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:

370
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

173
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

CYTOPLASMIC EXPRESSION OF RECOMBINANT INTERLEUKIN-2 AND INTERLEUKIN-4 PROTEINS RESULTS IN HYDROGEN PEROXIDE ACCUMULATION AND REDUCTION IN CATALASE ACTIVITY IN ESCHERICHIA COLI

Pages

  64-71

Abstract

 Background and the purpose of the study: The Reactive oxygen species (ROS) is induced in the cells following various stresses but the effect of RECOMBINANT PROTEIN expression on ROS generation has not been studied yet. In this study, H2O2 concentration and CATALASE ACTIVITY variations and their correlation with cell growth following CYTOPLASMIC EXPRESSION of human interleukin-2 (hIL-2) and mouse interleukin-4 (mIL-4) in ESCHERICHIA COLI were investigated. Additionally, the effect of RECOMBINANT PROTEIN expression under different conditions was compared to the effect of foreign DNA introduction on these factors.Methods: Plasmids pEThIL-2 and pETmIL-4 were used for expression of human interleukin-2 (hIL-2) and mouse interleukin-4 (mIL-4) inside the cytoplasm of the cells. Having confirmed protein expression using SDS-PAGE analysis and ELISA assay, H2O2 concentration and CATALASE ACTIVITY were measured at various ODs.Results and major conclusion: Empty vector introduction increased significantly H2O2 concentration of the cells. However, H2O2 concentration in hIL-2 and mIL-4 expressing cells was significantly higher than its concentration in empty vector transformed cells. CATALASE ACTIVITY was reduced in foreign DNA introduced cells. It was more lowered following expression of RECOMBINANT PROTEINs. Results of this study revealed the relationship between foreign DNA introduction and protein expression with H2O2 elevation and CATALASE ACTIVITY reduction. There was also correlation between H2O2 elevation and reduction in CATALASE ACTIVITY with the cell growth depression.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    HEJAZI, M.S., KARIMI, F., MAHDIZADEH AGHDAM, E., BARZEGARI, A., FARSH DOUSTI HAGH, M., PARVIZI, M., MAHMOUDI AZAR, L., & HEJAZI, M.A.. (2009). CYTOPLASMIC EXPRESSION OF RECOMBINANT INTERLEUKIN-2 AND INTERLEUKIN-4 PROTEINS RESULTS IN HYDROGEN PEROXIDE ACCUMULATION AND REDUCTION IN CATALASE ACTIVITY IN ESCHERICHIA COLI. DARU JOURNAL OF PHARMACEUTICAL SCIENCE, 17(2), 64-71. SID. https://sid.ir/paper/275496/en

    Vancouver: Copy

    HEJAZI M.S., KARIMI F., MAHDIZADEH AGHDAM E., BARZEGARI A., FARSH DOUSTI HAGH M., PARVIZI M., MAHMOUDI AZAR L., HEJAZI M.A.. CYTOPLASMIC EXPRESSION OF RECOMBINANT INTERLEUKIN-2 AND INTERLEUKIN-4 PROTEINS RESULTS IN HYDROGEN PEROXIDE ACCUMULATION AND REDUCTION IN CATALASE ACTIVITY IN ESCHERICHIA COLI. DARU JOURNAL OF PHARMACEUTICAL SCIENCE[Internet]. 2009;17(2):64-71. Available from: https://sid.ir/paper/275496/en

    IEEE: Copy

    M.S. HEJAZI, F. KARIMI, E. MAHDIZADEH AGHDAM, A. BARZEGARI, M. FARSH DOUSTI HAGH, M. PARVIZI, L. MAHMOUDI AZAR, and M.A. HEJAZI, “CYTOPLASMIC EXPRESSION OF RECOMBINANT INTERLEUKIN-2 AND INTERLEUKIN-4 PROTEINS RESULTS IN HYDROGEN PEROXIDE ACCUMULATION AND REDUCTION IN CATALASE ACTIVITY IN ESCHERICHIA COLI,” DARU JOURNAL OF PHARMACEUTICAL SCIENCE, vol. 17, no. 2, pp. 64–71, 2009, [Online]. Available: https://sid.ir/paper/275496/en

    Related Journal Papers

  • No record.
  • 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