Influence of genotype, explant source, and gelling agent on in vitro shoot regeneration of chrysanthemum
详细信息    查看全文
  • 作者:Ki-Byung Lim (1)
    Soo Jin Kwon (2)
    Soo In Lee (2)
    Yoon-Jung Hwang (1)
    Aung Htay Naing (1)
  • 关键词:6 ; benzyladenine ; adventitious shoots formation ; in vitro propagation ; naphthaleneacetic acid ; ornamental plant
  • 刊名:Horticulture, Environment, and Biotechnology
  • 出版年:2012
  • 出版时间:August 2012
  • 年:2012
  • 卷:53
  • 期:4
  • 页码:329-335
  • 全文大小:148KB
  • 参考文献:1. Annadana, S., W. Rademaker, M. Ramanna, M. Udayakumar, and J. de Jong. 2000. Response of stem explants to screening and explants source as a basis for methodical advancing of regeneration protocols for chrysanthemum. Plant Cell Tiss. Org. Cult. 62:47-5. CrossRef
    2. Baroncelli, S., S. Buittiet, M. Bennici, W. Foroughi, G. Mix, H. Gaul, A.M. Tagliasacchi, M. Loiero, and B. Giorgi. 1978. Genetic control of in vitro and in vivo growth of hexaploid wheat. Z Pflanzenzuecht. 80:109-16.
    3. Berrios, E.F., L. Gentzbittel, H. Serieys, G. Alibert, and A. Sarrafi. 1999. Influence of genotype and gelling agents on in vitro regeneration by organogenesis in sunflower. Plant Cell Tiss. Org. Cult. 59:65-9. CrossRef
    4. Bliss, B.J., L. Landherr, C.W. de Pamphilis, H. Ma, Y. Hu, and S.N. Maximova. 2009. Regeneration and plantlet development from somatic tissues of / Aristolochia fimbriata. Plant Cell Tiss. Org. Cult. 98:105-14. CrossRef
    5. Bornam, C.H. and T.C. Vogelman. 1984. Effect of rigidity of gel medium on benzyladenine-induced adventitious bud formation and vitrification in vitro in / Picea abies. Physiol. Plant. 61:505-12. CrossRef
    6. Debergh, P.C. 1983. Effects of agar brand and concentration on the tissue culture medium. Physiol. Plant. 59:270-76. CrossRef
    7. Debergh, P.C., J. Aitken-Christie, D. Cohen, B. Grout, S. Von Arnold, R. Zimmerman, and M. Ziv. 1992. Reconsideration of the term vitrification as used in micropropagation. Plant Cell. Tiss. Org. Cult. 30:135-40. CrossRef
    8. Dhar, U. and M. Joshi. 2005. Efficient plant regeneration protocol through callus for / Saussurea obvallata (dc.) Edgew. (Asteraceae): Effect of explant type, age and plant growth regulators. Plant Cell Rep. 24:195-00. CrossRef
    9. Dolgov, S.V., T. Yu. Mitiouchiina, and K.G. Skryabin. 1997. / Agrobacterial transformation of / Chrysanthemum. Acta Hort. 447:329-34.
    10. Gao, Y., Z. Bo, D. Guoxun, and Z. Qixiang. 2001. Shoot regeneration from stem and leaf explants of / Dendrathema grandiflorum.] J. Beijing For. Univ. 23:32-3.
    11. Himstedt, J.P., H.J. Jacobsen, and K.G. Fischer. 2001. Shoot regeneration from stem and leaf explants of chrysanthemum ( / Dendranthema × / grandiflorum). Acta Hort. 560:421-24.
    12. Hodson de Jaramillo, E., A. Forero, G. Cancino, A.M. Moreno, L.E. Monsalve, and W. Acero. 2008. In vitro regeneration of three chrysanthemum ( / Dendrathema grandiflora) varieties via organogenesis and somatic embryogenesis. Universitas Scientiarum 13:118-27.
    13. Kaul, V., R.M. Miller, J.F. Hutchinson, and D. Richardsm. 1990. Shoot regeneration from stem and leaf explants of / Dendranthema grandiflora Tzvelev (syn. / Chrysanthemum morifolium Ramat.). Plant Cell. Tiss. Org. Cult. 21:21-0. CrossRef
    14. Lee, T., M.E.E. Huang, and E.C. Pua. 1997. High frequency shoot regeneration from leaf disc explants of garland chrysanthemum ( / Chrysanthemum coronarium L.) in vitro. Plant Sci. 126:219-26. CrossRef
    15. Lu, C.Y., G. Nugent, and T. Wardley. 1990. Efficient, direct plant regeneration from stem segments of chrysanthemum ( / Chrysanthemum morifolium Ramat. cv. Royal Purple). Plant Cell Rep. 8:733-36. CrossRef
    16. Murashige, T. and F. Skoog, 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant 15:473-97. CrossRef
    17. Nagarathna, K.C., H.S. Prakash, and H.S. Shetty. 1991. Genotypic effects on the callus formation from different explants of pearl millet B lines. Adv Plant Sci. 4:82-6.
    18. Nahid, J.S., S. Shyamali, and H. Kazumi. 2007. High frequency shoot regeneration from petal explants of / Chrysanthemum morifolium Ramat. in vitro. Pakistan J. Biolog Sci. 10:3356-361. CrossRef
    19. Palmer, C.D. and W.A. Keller. 2011. Plant regeneration from petal explants of / Hypericum perforatum L. Plant Cell. Tiss. Org. Cult. 105:129-34. CrossRef
    20. Pereira, A.M.S., B.W. Bertoni, B.A. Gloria, R.B.A. Araiyo, A.H. Janauario, M.V. Loureno, and S.C. Franca. 2000. Micropropagation of / Pathomorphe umbellate via direct organogenesis from leaf explants. Plant Cell. Tiss. Org. Cult. 60:47-3. CrossRef
    21. Petty, L.M., N.P. Harberd, I.A. Carre, B. Thomas, and S.D. Jackson. 2003. Expression of the Arabidopsis gai gene under its own promoter causes a reduction in plant height in chrysanthemum by attenuation of the gibberellins response. Plant Sci. 164:175-82. CrossRef
    22. Pochet, B., V. Scoman, M.M. Mestdagh, B. Moreau, and P. Andre. 1991. Influence of agar gel properties on the in vitro micropropagation of different clones of / Thuja plicata. Plant Cell. Rep. 10:406-09. CrossRef
    23. Prasad, R.N., A.K. Sharma, and H.C. Chaturvedi. 1983. Clonal multiplication of / Chrysanthemum morifolium otome zakurain long-term culture. Bangladesh J. Bot. 2:96-02.
    24. Rout, G.R., P. Panday, and P. Das. 1996. Direct plant regeneration of / Chrysanthemum morifolium Ramat. cv. Deep Pink. Proc. Natl. Acad. Sci. (India). 67:57-6.
    25. Sauvadet, M.A., P. Brochard, and J.B. Gibod. 1990. A protoplast to plant system in chrysanthemum: Differential responses among several commercial clones. Plant Cell Rep. 8:692-95. CrossRef
    26. Sharma, G. and A.R. Nautiyal. 2009. Influence of explants type and plant growth regulators on in vitro multiple shoots regeneration of a laurel from Himalaya. Nature Sci. 7:1-.
    27. Singha, S. 1984. Influence of two commercial agars on in vitro shoot proliferation of ‘Almey-crabapple and ’seckel-pear. HortScience 19:227-28.
    28. Soh, H.S., Y.H. Han, G.Y. Lee, J.W. Lim, B.Y. Yi, Y.H. Lee, G.W. Choi, and Y.D. Park. 2009. Transformation of / Chrysanthemum morifolium with insecticidal gene ( / Cry1Ac) to develop pest resistance. Hort. Environ. Biotechnol. 50:57-2.
    29. Teixeira da Silva, J.A. 2004. Ornamental chrysanthemums: Improvement by biotechnology. Plant Cell. Tiss. Org. Cult. 79:1-8. CrossRef
    30. van Wordragen, M.F., G. Honée, and H.J.M. Dons. 1993. Insect resistant chrysanthemum calluses by introduction of a / Bacillus thuringiensis crystal protein gene. Transgenic Res. 2:170-80. CrossRef
    31. Zalewska, M. and M. Jerzy. 1997. Mutation spectrum in / Dendranthema grandiflora Tzvelev after in vivo and in vitro regeneration of plants from irradiated leaves. Acta Hort. 447:615-18.
    32. Zheng, Z.L., Z. Yang, J.C. Jang, and J.D. Metzger. 2001. Modification of plant architecture in chrysanthemum by ectopic expression of the tobacco phytochrome B1 gene. J. Amer. Soc. Hort. Sci. 126:19-6.
  • 作者单位:Ki-Byung Lim (1)
    Soo Jin Kwon (2)
    Soo In Lee (2)
    Yoon-Jung Hwang (1)
    Aung Htay Naing (1)

    1. Department of Horticultural Science, Kyungpook National University, Daegu, 702-701, Korea
    2. Department of Agricultural Biotechnology, National Academy of Agricultural Science, Rural Development Administration, Suwon, 441-707, Korea
文摘
The capacity for shoot regeneration of leaf, petiole, and stem explants of eleven chrysanthemum cultivars was examined on the MS medium containing 1 μM naphthaleneacetic acid and 10 μM 6-benzyladenine solidified with 0.8% Agar, 0.4% Agarose, or 0.25% Gelrite. Significant differences in frequency of callus formation and regeneration from the different explants were observed among the different cultivars when grown on the media solidified with the different gelling agents. Gelrite was found to be the most effective gelling agent in promoting of the shoot. Of the different explants used, in general, stem exhibited the highest frequencies of shoot organogenesis and mean number of shoots per explant regardless of cultivar and gelling agent. However, the highest frequency of regeneration (11.67 shoots per explant) was noted from leaf explants of cv. Borami followed by (4.33 shoots per explant) from stem explants of cv. Yes Nuri. Shoots were directly developed from the surface of explants, not through callus formation. Low frequencies of shoot organogenesis were observed for the remaining cultivars except for cvs. Yes Time and Yes Star, which exhibits no shoot formation at all. In this study, we have developed an efficient in vitro protocol for cvs. Borami and Yes Nuri from suitable explant.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700