Cloning and expression of ESAT cDNA coding region of mycobacterium tuberculosis in E.Coli
- VernacularTitle:结核抗原ESAT-6基因的克隆及在大肠埃希菌中的表达
- Author:
Qingmin WANG
;
Zhenlin HU
;
Shuhan SUN
;
Al ET
;
- Publication Type:Journal Article
- Keywords:
Mycobacterium tuberculosis;
ESAT-6;
Gene expression;
Cloning, molecular
- From:
Chinese Journal of Infectious Diseases
1999;0(01):-
- CountryChina
- Language:Chinese
-
Abstract:
Objective To clone and express the gene encoding ESAT antigen of Mycobacterium tuberculosis (chinese stain). Methods Genome of mycobacterium tuberculosis was extracted. Then, the full length cDNA encoding ESAT protein was amplified by PCR and cloned into prokaryotic expressing vector pGEX5T and sequenced. pGEX5T ESAT was expressed in k802 Ecoli, and the expressed protein was determined by western blot using the sera from ten patients with tuberculosis. Results One specific band of 0.3kb or so was obtained and sequencing result was identical to that reported from Genbank. The expressed protein could be specifically recognized by the sera from tuberculosis patients. Conclusions The full length cDNA of Mycobacterium tuberculosis (Chinese strain) ESAT protein was cloned and expressed successfully, which will be helpful in further studies on diagnosis and treatment of tuberculosis.
