Doustdar Farahnoosh, Pazhang Mohammad, Mehrnejad Faramarz, Safarzadeh Mehrnoosh, Rabiei Davod, Chaparzadeh Nader, Falahati Hanieh, Mir-Derikvand Mohammad
Infectious Diseases and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences, P. O. Box 1985717443, Tehran, Iran.
Protein J. 2015 Jun;34(3):181-92. doi: 10.1007/s10930-015-9610-5.
Pyrazinamide (PZA) is one the first line anti-tuberculosis drugs that require activation by the pyrazinamidase (PZase). Most PZA-resistant Mycobacterium tuberculosis strains have mutations in the pncA gene which encoding PZase that result in the reduction or loss of the enzyme activity. Herein, we have examined how various mutations, which have been found from the PZA-resistant M. tuberculosis strains in Iran, modify the PZase activity. To elucidate the possible role of these mutations, namely A143T (MUT1), L151S (MUT2), A143T/T168A/E173K (MUT3), in the bioactivity of the enzyme, the PZase and mutant genes were cloned, functionally expressed and biochemically and computationally characterized. In comparison to the PZase enzyme, the enzymatic efficiency of mutant enzymes was decreased, with MUT2 indicating the largest enzymatic efficiency reduction. Homology models of mutants were constructed based on the PZase X-ray crystal structure. Molecular modeling and substrate docking revealed that the wild-type has much stronger binding affinity to PZA than the mutants whereas MUT2 has the weakest binding affinity. In addition, the molecular dynamics simulations and the essential dynamics results illustrated that the positions of the 51st to 71st residues were more dynamics in MUT2 as compared to the other atoms in PZase, MUT1 and MUT3 which could decrease the K(m) and k(cat) values of the enzymes.
吡嗪酰胺(PZA)是一线抗结核药物之一,需要吡嗪酰胺酶(PZase)激活。大多数耐PZA的结核分枝杆菌菌株在编码PZase的pncA基因中发生突变,导致酶活性降低或丧失。在此,我们研究了在伊朗耐PZA的结核分枝杆菌菌株中发现的各种突变如何改变PZase活性。为了阐明这些突变,即A143T(MUT1)、L151S(MUT2)、A143T/T168A/E173K(MUT3)在酶生物活性中的可能作用,对PZase和突变基因进行了克隆、功能表达,并进行了生化和计算表征。与PZase酶相比,突变酶的酶促效率降低,其中MUT2的酶促效率降低最大。基于PZase X射线晶体结构构建了突变体的同源模型。分子建模和底物对接显示,野生型对PZA的结合亲和力比突变体强得多,而MUT2的结合亲和力最弱。此外,分子动力学模拟和主成分动力学结果表明,与PZase、MUT1和MUT3中的其他原子相比,MUT2中第51至71位残基的位置更具动态性,这可能会降低酶的K(m)和k(cat)值。