Skip to main content
Log in

Endosperm culture: a facile and efficient biotechnological tool to generate passion fruit (Passiflora cincinnata Mast.) triploid plants

  • Original Article
  • Published:
Plant Cell, Tissue and Organ Culture (PCTOC) Aims and scope Submit manuscript

Abstract

Triploid plants represent an important resource for the breeding of fruit and ornamental plants. Here, we report a facile and robust system for regenerating passion fruit triploid plants (Passiflora cincinnata Mast.) through in vitro endosperm culture. We describe the histological and biochemical aspects associated with the de novo shoot organogenesis. Endosperms were cultured on Murashige and Skoog medium supplemented with 1.5, 2.0, and 3.0 mg L−1 of 6-benzyladenine or thidiazuron, while a cytokinin-free medium was used as control. The highest percentage of organogenic calli (56%) was estimated at 1.7 mg L−1 6-benzyladenine, whereas the highest average number of shoots (24.85) per explant was estimated at 1.6 mg L−1 6-benzyladenine. Flow cytometry and chromosomal analysis confirmed that endosperm-derived plants were triploid, with a chromosome count of 27 (2n = 3x = 27) as well as a DNA amount similar to that of endosperm and 1.5 times greater than in diploid counterparts (2n = 2x = 18). The regeneration of adventitious shoots was evident 30 days after culture and occurred from the reprogramming of edge cells of the endosperm. During this process, lipids and proteins were quickly mobilized in the early stages of shoot organogenesis, whereas carbohydrates were synthesized throughout the development of adventitious shoots. This observation illustrates the mobilization dynamics of endosperm reserves during de novo shoot organogenesis in P. cincinnata.

Key message

Adventitious shoots induced by reprogramming of the outer cell layers of the endosperm generate true-to-type triploid passion fruit plants.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

Download references

Acknowledgements

This work was supported by “Fundação de Amparo à Pesquisa do Estado de Mato Grosso” (FAPEMAT) (Cuiabá, MT); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brazil (CAPES)—Finance Code 001; and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (420913/2018-1). We also thank the CNPq for granting a scholarship to MM (DCR-314905/2018-9). We would like to thank Editage (www.editage.com) for English language editing.

Funding

This work was supported by “Fundação de Amparo à Pesquisa do Estado de Mato Grosso” (FAPEMAT) (Cuiabá, MT), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brazil (CAPES)—Finance Code 001, and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (420913/2018-1).

Author information

Authors and Affiliations

Authors

Contributions

NTS established organogenic cultures and wrote the paper; LASS assisted with histological evaluations; MM performed biochemical analyses and revised the paper; ACR and EMM carried out the chromosome count and flow cytometry analyses; IFC designed the research and revised the paper; WCO and LFV revised the paper; DIR and MLS designed the research and wrote the paper.

Corresponding author

Correspondence to Maurecilne Lemes da Silva.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Consent for publication

All co-authors listed have approved the final version of the manuscript.

Additional information

Communicated by Sergio J. Ochatt.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

da Silva, N.T., Silva, L.A.S., Reis, A.C. et al. Endosperm culture: a facile and efficient biotechnological tool to generate passion fruit (Passiflora cincinnata Mast.) triploid plants. Plant Cell Tiss Organ Cult 142, 613–624 (2020). https://doi.org/10.1007/s11240-020-01887-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11240-020-01887-2

Keywords

Navigation