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Registro Completo |
Biblioteca(s): |
Embrapa Acre. |
Data corrente: |
10/01/2012 |
Data da última atualização: |
01/11/2023 |
Tipo da produção científica: |
Artigo em Anais de Congresso |
Autoria: |
CARVALHO, C. A. C. de; COSTA, D. de A. da; ALVARES, V. de S.; NOGUEIRA, R. M.; LIMA, A. C. de; MADRUGA, A. L. S. |
Afiliação: |
CRISTHYAN ALEXANDRE CARCIA DE CARVALHO, UFAC; DAVID DE AQUINO DA COSTA; VIRGINIA DE SOUZA ALVARES, CPAF-AC; ROBERTA MARTINS NOGUEIRA, UFMT; ANGELICA COSTA DE LIMA, UNINORTE; AILSON LUIZ SUDAN MADRUGA, CPAF-AC. |
Título: |
Fungos produtores de aflatoxina na castanha-do-brasil (Bertholletia excelsa) após a secagem em secador a alta temperatura por convecção natural. |
Ano de publicação: |
2011 |
Fonte/Imprenta: |
In: SIMPÓSIO BRASILEIRO DE PÓS-COLHEITA DE FRUTAS, HORTALIÇAS E FLORES, 3., 2011, Nova Friburgo. Anais... Rio de Janeiro: Embrapa Agroindústria Tropical, 2011. |
Páginas: |
p. 264-267. |
Descrição Física: |
1 CD-ROM. |
Idioma: |
Português |
Conteúdo: |
O presente trabalho objetivou analisar a qualidade da castanha-do-brasil após a secagem em secador à alta temperatura por convecção natural. |
Palavras-Chave: |
Aflatoxinas; Calidad de la fruta; Castanha do brasil; Convecção natural; Madera tropical; Micotoxinas; Natural convection; Nuez del Brasil; Secadores de convección; Temperatura de secado. |
Thesagro: |
Aflatoxina; Aspergillus flavus; Bertholletia excelsa; Castanha do pará; Contaminação fúngica; Essência florestal; Fruto; Micotoxina; Qualidade; Resistência a temperatura; Secagem artificial. |
Thesaurus Nal: |
Aflatoxins; Aspergillus parasiticus; Brazil nuts; Convection dryers; Drying temperature; Fruit quality; Fungi; Mycotoxins; Tropical wood. |
Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/115604/1/24065.pdf
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Marc: |
LEADER 01868nam a2200541 a 4500 001 1912155 005 2023-11-01 008 2011 bl uuuu u00u1 u #d 100 1 $aCARVALHO, C. A. C. de 245 $aFungos produtores de aflatoxina na castanha-do-brasil (Bertholletia excelsa) após a secagem em secador a alta temperatura por convecção natural.$h[electronic resource] 260 $aIn: SIMPÓSIO BRASILEIRO DE PÓS-COLHEITA DE FRUTAS, HORTALIÇAS E FLORES, 3., 2011, Nova Friburgo. Anais... Rio de Janeiro: Embrapa Agroindústria Tropical$c2011 300 $ap. 264-267.$c1 CD-ROM. 520 $aO presente trabalho objetivou analisar a qualidade da castanha-do-brasil após a secagem em secador à alta temperatura por convecção natural. 650 $aAflatoxins 650 $aAspergillus parasiticus 650 $aBrazil nuts 650 $aConvection dryers 650 $aDrying temperature 650 $aFruit quality 650 $aFungi 650 $aMycotoxins 650 $aTropical wood 650 $aAflatoxina 650 $aAspergillus flavus 650 $aBertholletia excelsa 650 $aCastanha do pará 650 $aContaminação fúngica 650 $aEssência florestal 650 $aFruto 650 $aMicotoxina 650 $aQualidade 650 $aResistência a temperatura 650 $aSecagem artificial 653 $aAflatoxinas 653 $aCalidad de la fruta 653 $aCastanha do brasil 653 $aConvecção natural 653 $aMadera tropical 653 $aMicotoxinas 653 $aNatural convection 653 $aNuez del Brasil 653 $aSecadores de convección 653 $aTemperatura de secado 700 1 $aCOSTA, D. de A. da 700 1 $aALVARES, V. de S. 700 1 $aNOGUEIRA, R. M. 700 1 $aLIMA, A. C. de 700 1 $aMADRUGA, A. L. S.
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Embrapa Acre (CPAF-AC) |
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Registro Completo
Biblioteca(s): |
Embrapa Agrobiologia. |
Data corrente: |
30/08/2007 |
Data da última atualização: |
18/03/2015 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
Internacional - A |
Autoria: |
FORLANO, M. D.; TEIXEIRA, K. R. dos S.; SCOFIELD, A.; ELISEI, C.; YOTOKO, K. S. C.; FERNANDES, K. R.; LINHARES, G. F. C.; EWING, S. A.; MASSARD, C. L. |
Afiliação: |
M. D. Forlano, UCLA; Kátia Regina dos Santos Teixeira, Embrapa Agrobiologia; A. Scofield, UFPA; C. Elisei, Embrapa Gado de Corte; K. S. C. Yotoko, PUCRS; K. R. Fernandes, UFRRJ; G. F. C. Linhares, UFGO; S. A. Ewing, Oklahoma State University; C. L. Massard, UFRRJ. |
Título: |
Molecular characterization of Hepatozoon sp. from Brazilian dogs and its phylogenetic relationship with other Hepatozoon spp. |
Ano de publicação: |
2007 |
Fonte/Imprenta: |
Veterinary Parasitology, Amsterdam, v. 145, n. 1-2, p. 21-30, apr. 2007. |
Idioma: |
Inglês |
Notas: |
Parceria: UCLA, Universidade Federal do Pará, Embrapa Gado de Corte, Universidade Católica do Rio Grande do Sul, UFRRJ, Universidade Federal de Goiás, Oklahoma State University |
Conteúdo: |
To characterize phylogenetically the species which causes canine hepatozoonosis at two rural areas of Rio de Janeiro State, Brazil, we used universal or Hepatozoon spp. primer sets for the 18S SSU rRNA coding region. DNA extracts were obtained from blood samples of thirteen dogs naturally infected, from four experimentally infected, and from five puppies infected by vertical transmission from a dam, that was experimentally infected. DNA of sporozoites of Hepatozoon americanum was used as positive control. The amplification of DNA extracts from blood of dogs infected with sporozoites of Hepatozoon spp. was observed in the presence of primers to 18S SSU rRNA gene of Hepatozoon spp., whereas DNA of H. americanum sporozoites was amplified in the presence of either universal or Hepatozoon spp.-specific primer sets; the amplified products were approximately 600 bp in size. Cloned PCR products obtained from DNA extracts of blood from two dogs experimentally infected with Hepatozoon sp. were sequenced. The consensus sequence, derived from six sequence data sets, were blasted against sequences of 18S SSU rRNA of Hepatozoon spp. available at GenBank and aligned to homologous sequences to perform the phylogenetic analysis. This analysis clearly showed that our sequence clustered, independently of H. americanum sequences, within a group comprising other Hepatozoon canis sequences. Our results confirmed the hypothesis that the agent causing hepatozoonosis in the areas studied in Brazil is H. canis, supporting previous reports that were based on morphological and morphometric analyses. MenosTo characterize phylogenetically the species which causes canine hepatozoonosis at two rural areas of Rio de Janeiro State, Brazil, we used universal or Hepatozoon spp. primer sets for the 18S SSU rRNA coding region. DNA extracts were obtained from blood samples of thirteen dogs naturally infected, from four experimentally infected, and from five puppies infected by vertical transmission from a dam, that was experimentally infected. DNA of sporozoites of Hepatozoon americanum was used as positive control. The amplification of DNA extracts from blood of dogs infected with sporozoites of Hepatozoon spp. was observed in the presence of primers to 18S SSU rRNA gene of Hepatozoon spp., whereas DNA of H. americanum sporozoites was amplified in the presence of either universal or Hepatozoon spp.-specific primer sets; the amplified products were approximately 600 bp in size. Cloned PCR products obtained from DNA extracts of blood from two dogs experimentally infected with Hepatozoon sp. were sequenced. The consensus sequence, derived from six sequence data sets, were blasted against sequences of 18S SSU rRNA of Hepatozoon spp. available at GenBank and aligned to homologous sequences to perform the phylogenetic analysis. This analysis clearly showed that our sequence clustered, independently of H. americanum sequences, within a group comprising other Hepatozoon canis sequences. Our results confirmed the hypothesis that the agent causing hepatozoonosis in the areas studied in Brazil i... Mostrar Tudo |
Thesaurus NAL: |
Hepatozoon canis. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02505naa a2200241 a 4500 001 1629413 005 2015-03-18 008 2007 bl uuuu u00u1 u #d 100 1 $aFORLANO, M. D. 245 $aMolecular characterization of Hepatozoon sp. from Brazilian dogs and its phylogenetic relationship with other Hepatozoon spp. 260 $c2007 500 $aParceria: UCLA, Universidade Federal do Pará, Embrapa Gado de Corte, Universidade Católica do Rio Grande do Sul, UFRRJ, Universidade Federal de Goiás, Oklahoma State University 520 $aTo characterize phylogenetically the species which causes canine hepatozoonosis at two rural areas of Rio de Janeiro State, Brazil, we used universal or Hepatozoon spp. primer sets for the 18S SSU rRNA coding region. DNA extracts were obtained from blood samples of thirteen dogs naturally infected, from four experimentally infected, and from five puppies infected by vertical transmission from a dam, that was experimentally infected. DNA of sporozoites of Hepatozoon americanum was used as positive control. The amplification of DNA extracts from blood of dogs infected with sporozoites of Hepatozoon spp. was observed in the presence of primers to 18S SSU rRNA gene of Hepatozoon spp., whereas DNA of H. americanum sporozoites was amplified in the presence of either universal or Hepatozoon spp.-specific primer sets; the amplified products were approximately 600 bp in size. Cloned PCR products obtained from DNA extracts of blood from two dogs experimentally infected with Hepatozoon sp. were sequenced. The consensus sequence, derived from six sequence data sets, were blasted against sequences of 18S SSU rRNA of Hepatozoon spp. available at GenBank and aligned to homologous sequences to perform the phylogenetic analysis. This analysis clearly showed that our sequence clustered, independently of H. americanum sequences, within a group comprising other Hepatozoon canis sequences. Our results confirmed the hypothesis that the agent causing hepatozoonosis in the areas studied in Brazil is H. canis, supporting previous reports that were based on morphological and morphometric analyses. 650 $aHepatozoon canis 700 1 $aTEIXEIRA, K. R. dos S. 700 1 $aSCOFIELD, A. 700 1 $aELISEI, C. 700 1 $aYOTOKO, K. S. C. 700 1 $aFERNANDES, K. R. 700 1 $aLINHARES, G. F. C. 700 1 $aEWING, S. A. 700 1 $aMASSARD, C. L. 773 $tVeterinary Parasitology, Amsterdam$gv. 145, n. 1-2, p. 21-30, apr. 2007.
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