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High-frequency plant regeneration from embryogenic cell suspension cultures of Gynura procumbens

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Abstract

The efficient plant regeneration system from embryogenic cell suspension cultures of Gynura procumbens (Lour.) Merr. is described. Leaf, stem and petiole explants were cultured on Murashige and Skoog (MS) medium supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D) in various concentrations (0, 0.1, 0.3, 1.0 and 3.0 mg l−1). Leaf, stem and petiole explants formed pale-yellow nodular callus and off-white calluses at a frequency of 100% when cultured on MS medium supplemented with more than 1 mg l−1 of 2,4-D after 4 weeks incubation. However, only 20% of pale-yellow nodular callus derived from petiole explants developed into white embryonic structures. Upon transfer to MS basal medium without growth regulators, these white embryonic structures differentiated into somatic embryos. Embryogenic cell suspension cultures were initiated from petiole-derived pale-yellow nodular calluses. More than 73.2% of regenerated plantlets via somatic embryogenesis produced roots on MS medium supplemented with 0.1 mg l−1 α-naphthaleneacetic acid and 1 mg l−1 indole-3-butyric acid (IBA), respectively. Rooted plantlets were successfully transplanted to soil mixture of sterile vermiculite and potting soil (1:1) and grown to maturity in a growth chamber, achieving a survival rate of > 95%. The plant regeneration system from embryogenic cell suspension cultures of G. procumbens established in this study could be applied as an alternative for mass proliferation as well as molecular breeding for quality improvement of G. procumbens.

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References

  • Akowuah GA, Sadikun A, Mariam A (2002) Flavonoid identification and hypoglycaemic studies of the butanol fraction from Gynura procumbens. Pharm Biol 40:405–410

    Article  CAS  Google Scholar 

  • Alizah Z, Nurulaishah Y (2015) Multiple shot regeneration from nodal explants of Gynura procumbens (Lour.) Merr. Annu Res Rev Biol 6:85–88

    Article  Google Scholar 

  • Chan LK, Lim SY, Pan LP (2009) Micropropagation of Gynura procumbens (Lour.) Merr. an important medicinal plant. J Med Plant Res 3:105–111

    Google Scholar 

  • Dai N, Yu YC, Ren TH, Wu JG, Jiang Y, Shen LG, Zhang J (2007) Gynura root induces hepatic veno-occlusive disease: a case report and review of the literature. World J Gastroenterol 13:1628–1631

    Article  PubMed  PubMed Central  Google Scholar 

  • De-la-Peña C, Nic-Can GI, Galaz-Ávalos RM, Avilez-Montalvo R, Loyola-Vargas VM (2015) The role of chromatin modifications in somatic embryogenesis in plants. Front Plant Sci 6:635

    Article  PubMed  PubMed Central  Google Scholar 

  • Hew CS, Khoo BY, Gam LH (2013) The anti-cancer property of proteins extracted from Gynura procumbens (Lour.) Merr. PLoS One 8:7 e68524

    Article  CAS  PubMed  Google Scholar 

  • Hoe SZ, Kamaruddin MY, Lam SK (2007) Inhibition of angiotensin-converting enzyme activity by a partially purified fraction of Gynura procumbens in spontaneously hypertensive rats. Med Princ Pract 16:203–208

    Article  PubMed  Google Scholar 

  • Iskander MN, Song Y, Coupar IM, Jiratchariyakul W (2002) Anti-inflammatory screening of the medicinal plant Gynura procumbens. Plant Food Hum Nutr 57:233–244

    Article  CAS  Google Scholar 

  • Jie EY, Ryu YB, Choi SA, Ahn MS, Liu JR, Min SR, Kim SW (2015) Mass propagation of microtubers from suspension cultures of Pinellia ternata cells and quantitative analysis of succinic acid in Pinellia tubers. Plant Biotechnol Rep 9:331–338

    Article  Google Scholar 

  • Kaewseejan N, Sutthikhum V, Siriamornpun S (2015) Potential of Gynura procumbens leaves as source of flavonoid-enriched fractions with enhanced antioxidant capacity. J Funct Foods 12:120–128

    Article  CAS  Google Scholar 

  • Keng CL, Yee LS, Pin PL (2009) Micropropagation of Gynura procumbens (Lour.) Merr. an important medicinal plant. Med Plant Res 3:105–111

    CAS  Google Scholar 

  • Ling APK, Chin MF, Hussein S (2009) Adventitious root production of Centella asiatica in response to plant growth regulator and sucrose concentrations. Med Aromat Plant Sci Biotechnol 3:36–41

    Google Scholar 

  • Min SR, Liu JR, Kim SW (2007) Plant regeneration from zygotic embryo-derived embryogenic cell suspension cultures of Ranunculus kazusensis. Plant Biotechnol Rep 1:57–60

    Article  Google Scholar 

  • Mithila J, Hall JC, Victor JMR, Saxena PK (2003) Thidiazuron induces shoot organogenesis at low concentrations and somatic embryogenesis at high concentrations on leaf and petiole explants of African violet (Saintpaulia ionantha Wendl). Plant Cell Rep 21:408–414

    Article  CAS  PubMed  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 

  • Oh MJ, Na HR, Choi HK, Liu JR, Kim SW (2008) High frequency plant regeneration from zygotic embryo derived embryogenic cell suspension cultures of watershield (Brasenia schreberi). Plant Biotechnol Rep 2:87–92

    Article  Google Scholar 

  • Oh MJ, Ahn MS, Jie EY, Liu JR, Min BW, Kim SW (2013) High-frequency plant regeneration from immature zygotic embryo cultures of Houttuynia cordata Thunb via somatic embryogenesis. Plant Biotechnol Rep 7:527–534

    Article  Google Scholar 

  • Parvin F, Md JI, Jahan N, Khan H, Md PES, Md AI, Rahaman MH, Md MR (2014) Efficient in vitro micropropagation of Gynura procumbens—an important rare medicinal plant, through shoot tip and nodal segments explants. J Res Biol 4:1444–1450

    Google Scholar 

  • Perry LM, Metzger J (1980) Medicinal plants of East and South East Asia: attributed properties and uses. The MIT Press, Cambridge

    Google Scholar 

  • Puangpronpitag D, Kaewseejan N, Nakornriab M (2012) Evaluation of phytochemical composition and antibacterial property of Gynura procumbens extract. Asian J Plant Sci 11:77–82

    Article  Google Scholar 

  • Qi X, Wu B, Cheng Y, Qu H (2009) Simultaneous characterization of pyrrolizidine alkaloids and N-oxides in Gynura segetum by liquid chromatography/ion trap mass spectrometry. Rapid Commun Mass Spectrom 23:291–302

    Article  CAS  PubMed  Google Scholar 

  • Saiman MZ, Mustafa NR, Schulte AE, Verpoorte R, Choi YH (2012) Induction, characterization, and NMR-based metabolic profiling of adventitious root cultures from leaf explants of Gynura procumbens. Plant Cell Tissue Organ Cult 109:465–475

    Article  CAS  Google Scholar 

  • Rosidah, Yam MF, Sadikun A, Ahmad M, Akowuah GA, Asmawi MZ (2009) Toxicology evaluation of standardized methanol extract of Gynura procumbens. J Ethnopharmacol 123:244–249

    Article  PubMed  Google Scholar 

  • Zahra AA, Kadir FA, Mahmood AA, Al hadi AA, Suzy SM, Sabri SZ, Latif II, Ketuly KA (2011) Acute toxicity study and wound healing potential of Gynura procumbens leaf extract in rats. J Med Plant Res 5:2551–2558

    Google Scholar 

  • Zhao J, Cui J, Liu J, Liao F, Henny RJ, Chen J (2012) Direct somatic embryogenesis from leaf and petiole explants of Spathiphyllum ‘Supreme’ and analysis of regenerants using flow cytometry. Plant Cell Tissue Organ Cult 110(2):239–249

    Article  Google Scholar 

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Acknowledgements

This work was supported by a grant from the KRIBB Research Initiative Program (KGM5281711).

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Correspondence to Suk Weon Kim.

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Jie, E.Y., Atong, N.S., Ahn, W.S. et al. High-frequency plant regeneration from embryogenic cell suspension cultures of Gynura procumbens. Plant Biotechnol Rep 13, 27–33 (2019). https://doi.org/10.1007/s11816-018-0507-6

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  • DOI: https://doi.org/10.1007/s11816-018-0507-6

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