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Mycobacterium tuberculosis cysteine biosynthesis genes mec+-cysO-cysM confer resistance to clofazimine.
Burns-Huang, Kristin; Mundhra, Shashirekha.
Afiliación
  • Burns-Huang K; Department of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065, USA. Electronic address: krb2013@med.cornell.edu.
  • Mundhra S; Department of Microbiology and Immunology, Weill Cornell Medicine, New York, NY 10065, USA.
Tuberculosis (Edinb) ; 115: 63-66, 2019 03.
Article en En | MEDLINE | ID: mdl-30948178
The Mycobacterium tuberculosis mec+-cysO-cysM gene cluster was shown to be part of a novel cysteine biosynthesis pathway in vitro, but little is known about its essentiality or role in M. tuberculosis physiology. In this study, we generate a knock out of the mec+-cysO-cysM gene cluster in M. tuberculosis and show that the gene cluster is not essential under a variety of conditions, suggesting redundancy in pathways for cysteine biosynthesis in M. tuberculosis. The cysteine biosynthesis gene cluster is essential for resistance for clofazimine, a peroxide-producing anti-leprosy drug. Therefore, although under most conditions the pathway is not essential, it likely has an important role in defense against oxidative stress in M. tuberculosis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Clofazimina / Cisteína / Genes Bacterianos / Mycobacterium tuberculosis / Antituberculosos Idioma: En Revista: Tuberculosis (Edinb) Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Clofazimina / Cisteína / Genes Bacterianos / Mycobacterium tuberculosis / Antituberculosos Idioma: En Revista: Tuberculosis (Edinb) Año: 2019 Tipo del documento: Article