Skip to main content
Log in

The effects of 1-naphthaleneacetic acid and N6-benzyladenine on the growth of Cymbidium forrestii rhizomes in vitro

  • Published:
Plant Cell, Tissue and Organ Culture Aims and scope Submit manuscript

Abstract

An Asiatic orchid, Cymbidium forrestii, was clonally propagated using seed-derived rhizomes as explants. The rhizomes were cultured and proliferated on Murashige and Skoog medium supplemented with various growth substances. Auxins stimulated rhizome growth by increasing branching and fresh weight of the explant, with 1-naphthaleneacetic acid (NAA) being the most effective auxin. All auxins tested suppressed normal shoot formation. The apical meristem of the rhizome reacted to exogenously applied auxin by reducing the cytoplasmic zone of the apical meristem and causing meristem derivatives to rapidly differentiate into vacuolated parenchyma cells. Leaf formation and development was retarded in the presence of auxin. Cytokinins generally reduced rhizome growth and the number of branches, but benzyladenine (BA) can induce shoot formation in vitro. BA induced the cytoplasmic zone of the apical meristem to enlarge and enhanced leaf development. A 5% (w/v) sucrose concentration was most effective in shoot induction when combined with 5 mg1-1 BA. Activated charcoal promoted rhizome growth; however, shoot formation was inhibited.

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.

Similar content being viewed by others

References

  1. Arditti J (1977) Clonal propagation of orchids by means of tissue culture—a manual. In: Arditti J (Ed) Orchid Biology, Vol 1 (pp 203–293). Cornell University Press

  2. Cutter EG (1978) Structure and development of the potato plant. In: Harris PM (Ed) The Potato Crop (pp 70–152). Chapman and Hall, London

    Google Scholar 

  3. Chung JD, Chun CK, Kim SS & Lee JS (1985) Factors affecting growth of rhizome and organogenesis of Korean native Cymbidium kanran. J. Kor. Soc. Hortic. Sci. 26: 281–288

    Google Scholar 

  4. Chung JD, Chun CK & Choi SO (1985) Asymbiotic germination of Cymbidium ensifolium. II. Effects of several supplements to the medium, pH values and light and/or dark culture periods on growth of rhizome and organogenesis from rhizome. J. Kor. Soc. Hortic. Sci. 26: 186–192

    Google Scholar 

  5. Ernst R (1974) The use of activated charocoal in a symbiotic seedling culture of Paphiopedilum. Am. Orchid Soc. Bull. 43: 35–38.

    Google Scholar 

  6. Hu SY (1971) Orchids in the life and culture of the Chinese people. Chung Chi. J. 10: 1–26

    Google Scholar 

  7. Jensen WA (1962) Botanical Histochemistry. W.H. Freeman and Co., San Francisco

    Google Scholar 

  8. Kokubu T, Kaieda Y, Higashi Y, Kitano T & Fukamizu F (1980) Organogenesis in sterile culture of oriental Cymbidium, Cymbidium kanran Makino. Mem. Fac. Agric. Kagoshima Univ 16: 53–64

    Google Scholar 

  9. Knudson L (1946) A new nutrient for the germination of orchid seeds. Am. Orchid Soc. Bull. 15: 214–217

    Google Scholar 

  10. Lee JS, Shim KK, Yoo MS, Lee JS & Kim YJ (1986) Studies on rhizome growth and organogenesis of Cymbidium kanran cultured in vitro. J. Kor. Soc. Hortic. Sci. 27: 174–180

    Google Scholar 

  11. Morel GM (1960) Producing virus-free cymbidiums. Am. Orchid Soc. Bull. 29: 495–497

    Google Scholar 

  12. Murashige T & Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. PHysiol. Plant. 15: 473–497

    Google Scholar 

  13. Paek KY, Shim GB & Hwang JK (1987) Asymbiotic germination and plantlet formation of rhizome through the aseptic culture of temperate Cymbidium seeds. J. Kor. Soc. Hortic. Sci. 28: 185–193.

    Google Scholar 

  14. Paek KY, Shim GB & Kim JJ (1989) Asymbiotic germination of temperate Cymbidiums and effect of media and growth regulators on organogenesis. J. Kor. Soc. Hortic. Sci. 30: 234–247.

    Google Scholar 

  15. Paek KY, Shim GB & Kim JJ (1990) Effect of natural products and BAP exposing periods on organogenesis of temperate Cymbidiums using rhizome. J. Kor. Soc. Hortic. Sci. 31: 74–80.

    Google Scholar 

  16. Paek KY, Ahn SY & Shim GB (1991) Anatomical observations on organogenesis,and polyphenol concent, isoenzyme analysis of in vitro cultured rhizomes in temperate Cymbidiums. J. Kor. Soc. Hortic. Sci. 31 (in press)

  17. Shimasaki K & Uemoto S (1987) Micropropagation of terrestrial cymbidims using the rhizome. Proc. 12th World Orchid Conference 1987, Tokyo, Japan, p. 285

  18. Sussex IM (1989) Developmental programming of the shoot meristem. Cell 56: 225–229

    Google Scholar 

  19. Ueda H & Torikata H (1969) Organogenesis in the meristem cultures of cymbidiums. III. Histological studies on the shoot formation at the rhizome-tips of Cymbidium goeringii Reichb. F. cultured in vitro. J. Jap. Soc. Hortic. Sci. 38: 262–265

    Google Scholar 

  20. Wang X (1988) Tissue culture of Cymbidium: plant and flower induction in vitro. Lindleyana 3: 184–189

    Google Scholar 

  21. Weatherhead MA, Burdon J & Henshaw GG (1978) Some effects of activated charcoal as an additive to plant tissue culture media. Z. Pflanzenphysiol. 89: 141–147

    Google Scholar 

  22. Wooley DJ & Wareing PF (1972) The role of roots, cytokinins and apical dominance in the control of lateral shoot form. Planta 105: 33–42

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Paek, K.Y., Yeung, E.C. The effects of 1-naphthaleneacetic acid and N6-benzyladenine on the growth of Cymbidium forrestii rhizomes in vitro. Plant Cell Tiss Organ Cult 24, 65–71 (1991). https://doi.org/10.1007/BF00039732

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00039732

Key words

Navigation