[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Editorial Board::
Executive Members::
Instruction to Authors::
Peer Review::
Articles Archive::
Indexing Databases::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 17, Issue 4 (12-2015) ::
J Gorgan Univ Med Sci 2015, 17(4): 112-118 Back to browse issues page
Cloning and expression soluble recombinant parathyroid hormone in E. coli
Aghajani MH * 1, Tahzibi A2 , Shahbazi M3
1- M.Sc Student in Medical Biotechnology, Faculty of Advanced Medical SciencesTechnologies, Golestan University of Medical Sience, Gorgan, Iran , shahbazim@goums.ac.ir
2- Assistant Professor, Food and Drug Organization, Tehran, Iran
3- Associate Professor, Head of Cellular and Molecular Research, Center of Taleghani Hospital, Golesatn University of Medical Sciences, Gorgan, Iran
Abstract:   (10289 Views)
Background and Objective: Parathyroid proteins involved in calcium homeostasis. With increasing age and other relevant factors, this hormone is not able to perform its role. Using recombinant parathyroid hormone prevent disease progression and effective in improvement of disease. This study was done to design and build the desired construct genes, cloning process and synthesis of soluble parathyroid hormone in E. coli. Methods: In this laboratory study, design and optimization sequence of the gene parathyroid hormone (PTH) was carried out for expression of soluble proteins in bacteria. The construct contining PTH gene (puc 57) transformed into bacteria and cultivation was done in SOB medium then Plasmid extraction was performed. Fragment encoding the PTH was isolated by digestion of the cloning vector and ligate to expression vector (PET-32a). Subcloning process followed by induction with IPTG 1mM. The recombinant parathyroid hormon was expressed in bacteria, subsequently. Results: After enzymatic digestion, the fragment encoding the protein of interest was properly localized. The process was confirmed by polymerase chain reaction (PCR). Following performing a transformation, induction process performed by IPTG with final concentration 1mM that caused the soluble parathyroid proteins to be expressed in bacteria and the process was confirmed by Western blot technique. Conclusion: Protein expression in bacteria due to its rapid growth and the need to inexpensive medium is cost-effective. Soluble recombinant protein expression reduces downstream of recombinant protein production.
Keywords: Recombinant parathyroid hormone, Expression vector, Enzymatic digestion, PCR
Full-Text [PDF 278 kb] [English Abstract]   (14133 Downloads)    
Type of Study: Original Articles | Subject: Medical Biotecnology
Send email to the article author


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Aghajani MH, Tahzibi A, Shahbazi M. Cloning and expression soluble recombinant parathyroid hormone in E. coli. J Gorgan Univ Med Sci 2015; 17 (4) :112-118
URL: http://goums.ac.ir/journal/article-1-2583-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 17, Issue 4 (12-2015) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.04 seconds with 36 queries by YEKTAWEB 4660
Creative Commons License
This work is licensed under a Creative Commons — Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)