Skip to main content
Log in

Seedling preconditioning in thidiazuron enhances axillary shoot proliferation and recovery of transgenic cowpea plants

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

Abstract

Lack of competence of seedling explants for efficient shoot proliferation in recalcitrant grain legume cowpea restricts its genetic manipulation for crop improvement. This study aimed at establishing a protocol to increase the shoot proliferation efficiency during the regeneration of transgenic cowpea plants. Here, we describe how seedling preconditioning in thidiazuron (TDZ) could stimulate the transformation process (by 3.5-fold), shoot proliferation potential of cotyledonary node (by a factor of fourfold) and accelerate the transgenic shoot regeneration. We investigated the effect of TDZ and 6-benzyladenine (BA) at high dose (5–20 μM) in the induction phase of regeneration by preconditioning seedlings for different durations (2–6 days) with the aim of improving shoot proliferation competence from cultured explants. Cotyledonary node explants from preconditioned seedlings were cultured on MSB5 medium supplemented with 5 μM BA and 0.5 μM kinetin for 4 weeks. Best response in terms of maximum shoot proliferation (7.1 shoots per explants), and greatest shoot length (2.6 cm) were obtained with explants derived from seedlings preconditioned in 10 μM TDZ for 4 days. This enhanced shoot proliferation ability was maintained through three subsequent 4-week long regeneration passages. On comparison of the transformation rate in absence and presence of seedling preconditioning (in 10 μM TDZ for 4 days), a significant enhancement from 0.6 to 2.1% was observed. The promotive effect of seedling preconditioning had a direct beneficial effect on transgenic plant recovery time leading to a reduction of more than 2 weeks. The protocol was found applicable to seven cowpea genotypes.

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
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  • Amutha S, Ganapathi A, Muruganantham M (2006) Thidiazuron-induced high-frequency axillary and adventitious shoot regeneration in Vigna radiata (L.) Wilczek. In Vitro Cell Dev Biol Plant 42:26–30

    Article  CAS  Google Scholar 

  • Chaudhury D, Madanpotra S, Jaiwal R, Saini R, Kumar PA, Jaiwal PK (2007) Agrobacterium tumefaciens-mediated high frequency genetic transformation of an Indian cowpea (Vigna unguiculata L. Walp.) cultivar and transmission of transgenes into progeny. Plant Sci 172:692–700

    Article  CAS  Google Scholar 

  • Chen WS, Huang KL, Yu HC (1997) Cytokinins from terminal buds of Euphoria longana during different growth stages. Physiol Plant 99:185–189

    Article  CAS  Google Scholar 

  • Chilton MD, Currier TC, Farrand SK, Bendich AJ, Gordon MP, Nester EW (1974) Agrobacterium tumefaciens DNA and PS8 bacteriophage DNA not detected in crown gall tumors. Proc Natl Acad Sci USA 71:3672–3676

    Google Scholar 

  • Christianson ML, Warnick DA (1983) Competence and determination in the process of in vitro shoot organogenesis. Dev Biol 95:288–293

    Article  PubMed  CAS  Google Scholar 

  • D’Onofrio C, Morini S (2006) Somatic embryo, adventitious root and shoot regeneration in in vitro grown quince leaves as influenced by treatments of different length with growth regulators. Sci Hortic Amsterdam 107:194–199

    Article  Google Scholar 

  • Dang W, Wei ZM (2009) High frequency plant regeneration from the cotyledonary node of common bean. Biol Plant 53(2):312–316

    Article  CAS  Google Scholar 

  • Dita MA, Rispail N, Prats E, Rubiales D, Singh KB (2006) Biotechnology approaches to overcome biotic and abiotic stress constraints in legumes. Euphytica 147:1–24

    Article  Google Scholar 

  • Dubois LAM, De Vries DP (1997) Genetic variation of rose cultivars for direct shoot organogenesis. Acta Hortic 447:79–85

    Google Scholar 

  • Fang J, Chao CT, Roberts PA, Ehlers JD (2007) Genetic diversity of cowpea [Vigna unguiculata (L.) Walp.] in four West African and USA breeding programs as determined by AFLP analysis. Genet Resour Crop Evol 54:1197–1209

    Article  CAS  Google Scholar 

  • Gamborg OL, Miller RA, Ojima K (1968) Nutrient requirements of suspension cultures of soybean root cell. Exp Cell Res 50:151–158

    Article  PubMed  CAS  Google Scholar 

  • Gomathinayagam P, Ganeshram S, Rathnaswamy R, Ramaswamy NM (1998) Interspecific hybridization between Vigna unguiculata (L.) Walp. and V. vexillata (L.) A. Rich. through in vitro embryo culture. Euphytica 102:203–209

    Article  Google Scholar 

  • Gordon-Kamm W, Dilkes BP, Lowe K, Hoerster G, Sun X, Ross M, Church L, Bunde C, Farrell J, Hill P, Maddock S, Snyder J, Sykes L, Li Z, Woo YM, Bidney D, Larkins BA (2002) Stimulation of the cell cycle and maize transformation by disruption of the plant retinoblastoma pathway. Proc Natl Acad Sci USA 99(18):11975–11980

    Article  PubMed  CAS  Google Scholar 

  • Gurel S, Baloglu MC, Gurel E, Oktem HA, Yucel M (2011) A two-stage pretreatment of seedlings improves adventitious shoot regeneration in sugar beet (Beta vulgaris L.). Plant Cell Tiss Organ Cult 106(2):261–268

    Google Scholar 

  • Ibrahim R, Debergh PC (2001) Factors controlling high efficiency adventitious bud formation and plant regeneration from in vitro leaf explants of roses (Rosa hybrida L.). Sci Hortic 88:41–57

    Article  Google Scholar 

  • Jahan AA, Anis M, Aref IM (2011) Preconditioning of axillary buds in thidiazuron-supplemented liquid media improves in vitro shoot multiplication in Nyctanthes arbor-tristis L. Appl Biochem Biotechnol 163(7):851–859

    Article  PubMed  CAS  Google Scholar 

  • Jefferson RA (1987) Assaying chimearic genes in plants: the GUS gene fusion system. Plant Mol Biol 204:387–405

    Google Scholar 

  • Jones MP, Yi Z, Murch SJ, Saxena PK (2007) Thidiazuron-induced regeneration of Echinacea purpurea L.: micropropagation in solid and liquid culture systems. Plant Cell Rep 26(1):13–19

    Article  PubMed  CAS  Google Scholar 

  • Kucharska D, Orlikowska T (2009) Enhancement of in vitro organogenetic capacity of rose by preculture of donor shoots on the medium with thidiazuron. Acta Physiol Plant 31:495–500

    Article  CAS  Google Scholar 

  • Lane WD, Iketani H, Hatashi T (1998) Shoot regeneration from cultured leaves of Japanese pear (Pyrus pyrifolia). Plant Cell Tiss Organ Cult 54(1):9–14

    Article  Google Scholar 

  • Meng R, Chen THH, Finn CE, Li Y (2004) Improving in vitro plant regeneration from leaf and petiole explants of ‘Marion’ blackberry. Hort Sci 39(2):316–320

    CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Murch SJ, Saxena PK (2001) Molecular fate of thidiazuron and its effects on auxin transport in hypocotyls tissues of Pelargonium × hortorum Bailey. Plant Growth Regul 35:269–275

    Article  CAS  Google Scholar 

  • Murthy BNS, Murch SJ, Saxena PK (1998) Thidiazuron: a potent regulator of in vitro plant morphogenesis. In Vitro Cell Dev Biol Plant 34:267–275

    Article  CAS  Google Scholar 

  • Orlikowska T, Dyer WE (1993) In vitro regeneration and multiplication of safflower (Carthamus tinctorius L.). Plant Sci 93:151–157

    Article  CAS  Google Scholar 

  • Orlikowska T, Nowak E, Marasek A, Kucharska D (1999) Effect of growth regulators and incubation period on in vitro regeneration of adventitious shoots from gerbera petioles. Plant Cell Tiss Org Cult 59:95–102

    Article  CAS  Google Scholar 

  • Paul S, Kundu A, Pal A (2011) Identification and validation of conserved microRNAs along with their differential expression in roots of Vigna unguiculata grown under salt stress. Plant Cell Tiss Organ Cult 105:233–242

    Article  CAS  Google Scholar 

  • Rosu A, Skirvin RM, Bein A, Norton AM, Kushad M, Otterbacher AG (1995) The development of putative adventitious shoots from a chimeral thornless rose (Rosa multiflora Thunb. ex. J. Murr.) in vitro. J Hort Sci 70:901–907

    Google Scholar 

  • Sambrook KJ, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, New York

    Google Scholar 

  • San Jose CM, Ballester A, Vieitez M (2001) Effect of thidiazuron on multiple shoot induction and plant regeneration from cotyledonary node of chestnut. J Hort Sci Biotech 76(5):588–595

    CAS  Google Scholar 

  • Sivanesan I, Song JY, Hwang SJ, Jeong BR (2011) Micropropagation of Cotoneaster wilsonii Nakai-a rare endemic ornamental plant. Plant Cell Tiss Organ Cult 105:55–63

    Article  Google Scholar 

  • Solleti SK, Bakshi S, Purkayastha J, Panda SK, Sahoo L (2008a) Transgenic cowpea (Vigna unguiculata) seeds expressing a bean α-amylase inhibitor 1 confer resistance to storage pests, bruchid beetles. Plant Cell Rep 27:1841–1850

    Article  PubMed  CAS  Google Scholar 

  • Solleti SK, Bakshi S, Sahoo L (2008b) Additional virulence genes in conjunction with efficient selection scheme, and compatible culture regime enhance recovery of stable transgenic plants in cowpea via Agrobacterium tumefaciens-mediated transformation. J Biotech 135:97–104

    Article  CAS  Google Scholar 

  • Somers DA, Samac DA, Olhoft PM (2003) Recent Advances in Legume Transformation. Plant Physiol 131(3):892–899

    Google Scholar 

  • Sovari S, Ulvinen S, Hietarante T, Hiirsalmi H (1993) Preculture medium promotes direct shoot regeneration from micro-propagated strawberry leaf discs. Hort Sci 28:55–57

    Google Scholar 

  • Srinivasan T, Kumar KRR, Kirti PB (2010) Establishment of efficient and rapid regeneration system for some diploid wild species of Arachis. Plant Cell Tiss Organ Cult 101:303–309

    Article  Google Scholar 

  • Sriskandarajah S, Goodwin P (1998a) Conditioning promotes regeneration and transformation in apple leaf explants. Plant Cell Tiss Org Cult 53:1–11

    Article  CAS  Google Scholar 

  • Sriskandarajah S, Goodwin P (1998b) Conditioning promotes regeneration and transformation in apple leaf. Plant Cell Tiss Org Cult 53:1

    Article  CAS  Google Scholar 

  • Swartz HJ, Bors R, Mohamed F, Naess SK (1990) The effect of in vitro pretreatments on subsequent shoot organogenesis from excised Rubus and Malus leaves. Plant Cell Tiss Org Cult 21:179–184

    Article  CAS  Google Scholar 

  • Thirukkumaran G, Ntui VO, Khan RS, Mii M (2009) Thidiazuron: an efficient plant growth regulator for enhancing Agrobacterium-mediated transformation in Petunia hybrid. Plant Cell Tiss Organ Cult 99:109–115

    Article  CAS  Google Scholar 

  • Timko MP, Ehlers JD, Roberts PA (2007) Cowpea. In: Kole C (ed) Pulses, sugar and tuber crops. Theoretical and applied genetics, genome mapping and molecular breeding in plants. Springer, Berlin, vol 3, pp 49–67

  • Tzfira T, Jensen CS, Wang W, Zuker A, Vinocur B, Altman A, Vainstein A (1997) Transgenic Populus tremula: a step-by-step protocol for its Agrobacterium-mediated transformation. Plant Mol Biol Rep 15:219–235

    Article  CAS  Google Scholar 

  • Villemont E, Dubois F, Sangwan RS, Vasseur G, Bourgeois Y, Sangwan-Norreel BS (1997) Role of the host cell cycle in the Agrobacterium-mediated genetic transformation of Petunia: evidence of an S-phase control mechanism for T-DNA transfer. Planta 20:160–172

    Article  Google Scholar 

  • Zhang CL, Chen DF, McCormac AC, Scott NW, Elliott MC, Slater A (2001) Use of the GFP reporter gene as a vital marker for Agrobacterium-mediated transformation of sugar beet (Beta vulgaris L.). Mol Biotechnol 17:109–117

    Article  PubMed  Google Scholar 

  • Zhang CG, Li W, Mao YF, Zhao DL, Dong W, Guo GQ (2005) Endogenous Hormonal levels in scutellaria baicalensis calli induced by thidiazuron. Russ J Plant Physiol 52(3):345–351

    Article  CAS  Google Scholar 

  • Zhihui S, Tzitzikas M, Raemakers K, Zhengqiang M, Visser R (2009) Effect of TDZ on plant regeneration from mature seeds in pea (Pisum sativum). In Vitro Cell Dev Biol-Plant 45:776–782

    Article  Google Scholar 

  • Zok A, Olah R, Hideg E, Horvath VG, Kos PB, Majer P, Varadi G, Szegedi E (2010) Effect of Medicago sativa ferritin gene on stress tolerance in transgenic grapevine. Plant Cell Tiss Organ Cult 100:339–344

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We thank Prof. K. Veluthambi, MKU, Madurai, India for Agrobacterium strain and Center for Appliaction of Molecular Biology to International Agriculture (CAMBIA), Australia for pCAMBIA2301. The research was supported in part by grants under Program Support from Department of Biotechnology (DBT), Government of India. SB and NKR are grateful to Council of Scientific and Industrial Research (CSIR) for Senior and Junior Research Fellowships, respectively.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lingaraj Sahoo.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bakshi, S., Roy, N.K. & Sahoo, L. Seedling preconditioning in thidiazuron enhances axillary shoot proliferation and recovery of transgenic cowpea plants. Plant Cell Tiss Organ Cult 110, 77–91 (2012). https://doi.org/10.1007/s11240-012-0132-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11240-012-0132-y

Keywords

Navigation