INVESTIGADORES
DOLCE natalia Raquel
artículos
Título:
Cryopreservation of Ilex dumosa (Aquifoliaceae) germplasm.
Autor/es:
DOLCE, NATALIA R.; REY, HEBE Y.; MROGINSKI, LUIS A.
Revista:
ACTA HORTICULTURAE
Editorial:
International Society for Horticultural Science
Referencias:
Lugar: Leuven; Año: 2011 vol. 908 p. 347 - 353
ISSN:
0567-7572
Resumen:
Most of the subtropical Ilex species have recalcitrant seeds and therefore not suitable for long term preservation using conventional seed storage methods. Thus, the germplasm of Ilex spp. is maintained in the field as genebanks. This work describes experiments demonstrating the feasibility of long term conservation of I. dumosa through cryopreservation of both whole seeds and zygotic rudimentary embryos. Lately, this species has received the most attention from plant breeders because, besides the quality of its leaves for making the stimulatory beverage named "mate" with less caffeine than the ones from I. paraguariensis, the plants are resistant to some pests. For cryopreservation of zygotic embryos and apical shoot-tips: the explants were aseptically removed, encapsulated in 3% calcium alginate beads and pregrown for 24 h intervals in liquid medium enriched with progressively increasing sucrose concentrations (0.5, 0.75 and 1 M). The beads were then dehydrated with silica gel to 25% water content and plunged rapidly in liquid nitrogen. The beads were rewarmed by immersion in a water bath at 30º C. Finally, the beads were transferred onto culture medium (1/4 MS, 3% sucrose, 0.1 mg/L zeatin, solidified with 0.8% agar) and incubated in a growth room at 27º C under a 14 h photoperiod (116 ìmol.m-2.s-1). By culturing cryopreserved embryos, as much as 42% of them produced plants. However, no plants were recovery when apical shoot-tips were cryopreserved. In addition, a procedure for cryopreservation of mature intact seeds of I. dumosa by desiccation with silica gel and rapid freezing was developed. As much as 40% of the cryopreserved seeds produced plants when they were cultivated in vitro in an appropriate culture medium.