PROPAGATION OF Plantago major L. BY PLANT TISSUE CULTURE TECHNIQUE

Ngày nhận bài: 29-09-2016

Ngày duyệt đăng: 20-12-2016

Ngày xuất bản: 06-08-2025

Chuyên mục:

KỸ THUẬT VÀ CÔNG NGHỆ

Cách trích dẫn:

Ay, N., V.Duy, M., Baatartsogt, O., Altantsetseg, K., & Enkhchimeg, V. (2025). PROPAGATION OF Plantago major L. BY PLANT TISSUE CULTURE TECHNIQUE. Tạp Chí Khoa học Nông nghiệp Việt Nam, 15(3), 282–289. https://doi.org/10.31817/tckhnnvn.2017.15.3.

PROPAGATION OF Plantago major L. BY PLANT TISSUE CULTURE TECHNIQUE

N. V. Ay 1, 2 , M. V.Duy 1, 2 , O. Baatartsogt 1, 2 , Kh. Altantsetseg 1, 2 , V. Enkhchimeg (*) 1, 2

  • Tác giả liên hệ: [email protected]
  • 1 Dept of Biotechnology and breeding, School of Animal Sciences and Biotechnology, Mongolian University of Life Sciences, Mongolia
  • 2 College of Agriculture and Applied Biology, Can Tho University, Vietnam
  • Từ khóa

    2, 4-D: 2, 4-Dichlorophenoxyacetic acid, ABBREVIATIONS, Acclimatization, BA: Benzyl adenine, NAA: α-Naphthaleneacetic acid, MS: Murashige and Skoog, Plantago major L, plant growth hormone, TDZ: Thidiazuron, tissue culture

    Tóm tắt


    Plantago major L., a species that originated in the Far East, has been used for medicinal aspects since ancient times. The technique for callus induction, growth, and plant regeneration from cultured young leaves and petiole explants of Plantago major was carried out. The best initiation and growth of calli was achieved on MS supplemented with 1 mgL-1 2,4-D and 0.5 mgL-1 BA. Shoot regeneration from the calli was obtained on MS medium containing
    1 mgL-1 TDZ alone or combined with 0.5 mgL-1 α-NAA (100 and 96%, respectively). Moreover, the optimum medium for shoot multiplication was MS medium comprising 5 mgL-1 BA, and root formation from the shoots was half-strength MS medium supplemented with 2 mgL-1 NAA. The regenerated plants were successfully transferred into pots containing a mixture of decayed straw: rice husk ashes, (1:1, v/v), sand: soil (1:1, v/v), soil, or sand and grown in nethouse. The phenotypes of regenerated plants were normal as a mother plant.

    Tài liệu tham khảo

    Basma, M.A.R., Hiba A.H. and Muna K.M. (2012). The study of antibacterial activity of Plantago major and Ceratonia siliqua. The Iraqi Postgraduate Medical Journal, 11(1): 130 - 135.

    Bekman P. and Lukens T. (1997). Simple step for pot calla success. Grower Talks, 60(12): 49 - 54.

    Chandra S., Bandopadhyay R., Kumar V. and Chandra R. (2010). Acclimatization of tissue cultured plantlets: from laboratory to land. Biotechnol Let, DOI 10.1007/s10529 - 010 - 0290 - 0, 32: 1199 - 1205.

    Chatfield J.M. and Armstrong D.J. (1986). Regulation of cytokinin oxidase activity in callus tissues of Phaseolus vulgaris L. cv. Great Northern. Physiol. Plant, 80: 493 - 499.

    Driver J.A. and Suttle G.R. (1987). Nursery handling of propagles. In: Cell and Tissue Culture in Forestry (Bonga J.M. & Durzan D.J., eds.). Dortrecht, Netherlands, pp. 320 - 335

    Fons F., Gargadennec A. and Rapior S. (2008). Culture of Plantago species as bioactive components resources: a 20 year review and recent applications. Acta Bot. Gallica., 155(2): 277 - 300.

    George E. F. (1993). Plant propagation by tissue culture (2nd. Ed.). Exegetic Ltd., UK. 709p.

    Ho P.H. (2000). Illustrated Flora of Viet Nam. Youth Publication House, pp. 879 - 880.

    Hutchinson J.M. and Saxena P.K. (1996). Acetylsalicylic acid enhances and synchronizes thidiazuron - induced somatic embryogenesis in geranium (Pelargonium × Hortorum Bailey) tissue cultures. Plant Cell Rep., 15: 512 - 515.

    IAEA. (2004). Low cost options for tissue culture technology in developing countries. IAEA - TECDOC - 1384, ISBN: 92 - 0 - 115903 - X, ISSN: 1011 - 4289

    Kalia R. K., Singh R., Rai M. K., Mishra G. P., Singh S. R. and Dhawan A. K. (2011). Biotechnological interventions in sea buckthorn (Hippophae L.): current status and future prospects. Trees: DOI: 10.1007/s00468 - 011 - 0543 - 0, 25(4): 559 - 575.

    Kende H. and Zeevaart J.A. A. (1997). The five classical plant hormones. The Plant Cell, 9: 1197 - 1210.

    Kolak U., Boga M., Urusak E.A. and Ulubelen A. (2011). Constituents of Plantago major subsp. intermedia with antioxidant and anticholinesterase capacities. Turk J Chem, 35: 637 - 645

    Li Y. and Li P. (2005). In vivo culture method of Plantago major. Patent written in Chinese CN 1701657, 9p.

    Makowczynska J. and Andrzejewska - Golec E. (2000). Somatic embryogenesis in in vitro culture of Plantago asiatica L. Acta Soc. Bot. Pol., 69: 245 - 250.

    Makowczynska J. and Andrzejewska - Golec E. (2003). Micropropagation of Plantago asiatica L. through culture of shoot tips. Acta Societatis Botanicorum Poloniae, 72(3): 191 - 194.

    Mok M.C., Mok D.W.S., Armstrong D.J., Shado K., Isogai Y. and Okomoto T. (1982). Cytokinin activity of N - phenyl N - 1,2,3 - thiadiazol - 5 - ylurea (thidiazuron). Phytochem, 21: 1509 - 1511.

    Murashige T. and Skoog F. (1962). A revised medium for rapid growth and bio - assays with tobaco tissue culture. Physiol. Plant., 15: 473 - 497.

    Murthy B. N. S., Murch S. J. and Saxena P. K. (1995). Thidiazuron - induced somatic embryogenesis in intact seedlings of peanut (Arachis hypogaea): endogenous growth regulator levels and significance of cotyledons. Physiol. Plant., 94: 268 - 276.

    Pourmorad F., Hosseinimehr S.J. and Shahabimajd N. (2006). Antioxidant activity, phenol and flavonoid contents of some selected Iranian medicinal plants, African J Biotechnol, 5(11): 1142 - 1145.

    Samuelsen A.B. (2000). The traditional uses, chemical constituents and biological activities of Plantago major L. A review. Journal of Ethnopharmacology, 71: 1 - 21.

    Souri E., Amin G., Farsam H. and Barazandeh Tehrani M. (2008). Screening of antioxidant activity and phenolic content of 24 medicinal plant extracts, DARU, 16(2): 83 - 87.

    Thomas J.C. and Ketterman F.R. (1986). Cytokinin activity induced by Thidiazuron. Plant Physiol., 81: 681 - 683.

    Tu Y. (1996). Tissue culture of asiatic plantain (Plantago asiatica). Zhongcaoyao, 27: 296 - 298.

    Van Huylenbroeck J.M. and Debergh P.C. (1996). Impact of sugar concentration in vitro on photosynthesis and carbon metabolism during ex vitro acclimatization of Spatiphyllum plantlets. Physiol. Plant., 96: 298 - 304.