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

LUIS A. MROGINSKI*, PEDRO A. SANSBERRO, ADRIANA M. SCOCCHI, CLAUDIA LUNA, HEBE Y. REY

Instituto de Botánica del Nordeste (IBONE), Facultad de Ciencias Agrarias (UNNE), C.C. 209. (3400) Corrientes, Argentina
Address correspondence to: Luis A. Mroginski. E-mail: luis@agr.unne.edu.ar

BIOCELL 2008, 32(1), 33-39. https://doi.org/10.32604/biocell.2008.32.033

Abstract

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 rudimentary 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 quarterstrength 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.

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APA Style
MROGINSKI*, L.A., SANSBERRO, P.A., SCOCCHI, A.M., LUNA, C., REY, H.Y. (2008). A cryopreservation protocol for immature zygotic embryos of species of ilex (aquifoliaceae). BIOCELL, 32(1), 33-39. https://doi.org/10.32604/biocell.2008.32.033
Vancouver Style
MROGINSKI* LA, SANSBERRO PA, SCOCCHI AM, LUNA C, REY HY. A cryopreservation protocol for immature zygotic embryos of species of ilex (aquifoliaceae). BIOCELL . 2008;32(1):33-39 https://doi.org/10.32604/biocell.2008.32.033
IEEE Style
L.A. MROGINSKI*, P.A. SANSBERRO, A.M. SCOCCHI, C. LUNA, and H.Y. REY, “A cryopreservation protocol for immature zygotic embryos of species of Ilex (Aquifoliaceae),” BIOCELL , vol. 32, no. 1, pp. 33-39, 2008. https://doi.org/10.32604/biocell.2008.32.033

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cc Copyright © 2008 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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