Isoniazid-Resistance Conferring Mutations in Mycobacterium tuberculosis KatG: Catalase, Peroxidase, and INH-NADH Adduct Formation Activities

tuberculosis;INH;KatG;Peroxidase;Catalase

Cade, Christine Elizabeth ; Dr. Elon Ison, Committee Member,Dr. Christian Melander, Committee Member,Dr. Reza Ghiladi, Committee Chair,Cade, Christine Elizabeth ; Dr. Elon Ison ; Committee Member ; Dr. Christian Melander ; Committee Member ; Dr. Reza Ghiladi ; Committee Chair

University:North Carolina State University

关键词: tuberculosis;    INH;    KatG;    Peroxidase;    Catalase;   

Others  :  https://repository.lib.ncsu.edu/bitstream/handle/1840.16/2478/etd.pdf?sequence=1&isAllowed=y

美国|英语

来源: null

【 摘 要 】

Mycobacterium tuberculosis catalase-peroxidase (KatG) is a bifunctional hemoprotein which activates isoniazid (INH), a pro-drug that is integral to frontline antituberculosis treatments. The activated species, an isonicotinoyl radical, couples to NAD+/NADH forming an isoniazid-NADH adduct that ultimately confers anti-tubercular activity. In order to better understand the mechanisms of isoniazid activation as well as the origins of KatG-derived INH-resistance, we have compared the catalytic properties of the wild-type enzyme to twenty-three KatG mutants which have been associated with isoniazid resistance in clinical M. tuberculosis isolates. Neither catalase nor peroxidase activities, the two inherent enzymatic functions of KatG, were found to correlate with isoniazid resistance. Furthermore, catalase function was lost in mutants which lacked the Met-Tyr-Trp crosslink, the biogenic cofactor in KatG which has been previously shown to be integral to this activity. The presence or absence of the crosslink itself, however, was also found to not correlate with INH resistance. The KatG resistance-conferring mutants were then assayed for their ability to generate the INH-NADH adduct in the presence of peroxide (t-BuOOH and H2O2), superoxide, and no exogenous oxidant (air-only). The results demonstrate that residue location plays a critical role in determining INH-resistance mechanisms associated with INH activation; however, different mutations at the same location can produce vastly different reactivities that are oxidant-specific. Furthermore, the data can be interpreted to suggest the presence of a second mechanism of INH-resistance that is not correlated with the formation of the INH-NADH adduct.