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Cloning, expression and characterization of histidine-tagged biotin synthase of Mycobacterium tuberculosis.
Magwamba, Clement Chedza; Rukseree, Kamolchanok; Palittapongarnpim, Prasit.
Afiliación
  • Magwamba CC; Department of Microbiology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400, Thailand; Ministry of Health, Private Bag 0038, Gaborone, Botswana. Electronic address: cmagwamba@yahoo.com.
  • Rukseree K; Mahidol University, Amnatcharoen Campus, Muang, Amnatcharoen 37000, Thailand. Electronic address: rukseree@gmail.com.
  • Palittapongarnpim P; Department of Microbiology, Faculty of Science, Mahidol University, Rama 6 Road, Bangkok 10400, Thailand; National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani 12120, Thailand. Electronic address: prasit.pal@mahidol.ac.th.
Tuberculosis (Edinb) ; 98: 42-9, 2016 05.
Article en En | MEDLINE | ID: mdl-27156617
The emergence of Mycobacterium tuberculosis strains that are resistant to the current anti-tuberculosis (TB) drugs necessitates a need to develop a new class of drugs whose targets are different from the current ones. M. tuberculosis biotin synthase (MtbBS) is one such target that is essential for the survival of the bacteria. In this study, MtbBS was cloned, overexpressed and purified to homogeneity for biochemical characterization. It is likely to be a dimer in its native form. Its pH and temperature optima are 8.0 and 37 °C, respectively. Km for DTB and SAM was 2.81 ± 0.35 and 9.95 ± 0.98 µM, respectively. The enzyme had a maximum velocity of 0.575 ± 0.015 µM min(-1), and a turn-over of 0.0935 min(-1). 5'-deoxyadenosine (dAH), S-(5'-Adenosyl)-l-cysteine (AdoCy) and S-(5'-Adenosyl)-l-homocysteine (AdoHcy) were competitive inhibitors of MtbBS with the following inactivation parameters: Ki = 24.2 µM, IC50 = 267.4 µM; Ki = 0.84 µM, IC50 = 9.28 µM; and Ki = 0.592 µM, IC50 = 6.54 µM for dAH, AdoCy and AdoHcy respectively. dAH could inhibit the growth of M. tuberculosis H37Ra with an MIC of 392.6 µg/ml. This information should be useful for the discovery of inhibitors of MtbBS.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sulfurtransferasas / Proteínas Bacterianas / Clonación Molecular / Histidina / Mycobacterium tuberculosis Idioma: En Revista: Tuberculosis (Edinb) Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sulfurtransferasas / Proteínas Bacterianas / Clonación Molecular / Histidina / Mycobacterium tuberculosis Idioma: En Revista: Tuberculosis (Edinb) Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido