Cultivo de protoplastos de yuca y Stylosanthes

cg.subject.ciatCASSAVAen_US
dc.contributor.authorSzabados, Laszloen_US
dc.date.accessioned2016-02-29T17:13:08Zen_US
dc.date.available2016-02-29T17:13:08Zen_US
dc.identifier.urihttps://hdl.handle.net/10568/71862en_US
dc.titleCultivo de protoplastos de yuca y Stylosanthesen_US
dcterms.abstractMethods of isolation and culture of cassava and Stylosanthes protoplasts are described. The application of these methods requires the routine regeneration of plants from isolated protoplasts. In cassava, protoplast isolation from leaves and shoot tips of plants cultured in vitro and from somatic embryos, differentiated from leaf segments, was possible with an enzyme mixture consisting of Onozuka cellulase, hemicellulase, and Pectolyase. Isolated protoplasts were purified by filtration and cultured in liquid medium; they regenerated cell wall after 1-2 days of culture and presented cell division after 3-4 days. Division frequency observed was 10- 20 percent in protoplast cultures from leaf mesophyll and shoot tips. In cultures of somatic embryos, this frequency was less than 5 percent. Within 3-4 wk., dividing protoplasts formed colonies. The plated colonies formed callus in several culture media. Protoplasts from 10 cassava var. have been isolated and cultured. (CIAT)en_US
dcterms.accessRightsOpen Accessen_US
dcterms.bibliographicCitationSZABADOS, L. 1985. Cultivo de protoplastos de yuca y Stylosanthes. Centro Internacional de Agricultura Tropical (CIAT), Cali, CO. 5 p. (Seminarios internos SE-5-85)en_US
dcterms.extent5 p.en_US
dcterms.issued1985en_US
dcterms.languageesen_US
dcterms.publisherInternational Center for Tropical Agricultureen_US
dcterms.subjectmanihot esculentaen_US
dcterms.subjecttissue cultureen_US
dcterms.subjectprotoplastsen_US
dcterms.subjectstarch cropsen_US
dcterms.subjectcultivo de tejidosen_US
dcterms.subjectprotoplastosen_US
dcterms.typeReporten_US

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