Log in

Recalcitrant effects associated with the development of basal callus-like tissue on caulogenesis and rhizogenesis in Sclerocarya birrea

  • SI : Tissue Culture
  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

In the micropropagation of woody plant species, adventitious root and shoot formation remain some of the major bottlenecks due to their recalcitrance to in vitro manipulation. Some plant growth regulators may ameliorate these recalcitrant effects and improve in vitro caulogenic and rhizogenic processes. Shoot induction on shoot meristems, hypocotyls and epicotyls was evaluated using equimolar concentrations of benzyladenine (BA), meta-topolin (mT), meta-topolin riboside (mTR), and meta-methoxytopolin riboside (MemTR). Three auxins, indole-3-acetic acid (IAA), indole-3-butyric acid (IBA) and α-naphthalene acetic acid (NAA) were used in the induction of adventitious roots. Moderately high shoot formation (62.7%) was achieved at a concentration of 8.0 μM mT after 8 weeks in culture. The highest number of adventitious shoots per explant (2.4 ± 0.3) and the longest shoots (23.5 ± 3.16 mm) were recorded on 8.0 μM mT, though not significantly different from BA treatments. Most shoots progressively produced brown basal callus, which is a potential sink for cytokinin conjugates that are inhibitory to further proliferation of adventitious shoots. Good adventitious shoot formation occurred in 55% of hypocotyl explants on 8.0 μM mT. The highest rooting (91.6%) was achieved with IBA-treated shoots at a concentration of 4.0 μM. The use of mT and IBA provide an efficient micropropagation method for S. birrea, though further research is required especially in overcoming ex vitro plantlet survival challenges.

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

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

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

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

Abbreviations

BA:

6-Benzyladenine

IAA:

Indole-3-acetic acid

IBA:

Indole-3-butyric acid

MemTR:

6-(-3-methoxybenzylamino)-9-β-D-ribofuranosylpurine

MS:

Murashige and Skoog (1962) basal medium

mT:

6-(3-hydroxybenzylamino)purine

mTR:

6-(-3-hydroxybenzylamino)-9-β-D-ribofuranosylpurine

NAA:

α-Naphthalene acetic acid

PVP:

Polyvinylpyrrolidone

References

  • Auer CA (1997) Cytokinin conjugation: recent advances and patterns in plant evolution. Plant Growth Regul 23:17–32

    Article  CAS  Google Scholar 

  • Baltierra XC, Montenegro G, De García E (2004) Ontogeny of in vitro rooting processes in Eucalyptus globules. In Vitro Cell Dev Biol Plant 40:499–503

    Article  Google Scholar 

  • Benson EE (2000) In vitro recalcitrance: an introduction. In Vitro Cell Dev Biol Plant 36:141–148

    Article  Google Scholar 

  • De Klerk GJ (2002) Rooting of microcuttings: theory and practice. In Vitro Cell Dev Biol Plant 38:415–422

    Article  Google Scholar 

  • De Klerk GJ, Keppel M, Terbrugge J, Meekes H (1995) Timing of the phases in adventitious root formation in apple microcuttings. J Exp Bot 46:965–972

    Article  Google Scholar 

  • De Klerk GJ, Van Der Krieken W, De Jong JC (1999) The formation of adventitious roots: new concepts, new possibilities. In Vitro Cell Dev Biol Plant 35:189–199

    Article  Google Scholar 

  • De Paiva Neto VB, Da Mota TR, Otoni WC (2003) Direct organogenesis from hypocotyl-derived explants of annatto (Bixa orellana). Plant Cell Tiss Organ Cult 75:159–167

    Article  Google Scholar 

  • Epstein E, Ludwig-Müller J (1993) Indole-3-butyric acid in plants: occurrence, biosynthesis, metabolism, and transport. Physiol Plant 88:382–389

    Article  CAS  Google Scholar 

  • Fehér A, Pasternak TP, Dudits D (2003) Transition of somatic plant cells to an embryogenic state. Plant Cell Tiss Organ Cult 74:201–228

    Article  Google Scholar 

  • Feito I, Gea MA, Fernández B, Rodríguez R (1996) Endogenous plant growth regulators and rooting capacity of different walnut tissues. Plant Growth Regul 19:101–108

    Article  CAS  Google Scholar 

  • Fogaça CM, Fett-Neto AG (2005) Role of auxin and its modulators in the adventitious rooting of Eucalyptus species differing in recalcitrance. Plant Growth Regul 45:1–10

    Article  Google Scholar 

  • Gueye B, Said-Ahmed H, Marcillo F, Borgel A, Sane D, Hibert J-L, Verdeil J-L, Blervacq A-S (2009) Callogenesis and rhizogenesis in the date palm leaf segments: are there similarities between the two auxin-induced pathways? Plant Cell Tiss Organ Cult 98:47–58

    Article  CAS  Google Scholar 

  • Hatzilazarou SP, Syros TD, Yupsanis TA, Bosabalidis AM, Economou AS (2006) Peroxidases, ligin and anatomy during in vitro and ex vitro rooting of gardenia (Gardenia jasminoides Ellis) microshoots. J Plant Physiol 163:827–836

    Article  PubMed  CAS  Google Scholar 

  • Huang LC, Lee YL, Huang BL, Kuo C, Shaw JE (2002) High polyphenol oxidase activity and low titratable acidity in browning bamboo tissue culture. In Vitro Cell Dev Biol Plant 38:358–365

    CAS  Google Scholar 

  • Ludwig-Müller J, Vertocnik A, Town CD (2005) Analysis of indole-3-butyric acid-induced adventitious root formation on Arabidopsis stem segments. J Exp Bot 56:2095–2105

    Article  PubMed  Google Scholar 

  • Magyar-Tábori K, Dobránszki J, Teixeira da Silva JA, Bulley SM, Hudák I (2010) The role of cytokinins in shoot organogenesis in apple. Plant Cell Tiss Organ Cult 101:251–267

    Article  Google Scholar 

  • Makunga NP, Van Staden J (2008) An efficient system for the production of clonal plantlets of the medicinally important aromatic plant: Salvia africana-lutea L. Plant Cell Tiss Organ Cult 92:63–72

    Article  Google Scholar 

  • McCown BH (2000) Recalcitrance of woody and herbaceous perennial plants: dealing with genetic predeterminism. In Vitro Cell Dev Biol Plant 36:149–154

    Article  Google Scholar 

  • Mollel HN, Goyvaerts EMA (2004) Preliminary examination of factors affecting Agrobacterium tumefaciens-mediated transformation of marula, Sclerocarya birrea subsp. caffra (Anacardiaceae). Plant Cell Tiss Organ Cult 79:321–328

    Article  CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Pullman GS, Timmis R (1992) Establishment of juvenile-like shoot cultures and plantlets from 4–16 year-old Douglas-fir (Pseudotsuga menziesii (Mirb. Franco) trees. Plant Cell Tiss Organ Cult 29:187–198

    Article  Google Scholar 

  • Schwarz OJ, Sharma AR, Beaty RM (2005) Propagation from nonmeristematic tissues: organogenesis. In: Trigiano RN, Gray DJ (eds) Plant development and biotechnology. CRS Press, Boca Raton, FL, pp 159–172

    Google Scholar 

  • Sharma P, Rajam MV (1995) Genotype, explant and position effects on organogenesis and somatic embryogenesis in eggplant (Solanum melongena L.). J Exp Bot 46:135–141

    Article  CAS  Google Scholar 

  • Strnad M (1997) The aromatic cytokinins. Physiol Plant 101:674–688

    Article  CAS  Google Scholar 

  • Sugiyama M (1999) Organogenesis in vitro. Curr Opin Plant Biol 2:61–64

    Article  PubMed  CAS  Google Scholar 

  • Tereso S, Miguel CM, Mascarenhas M, Roque A, Trindade H, Maroco J, Oliveira MM (2008) Improved in vitro rooting of Prunus dulcis Mill. cultivars. Biol Plant 52:437–444

    Article  CAS  Google Scholar 

  • Tilkat E, Onay A (2009) Direct shoot organogenesis from in vitro-derived mature leaf explant of pistachio. In Vitro Cell Dev Biol Plant 45:92–98

    Article  CAS  Google Scholar 

  • Towfik AA, Noga G (2001) Adventitious shoot proliferation from hypocotyls and internodal stem explants from cumin. Plant Cell Tiss Organ Cult 66:141–147

    Article  Google Scholar 

  • Van Staden J, Crouch NR (1996) Benzyladenine and derivatives—their significance and interconversion in plants. Plant Growth Regul 19:153–175

    Article  Google Scholar 

  • Vieitez AM, Corredoira E, Ballester A, Muñoz F, Durán J, Ibarra M (2009) In vitro regeneration of the important North American oak species Quercus alba, Quercus bicolour and Quercus rubra. Plant Cell Tiss Organ Cult 98:135–145

    Article  CAS  Google Scholar 

  • Viljoen AM, Kamatou GPP, Başer KHC (2008) Head-space volatiles of marula (Sclerocarya birrea subsp. caffra). S Afr J Bot 74:325–326

    Article  CAS  Google Scholar 

  • Werbrouck SPO, Van Der Jeugt B, Dewitte W, Prinsen E, Van Onckelen HA, Debergh PC (1995) The metabolism of benzyladenine in Spathiphyllum floribundum ‘Schott Petite’ in relation to acclimatisation problems. Plant Cell Rep 14:662–665

    Article  CAS  Google Scholar 

  • Werbrouck SPO, Strnad M, Van Onckelen HA, Debergh PC (1996) Meta-topolin, an alternative to benzyladenine in tissue culture? Physiol Plant 98:291–297

    Article  CAS  Google Scholar 

  • Werner T, Motyka V, Strnad M, Schmülling T (2001) Regulation of plant growth by cytokinin. Proc Natl Acad Sci USA 98:10487–10492

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The financial support by the National Research Foundation (NRF), Pretoria and the University of KwaZulu-Natal.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Johannes Van Staden.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Moyo, M., Finnie, J.F. & Van Staden, J. Recalcitrant effects associated with the development of basal callus-like tissue on caulogenesis and rhizogenesis in Sclerocarya birrea . Plant Growth Regul 63, 187–195 (2011). https://doi.org/10.1007/s10725-011-9562-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10725-011-9562-5

Keywords

Navigation