007/s00203-021-02307-5 |
Idioma: |
Inglês |
Conteúdo: |
This study aimed to identify four isolates of Trichoderma sp. (Ufra.T06, Ufra.T09, Ufra.T12, and Ufra.T52) and characterize their interaction with Magnaporthe oryzae in vitro and in vivo conditions. The four isolates of Trichoderma sp. were sequenced, investigated as an antagonist against M. oryzae in five Petri plate assays, and as an inhibitor of conidial germination appressoria formation. Finally, were quantified the lytic activity of chitinase (CHI), glucanase (GLU), and protease (PRO) during co-cultivation of Trichoderma sp. and M. oryzae. In vivo, leaf blast suppression was evaluated intwo assays: simultaneous and curative application. Both in vitro and in vivo assays were scanned by electron microscopy (SEM). All isolates were identified as Trichoderma asperellum. All in vitro Petri plates assays reduced M. oryzae colony growth (paired?91.18% by Ufra.T09, volatile metabolites?all isolates equally reduced, non-volatile?68.33% by Ufra.T06,thermostability?99.77% by Ufra.T52 and co-cultivate?64.25% by Ufra.T52). The filtrates and conidia suspensions for T. asperellum isolates inhibited the conidia germination and appressoria formation significantly. In co-cultivate (mycelial or cell wall), all enzymes (GLU, CHI, and PRO) and times (24, 48, and 72 h) showed increased activity. In vivo, reduced leafblast severity until 94.64% (Ufra.T52cs) in a simultaneous and until 85% (Ufra.T09 24 and 48 hasi) in a curative application. T. asperellum isolates showed efficient control of M. oryzae by mycoparasitism, and antibiosis mechanisms were interfered with by the M. oryzae infection process. MenosThis study aimed to identify four isolates of Trichoderma sp. (Ufra.T06, Ufra.T09, Ufra.T12, and Ufra.T52) and characterize their interaction with Magnaporthe oryzae in vitro and in vivo conditions. The four isolates of Trichoderma sp. were sequenced, investigated as an antagonist against M. oryzae in five Petri plate assays, and as an inhibitor of conidial germination appressoria formation. Finally, were quantified the lytic activity of chitinase (CHI), glucanase (GLU), and protease (PRO) during co-cultivation of Trichoderma sp. and M. oryzae. In vivo, leaf blast suppression was evaluated intwo assays: simultaneous and curative application. Both in vitro and in vivo assays were scanned by electron microscopy (SEM). All isolates were identified as Trichoderma asperellum. All in vitro Petri plates assays reduced M. oryzae colony growth (paired?91.18% by Ufra.T09, volatile metabolites?all isolates equally reduced, non-volatile?68.33% by Ufra.T06,thermostability?99.77% by Ufra.T52 and co-cultivate?64.25% by Ufra.T52). The filtrates and conidia suspensions for T. asperellum isolates inhibited the conidia germination and appressoria formation significantly. In co-cultivate (mycelial or cell wall), all enzymes (GLU, CHI, and PRO) and times (24, 48, and 72 h) showed increased activity. In vivo, reduced leafblast severity until 94.64% (Ufra.T52cs) in a simultaneous and until 85% (Ufra.T09 24 and 48 hasi) in a curative application. T. asperellum isolates showed efficient control of M... Mostrar Tudo |
Palavras-Chave: |
Antagonism; Bioagent; Mycoparasitism. |
Thesagro: |
Antagonismo; Arroz; Brusone; Controle Biológico; Marcador Molecular; Oryza Sativa; Trichoderma. |
Thesaurus NAL: |
Biological control; Mycoparasites; Rice. |
Categoria do assunto: |
H Saúde e Patologia |
Marc: |
LEADER 02690naa a2200373 a 4500 001 2131247 005 2021-04-13 008 2021 bl uuuu u00u1 u #d 022 $a0302-8933 024 7 $ahttps://doi.org/10.1007/s00203-021-02307-5$2DOI 100 1 $aSOUSA, T. P. de 245 $aMolecular identification of Trichoderma sp. isolates and biochemical characterization of antagonistic interaction against rice blast.$h[electronic resource] 260 $c2021 520 $aThis study aimed to identify four isolates of Trichoderma sp. (Ufra.T06, Ufra.T09, Ufra.T12, and Ufra.T52) and characterize their interaction with Magnaporthe oryzae in vitro and in vivo conditions. The four isolates of Trichoderma sp. were sequenced, investigated as an antagonist against M. oryzae in five Petri plate assays, and as an inhibitor of conidial germination appressoria formation. Finally, were quantified the lytic activity of chitinase (CHI), glucanase (GLU), and protease (PRO) during co-cultivation of Trichoderma sp. and M. oryzae. In vivo, leaf blast suppression was evaluated intwo assays: simultaneous and curative application. Both in vitro and in vivo assays were scanned by electron microscopy (SEM). All isolates were identified as Trichoderma asperellum. All in vitro Petri plates assays reduced M. oryzae colony growth (paired?91.18% by Ufra.T09, volatile metabolites?all isolates equally reduced, non-volatile?68.33% by Ufra.T06,thermostability?99.77% by Ufra.T52 and co-cultivate?64.25% by Ufra.T52). The filtrates and conidia suspensions for T. asperellum isolates inhibited the conidia germination and appressoria formation significantly. In co-cultivate (mycelial or cell wall), all enzymes (GLU, CHI, and PRO) and times (24, 48, and 72 h) showed increased activity. In vivo, reduced leafblast severity until 94.64% (Ufra.T52cs) in a simultaneous and until 85% (Ufra.T09 24 and 48 hasi) in a curative application. T. asperellum isolates showed efficient control of M. oryzae by mycoparasitism, and antibiosis mechanisms were interfered with by the M. oryzae infection process. 650 $aBiological control 650 $aMycoparasites 650 $aRice 650 $aAntagonismo 650 $aArroz 650 $aBrusone 650 $aControle Biológico 650 $aMarcador Molecular 650 $aOryza Sativa 650 $aTrichoderma 653 $aAntagonism 653 $aBioagent 653 $aMycoparasitism 700 1 $aCHAIBUB, A. A. 700 1 $aCORTES, M. V. de C. B. 700 1 $aBATISTA, T. F. C. 700 1 $aBEZERRA, G. de A. 700 1 $aSILVA, G. B. da 700 1 $aFILIPPI, M. C. C. de 773 $tArchives of Microbiology, 2021.
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