A cryopreservation protocol for immature zygotic embryos of species of Ilex (aquifoliaceae)

• Autores: Mroginski, Luis Amado; Sansberro, Pedro Alfonso; Scocchi, Adriana M.; Luna, Claudia Verónica; Rey, Hebe Yolanda
• Año de publicación: 2008
• Idioma: español castellano
• Tipo de recurso: artículo
• Fuente: Biocell, 2008, vol. 32, no. 1, p. 33-39.
• Materia: Encapsulation-dehydration; Germplasm preservation; Liquid nitrogen; Llex
• Institución: Universidad Nacional del Nordeste

Fil: Mroginski, Luis Amado. Universidad Nacional del Nordeste. Facultad de Ciencias Agrarias; Argentina.
Fil: Sansberro, Pedro Alfonso. Universidad Nacional del Nordeste. Facultad de Ciencias Agrarias; Argentina.
Fil: Scocchi, Adriana M. Universidad Nacional del Nordeste. Facultad de Ciencias Agrarias; Argentina.
Fil: Luna, Claudia Verónica. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Botánica del Nordeste; Argentina.
Fil: Luna Claudia Verónica. Universidad Nacional del Nordeste. Facultad de Ciencias Agrarias; Argentina.
Fil: Rey, Hebe Yolanda. Universidad Nacional del Nordeste. Faculta de Ciencias Agrarias; Argentina.
Tropical Ilex species have recalcitrant seeds. This work describes experiments demonstrating the feasibility of long-term conservation of Ilex brasiliensis, I. brevicuspis, I. dumosa, I. intergerrima, I. paraguariensis, I. pseudoboxus, I. taubertiana, and I. theezans through cryopreservation of zygotic rudimen- tary embryos at the heart developmental stage. The embryos were aseptically removed from the seeds and precultured (7 days) in the dark, at 27± 2oC on solidified (0.8% agar) 1/4MS medium, [consisting of quarter- strength salts and vitamins of Murashige and Skoog (1962) medium] with 3% sucrose and 0.1 mg/l Zeatin. The embryos were then encapsulated in 3% calcium alginate beads and pretreated at 24 h intervals in liquid medium supplemented with progressively increasing sucrose concentrations (0.5, 0.75 and 1 M). Beads were dehydrated for 5 h with silicagel to 25% water content (fresh weight basis) and then placed in sterile 5 ml cryovials. Then the beads were either plunged rapidly in liquid nitrogen were they were kept for 1 h (rapid cooling) or cooled at 1oC min-1 to -30oC. Then the beads were immersed in liquid nitrogen for 1 h (slow cooling). The beads were rewarmed by immersion of the cryovials for 1 min in a water bath thermostated at 30oC. Finally, beads were transferred onto culture medium (1/4MS, 3% sucrose, 0.1 mg/l zeatin, solidified with 0.8% agar) and incubated in a growth room at 27 ± 2oC under a 14 h light (116 μmol. m-2.s-1)/ 10 h dark photoperiod. Maximum recovery percentages between 15 and 83% (depending on de the species and the treatment) were obtained with the cryopreserved embryos.