Abstract: To exhibit an incorporated atomic science devoted system for tuberculosis diagnosis. Mycobacterium tuberculosis (MTB) instigates putrefaction of infected cells to avoid immune reactions. As of late we found that MTB uses the protein CpnT to execute human macrophages by discharging its C-terminal area, named Tuberculosis Necrotizing Toxin (TNT) that incites putrefaction by an obscure component. The TNT controls the cytosol of MTB-infected macrophages where it hydrolyzes the main element co-catalyst Nicotinamide Adenine Dinucleotide (NAD+). Articulation or infusion of a non-synergist TNT mutant demonstrated no cytotoxicity in macrophages or zebrafish zygotes, separately, exhibiting that the NAD+-glycohydrolase action is required for TNT-prompted cell demise. To anticipate self-harming, MTB produces a Immunity Factor for TNT (IFT) that ties TNT and represses its action. The precious stone structure of the TNT-IFT complex uncovered a novel NAD+-glycohydrolase overlap of TNT which constitutes the establishing individual from a toxin family across the board in pathogenic micro-organisms.