ISSN: 0973-7510

E-ISSN: 3015-3018

Ramane Sangram Pandit ,1, Rishendra Verma1, Tista Mondal1 and Vikramaditya Upmanyu2
1Mycobacteria Laboratory, Division of Bacteriology and Mycology, 2Division of Biological Standardization, Indian Veterinary Research Institute (IVRI), Izatnagar, Bareilly – 243122, India.
© The Author(s). 2015
J. Pure Appl. Microbiol., 2015, 9 (4): 3015-3018
Received: 20/06/2015 | Accepted: 19/08/2015 | Published: 31/12/2015
Abstract

The mpb83 and cfp2 genes encoding MPB83 and CFP2 immunodominant proteins were amplified from Mycobacterium bovis field strain 3/86 by polymerase chain reaction. The recombinant plasmids were constructed via inserting the mpb83 and cfp2 genes into the pET vector and named pET28b-mpb83 and pET28b-cfp2, respectively. The nucleotide sequences of the insert PCR products showed an open reading frame of 600 and 360 base pairs for mpb83 and cfp2, respectively. The sequenced genes and its deduced amino acid sequences were compared with the published sequences of reference strains. The sequences of the mpb83 and cfp2 genes share more than 99% similarity at both nucleotide and deduced amino acid level with published reference M. tuberculosis complex strains indicating their conserved nature.

Keywords

Rice germ lectin; Nitrogen-fixation bacteria; 16Sr RNA; Bicillus megaterium.

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