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Identification of a Mycothiol-Dependent Nitroreductase from Mycobacterium tuberculosis
[Image: see text] The success of Mycobacterium tuberculosis (Mtb) as a pathogen depends on the redundant and complex mechanisms it has evolved for resisting nitrosative and oxidative stresses inflicted by host immunity. Improving our understanding of these defense pathways can reveal vulnerable poin...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952258/ https://www.ncbi.nlm.nih.gov/pubmed/29465985 http://dx.doi.org/10.1021/acsinfecdis.7b00111 |
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author | Negri, Ana Javidnia, Prisca Mu, Ran Zhang, Xiaojie Vendome, Jeremie Gold, Ben Roberts, Julia Barman, Dipti Ioerger, Thomas Sacchettini, James C. Jiang, Xiuju Burns-Huang, Kristin Warrier, Thulasi Ling, Yan Warren, J. David Oren, Deena A. Beuming, Thijs Wang, Hongyao Wu, Jie Li, Haitao Rhee, Kyu Y. Nathan, Carl F. Liu, Gang Somersan-Karakaya, Selin |
author_facet | Negri, Ana Javidnia, Prisca Mu, Ran Zhang, Xiaojie Vendome, Jeremie Gold, Ben Roberts, Julia Barman, Dipti Ioerger, Thomas Sacchettini, James C. Jiang, Xiuju Burns-Huang, Kristin Warrier, Thulasi Ling, Yan Warren, J. David Oren, Deena A. Beuming, Thijs Wang, Hongyao Wu, Jie Li, Haitao Rhee, Kyu Y. Nathan, Carl F. Liu, Gang Somersan-Karakaya, Selin |
author_sort | Negri, Ana |
collection | PubMed |
description | [Image: see text] The success of Mycobacterium tuberculosis (Mtb) as a pathogen depends on the redundant and complex mechanisms it has evolved for resisting nitrosative and oxidative stresses inflicted by host immunity. Improving our understanding of these defense pathways can reveal vulnerable points in Mtb pathogenesis. In this study, we combined genetic, structural, computational, biochemical, and biophysical approaches to identify a novel enzyme class represented by Rv2466c. We show that Rv2466c is a mycothiol-dependent nitroreductase of Mtb and can reduce the nitro group of a novel mycobactericidal compound using mycothiol as a cofactor. In addition to its function as a nitroreductase, Rv2466c confers partial protection to menadione stress. |
format | Online Article Text |
id | pubmed-5952258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-59522582018-05-16 Identification of a Mycothiol-Dependent Nitroreductase from Mycobacterium tuberculosis Negri, Ana Javidnia, Prisca Mu, Ran Zhang, Xiaojie Vendome, Jeremie Gold, Ben Roberts, Julia Barman, Dipti Ioerger, Thomas Sacchettini, James C. Jiang, Xiuju Burns-Huang, Kristin Warrier, Thulasi Ling, Yan Warren, J. David Oren, Deena A. Beuming, Thijs Wang, Hongyao Wu, Jie Li, Haitao Rhee, Kyu Y. Nathan, Carl F. Liu, Gang Somersan-Karakaya, Selin ACS Infect Dis [Image: see text] The success of Mycobacterium tuberculosis (Mtb) as a pathogen depends on the redundant and complex mechanisms it has evolved for resisting nitrosative and oxidative stresses inflicted by host immunity. Improving our understanding of these defense pathways can reveal vulnerable points in Mtb pathogenesis. In this study, we combined genetic, structural, computational, biochemical, and biophysical approaches to identify a novel enzyme class represented by Rv2466c. We show that Rv2466c is a mycothiol-dependent nitroreductase of Mtb and can reduce the nitro group of a novel mycobactericidal compound using mycothiol as a cofactor. In addition to its function as a nitroreductase, Rv2466c confers partial protection to menadione stress. American Chemical Society 2018-02-21 2018-05-11 /pmc/articles/PMC5952258/ /pubmed/29465985 http://dx.doi.org/10.1021/acsinfecdis.7b00111 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Negri, Ana Javidnia, Prisca Mu, Ran Zhang, Xiaojie Vendome, Jeremie Gold, Ben Roberts, Julia Barman, Dipti Ioerger, Thomas Sacchettini, James C. Jiang, Xiuju Burns-Huang, Kristin Warrier, Thulasi Ling, Yan Warren, J. David Oren, Deena A. Beuming, Thijs Wang, Hongyao Wu, Jie Li, Haitao Rhee, Kyu Y. Nathan, Carl F. Liu, Gang Somersan-Karakaya, Selin Identification of a Mycothiol-Dependent Nitroreductase from Mycobacterium tuberculosis |
title | Identification of a Mycothiol-Dependent Nitroreductase
from Mycobacterium tuberculosis |
title_full | Identification of a Mycothiol-Dependent Nitroreductase
from Mycobacterium tuberculosis |
title_fullStr | Identification of a Mycothiol-Dependent Nitroreductase
from Mycobacterium tuberculosis |
title_full_unstemmed | Identification of a Mycothiol-Dependent Nitroreductase
from Mycobacterium tuberculosis |
title_short | Identification of a Mycothiol-Dependent Nitroreductase
from Mycobacterium tuberculosis |
title_sort | identification of a mycothiol-dependent nitroreductase
from mycobacterium tuberculosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952258/ https://www.ncbi.nlm.nih.gov/pubmed/29465985 http://dx.doi.org/10.1021/acsinfecdis.7b00111 |
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