Cloning and characterization of the gene for immunogenic protein MPB64 of Mycobacterium bovis BCG

Author:

Yamaguchi R1,Matsuo K1,Yamazaki A1,Abe C1,Nagai S1,Terasaka K1,Yamada T1

Affiliation:

1. Central Research Laboratories, Ajinomoto Co., Inc., Kawasaki, Japan.

Abstract

The gene for immunogenic protein MPB64 found in culture filtrates of only Mycobacterium tuberculosis and some strains of Mycobacterium bovis BCG was cloned by using a single-probe method and was sequenced. The gene analysis revealed that the structural gene for MPB64 consisted of 618 base pairs, and its deduced molecular weight was 22,400. Twenty-two amino acids for a putative signal peptide and 205 amino acids for the MPB64 protein were observed. In the coding region, the third letter of the codon showed a biased codon and a high G+C content (78.5%). The gene was expressed in Escherichia coli by using an E. coli expression vector. The product showed migration similar to that of the authentic MPB64 protein by electrophoresis and reacted with the polyclonal and the monoclonal antibodies raised against the MPB64 protein. The strict specificity of MPB64 could be applied to immunodiagnosis of tuberculosis.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference32 articles.

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3. Characterization of antibodyreactive epitopes on the 65-kilodalton protein of Mycobacterium leprae;Buchanan T. M.;Infect. Immun.,1987

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5. Nucleotide sequence of a streptomycete amino glycoside phosphotransferase gene and its relationship to phosphotransferases encoded by resistance plasmids;Gray G.;Proc. Natl. Acad. Sci. USA,1985

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