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Registro Completo
Biblioteca(s):  Embrapa Mandioca e Fruticultura.
Data corrente:  16/04/2004
Data da última atualização:  16/04/2004
Autoria:  GOMEZ-VASQUEZ, R.; DAY, R. C.; BEECHING, J. R.; COOPER, R. M.
Título:  Biochemical components of disease resistance of cassava.
Ano de publicação:  1998
Fonte/Imprenta:  Revista Brasileira de Mandioca, Salvador, v. 17, p. 40, nov., 1998., Suplemento.
Idioma:  Inglês
Conteúdo:  Resistant genotypes offer the only durable, practicable means of controlling Xanthomonas bacterial bligth, but the nature of defences of cassava to this and to other diseases are virtually unknown. Suspension cultured cells in vitro show a series of resistance related responses to a range of microbial elicitors such as glucans from yeast and Colletotrichum, and to certain endogenous elicitors such as oligogalacturonides, jasmonic acid and glutathione. Surprisingly, pure LPS was ineffective but crude commercial EPS [xanthan] had effect. Auxin levels had a profound influence on intensity of cellular responses. This facile system has revealed a rapid [from 3 mins] and intensive, extracellular oxidative burst [as MO2] which can function as a first fine of defence by creating toxic Conditions, cross-linking cell wall components and as a diffusible signal. Subsequently, defence-related genes such as PAL are induced which may contribute to formation of flavonoids and antibacterial compounds. The oxidative burst may derive in part from the increased activity or production of peroxidase or from xanthine oxidase which is constitutive; gene[s] for the latter are under study. Similarly, in plants in response to incompatible bacterial pathogens, there is rapid generation of peroxide associated with plant cell walls, as revealed by cerium chloride and transmission EM; other localised increased were in peroxidase, PAL and its mRNA [revealed by in situ hybridisation], flavonoids and unknow... Mostrar Tudo
Categoria do assunto:  --
Marc:  Mostrar Marc Completo
Registro original:  Embrapa Mandioca e Fruticultura (CNPMF)
Biblioteca ID Origem Tipo/Formato Classificação Cutter Registro Volume Status URL
CNPMF20986 - 1ADDAP - --633.68205
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Registro Completo

Biblioteca(s):  Embrapa Cerrados.
Data corrente:  20/03/2008
Data da última atualização:  20/10/2009
Tipo da produção científica:  Documentos
Autoria:  ANJOS, J. de R. N. dos; CHARCHAR, M. J. d'A.
Afiliação:  José de Ribamar Nazareno dos Anjos, CPAC; Maria José d'Ávila Charchar, CPAC.
Título:  Patogenicidade de isolados de fusarium sacchari de mangueira do Cerrado do Brasil Central.
Ano de publicação:  2007
Fonte/Imprenta:  Planaltina, DF: Embrapa Cerrados, 2007.
Páginas:  16 p.
Série:  (Embrapa Cerrados. Documentos, 180).
Idioma:  Português
Conteúdo:  ABSTRACT: The fungus Fusarium sacchari (E.J. Butler & Hafiz Kahn) W. Gams, was consistently isolated from infected malformed shoots and panicles of mango in the Cerrado Region of Central Brazil, from 1998 to 2000. Pathogenicity tests of the F. sacchari isolates were carried out on potted six month-old Tommy Atkins seedlings by introducting a PDA disk with fungal mycelium and conidia in a vertical slit at the tip. F. sacchari is almost completely restricted to shoot tissues in malformed trees. The levels of colonization are highest in malformed vegetative and floral shoots and are much lower in asymptomatic shoots. Treatment of mango malformation with fungicides is ineffective. The only viable control option is the removal and burning of the affected shoot tissue.
Palavras-Chave:  Control; Controle; Fusarium sacchari; Plant diseases.
Thesagro:  Doença de Planta; Doença Fúngica; Fungo; Malformação; Manga; Mangifera Indica; Patogenicidade.
Thesaurus NAL:  fungi; mangoes; pathogenicity.
Categoria do assunto:  --
URL:  https://ainfo.cnptia.embrapa.br/digital/bitstream/CPAC-2009/28635/1/doc_180.pdf
Marc:  Mostrar Marc Completo
Registro original:  Embrapa Cerrados (CPAC)
Biblioteca ID Origem Tipo/Formato Classificação Cutter Registro Volume Status
CPAC28635 - 1UMTFL - --FOL7815CRI7329
CPAC28635 - 2UMTFL - --FOL7815DOC217
CPAC28635 - 3UMTFL - --FOL7815FOL7815
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