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In vitro establishment and multiplication of Nymphaea hybrid ‘James Brydon’

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Abstract

Rhizome tips were the most suitable explants for in vitro plant regeneration and multiplication of Nymphaea hybrid ‘James Brydon’ on Murashige and Skoog medium containing different concentrations and combinations of indole-3-acetic acid, 1-naphthaleneacetic acid (NAA), 2,4-dichlorophenoxyacetic acid, 6-benzyladenine (BA), kinetin, 2-isopentenyladenine (2iP) and gibberellic acid (GA3). A combination of 2iP, BA, and NAA strongly favored induction of shoot buds and shoot proliferation. Pretreatment of shoot cultures at 8°C for 30 days or with 14.4 or 28.9 μM GA3 for 15 days did not improve shoot multiplication. A 16-h photoperiod with photosynthetic photon flux of 30 μmol m-2 s-1 was found to be the optimum light condition for shoot growth and multiplication. Multiple shoots produced well developed root systems within 4 weeks after transfer to a plant growth regulator-free medium containing activated charcoal.

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Abbreviations

BA:

6-benzyladenine

2,4-d :

2,4-dichlorophenoxyacetic acid

GA3 :

gibberellic acid

IAA:

indole-3-acetic acid

2iP:

2-isopentenyladenine

MS:

Murashige and Skoog medium

NAA:

1-naphthaleneacetic acid

References

  • George EF & Sherrington PD (1984) Plant Propagation by Tissue Culture. Exegetics Ltd, Reading, England

    Google Scholar 

  • Huetteman CA & Preece JE (1993) Thidiazuron: a potent cytokinin for woody plant tissue culture. Plant Cell Tiss. Org. Cult. 33: 105–119

    Google Scholar 

  • Jenks M, Kane M, Marousky F, McConnell D & Sheehan T (1990) In vitro establishment and epiphyllous regeneration of Nymphaea ‘Daubeniana’. HortScience 25: 1664

    Google Scholar 

  • Jordan M & Oyanedel E (1992) Regeneration of Pouteria lucuma (Sapotaceae) plants in vitro. Plant Cell Tiss. Org. Cult. 31: 249–252

    Google Scholar 

  • Kane ME, Sheehan TJ & Ferwerda FH (1988) In vitro growth of American lotus embryos. HortScience 23: 611–613

    Google Scholar 

  • Kelly JW & Frett JJ (1986) Photoperiodic control of growth of water lilies. HortScience 21: 151

    Google Scholar 

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

    Google Scholar 

  • Rao S & Mohan Ram HY (1981) Regeneration of whole plants from cultured shoot tips of Limnophila indica. Can. J. Bot. 59: 969–973

    Google Scholar 

  • Swindells P (1983) Waterlilies. Timber Press, Portland, Oregon

    Google Scholar 

  • Zar JH (1984) Biostatistical Analysis, 2nd edition, Prentice-Hall, Inc., New Jersey

    Google Scholar 

Download references

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Lakshmanan, P. In vitro establishment and multiplication of Nymphaea hybrid ‘James Brydon’. Plant Cell Tiss Organ Cult 36, 145–148 (1994). https://doi.org/10.1007/BF00048326

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  • DOI: https://doi.org/10.1007/BF00048326

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