Cloning, expression and purification of early secretory antigenic target 6kDa protein (ESAT-6) of Mycobacterium tuberculosis
| Author | Zahra Farshadzadeh | en |
| Author | Mojtaba Sankian | en |
| Author | Forough Yousefi | en |
| Author | Aida Gholobi | en |
| Author | Reza Zarif | en |
| Author | Mahboobeh Naderi nasab | en |
| Author | Tahereh Rashed | en |
| Author | Abdolreza Varasteh | en |
| Issued Date | 2010-04-30 | en |
| Abstract | Introduction and objective: The early secretory antigenic target 6kDa protein (ESAT-6) antigen from Mycobacterium tuberculosis is a dominant target for cell-mediated immunity in the early phase of tuberculosis (TB) in TB patients. ESAT-6 was found to distinguish TB patients from BCG-vaccinated donors. The aim of this study was cloning and expression of ESAT-6 of M. tuberculosis. Materials and methods: DNA was extracted from M. tuberculosis H37Rv. PCR was performed using gene-specific oligonucleotide primers and the PCR products were inserted into the pET102/D vector and transferred into Escherichia coli strain TOPO10. The recombinant plasmids transferred into E. coli strain BL21. Results: The transformed plasmid into E. coli strain BL21 was effectively expressed. The expressed fusion protein (23kDa on SDS-PAGE) was found almost entirely in the soluble form and the recombinant protein was purified by Ni-NTA column. Conclusion: We successfully cloned and expressed ESAT-6 protein of M. tuberculosis in E. coli. As a specific antigen, it can be useful for diagnosis of both active and latent tuberculosis with ELISA in future. | en |
| DOI | https://doi.org/ | en |
| Keyword | ESAT6 antigen | en |
| Keyword | Cloning | en |
| Keyword | Mycobacterium tuberculosis | en |
| Publisher | Brieflands | en |
| Title | Cloning, expression and purification of early secretory antigenic target 6kDa protein (ESAT-6) of Mycobacterium tuberculosis | en |
| Type | Research Article | en |
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