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:

313
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

295
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

CLONING, EXPRESSION AND PURIFICATION OF PSEUDOMONAS PUTIDA ATCC12633 CREATINASE

Pages

  169-175

Abstract

 Background: PSEUDOMONAS PUTIDA (P. putida) ATCC12633 can produce CREATINASE. It is a microbial enzyme which degrades creatinine in bacteria and provides source of carbon and nitrogen. Also, this enzyme is used in the enzymatic measurement of creatinine concentration for diagnosis of renal and muscles functions and diseases. Our purpose was recombinant production of CREATINASE for using in clinical measurement of serum or urine creatinine.Methods: A 1209bp of open reading frame of CREATINASE was amplified by PCR from P. putida ATCC12633genome and cloned into pET28a expression vector which was digested using NheI and XhoI restriction enzymes. Cloning was confirmed by colony PCR, double digestion analysis and sequencing. Recombinant pET28a vector was transformed toEscherichia coli (E. coli) BL21 (DE3). CREATINASE expression was induced inE.coli BL21 (DE3) using IPTG and confirmed by SDS-PAGE and western blotting.Purification of CREATINASE was performed using Ni-NTA column. The specific activity of this enzyme was also investigated.Results: The CREATINASE gene cloning was confirmed by DNA sequencing. Successful expression of CREATINASE was performed inE. coli (57.4% of total protein). SDS-PAGE and western blot analysis showed a 45kDa CREATINASE protein. Purification of CREATINASE was done with high purity. The specific activity of recombinant enzyme is 26.54 unit/mgthat is much higher than other CREATINASE used in the commercial kits (9 unit/mg).Conclusion: The P. putida ATCC12633 recombinant CREATINASE was expressed efficiently inE. coli BL21 and 57% of total protein was the recombinant CREATINASE. Also, expressed CREATINASE has high solubility and also the enzyme has good activity compared to enzymes used in commercial kits, so a new source of CREATINASE was produced for creatinine assay kit in this study.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    Afshari, Elnaz, Amini Bayat, Zahra, HOSSEINKHANI, SAMAN, & BAKHTIARI, NAHID. (2017). CLONING, EXPRESSION AND PURIFICATION OF PSEUDOMONAS PUTIDA ATCC12633 CREATINASE. AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB), 9(4), 169-175. SID. https://sid.ir/paper/313978/en

    Vancouver: Copy

    Afshari Elnaz, Amini Bayat Zahra, HOSSEINKHANI SAMAN, BAKHTIARI NAHID. CLONING, EXPRESSION AND PURIFICATION OF PSEUDOMONAS PUTIDA ATCC12633 CREATINASE. AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB)[Internet]. 2017;9(4):169-175. Available from: https://sid.ir/paper/313978/en

    IEEE: Copy

    Elnaz Afshari, Zahra Amini Bayat, SAMAN HOSSEINKHANI, and NAHID BAKHTIARI, “CLONING, EXPRESSION AND PURIFICATION OF PSEUDOMONAS PUTIDA ATCC12633 CREATINASE,” AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB), vol. 9, no. 4, pp. 169–175, 2017, [Online]. Available: https://sid.ir/paper/313978/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