Plant Cell, Tissue and Organ Culture (PCTOC)

, Volume 115, Issue 3, pp 385–393 | Cite as

Repetitive somatic embryogenesis from leaves of the medicinal plant Petiveria alliacea L.

  • L. Cantelmo
  • B. O. Soares
  • L. P. Rocha
  • J. A. Pettinelli
  • C. H. Callado
  • E. Mansur
  • A. Castellar
  • R. F. Gagliardi
Original Paper

Abstract

Leaf segments from in vitro-grown shoot cultures of Petiveria alliacea were incubated on Murashige and Skoog (MS) medium supplemented with different concentrations of zeatin, thidiazuron, 2,4-dichlorophenoxyacetic acid (2,4-D) or picloram (PIC). Direct somatic embryogenesis was induced in response to all tested concentrations of 2,4-D and PIC. Primary somatic embryos displayed highly repetitive embryogenesis, both on the induction medium and in liquid hormone-free MS medium. Plantlets were obtained from these secondary embryos at an estimated frequency of 5 %, after 180 days of culture on half-strength MS medium gelled with 0.2 % Phytagel. Simultaneous development of friable non-embryogenic callus was also observed on media containing PIC or 2,4-D at different concentrations. Cell suspension cultures initiated from these callus tissues did not show an increase in biomass. The embryogenic portions formed at the surface of the explants in response to 20.0 μM PIC were inoculated in hormone-free full-or half-strength liquid MS medium (MS0) and showed high rates of secondary embryogenesis, resulting in the production of a mean of 35 embryos for each embryo inoculated at the culture initiation. Embryos that started the conversion process in the liquid MS0 medium originated whole plants at a frequency of 100 % when transferred to MS0 medium solidified with 0.7 % agar. Acclimatization was achieved in 90 % of the converted plantlets, with the production of phenotypically normal plants. This system is potentially useful for the micropropagation of this species, as well as for the production of substances with pharmacological interest, such as dibenzyl trisulfide.

Keywords

Phytolaccacea Embryogenic cell suspension Direct somatic embryogenesis Callus Dibenzyl trisulfide Picloram 

Notes

Acknowledgments

This work was sponsored by the Carlos Chagas Filho Foundation for Research Support of Rio de Janeiro (FAPERJ), the National Council for Scientific and Technological Development (CNPq/Brazil), and the Foundation for the Coordination of Improvement of Higher Education Personnel (CAPES).

References

  1. Ahmed ABA, Rao AS, Rao MV, Taha RM (2011) Effect of Picloran, additives and plant growth regulators on somatic embryogenesis of Phyla nodiflora (L.) Greene. Braz Arch Biol Technol 54:7–13CrossRefGoogle Scholar
  2. An H, Zhu J, Wang X, Xu X (2006) Synthesis and anti-tumor evaluations of new trisulfide derivatives. Bioorg Med Chem Lett 16:4826–4829PubMedCrossRefGoogle Scholar
  3. Arnold S, Sabala I, Bozhkov P, Dyachok J, Filonova L (2002) Developmental pathways of somatic embryogenesis. Plant Cell Tissue Organ Cult 69:233–249CrossRefGoogle Scholar
  4. Aslam J, Mujib A, Nasim SA, Sharma MP (2009) Screening of vincristine yield in ex vitro and in vitro somatic embryos derived plantlets of Catharanthus roseus L. (G) Don. Sci Hortic 119:325–329CrossRefGoogle Scholar
  5. Ayedoun MA, Moudachirou M, Sossou PV, Garneau F-X, Gagnon H, Jean F-I (1998) Volatile constituents of the root oil of Petiveria alliacea L. from Benin. J Essent Oil Res 10:645–646CrossRefGoogle Scholar
  6. Bourgaud F, Gravot A, Milesi S, Gontier E (2001) Production of plant secondary metabolites: a historical perspective. Plant Sci 161:839–851Google Scholar
  7. Castellar A, Gagliardi RF, Mansur E (2011) In vitro propagation and establishment of callus and cell suspension cultures of Petiveria alliacea L., a valuable medicinal plant. J Med Plant Res 5:1113–1120Google Scholar
  8. Castellar A, Gagliardi RF, Mansur E, Bizzo HR, Souza AM, Leitão SG (2013) Essential Oils and volatile constituents from in vitro and ex vitro plants of Petiveria alliacea L. J Essent Oil Res. doi: 10.1080/10412905.2013.820673
  9. Chen JT, Hong PI (2012) Cellular origin and development of secondary somatic embryos in Oncidium leaf cultures. Biol Plantarum 56:215–220CrossRefGoogle Scholar
  10. Chirinos DN (1992) El milagro de los vegetales: Petiveria alliacea, 3rd edn. Bienes Lacónica, Caracas, pp 39–46Google Scholar
  11. De Sousa JR, Demuner AJ, Pinheiro JA, Breitmaier E, Cassels BK (1990) Dibenzyl trisulphide and trans-N-methyl-4-methoxyproline from Petiveria alliacea. Phytochemistry 29:3653–3655CrossRefGoogle Scholar
  12. Delle-Monache F, Suarez LEC (1992) 6-c-formil and 6-c-hydroxymethyl flavanones from Petiveria alliacea. Phytochemistry 31:2481–2482CrossRefGoogle Scholar
  13. Delle-Monache F, Menichini F, Suarez LEC (1996) Substances from Petiveria alliacea: II. Further flavonoids and triterpenes. Gaz Chim Ital 126:275–278Google Scholar
  14. Devi BC, Narmathabai V (2011) Somatic embryogenesis in the medicinal legume Desmodium motorium (Houtt.) Merr. Plant Cell Tissue Organ Cult 106:409–418CrossRefGoogle Scholar
  15. Feder N, O’Brien TP (1968) Plant microtechnique: some principles and new methods. Am J Bot 55:123–142CrossRefGoogle Scholar
  16. Fehér A, Pasternak TP, Dudits D (2003) Transition of somatic plant cells to an embryogenic state. Plant Cell Tissue Organ Cult 74:201–228CrossRefGoogle Scholar
  17. George EF, Hall MA, Klerk GJD (2008) Plant propagation by tissue culture: vol. 1. The background, 3rd edn. Springer, DordrechtGoogle Scholar
  18. Gill R, Saxena PK (1993) Somatic embryogenesis in Nicotiana-tabacum L.: induction by thidiazuron of direct embryo differentiation from cultured leaf discs. Plant Cell Rep 12:154–159PubMedCrossRefGoogle Scholar
  19. Goebel-Tourand I, Mauro MC, Sossountzov L, Miginiac E, Deioire A (1993) Arrest of somatic embryo development in grapevine: histological characterization and the effect of ABA, BAP and zeatin in stimulating plantlet development. Plant Cell Tissue Organ Cult 33:91–103CrossRefGoogle Scholar
  20. Hankoua BB, Taylor NJ, Ng SYC, Fawole I, Puonti-Kaerlas J, Padmanabhan C, Yadav JS, Fauquet CM, Dixon AGO, Fondong VN (2006) Production of the first transgenic cassava in Africa via direct shoot organogenesis from friable embryogenic calli and germination of maturing somatic embryos. Afr J Biotechnol 5:1700–1712Google Scholar
  21. Jimenez VM (2005) Involvement of plant hormones and plant growth regulators on in vitro somatic embryogenesis. Plant Growth Regul 47:91–110CrossRefGoogle Scholar
  22. Johansen DA (1940) Plant microtechnique. McGraw-Hill, New YorkGoogle Scholar
  23. Karami O, Deljou A, Pour AM (2007) Repetitive somatic embryogenesis in carnation on picloram supplemented medium. Plant Growth Regul 51:33–39CrossRefGoogle Scholar
  24. Kaur P, Kothari SL (2004) In vitro culture of kodo millet: influence of 2,4-D and picloram in combination with kinetin on callus initiation and regeneration. Plant Cell Tissue Organ Cult 77:73–79CrossRefGoogle Scholar
  25. Kubec R, Musah RA (2001) Cysteine sulfoxide derivatives in Petiveria alliacea. Phytochemistry 58:981–985PubMedCrossRefGoogle Scholar
  26. Lee W-L, Chan L-K (2004) Establishment of Orthosiphon stamineus cell suspension culture for cell growth. Plant Cell Tissue Organ Cult 78:101–106CrossRefGoogle Scholar
  27. Maharik N, Elgengaihib S, Taha H (2009) Anthocyanin production in callus cultures of Crataegus sinaica Boiss. Int J Acad Res 1:30–34Google Scholar
  28. Mata-Greenwood E, Ito A, Westenburg H, Cui BL, Mehta RG, Kinghorn AD, Pezzuto JN (2001) Discovery of novel inducers of cellular differentiation using HL-60 promyelocytic cells. Anticancer Res 21:1763–1770PubMedGoogle Scholar
  29. Mendoza MG, Kaeppler HF (2002) Auxin and sugar effects on callus induction and plant regeneration frequencies from mature embryos of wheat (Triticum aestivum L.). In Vitro Cell Dev Biol Plant 38:39–45Google Scholar
  30. Mitchell SA, Ahmad MH (2006) A review of medicinal plant research at the University of the West Indies, Jamaica, 1948–2001. West Indian Med J 55:243–269Google Scholar
  31. Morini S, D’Onofrio C, Bellocchi G, Fisichella M (2000) Effect of 2,4-D and light quality on callus production and differentiation from in vitro cultured quince leaves. Plant Cell Tissue Organ Cult 63:47–55CrossRefGoogle Scholar
  32. Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–497CrossRefGoogle Scholar
  33. Okada Y, Tanaka K, Sato E, Okajima H (2008) Antioxidant activity of the new thiosulfinate derivative, S-benzyl phenylmethanethiosulfinate, from Petiveria alliacea L. Org Biomol Chem 6:1097–1102PubMedCrossRefGoogle Scholar
  34. Ooi SE, Choo C-N, Ishak Z, Ong-Abdullah M (2012) A candidate auxin-responsive expression marker gene, EgIAA9, for somatic embryogenesis in oil palm (Elaeis guineensis Jacq.). Plant Cell Tissue Organ Cult 110:201–212CrossRefGoogle Scholar
  35. Pacheco G, Gagliardi RF, Carneiro LA, Callado CH, Valls JFM, Mansur E (2007) The role of BAP in somatic embryogenesis induction from seed explants of Arachis species from Sections Erectoides and Procumbentes. Plant Cell Tissue Organ Cult 88:121–126CrossRefGoogle Scholar
  36. Pinto DLP, De Almeida AMR, Rêgo MM, Da Silva ML, De Oliveira EJ, Otoni WC (2011) Somatic embryogenesis from mature zygotic embryos of commercial passionfruit (Passiflora edulis Sims) genotypes. Plant Cell Tissue Organ Cult 107:521–530CrossRefGoogle Scholar
  37. Roeser KR (1972) Die Nadel der Schwarzkiefer–Massenprodukt und Kunstwert der Natur. Mikrokosmos 61:33–36Google Scholar
  38. Rösner H, Williams LAD, Jung A, Kraus W (2001) Disassembly of microtubules and inhibition of neurite outgrowth, neuroblastoma cell proliferation, and MAP-kinase tyrosine dephosphorylation by dibenzyl trisulphide. Biochim Biophys Acta 1540:166–177PubMedCrossRefGoogle Scholar
  39. Ruffa MJ, Ferraro G, Wagner ML, Calcagno ML, Campos RH, Cavallaro L (2002) Cytotoxic effect of Argentine medicinal plant extracts on human hepatocellular carcinoma cell line. J Ethnopharmacol 79:335–339PubMedCrossRefGoogle Scholar
  40. Sass JE (1958) Elements of Botanical Microtechnique. McGraw-Hill, LondonGoogle Scholar
  41. Shohael MA, Ali MB, Yu EH, Paek K (2006) Effect of temperature on secondary metabolites production and antioxidant enzyme activities in Eleutheococcus senticosus somatic embryos. Plant Cell Tissue Organ Cult 85:219–228CrossRefGoogle Scholar
  42. Shohael MA, Ali MB, Ali JE, Paek K (2007) Glutathione metabolism and antioxidant responses during Eleutherococcus senticosus somatic embryo development in a bioreactor. Plant Cell Tissue Organ Cult 89:121–129CrossRefGoogle Scholar
  43. Szypula W, Pietrosiuk A, Suchocki P, Furmanowa M, Kazimierska O (2005) Somatic embryogenesis and in vitro culture of Huperzia selago shoots as a potential source of huperzine. Plant Sci 168:1443–1452CrossRefGoogle Scholar
  44. Taylor L (2005) The Healing Power of Rainforest Herbs: A Guide to Understanding and Using Herbal Medicinals. Square One Publishers http//www.rain-tree.com/paudarco.htm. Accessed 24 Sept 2010
  45. Urueña C, Cifuentes C, Castañeda D, Arango A, Kaur P, Asea A, Fiorentino S (2008) Petiveria alliacea extracts uses multiple mechanisms to inhibit growth of human and mouse tumoral cells. BMC Complement. Altern Med 8:1–17Google Scholar
  46. Vargas TE, De García E, Oropeza M (2005) Somatic embryogenesis in Solanum tuberosum from cell suspension cultures: histological analysis and extracellular protein patterns. J Plant Physiol 162:449–456PubMedCrossRefGoogle Scholar
  47. Webster SA, Mitchell SA, Ahmad MH (2004) Somatic embryogenic response of Petiveria alliacea leaf explant-derived callus to sucrose and glucose enriched media supplemented with NAA and BAP. Abstract Issue—World Congress on In Vitro Biology. In Vitro Cell Dev Biol 40:33Google Scholar
  48. Webster SA, Mitchel SA, Gallimore WA, Williams LAD, Ahmad MH (2008) Biosynthesis of Dibenzyl Trisulfide (DTS) from somatic embryos and rhizogenous/embryogenic callus derived from Guinea hen weed (Petiveria alliacea L.) leaf explants. In Vitro Cell Develop Biol 44:112–118Google Scholar
  49. Williams LAD, The TL, Gardener MT, Fletcher CK, Naravane A, Gibbs N, Fleishacker R (1997) Immunomodulatory activities of Petiveria alliacea L. Phytother Res 11:251–253CrossRefGoogle Scholar
  50. Williams LAD, Vasquez E, Klaiber I, Kraus W, Rosner H (2003) A sulfonic anhydride derivative from dibenzyl trisulphide with agro-chemical activities. Chemosphere 51:701–706PubMedCrossRefGoogle Scholar
  51. Williams LAD, Rösner H, Möller W, Conrad J, Nkurunziza JP, Kraus W (2004) In vitro anti-proliferation/cytotoxic activity of sixty natural products on the human’s SH-SY5Y neuroblastoma cells with specific reference to dibenzyl trisulphide. West Indian Med J 53:208–219PubMedGoogle Scholar
  52. Williams LAD, Rösner H, Levy HG, Barton EN (2007) A critical review of the therapeutic potential of dibenzyl trisulphide from Petiveria alliacea L. (Guinea hen weed, Anamu). West Indian Med J 56:17–21PubMedGoogle Scholar
  53. Williams LAD, Rösner H, Kraus W (2012) Molecules with potential for cancer therapy in the developing world: dibenzyl trisulfide (DTS). In: Nelson KE, Jones-Nelson B (eds) Genomics applications for the developing world, advances in microbial ecology. Springer, New York, pp 273–278CrossRefGoogle Scholar
  54. Yeung EC (1995) Structural and developmental patterns in somatic embryogenesis. In: Thorp TA (ed) In vitro embryogenesis in plants. Kluwer Academic, Dordrecht, pp 205–247CrossRefGoogle Scholar
  55. You CR, Fan TJ, Gong XQ, Bian FH, Liang LK, Qu FN (2011) A high-frequency cyclic secondary somatic embryogenesis system for Cyclamen persicum Mill. Plant Cell Tissue Organ Cult 107:233–242CrossRefGoogle Scholar
  56. You XL, Tan X, Dai JL, Li YH, Choi YE (2012) Large-scale somatic embryogenesis and regeneration of Panax notoginseng. Plant Cell Tissue Organ Cult 108:333–338CrossRefGoogle Scholar
  57. Zoghbi MGB, Andrade EHA, Maia JGS (2002) Volatile constituents from Adenocalymma alliaceum Miers and Petiveria alliacea L. Two medicinal herbs of the Amazon. Flavour Frag J 17:133–135CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media Dordrecht 2013

Authors and Affiliations

  • L. Cantelmo
    • 1
  • B. O. Soares
    • 1
  • L. P. Rocha
    • 1
  • J. A. Pettinelli
    • 1
  • C. H. Callado
    • 2
  • E. Mansur
    • 1
  • A. Castellar
    • 3
  • R. F. Gagliardi
    • 1
  1. 1.Núcleo de Biotecnologia VegetalUniversidade do Estado do Rio de JaneiroRio de JaneiroBrazil
  2. 2.Laboratório de Anatomia VegetalUniversidade do Estado do Rio de JaneiroRio de JaneiroBrazil
  3. 3.Laboratório de Produtos Naturais e AlimentosUniversidade Federal do Rio de JaneiroRio de JaneiroBrazil

Personalised recommendations