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Factors affecting direct organogenesis from flower explants of Allium giganteum

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Abstract

A novel method is described for the propagation of Allium giganteum Regel using direct organogenesis resulting in multiple shoot structures formed on mature flower buds or ovaries. A two step induction and differentiation procedure, similar to that described earlier in onion, was tested. Flowers were inoculated on the induction medium for 6 days and extracted ovaries were placed on the differentiation medium. Optimal formation of multiple shoot structures was obtained using modified BDS medium containing 50 g l−1 sucrose solidified by a mixture of agar/gellan-gum, with 8.88 μM benzylaminopurine (BA) and 9.05 μM 2,4 dichlorophenoxyacetic acid (2,4-D) in induction medium and 9.08 μM tidiazuron (TDZ) in the differentiation medium. Five plant sources obtained from different European retailers of ornamental bulbs were tested separately. All tested genotypes produced multiple organogenic structures, although induction percentages clustered in two distinctive groups. Shoots formed tended to become dormant, and attempts to improve their growth and rooting included treatment with fluridone. Dormancy was partly broken when shoots were briefly dipped in 1 μM fluridone. Genetic analysis of plant sources using random amplified polymorphic DNA method showed that 5 retailers actually distribute only two different clones, one of them more and the other less responsive to shoot organogensis.

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References

  • Barandiaran X, Martin N, Rodriguez-Conde ME, Di Pietro A & Martin J (1999) An efficient method for callus culture and shoot regeneration of garlic (Allium sativum L.) Hortscience 34: 348–349

    Google Scholar 

  • Campion B, Bohanec B & Javornik B (1995) Gynogenic lines of onion (Allium cepa L.): evidence of their homozygosity. Theor. Appl. Genet. 91: 598–602

    Google Scholar 

  • DeHertogh AA & Zimmer K (1993) Allium – ornamental species. In: DeHertogh AA & Le Nard M (eds) The Physiology of Flower Bulbs (pp 187–200). Elsevier Science Publishers, Amsterdam

    Google Scholar 

  • Do GS, Sco BE, Ko JM, Lee SH, Pak JH, Kim IS & Song SD (1999) Analysis of somaclonal variation through tissue culture and chromosomal localization of rDNA sites by fluorescent in situ hybridization in wild Allium tuberosum and a regenerated variant. Plant Cell Tiss. Org. Cult. 57: 113–119

    Google Scholar 

  • Dunstan DI & Short KC (1977) Improved growth of tissue cultures of onion, Alllium cepa. Physiol. Plant 41: 70–72

    Google Scholar 

  • Inagaki N, Matsunaga H, Kanechi M & Maekawa S (1994) In vitro micropropagation of Allium giganteum R. 2. Embryoid and plantlet regeneration through the anther culture of Allium giganteum R. Science Report of Faculty of Agriculture, Kobe University 21: 23–30

  • Inagaki N, Matsunaga H, Kawano T, Maekawa S & Terabun M (1992) In vitro micropropagation of Allium giganteum R. 1. Callus and shoot formation, and regeneration of plantlet through in vitro culture of emerged young leaves. Science report of Faculty of Agriculture, Kobe University 20: 47–53

  • Javornik B, Bohanec B & Campion B (1998) Second cycle gyn-ogenesis in onion, Allium cepa L., and genetic analysis of the plants. Plant Breeding 117: 275–278

    Google Scholar 

  • Kahane R, Rancillac M & Teyssendier-de-la-Serve B (1992) Long-term multiplication of onion (Allium cepa L.) by cyclic shoot regeneration in vitro. Plant Cell Tiss. Org. Cult. 28: 281–288

    Google Scholar 

  • Kim KS, Davelaar E & De Klerk GJ (1994) Abscisic acid controls dormancy development and bulb formation in lily plantlets regenerated in vitro. Physiol. Plant. 90: 59–64

    Google Scholar 

  • Lee KS & Ono K (1999) Chromosomal variation in callus lines and regenerated plantlets from three cultivars of Allium fistulosum L. (2 = 16). Cytologia 64: 465–478

    Google Scholar 

  • Lee SH, Ryu JA, Do GS, Seo BB, Pak JH, Kim IS & Song SD (1998) Chromosome analysis by fluorescence in situ hybridization of callus-derived regenerants in Allium cyaneum R. Plant Cell Rep. 18: 209–213

    Google Scholar 

  • Luthar Z & Bohanec B (1999) Induction of direct somatic organo-genesis in onion (Allium cepa L.) using a two step flower or ovary culture. Plant Cell Rep. 18: 797–802

    Google Scholar 

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

    Google Scholar 

  • Pierik RLM (1987) In vitro Culture of Higher Plants (pp 183-230). Kluwer Academic Publishers, Dordrecht, The Netherlands

    Google Scholar 

  • Popova LP & Riddle KA (1996) Development and accumulation of ABA in fluridone-treated and drought-stressed Vicia faba plants under different light conditions. Physiol. Plant. 98: 791–797

    Google Scholar 

  • Seabrook JEA (1994) In vitro propagation and bulb formation of garlic. Can. J. Plant Sci. 74: 155–158

    Google Scholar 

  • Silvertand B, van Rooyen A, Lavrijsen P, Van Harten AM & Jacobsen E (1996) Plant regeneration via organogenesis and somatic embryogenesis in callus cultures derived from mature zygotic embryos of leek (Allium ampeloprasum L.). Euphytica 91: 261–270

    Google Scholar 

  • VanScheepen J (1991) International Checklist for Hyacinths and Miscellaneous Bulbs. Royal General Bulb Growers Association, The Netherlands

    Google Scholar 

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Correspondence to Borut Bohanec.

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Šušek, A., Javornik, B. & Bohanec, B. Factors affecting direct organogenesis from flower explants of Allium giganteum. Plant Cell, Tissue and Organ Culture 68, 27–33 (2002). https://doi.org/10.1023/A:1012950601175

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  • DOI: https://doi.org/10.1023/A:1012950601175

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