DOI QR코드

DOI QR Code

Factors influencing efficiency of somatic embryogenesis of Gentiana kurroo (Royle) cell suspension

  • Fiuk, Agnieszka (Botanical Garden, Center for Biological Diversity Conservation, Polish Academy of Sciences) ;
  • Rybczynski, Jan J. (Botanical Garden, Center for Biological Diversity Conservation, Polish Academy of Sciences)
  • Received : 2007.12.21
  • Accepted : 2008.01.19
  • Published : 2008.04.30

Abstract

In this paper, we would like to show unexpected morphogenic potential of cell suspensions derived from seedling explants of Gentiana kurroo (Royle). Suspension cultures were established with the use of embryogenic callus derived from seedling explants (root, hypocotyl and cotyledons). Proembryogenic mass proliferated in liquid MS medium supplemented with $0.5mg\;l^{-1}$ 2,4-D and $1.0mg\;l^{-1}$ Kin. The highest growth coefficient was achieved for root derived cell suspensions. The microscopic analysis showed differences in aggregate structure depending on their size. To assess the embryogenic capability of the particular culture, 100 mg of cell aggregates was implanted on MS agar medium supplemented with Kin ($0.0-2.0mg\;l^{-1}$), $GA_3$ ($0.0-2.0mg\;l^{-1}$) and AS ($80.0mg\;l^{-1}$). The highest number of somatic embryos was obtained for cotyledon-derived cell suspension on $GA_3$-free medium, but the best morphological quality of embryos was observed in the presence of $0.5-1.0mg\;l^{-1}$ Kin, $0.5mg\;l^{-1}$ $GA_3$ and $80.0mg\;l^{-1}$ AS. The morphogenic competence of cultures also depended on the size of the aggregate fraction and was lower when size of aggregates decreased. Flow cytometry analysis reveled luck of uniformity of regenerants derived from hypocotyl suspension and 100% of uniformity for cotyledon suspension.

Keywords

Cited by

  1. Rapid and efficient callus induction and plant regeneration from seeds of zoysiagrass (Zoysia japonica Steud.) : In vitro culture of zoysiagrass vol.56, pp.4, 2008, https://doi.org/10.1111/j.1744-697x.2010.00195.x
  2. Cryopreservation enhances embryogenic capacity of Gentiana cruciata (L.) suspension culture and maintains (epi)genetic uniformity of regenerants vol.30, pp.4, 2008, https://doi.org/10.1007/s00299-010-0970-1
  3. Autotetraploid plant regeneration by indirect somatic embryogenesis from leaf mesophyll protoplasts of diploid Gentiana decumbens L.f. vol.51, pp.3, 2008, https://doi.org/10.1007/s11627-015-9674-0
  4. Comparison of the morphogenic potential of five Gentiana species in leaf mesophyll protoplast culture and ploidy stability of regenerated calli and plants vol.126, pp.2, 2008, https://doi.org/10.1007/s11240-016-1000-y
  5. Somatic embryogenesis and de novo shoot organogenesis can be alternatively induced by reactivating pericycle cells in Lisianthus (Eustoma grandiflorum (Raf.) Shinners) root explants vol.53, pp.3, 2008, https://doi.org/10.1007/s11627-017-9800-2
  6. Genetic transformation of gentian Gentiana tibetica (King) leaf explants with Agrobacterium tumefaciens strain C58C1 vol.39, pp.1, 2008, https://doi.org/10.1007/s11738-016-2327-z
  7. Somatic Embryogenesis of Immature Cunninghamia lanceolata (Lamb.) Hook Zygotic Embryos vol.7, pp.None, 2008, https://doi.org/10.1038/s41598-017-00156-1
  8. Analytical Methods of Phytochemicals from the Genus Gentiana vol.22, pp.12, 2008, https://doi.org/10.3390/molecules22122080
  9. Flow cytometry - a modern method for exploring genome size and nuclear DNA synthesis in horticultural and medicinal plant species vol.30, pp.1, 2008, https://doi.org/10.2478/fhort-2018-0011
  10. Somatic Embryogenesis in the Family Gentianaceae and Its Biotechnological Application vol.10, pp.None, 2008, https://doi.org/10.3389/fpls.2019.00762