Induction of somatic embryogenesis and cryopreservation of Abies pinsapo Boiss.

<i>Abies pinsapo</i> is an endangered species, endemic to southern Spain. Somatic embryogenesis and cryopreservation constitute important biotechnological tools, which can be used in order to improve the management and conservation of threatened species. The objective of this work was to develop somatic embryogenesis and cryopreservation protocols for <i>A. pinsapo</i>. Somatic embryogenesis was induced from mature zygotic embryos of <i>A. pinsapo</i> cultured on solid MS medium with macroelements at half-strength and supplemented with 20 g L<sup>-1</sup> sucrose and 5 mg L<sup>-1</sup> 6-benzylaminopurine (BA). Embryogenic cultures successfully proliferated on solid medium with the same formulation supplemented with 20 g L<sup>-1</sup> sucrose, 500 mg L<sup>-1</sup> L-glutamine, 1 g L<sup>-1</sup> casein hydrolysate and 1 mg L<sup>-1</sup> BA. Different preconditioning and cryoprotective treatments were tested in order to optimize cryopreservation of embryogenic tissues by using the slow-cooling technique. Embryogenic cultures at their exponential growth phase, i.e. 12-14 days after the last subculture, were used as cryopreservation explants. The best results were achieved after sucrose preculture and cryoprotecion with PGD I (mixture of polyethylene glycol, glucose and DMSO I), with 100% of explants resuming somatic embryogenesis after thawing. Following fluorescein diacetate (FDA) staining, more intense and abundant green fluorescence could be observed in these samples, compared to those subjected to other preconditioning and cryoprotective treatments, thus evincing a higher proportion of viable cells after freezing in liquid nitrogen. Cold hardening did not improve cryotolerance. In fact, incubation at 5 °C for two weeks appeared to affect explants response, delaying tissue regrowth after cryopreservation. This is the first time in which somatic embryogenesis and cryopreservation have been reported in Spanish fir. The results obtained allow to establish the bases for the integration of these techniques into <i>in situ</i> and <i>ex situ</i> conservation strategies.

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Publication Details

Journal
Frontiers in Plant Science
Published
2025-01-29
DOI
https://doi.org/10.3389/fpls.2025.1535113
Citations
1
Primary Topic
Plant tissue culture and regeneration
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article
Field-Weighted Citation Impact
0.81
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article

Induction of somatic embryogenesis and cryopreservation of Abies pinsapo Boiss.

María Victoria Bravo-Navas, Carolina Sánchez‐Romero, Laura Cabero-Moreno, Ignacio Landeras-López
1 citations
Frontiers in Plant Science
Plant tissue culture and regeneration
0.81
article

Induction of somatic embryogenesis and cryopreservation of Abies pinsapo Boiss.

María Victoria Bravo-Navas, Carolina Sánchez‐Romero, Laura Cabero-Moreno, Ignacio Landeras-López
article en
1 citations

Abstract

<i>Abies pinsapo</i> is an endangered species, endemic to southern Spain. Somatic embryogenesis and cryopreservation constitute important biotechnological tools, which can be used in order to improve the management and conservation of threatened species. The objective of this work was to develop somatic embryogenesis and cryopreservation protocols for <i>A. pinsapo</i>. Somatic embryogenesis was induced from mature zygotic embryos of <i>A. pinsapo</i> cultured on solid MS medium with macroelements at half-strength and supplemented with 20 g L<sup>-1</sup> sucrose and 5 mg L<sup>-1</sup> 6-benzylaminopurine (BA). Embryogenic cultures successfully proliferated on solid medium with the same formulation supplemented with 20 g L<sup>-1</sup> sucrose, 500 mg L<sup>-1</sup> L-glutamine, 1 g L<sup>-1</sup> casein hydrolysate and 1 mg L<sup>-1</sup> BA. Different preconditioning and cryoprotective treatments were tested in order to optimize cryopreservation of embryogenic tissues by using the slow-cooling technique. Embryogenic cultures at their exponential growth phase, i.e. 12-14 days after the last subculture, were used as cryopreservation explants. The best results were achieved after sucrose preculture and cryoprotecion with PGD I (mixture of polyethylene glycol, glucose and DMSO I), with 100% of explants resuming somatic embryogenesis after thawing. Following fluorescein diacetate (FDA) staining, more intense and abundant green fluorescence could be observed in these samples, compared to those subjected to other preconditioning and cryoprotective treatments, thus evincing a higher proportion of viable cells after freezing in liquid nitrogen. Cold hardening did not improve cryotolerance. In fact, incubation at 5 °C for two weeks appeared to affect explants response, delaying tissue regrowth after cryopreservation. This is the first time in which somatic embryogenesis and cryopreservation have been reported in Spanish fir. The results obtained allow to establish the bases for the integration of these techniques into <i>in situ</i> and <i>ex situ</i> conservation strategies.

Frontiers in Plant ScienceVol. 16
Universidad de Málaga (ES)
Life in Land
Openalex Percentile: Top 31%
Plant tissue culture and regeneration
0.81
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