Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection

Amino acid biosynthetic pathways are an attractive alternative to treat chronic infections such as Mycobacterium tuberculosis (Mtb). Here, the authors investigate the metabolic response to disruption of the aspartate pathway in persistent Mtb and identify essential enzymes as potential new targets f...

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Auteurs principaux: Erik J. Hasenoehrl, Dannah Rae Sajorda, Linda Berney-Meyer, Samantha Johnson, JoAnn M. Tufariello, Tobias Fuhrer, Gregory M. Cook, William R. Jacobs, Michael Berney
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Langue:EN
Publié: Nature Portfolio 2019
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Accès en ligne:https://doaj.org/article/9a443ee14abc47879b6eef91b9b88f3a
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spelling oai:doaj.org-article:9a443ee14abc47879b6eef91b9b88f3a2021-12-02T17:01:27ZDerailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection10.1038/s41467-019-12224-32041-1723https://doaj.org/article/9a443ee14abc47879b6eef91b9b88f3a2019-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-12224-3https://doaj.org/toc/2041-1723Amino acid biosynthetic pathways are an attractive alternative to treat chronic infections such as Mycobacterium tuberculosis (Mtb). Here, the authors investigate the metabolic response to disruption of the aspartate pathway in persistent Mtb and identify essential enzymes as potential new targets for drug development.Erik J. HasenoehrlDannah Rae SajordaLinda Berney-MeyerSamantha JohnsonJoAnn M. TufarielloTobias FuhrerGregory M. CookWilliam R. JacobsMichael BerneyNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Erik J. Hasenoehrl
Dannah Rae Sajorda
Linda Berney-Meyer
Samantha Johnson
JoAnn M. Tufariello
Tobias Fuhrer
Gregory M. Cook
William R. Jacobs
Michael Berney
Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
description Amino acid biosynthetic pathways are an attractive alternative to treat chronic infections such as Mycobacterium tuberculosis (Mtb). Here, the authors investigate the metabolic response to disruption of the aspartate pathway in persistent Mtb and identify essential enzymes as potential new targets for drug development.
format article
author Erik J. Hasenoehrl
Dannah Rae Sajorda
Linda Berney-Meyer
Samantha Johnson
JoAnn M. Tufariello
Tobias Fuhrer
Gregory M. Cook
William R. Jacobs
Michael Berney
author_facet Erik J. Hasenoehrl
Dannah Rae Sajorda
Linda Berney-Meyer
Samantha Johnson
JoAnn M. Tufariello
Tobias Fuhrer
Gregory M. Cook
William R. Jacobs
Michael Berney
author_sort Erik J. Hasenoehrl
title Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
title_short Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
title_full Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
title_fullStr Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
title_full_unstemmed Derailing the aspartate pathway of Mycobacterium tuberculosis to eradicate persistent infection
title_sort derailing the aspartate pathway of mycobacterium tuberculosis to eradicate persistent infection
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/9a443ee14abc47879b6eef91b9b88f3a
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