Expression of 19-kDa Protein of Mycobacterium Tuberculosis in Escherchia Coli
Xueqiong Wu
Abstract
Xueqiong Wu
Abstract
Objective To obtain recombinant 19-kDa protein from Mycobacterium tuberculosis by using gene engineering technology.Methods The gene coding 19-kDa protein inserted into a expression vector pET24b,and then transferred E.coli BL21(DE3).The expressed product was identified by SDS-PAGE,Plasmid pET24b containing19-kDa gene was transferred into competent Escherichia coli BL21(DE3) and 19-kDa gene was over expressed by the inducement of IPTG.Results The recombinant 19-kDa protein was expressed in soluble form in E.coli. When the culture was induced for 3~4 hours,the recombinant 19-KDa protein was produced in highest quantity .Conclusion Escherichia coli containing recombinant plasmid pET24b-19-kDa gene could express recombinant 19-KDa protein in high level.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To obtain recombinant 19-kDa protein from Mycobacterium tuberculosis by using gene engineering technology.Methods The gene coding 19-kDa protein inserted into a expression vector pET24b,and then transferred E.coli BL21(DE3).The expressed product was identified by SDS-PAGE,Plasmid pET24b containing19-kDa gene was transferred into competent Escherichia coli BL21(DE3) and 19-kDa gene was over expressed by the inducement of IPTG.Results The recombinant 19-kDa protein was expressed in soluble form in E.coli. When the culture was induced for 3~4 hours,the recombinant 19-KDa protein was produced in highest quantity .Conclusion Escherichia coli containing recombinant plasmid pET24b-19-kDa gene could express recombinant 19-KDa protein in high level.
Key concepts: Recombinant DNA, Escherichia coli, lac operon, Mycobacterium tuberculosis, Molecular biology, Gene, Plasmid, HSPA2