مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

1,408
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

STUDYING THE EFFICIENCY OF FLORAL DIP METHOD FOR GENETIC TRANSFORMATION OF APIACEAEPLANTS

Pages

  139-147

Abstract

 Plant tissue culture techniques are used as basic requirement of common PLANT TRANSFORMATION systems. In most cases of PLANT TRANSFORMATION, a reproducible regeneration protocol is the limiting step due to long time lasting, specialized facilities and well experienced persons. Furthermore, tissue culture procedures induce somaclonal variation among regenerated transgenic plants. Therefore, recently current studies in plant molecular biology prefer PLANT TRANSFORMATION procedures avoiding tissue culture phase. Various in plant a transformation procedures have been explored, among which the FLORAL DIP method is the most reliablein vivo transformation method. In this research, with the aim of evaluating the ability of FLORAL DIP method for genetic transformation of someApiaceae plants, we studied Dill (Anethum graveolens), Fennel (Foeniculum vulgare), Coriander (Coriandrum sativum), Carrot (Daucus carrota), Parsley (Petrocelium sativum) and Celery (Apium graveolens).Arabidopsis thalianawas used as a model plant of experimental procedure. Flowers, in different stages of inflorescence development, were immersed in different suspension ofAgrobacterium tumefaciens carrying the plant binary vector pBI121. This vector carries plant reporter geneuidA (gus) and the plant selectable marker genenpt II. Although, producing transgenic ARABIDOPSIS plants with a high transformation rate of 4% verified the accuracy of experimental procedure, FLORAL DIP method was not successful for transformation ofApiaceae plants. Only one transformed celery plantlet, carryingnpt II gene with no expression of GUS, was obtained bby screening more than 10000 seeds produced by treated plants from all the species. Transgenic ARABIDOPSIS plants expressinggus reporter gene were confirmed through PCR and histochemical assays.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    GHABOULI, M., BAHRAMI, A.R., SHAHRIARI, F.A., ZOLALA, J., & MOHAMMADI, A.. (2013). STUDYING THE EFFICIENCY OF FLORAL DIP METHOD FOR GENETIC TRANSFORMATION OF APIACEAEPLANTS. JOURNAL OF HORTICULTURE SCIENCE (AGRICULTURAL SCIENCES AND TECHNOLOGY), 27(2), 139-147. SID. https://sid.ir/paper/142256/en

    Vancouver: Copy

    GHABOULI M., BAHRAMI A.R., SHAHRIARI F.A., ZOLALA J., MOHAMMADI A.. STUDYING THE EFFICIENCY OF FLORAL DIP METHOD FOR GENETIC TRANSFORMATION OF APIACEAEPLANTS. JOURNAL OF HORTICULTURE SCIENCE (AGRICULTURAL SCIENCES AND TECHNOLOGY)[Internet]. 2013;27(2):139-147. Available from: https://sid.ir/paper/142256/en

    IEEE: Copy

    M. GHABOULI, A.R. BAHRAMI, F.A. SHAHRIARI, J. ZOLALA, and A. MOHAMMADI, “STUDYING THE EFFICIENCY OF FLORAL DIP METHOD FOR GENETIC TRANSFORMATION OF APIACEAEPLANTS,” JOURNAL OF HORTICULTURE SCIENCE (AGRICULTURAL SCIENCES AND TECHNOLOGY), vol. 27, no. 2, pp. 139–147, 2013, [Online]. Available: https://sid.ir/paper/142256/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button