Two Escherichia coli clones expressing Mycobacterium tuberculosis antigens were isolated from a gene-bank in the plasmid vector pBR 325. ‘Western blot’ analysis revealed the presence of a unique protein band of molecular weight 68,000 and 38,000, respectively in cell extracts from each clone. The 68,000 dalton antigen was found to be expressed on Escherichia coli outer surface. Plasmid DNA from a third clone could confer leucine independence on two different leu B mutants of Escherichia coli but not on mutants in other leu genes, pointing to the possibility of genetic complementation. Thus, Mycobacterium tuberculosis DNA is capable of expression in Escherichia coli
An investigation into the presence of plasmids in Mycobacterium tuberculosis was conducted. No extra...
The first part of the thesis describes the characterization of 19 kDa antigen from M. bovis BCG. The...
Recombinant mycobacteria expressing Mycobacterium tuberculosis extracellular proteins are leading ca...
Abstract.Two Escherichia coli clones expressing Mycobacterium tuberculosis antigens were isolated fr...
The ability of Escherichia coli to use the expression signals of mycobacterial genes was tested by i...
A gene bank of Mycobacterium bovis BCG DNA in Escherichia coli was constructed by cloning Sau3A-clea...
Screening of a Mycobacterium tuberculosis genomic DNA library in the lambda gt11 expression vector w...
A gene responsible for the biosynthesis of leucine has been cloned by the complementation of the Esc...
The mechanism(s) used by Mycobacterium tuberculosis to establish disease in the human host are not w...
A gene responsible for the biosynthesis of leucine has been cloned by the complementation of the Esc...
The identification of Mycobacterium tuberculosis genes, specifically expressed during infection is a...
AbstractObjective/backgroundMycobacterium tuberculosis is an obligate pathogenic bacterial species i...
The first part of the thesis describes the characterization of 19 kDa antigen from M. bovis BCG. The...
This study was aimed at the molecular cloning and expression of the gene coding for FtsH protease of...
This study was aimed at the molecular cloning and expression of the gene coding for FtsH protease of...
An investigation into the presence of plasmids in Mycobacterium tuberculosis was conducted. No extra...
The first part of the thesis describes the characterization of 19 kDa antigen from M. bovis BCG. The...
Recombinant mycobacteria expressing Mycobacterium tuberculosis extracellular proteins are leading ca...
Abstract.Two Escherichia coli clones expressing Mycobacterium tuberculosis antigens were isolated fr...
The ability of Escherichia coli to use the expression signals of mycobacterial genes was tested by i...
A gene bank of Mycobacterium bovis BCG DNA in Escherichia coli was constructed by cloning Sau3A-clea...
Screening of a Mycobacterium tuberculosis genomic DNA library in the lambda gt11 expression vector w...
A gene responsible for the biosynthesis of leucine has been cloned by the complementation of the Esc...
The mechanism(s) used by Mycobacterium tuberculosis to establish disease in the human host are not w...
A gene responsible for the biosynthesis of leucine has been cloned by the complementation of the Esc...
The identification of Mycobacterium tuberculosis genes, specifically expressed during infection is a...
AbstractObjective/backgroundMycobacterium tuberculosis is an obligate pathogenic bacterial species i...
The first part of the thesis describes the characterization of 19 kDa antigen from M. bovis BCG. The...
This study was aimed at the molecular cloning and expression of the gene coding for FtsH protease of...
This study was aimed at the molecular cloning and expression of the gene coding for FtsH protease of...
An investigation into the presence of plasmids in Mycobacterium tuberculosis was conducted. No extra...
The first part of the thesis describes the characterization of 19 kDa antigen from M. bovis BCG. The...
Recombinant mycobacteria expressing Mycobacterium tuberculosis extracellular proteins are leading ca...