Development of a bioassay to quantify the ricin toxin content of castor bean (Ricinus communis L.) seeds - doi: 10.4025/actasciagron.v34i4.11284

In this study, we developed a bioassay to quantify the ricin toxin content of castor bean seeds. Existing quantification methods do not always reflect actual toxicity of the seeds analyzed, which may present lower ricin content even though they are more toxic than seeds presenting a higher content o...

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Detalles Bibliográficos
Autores: Demant, Carlos Alberto Rauer, Auld, Dick, Demant, Aline Rodrigues de Mello
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:Brasil
Institución:Universidade Estadual de Maringá (UEM)
Repositorio:Acta Scientiarum. Agronomy (Online)
Idioma:portugués
inglés
OAI Identifier:oai:periodicos.uem.br/ojs:article/11284
Acceso en línea:http://www.periodicos.uem.br/ojs/index.php/ActaSciAgron/article/view/11284
Access Level:acceso abierto
Palabra clave:Microbiologia e melhoramento genético de plantas
toxin
C. elegans
selection
Ricinus
microbiologia e melhoramento genetico de plantas
Descripción
Sumario:In this study, we developed a bioassay to quantify the ricin toxin content of castor bean seeds. Existing quantification methods do not always reflect actual toxicity of the seeds analyzed, which may present lower ricin content even though they are more toxic than seeds presenting a higher content of ricin. This is because these methods actually measure the addition of ricin RCA, which is a compound less toxic than pure ricin. We decided to use in this study, the nematode Caenorhabditis elegans, which has been widely used by the pharmaceutical industry. We tested two strains of C. elegans using different methods in 8 experiments. We examined 4 methods of extracting the ricin complex and 3 methods of exposing the nematodes. Among the nematode strains and ricin extraction methods tested, we concluded that the best strain for testing ricin toxicity was the strain called N2 and that the best method for ricin extraction was a rotating bath followed by centrifugation and exposing the nematodes in 24 well plates with a solution of nematodes extracted from the media with destilated waterexposing the nematodes in 24-well plates This method is inexpensive, quick and adequate for the selection of offspring with lower RIP content.