Skip to main content
Log in

In vitro cultures of Drosera aliciae as a source of a cytotoxic naphthoquinone: ramentaceone

  • Original Research Paper
  • Published:
Biotechnology Letters Aims and scope Submit manuscript

Abstract

A protocol for the in vitro propagation of Drosera aliciae to increase the yield of the naphthoquinone, ramentaceone, was developed. The highest micropropagation coefficient was obtained using half-strength Murashige–Skoog medium supplemented with 0.4 μM 6-benzyladenine (BA). The genetic fidelity and stability of the regenerated plants was confirmed with RAPD markers. The activity of the isolated ramentaceone was determined against four human tumor cell lines: U937, HeLa, MCF-7, HCT-116 with the highest cytotoxic activity towards the leukemic U937 cell line with an IC50 value of 3.2 μM.

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

Similar content being viewed by others

References

  • Ahmad A, Banerjee S, Wang Z, Kong D, Sarkar FH (2008) Plumbagin-induced apoptosis of human breast cancer cells is mediated by inactivation of NF-κB and Bcl-2. J Cell Biochem 105:1461–1471

    Article  PubMed  CAS  Google Scholar 

  • Aziz MH, Dreckschmidt NE, Verma AK (2008) Plumbagin, a medicinal plant-derived naphthoquinone, is a novel inhibitor of the growth and invasion of hormone-refractory prostate cancer. Cancer Res 68:9024–9032

    Article  PubMed  CAS  Google Scholar 

  • Babula P, Mikelova R, Adam V, Kizek R, Havel L, Sladky Z (2006) Using of liquid chromatography coupled with diode array detector for determination of naphthoquinones in plants and for investigation of influence of pH of cultivation medium on content of plumbagin in Dionaea muscipula. J Chromatogr B 842:28–35

    Article  CAS  Google Scholar 

  • Bapela NB, Lall N, Fourie PB, Franzblau SG, Van Rensburg CE (2006) Activity of 7-methyljuglone in combination with antituberculous drugs against Mycobacterium tuberculosis. Phytomedicine 13:630–635

    Article  PubMed  CAS  Google Scholar 

  • Bekesiova I, Nap JP, Mlynarova L (1999) Isolation of high quality DNA and RNA from leaves of the carnivorous plant Drosera rotundifolia. Plant Mol Biol Rep 17:269–277

    Article  CAS  Google Scholar 

  • Bobak M, Blehova A, Kristin J, Ovecka M, Samaj J (1995) Direct plant regeneration from leaf explants of Drosera rotundifolia cultured in vitro. Plant Cell Tiss Org Cult 43:43–49

    Article  Google Scholar 

  • Finnie JF, van Staden J (1993) Biotechnology and agriculture and forestry. In: Bajaj YPS (ed) Medicinal and aromatic plants V. Springer-Verlag, Berlin, pp 164–177

    Chapter  Google Scholar 

  • Gu JQ, Graf TN, Lee D, Chai HB, Mi Q, Kardono LBS et al (2004) Cytotoxic and antimicrobial constituents of the bark of Diospyros maritima collected in two geographical locations in Indonesia. J Nat Prod 67:1156–1161

    Article  PubMed  CAS  Google Scholar 

  • Hook IL (2001) Naphthoquinone contents of in vitro cultured plants and cell suspensions of Dionaea muscipula and Drosera species. Plant Cell Tiss Org Cult 67:281–285

    Article  CAS  Google Scholar 

  • Jayaram K, Prasad MNV (2007) Rapid in vitro multiplication of Drosera indica L.: a vulnerable, medicinally important insectivorous plant. Plant Biotechnol Rep 1:79–84

    Article  Google Scholar 

  • Juniper BE, Robins RJ, Joel DM (1989) Phytochemical aspects. In: The Carnivorous Plants. Harcourt Brace Jovanovich, Academic Press, London, pp 229–240

  • Kawiak A, Lojkowska E (2004) Application of RAPD in the determination of genetic fidelity in micropropagated Drosera plantlets. In Vitro Cell Dev Biol Plant 40:592–595

    Article  CAS  Google Scholar 

  • Kawiak A, Krolicka A, Lojkowska E (2003) Direct regeneration of Drosera from leaf explants and shoot tips. Plant Tiss Organ Cult 75:175–178

    Article  CAS  Google Scholar 

  • Kawiak A, Piosik J, Stasilojc G, Gwizdek-Wisniewska A, Marczak L, Stobiecki M, Bigda J, Lojkowska E (2007) Induction of apoptosis by plumbagin through reactive oxygen species-mediated inhibition of topoisomerase II. Toxicol Appl Pharmacol 223:267–276

    Article  PubMed  CAS  Google Scholar 

  • Khoddamzadeh AA, Sinniah UR, Kadir MA, Kadzimin SB, Mahmood M, Sreeramanan S (2010) Detection of somaclonal variation by random amplified polymorphic DNA analysis during micropropagation of Phalaenopsis bellina (Rchb.f.) Christenson. Afr J Biotechnol 9:6632–6663

    CAS  Google Scholar 

  • Kim KS, Jang GW (2004) Micropropagation of Drosera peltata, a tuberous sundew, by shoot tip culture. Plant Cell Tiss Org Cult 77:211–214

    Article  CAS  Google Scholar 

  • Krolicka A, Szpitter A, Maciag M, Biskup E, Gilgenast E, Romanik G, Kaminski M, Wegrzyn G, Lojkowska E (2009) Antibacterial and antioxidant activity of the secondary metabolites from in vitro cultures of Drosera aliciae. Biotechnol Appl Biochem 53:175–184

    CAS  Google Scholar 

  • Larkin PJ, Scowcroft WR (1981) Somaclonal variation: a novel source of variability from cell cultures for plant improvement. Theor Appl Genet 60:197–214

    Article  Google Scholar 

  • Larkin PJ, Banks PM, Bhati R, Bretell RS, Davies PA, Rayan SA, Scowcroft WR, Spidler LH, Tanner GH (1989) From somatic variation to variant plants: mechanisms and applications. Genome 31:705–711

    Article  Google Scholar 

  • Mahmood T, Nazar N, Abbasi BH, Khan MA, Ahmad M, Zafar M (2010) Detection of somaclonal variations using RAPD fingerprinting in Silybum marianum L. J Med Plants Res 4:1822–1824

    CAS  Google Scholar 

  • Marczak L, Kawiak A, Lojkowska E, Stobiecki M (2005) Secondary metabolites in in vitro cultured plants from the Drosera genus. Phytochem Anal 16:143–149

    Article  PubMed  CAS  Google Scholar 

  • Mebe PP, Cordel GA, Pezzuto JM (1998) Pentacyclic triterpenes and naphthoquinones from Euclea divinorum. Phytochemistry 47:311–313

    Article  CAS  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 

  • Rout GR, Samantaray S, Das P (2000) In vitro manipulation and propagation of medicinal plants. Biotechnol Adv 18:91–120

    Article  PubMed  CAS  Google Scholar 

  • Shieh JM, Chiang TA, Chang WT, Chao CH, Lee YC, Huang GY, Shih YX, Shih YW (2010) Plumbagin inhibits TPA-induced MMP-2 and u-PA expressions by reducing binding activities of NF-kappaB and AP-1 via ERK signaling pathway in A549 human lung cancer cells. Mol Cell Biochem 335:181–193

    Article  PubMed  CAS  Google Scholar 

  • Varshney A, Lakshmikumaran M, Srivastava PS, Dhawan V (2001) Establishment of genetic fidelity of in vitro-raised Lilium bulblets through RAPD markers. In Vitro Cell Dev Biol Plant 37:227–231

    Article  CAS  Google Scholar 

  • Wang CCC, Chiang YM, Sung SC, Hsu YL, Chang JK, Kuo PL (2008) Plumbagin induces cell cycle arrest and apoptosis through reactive oxygen species/c-Jun N-terminal kinase pathways in human melanoma A375.S2 cells. Cancer Lett 259:82–98

    Article  PubMed  CAS  Google Scholar 

  • Williams JGK, Kubelik AR, Livak KJ, Rafalski JA, Tingey SV (1990) DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Res 18:6531–6535

    Article  PubMed  CAS  Google Scholar 

  • Ziaratnia SM, Kunert KJ, Lall N (2009) Elicitation of 7-methyljuglone in Drosera capensis. S Afr J Bot 75:97–103

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by the grant of the Ministry of Science and Higher Education no. 3021/B/P01/2009/36. This publication is also financed by European Social Fund as a part of the project “Educators for the elite—integrated training program for PhD students, post-docs and professors as academic teachers at University of Gdansk” within the framework of Human Capital Operational Programme, Action 4.1.1, Improving the quality of educational offer of tertiary education institutions. We express our gratitude to Prof. M. Stobiecki (Institute of Bioorganic Chemistry, PAS, Poznan) for the isolation and identification of ramentaceone.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anna Kawiak.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kawiak, A., Królicka, A. & Łojkowska, E. In vitro cultures of Drosera aliciae as a source of a cytotoxic naphthoquinone: ramentaceone. Biotechnol Lett 33, 2309–2316 (2011). https://doi.org/10.1007/s10529-011-0700-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10529-011-0700-y

Keywords

Navigation