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Cloning and Sequencing of a Unique Antigen MPT70 from Mycobacterium tuberculosis H37Rv and Expression in BCG Using E. coli‐Mycobacteria Shuttle Vector
Author(s) -
MATSUMOTO S.,
MATSUO T.,
OHARA N.,
HOTOKEZAKA H.,
NAITO M.,
MINAMI J.,
YAMADA T.
Publication year - 1995
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1995.tb03565.x
Subject(s) - shuttle vector , mycobacterium bovis , biology , mycobacterium tuberculosis , gene , escherichia coli , peptide sequence , expression vector , cloning (programming) , signal peptide , microbiology and biotechnology , epitope , antigen , vector (molecular biology) , recombinant dna , tuberculosis , genetics , medicine , pathology , computer science , programming language
MPB70 is known to be an immunogenic mycobacterial protein secreted in large amounts from Mycobacterium bovis BCG (BCG) Tokyo. The analogous gene for MPT70 was cloned from Mycobacterium tuberculosis H37Rv which produces this protein in only a small amount. The gene encoding 193 amino acid residues inciuding 30 amino acids for the signal peptide. the promoter‐like sequence, and the ribosome‐binding site, was completely identical to that of BCG Tokyo. Computer analysis revealed that the carboxy‐terminal half of MPT70 was homologous to amino acid sequences of fasciclin 1, osteoblast‐specific factor 2 (OSF‐2), and human transforming growth factor‐beta induced gene product (βIG‐H3). Escherichia coli (E. coli) ‐mycobacteria shuttle vectors containing mpt70 or mpb70 genes 0.7kbp upstream of the 5′ end of them were able to be expressed in BCG Pasteur which is a MPB70 low‐producer, but the extent of the expression was not that of a high‐producer.

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