@article {5365,
	title = {Redox potential measurements of the Mycobacterium tuberculosis heme protein KatG and the isoniazid-resistant enzyme KatG(S315T): Insights into isoniazid activation},
	journal = {Biochemistry},
	volume = {39},
	number = {37},
	year = {2000},
	note = {<p>Times Cited: 28 Wengenack, NL Lopes, H Kennedy, MJ Tavares, P Pereira, AS Moura, I Moura, JJG Rusnak, F</p>
},
	pages = {11508-11513},
	type = {Journal Article},
	abstract = {<p>Mycobacterium tuberculosis KatG is a multifunctional heme enzyme responsible for activation of the antibiotic isoniazid. A KatG(S315T) point mutation is found in \&gt;50\% of isoniazid-resistant clinical isolates. Since isoniazid activation is thought to involve an oxidation reaction, the redox potential of KatG was determined using cyclic voltammetry, square wave voltammetry, and spectroelectrochemical titrations. Isoniazid activation may proceed via a cytochrome P450-like mechanism. Therefore, the possibility that substrate binding by KatG leads to an increase in the heme redox potential and the possibility that KatG(S315T) confers isoniazid resistance by altering the redox potential were examined. Effects of the heme spin state on the reduction potentials of KatG and KatG(S315T) were also determined. Assessment of the Fe3+/Fe2+ couple gave a midpoint potential of ca. -50 mV for both KatG and KatG(S315T). In contrast to cytochrome P450s, addition of substrate had no significant effect on either the KatG or KatG(S315T) redox potential. Conversion of the heme to a low-spin configuration resulted in a -150 to -200 mV shift of the KatG and KatG(S315T) redox potentials. These results suggest that isoniazid resistance conferred by KatG(S315T) is not mediated through changes in the heme redox potential. The redox potentials of isoniazid were also determined using cyclic and square wave voltammetry, and the results provide evidence that the ferric KatG and KatG(S315T) midpoint potentials are too low to promote isoniazid oxidation without formation of a high-valent enzyme intermediate such as compounds I and IT or oxyferrous KatG.</p>
},
	issn = {0006-2960},
	doi = {10.1021/bi001239v},
	url = {<Go to ISI>://WOS:000089436600036},
	author = {Wengenack, NL and Lopes, H and Kennedy, MJ and Tavares, P. and Pereira, AS and Moura, I and Moura, JJG and Rusnak, F}
}
