Identification Of Taxa and Functional Pathway Information Of Mycobacterium tuberculosis Microbiome And High Throughput Simulation Studies With Mycobacteriophage

Tuberculosis caused by bacteria Mycobacterium tuberculosis. The bacteria usually attack the lungs, but TB bacteria can attack any part of the body such as the kidney, spine and brain. Mycobacterium tuberculosis in lungs microbiome can be studied by metamorphic mechanization specifically metatransriptomics sequencing. These sequencing allow us to investigate the DNA content, RNA content, bacterial taxa and functional pathways. Further by taking antibiotic resistant protein from bacteria, we establish that bacteriophage lysine B D29(PDB-3HC7)can lyse mycolylarabinogalactan bonds and releases free mycolic acid. It do not show action on peptidoglycan bond. Based on information a full surface docking was performed. To verify assignment, a molecular dynamics simulations was performed to assess the stability of the docked substrates. MD simulation suggested hydrolytic activity of amino acids residues on Mycobacterium tuberculosis. Docking and simulation of bacteriophage D29 lysin B gene protein 12 with multiple antibiotic resistant proteins which takes part in transcription process in bacteria. Here, mycobacteriophage D29 showed a potent inhibition on action of antibiotic resistant protein during transcription process. This action resulted by modification or deactivation of amino acid residues.