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An efficient regeneration system via direct and indirect somatic embryogenesis for the medicinal tree Murraya koenigii

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Abstract

A reproducible protocol for direct and indirect somatic embryogenesis was established in a small aromatic tree, Murraya koenigii. Embryogenic callus was obtained from 90% zygotic embryonic axis (ZE) and 70% cotyledon (COT) explants in Murashige and Skoog (MS) basal medium supplemented with 8.88 μM 6-benzyladenine (BA) and 2.675 μM α-naphthaleneacetic acid (NAA). Globular somatic embryos were induced and further matured from such embryogenic callus by subsequent culture on the same basal media containing thidiazuron (TDZ) (2.27–9.08 μM). The highest frequency of somatic embryos (14.58 ± 0.42) was recovered from ZE-derived callus after 6 weeks. The age and type of explant and concentration of TDZ played an important role in the development of somatic embryos. Explants excised from 60-day-old seed differentiated from 96.67% of ZE explants and 86.67% from COT explants when cultured on MS basal medium supplemented with 4.54 and 9.08 μM TDZ, respectively, after 4 weeks. The best result obtained for the average frequency of somatic embryos (11.28 ± 0.32) was from ZE explants, which was significantly higher than COT explants (7.34 ± 0.97). Most of the somatic embryos (above 95%), irrespective of their origin, germinated after 4 weeks in 1/2 MS basal media containing 2.32 μM kinetin (KN) and 1.07 μM NAA. Well-rooted plantlets were successfully acclimatized. Histological analysis and scanning electron micrographs confirmed the initiation, development, and germination of somatic embryos from both explants.

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References

  • Adebajo AC, Ayoola OF, Iwalewa EO, Akindahunsi AA, Omisore NO, Adewunmi CO et al (2006) Anti-trichomonal, biochemical and toxicological activities of methanolic extract and some carbazole alkaloids isolated from the leaves of Murraya koenigii growing in Nigeria. Phytomedicine 13:246–254

    Article  PubMed  CAS  Google Scholar 

  • Bhuyan AK, Pattanaik S, Chand PK (1997) Micropropagation of curry leaf tree [Murraya koenigii (L.) Spreng.] by axillary proliferation using intact seedlings. Plant Cell Rep 16:779–782

    Article  CAS  Google Scholar 

  • Bilyeu KD, Cole JL, Laskey JG, Riekhof WR, Esparza TJ, Kramer MD et al (2001) Molecular and biochemical characterization of a cytokinin oxidase from maize. Plant Physiol 125:378–386

    Article  PubMed  CAS  Google Scholar 

  • Carimi F, De Pasquale F, Crescimanno FG (1995) Somatic embryogenesis in Citrus from styles culture. Plant Sci 105:81–86

    Article  CAS  Google Scholar 

  • Carra A, De Pasquale F, Ricci A, Carimi F (2006) Diphenylurea derivatives induce somatic embryogenesis in Citrus. Plant Cell Tissue Organ Cult 87:41–48

    Article  CAS  Google Scholar 

  • Chakrabarty M, Nath AC, Khasnobis S, Chakrabarty M, Konda Y, Harigaya Y et al (1997) Carbazole alkaloids from Murraya koenigii. Phytochemistry 46:751–755

    Article  PubMed  CAS  Google Scholar 

  • Da Silva ML, Pinto DLP, Guerra MP, Iochevet E, Floh S, Bruckner CH et al (2009) A novel regeneration system for a wild passion fruit species (Passiflora cincinnata Mast.) based on somatic embryogenesis from mature zygotic embryos. Plant Cell Tissue Organ Cult 99:47–54

    Article  Google Scholar 

  • Dam A, Paul S, Bandyopadhyay TK (2010) Direct somatic embryogenesis and plant regeneration from leaf explants of Limonium sinensis (Girard) Kuntze. Sci Hortic 126:253–260

    Article  CAS  Google Scholar 

  • Etienne H, Montoro P, Michaux-Ferriere N, Carron MP (1993) Effects of desiccation, medium osmolarity and abscisic acid on the maturation of Hevea brasiliensis somatic embryos. J Exp Bot 44:1613–1619

    Article  CAS  Google Scholar 

  • Fan GQ, Zhai XQ, Zhai CJ, Bi HT (2001) Callus induction from leaves of different Paulownia species and its plantlet regeneration. J For Res 12:209–214

    Article  Google Scholar 

  • Gaj MD (2004) Factors influencing somatic embryogenesis induction and plant regeneration with particular reference to Arabidopsis thaliana (L.) Heynh. Plant Growth Regul 43:27–47

    Article  CAS  Google Scholar 

  • Gupta GL, Nigam SS (1970) Chemical examination of the leaves of Murraya koenigii. Planta Med 19:83–86

    Article  PubMed  CAS  Google Scholar 

  • Ito C, Itoigawa M, Nakao K, Murata T, Tsuboi M, Kaneda N et al (2006) Induction of apoptosis by carbazole alkaloids isolated from Murraya koenigii. Phytomedicine 13:359–365

    Article  PubMed  CAS  Google Scholar 

  • Jiménez VM, Bangerth F (2001) Endogenous hormone levels in explants and in embryogenic and non-embryogenic cultures of carrot. Physiol Plant 111:389–395

    Article  PubMed  Google Scholar 

  • Jumin HB, Nito N (1996) Plant regeneration via somatic embryogenesis from protoplasts of six plant species related to Citrus. Plant Cell Rep 15:332–336

    Article  CAS  Google Scholar 

  • Kesari AN, Kesari S, Singh SK, Gupta RK, Watal G (2007) Studies on the glycemic and lipidemic effect of Murraya koenigii in experimental animals. J Ethnopharmacol 112:305–311

    Article  PubMed  Google Scholar 

  • Langhansová L, Konrádová H, Vaněk T (2004) Polyethylene glycol and abscisic acid improve maturation and regeneration of Panax ginseng somatic embryos. Plant Cell Rep 22:725–730

    Article  PubMed  Google Scholar 

  • Martin KP, Madassery J (2005) Direct and indirect somatic embryogenesis on cotyledon explants of Quassia amara L., an antileukaemic drug plant. In Vitro Cell Dev Biol Plant 41:54–57

    Article  Google Scholar 

  • Mauri PV, Manzanera JA (2004) Effect of abscisic acid and stratification on somatic embryo maturation and germination of holm oak (Quercus ilex L.). In Vitro Cell Dev Biol Plant 40:495–498

    Article  CAS  Google Scholar 

  • McCown B, Amos R (1979) Initial trials with commercial micropropagation of birch selections. Comb Proc Int Plant Prop Soc 29:387–393

    Google Scholar 

  • Mechanda SM, Baum BR, Johnson DA, Arnason JT (2003) Direct shoot regeneration from leaf segments of mature plants of Echinacea purpurea (L.) moench. In Vitro Cell Dev Biol Plant 39:505–509

    Article  Google Scholar 

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

    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 34:268–276

    Google Scholar 

  • Nanda RM, Rout GR (2003) In vitro somatic embryogenesis and plant regeneration in Acacia arabica. Plant Cell Tissue Organ Cult 73:131–135

    Article  CAS  Google Scholar 

  • Ningappa MB, Dinesha R, Srinivas L (2008) Antioxidant and free radical scavenging activities of polyphenol-enriched curry leaf (Murraya koenigii L.) extracts. Food Chem 106:720–728

    Article  CAS  Google Scholar 

  • Nirmal Babu K, Anu A, Remashree AB, Praveen K (2000) Micropropagation of curry leaf tree. Plant Cell Tissue Organ Cult 61:199–203

    Article  Google Scholar 

  • Nutan MTH, Hasnat A, Rashid MA (1998) Antibacterial and cytotoxic activities of Murraya koenigii. Fitoterapia 69:173–175

    CAS  Google Scholar 

  • Okamura M, Taniguchi T, Kondo T (2001) Efficient embryogenic callus induction and plant regeneration from embryonic axis explants in Quercus acutissima. J For Res 6:63–66

    Article  Google Scholar 

  • Prakash MG, Gurumurthi K (2010) Effects of type of explant and age, plant growth regulators and medium strength on somatic embryogenesis and plant regeneration in Eucalyptus camaldulensis. Plant Cell Tissue Organ Cult 100:13–20

    Article  CAS  Google Scholar 

  • Rahman MM, Gray AI (2005) A benzoisofuranone derivative and carbazole alkaloids from Murraya koenigii and their antimicrobial activity. Phytochemistry 66:1601–1606

    Article  PubMed  CAS  Google Scholar 

  • Rao LJM, Ramalakshmi K, Borse BB, Raghavan B (2007) Antioxidant and radical-scavenging carbazole alkaloids from the oleoresin of curry leaf (Murraya koenigii Spreng.). Food Chem 100:742–747

    Article  CAS  Google Scholar 

  • Roy MK, Thalang VN, Trakoontivakorn G, Nakahara K (2004) Mechanism of mahanine-induced apoptosis in human leukemia cells (HL-60). Biochem Pharmacol 67:41–51

    Article  PubMed  CAS  Google Scholar 

  • Sakai WS (1973) Simple method for differential staining of paraffin embedded plant material using toluidine blue O. Stain Technol 48:247–249

    PubMed  CAS  Google Scholar 

  • Shaw G (1994) Chemistry of adenine cytokinins. In: Mok DWS, Mok MC (eds) Cytokinins: chemistry, activity, and function. CRC Press, Boca Raton, FL, pp 15–34

    Google Scholar 

  • Shee C, Islam A, Ahmad F, Sharma AK (2007) Structure–function studies of Murraya koenigii trypsin inhibitor revealed a stable core beta sheet structure surrounded by α-helices with a possible role for α-helix in inhibitory function. Int J Biol Macromol 41(4):410–414

    Article  PubMed  CAS  Google Scholar 

  • Shudo K (1994) Chemistry of diphenylurea cytokinins. In: Mok DWS, Mok MC (eds) Cytokinins: chemistry, activity, and function. CRC Press, Boca Raton, FL, pp 35–42

    Google Scholar 

  • Tachibana Y, Kikuzaki H, Lajis NH, Nakatani N (2003) Antioxidative activity of carbazoles from Murraya koenigii leaves. J Agric Food Chem 49:5589–5594

    Article  Google Scholar 

  • Vila SK, Rey HY, Mroginski LA (2007) Factors affecting somatic embryogenesis induction and conversion in “paradise tree” (Melia azedarach L.). J Plant Growth Regul 26:268–277

    Article  CAS  Google Scholar 

  • Woo SH, Nair A, Adachi T, Campbell CG (2000) Plant regeneration from cotyledon tissues of common buckwheat (Fagopyrum esculentum Moench). In Vitro Cell Dev Biol Plant 36:358–361

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We are grateful to Dr. S. Banerjee, Editor, Australian Journal of Agricultural Research, for suggesting the necessary modifications to the manuscript. We thank Dr. P. S. Basu and Mr. K. Mukherjee for their valuable suggestions during the manuscript revision. Personal research grants (PRGs) provided by the University of Kalyani, Kalyani, West Bengal, India, are also gratefully acknowledged.

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Correspondence to T. K. Bandyopadhyay.

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Paul, S., Dam, A., Bhattacharyya, A. et al. An efficient regeneration system via direct and indirect somatic embryogenesis for the medicinal tree Murraya koenigii . Plant Cell Tiss Organ Cult 105, 271–283 (2011). https://doi.org/10.1007/s11240-010-9864-8

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  • DOI: https://doi.org/10.1007/s11240-010-9864-8

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