Kapetanaki Sofia M, Chouchane Salem, Yu Shengwei, Magliozzo Richard S, Schelvis Johannes P M
Department of Chemistry, New York University, 31 Washington Place, Room 1001, New York, NY 10003, USA.
J Inorg Biochem. 2005 Jun;99(6):1401-6. doi: 10.1016/j.jinorgbio.2005.03.016.
The reaction of Mycobacterium tuberculosis KatG and the mutant KatG(S315T) with two different organic peroxides is studied using resonance Raman spectroscopy. For the first time, an intermediate is observed in a catalase-peroxidase with vibrations that are characteristic of Compound II. The observation of this intermediate is consistent with photoreduction of Compound I and is in agreement with the formation of Compound I during the catalytic cycle of KatG. The same intermediate is detected in KatG(S315T), a mutant associated with resistance to isoniazid (INH), but with a lower yield, indicating that the organic peroxides cannot react with the heme iron in KatG(S315T) as efficiently as in wild-type KatG. Our results are consistent with catalytic competence of the S315T mutant and support the model that the S315T mutation confers antibiotic resistance by modifying the interaction between the enzyme and the drug.
利用共振拉曼光谱研究了结核分枝杆菌KatG和突变体KatG(S315T)与两种不同有机过氧化物的反应。首次在过氧化氢酶-过氧化物酶中观察到一种中间体,其振动具有化合物II的特征。该中间体的观察结果与化合物I的光还原一致,并且与KatG催化循环中化合物I的形成相符。在与异烟肼(INH)耐药相关的突变体KatG(S315T)中检测到相同的中间体,但产率较低,这表明有机过氧化物与KatG(S315T)中的血红素铁反应效率不如野生型KatG。我们的结果与S315T突变体的催化活性一致,并支持S315T突变通过改变酶与药物之间的相互作用赋予抗生素耐药性的模型。