Skip to main content
Log in

Plantlet regeneration via somatic embryogenesis from subcultured callus of mature embryos ofPicea abies (Norway spruce)

  • Rapid Communications in Cell Biology
  • Published:
In Vitro Cellular & Developmental Biology Aims and scope Submit manuscript

Editor's Statement This paper presents advances in the in vitro regeneration of a commercially useful plant species from stored seeds. In addition, data is presented on short-term storage of the plantlets, and long-term proliferation of the embryonal mass in vitro.

Summary

Embryogenic callus was initiated from radicles of mature embryos removed from imbibed seeds (24 h). Embryogenic and other nonembryogenic types of callus proliferated on a modified half-strength Murashige-Skoog medium (MS) basal medium (BM) supplemented withmyo-inositol, casein hydrolysate (CH), L-glutamine (gln) and growth regulators kinetin (KN), N6-benzyladenine (BAP) each (20×10−6 M), 2,4-dichlorophenoxyacetic acid (2,4-D) (50×10−6 M) Embryogenic callus bearing suspensor-like cells in a mucilaginous gel matrix was isolated and maintained by subculture every 10 to 12 days on BM with KN, BAP each (2×10−6 M) and 2,4-D (5×10−6 M). Somatic embryos developed spontaneously from the callus on this medium at 23±1° C. Closer examination revealed that numerous polyembryonic clusters, comprised of elongated cells (suspensors) and small dense cells with large nuclei (somatic embryos), occurred in the viscous gel. When this enriched embryonal-suspensor mass was subcultured to low 2,4-D (1×10−6 M), globular embryos developed by 40 to 60 days. Upon transfer to a liquid medium without growth regulators, the embryos elongated and developed cotyledons and shoots with needles. Plantlet development was completed by 30 days in a basal medium without CH, gln and growth regulators. The total culture time was 150 days. Approximately 40±10 embryos were formed from 500 mg of initial callus. Somatic embryogenesis became aberrant if embryos remained attached to the callus mass and were not subcultured within 10 to 12 days according to the described protocol. Somatic embryos were encapsulated in an alginate gel and stored at 4° C for nearly two months without visible adverse effects on viability.

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.

References

  1. Durzan, D. J. Progress and promise in forest genetics. In: Paper Science and Technology: The Cutting Edge, 50th Anniversary, May 8–10, 1979. Appleton, WI: The Institute of Paper Chemistry; 1980:31–60.

    Google Scholar 

  2. Durzan, D. J. Somatic embryogenesis and sphaeroblasts in conifer suspensions. In: Fujiwara, A. ed. Plant Tissue Culture. Tokyo, Japan: Proc. 5th Intl. Cong. Plant Tissue Culture; 1982:113–114.

  3. Feder, N.; O'Brien, T. P. Plant microtechnique: some principles and methods. Am. J. Bot. 55:123–142; 1968.

    Article  Google Scholar 

  4. Gupta, P. K.; Durzan, D. J. Shoot multiplication from mature trees of Douglas-fir (Pseudotsuga menziesii) and sugar pine (Pinus lambertiana). Plant Cell Repts 4:177–179; 1985.

    Article  CAS  Google Scholar 

  5. Gupta, P. K.; Durzan, D. J. Somatic polyembryogenesis from callus of mature sugar pine embryos. Bio/Technology; 1986:4:643–645.

    Article  Google Scholar 

  6. Gupta, P. K.; Shaw, D.; Durzan, D. J. Loblolly pine: micropropagation, somatic embryogenesis and encapsulation. In: Bonga, J. M.; Durzan, D. J., eds. Cell and Tissue Culture in Forestry. Martinus Nijhoff/Dr. W. Junk. The Hague. Vol. 3 (in press) 1987.

    Google Scholar 

  7. Hakman, I.; Fowke, L. C.; Von Arnold, S.; Ericksson, T. The development of somatic embryos in tissue cultures initiated from immature embryos ofPicea abies (Norway spruce). Plant. Sci. 38:53–59; 1985.

    Article  Google Scholar 

  8. Hakman, I.; Von Arnold, S. Plantlet regeneration through somatic embryogenesis inPicea abies (Norway spruce). J. Plant Physiol. 121:149–158; 1985.

    CAS  Google Scholar 

  9. Von Arnold, S.; Hakman, I. Effect of sucrose on initiation of embryogenic callus cultures from mature zygotic embryos ofPicea abies. J. Plant Physiol. 122:261–265; 1986.

    Google Scholar 

  10. Krogstrup, P. Embryo-like structures from cotyledons and ripe embryos of Norway spruce (Picea abies). Can. J. For. Res. 16:664–668.

  11. Murashige, T.; Skoog, F. A revised medium for the rapid growth and bioassay with tobacco tissue cultures. Physiol. Plant. 15:473–497; 1962.

    Article  CAS  Google Scholar 

  12. Nagmani, R.; Bonga, J. M. Embryogenesis in subcultured callus ofLarix decidua. Can. J. For. Res.; 15:1008–1091; 1985.

    Google Scholar 

  13. Norstog, K. Experimental embryology of gynmosperms. Johri, B. M. ed. Experimental embryology of vascular plants. Springer-Verlag: Berlin-Heidelberg: New York; 1982:25–48.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gupta, P.K., Durzan, D.J. Plantlet regeneration via somatic embryogenesis from subcultured callus of mature embryos ofPicea abies (Norway spruce). In Vitro Cell Dev Biol 22, 685–688 (1986). https://doi.org/10.1007/BF02623484

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02623484

Key words

Navigation