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

Journal Paper

Paper Information

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:

1,210
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

PRODUCTION OF A RECOMBINANT ANTIMICROBIAL DERMASEPTINE B1 PEPTIDE INNICOTIANA TABACUM L. HAIRY ROOTS WITH ANTIBACTERIAL ACTIVITY

Pages

  103-118

Abstract

 Background: Root hair culture is a valuable system to produce recombinant proteins in planta. ANTIMICROBIAL PEPTIDES (AMPs) are vital parts of the innate immune response found in almost allforms of life. Precise target activity and limited toxicity towards mammalian cells make themsuitable candidate molecules to combat evolving drug-resistant microorganisms. The aim of thepresent study was to produce a Dermaseptin B1 recombinant antimicrobial peptide in Nicotianatabacum root hair and assess the antibacterial activity of the protein extract from transgenic roothairs. Materials and Methods: A Dermaseptin B1 encoding gene sequence was C-terminally fused to aChitin Binding Domain (CBD) encoding sequence and cloned in a plant binary vector used forAgrobacterium rhizogenes-mediated transformation to generate root hairs in tobacco. Transgenicroot hairs were produced, and protein extracts were used to assess antimicrobial activity against anumber of microbes. Results: PCR and RT-PCR analysis confirmed the integration of the Dermaseptin B1 gene in a roothair cell genome and the presence of Dermaseptin B1 mRNA transcripts, respectively. Recombinantprotein had a significant (P<0. 05) antibacterial effect towards gram-positive and gram-negativebacteria. Conclusion: DERMASEPTINE B1 recombinant peptide was successfully produced in tobacco root haircells and its antibacterial effects was confirmed. These results suggest that the recombinant proteinmay have a therapeutic effect to control bacterial pathogens. It can be concluded that root hair cellscan be used to produce and purify valuable recombinant proteins with pharmaceutical applications.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    NAZARI, Z., NAZARIAN FIROUZABADI, F., ISMAILI, A., & DARVISHNIA, M.. (2018). PRODUCTION OF A RECOMBINANT ANTIMICROBIAL DERMASEPTINE B1 PEPTIDE INNICOTIANA TABACUM L. HAIRY ROOTS WITH ANTIBACTERIAL ACTIVITY. YAFTEH, 20(2 (76) ), 103-118. SID. https://sid.ir/paper/80261/en

    Vancouver: Copy

    NAZARI Z., NAZARIAN FIROUZABADI F., ISMAILI A., DARVISHNIA M.. PRODUCTION OF A RECOMBINANT ANTIMICROBIAL DERMASEPTINE B1 PEPTIDE INNICOTIANA TABACUM L. HAIRY ROOTS WITH ANTIBACTERIAL ACTIVITY. YAFTEH[Internet]. 2018;20(2 (76) ):103-118. Available from: https://sid.ir/paper/80261/en

    IEEE: Copy

    Z. NAZARI, F. NAZARIAN FIROUZABADI, A. ISMAILI, and M. DARVISHNIA, “PRODUCTION OF A RECOMBINANT ANTIMICROBIAL DERMASEPTINE B1 PEPTIDE INNICOTIANA TABACUM L. HAIRY ROOTS WITH ANTIBACTERIAL ACTIVITY,” YAFTEH, vol. 20, no. 2 (76) , pp. 103–118, 2018, [Online]. Available: https://sid.ir/paper/80261/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