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Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon

Bacteria adapt to changing environments by means of tightly coordinated regulatory circuits. The use of synthetic lethality, a genetic phenomenon in which the combination of two nonlethal mutations causes cell death, facilitates identification and study of such circuitry. In this study, we show that...

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Detalles Bibliográficos
Autores principales: Reimann, Sylvia A., Wolfe, Alan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161199/
https://www.ncbi.nlm.nih.gov/pubmed/21912549
http://dx.doi.org/10.1155/2011/107023
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author Reimann, Sylvia A.
Wolfe, Alan J.
author_facet Reimann, Sylvia A.
Wolfe, Alan J.
author_sort Reimann, Sylvia A.
collection PubMed
description Bacteria adapt to changing environments by means of tightly coordinated regulatory circuits. The use of synthetic lethality, a genetic phenomenon in which the combination of two nonlethal mutations causes cell death, facilitates identification and study of such circuitry. In this study, we show that the E. coli ompR malT (con) double mutant exhibits a synthetic lethal phenotype that is environmentally conditional. MalT(con), the constitutively active form of the maltose system regulator MalT, causes elevated expression of the outer membrane porin LamB, which leads to death in the absence of the osmoregulator OmpR. However, the presence and metabolism of glycolytic carbon sources, such as sorbitol, promotes viability and unveils a novel layer of regulation within the complex circuitry that controls maltose transport and metabolism.
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spelling pubmed-31611992011-09-12 Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon Reimann, Sylvia A. Wolfe, Alan J. Int J Microbiol Research Article Bacteria adapt to changing environments by means of tightly coordinated regulatory circuits. The use of synthetic lethality, a genetic phenomenon in which the combination of two nonlethal mutations causes cell death, facilitates identification and study of such circuitry. In this study, we show that the E. coli ompR malT (con) double mutant exhibits a synthetic lethal phenotype that is environmentally conditional. MalT(con), the constitutively active form of the maltose system regulator MalT, causes elevated expression of the outer membrane porin LamB, which leads to death in the absence of the osmoregulator OmpR. However, the presence and metabolism of glycolytic carbon sources, such as sorbitol, promotes viability and unveils a novel layer of regulation within the complex circuitry that controls maltose transport and metabolism. Hindawi Publishing Corporation 2011 2011-08-14 /pmc/articles/PMC3161199/ /pubmed/21912549 http://dx.doi.org/10.1155/2011/107023 Text en Copyright © 2011 S. A. Reimann and A. J. Wolfe. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Reimann, Sylvia A.
Wolfe, Alan J.
Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title_full Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title_fullStr Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title_full_unstemmed Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title_short Exposure to Glycolytic Carbon Sources Reveals a Novel Layer of Regulation for the MalT Regulon
title_sort exposure to glycolytic carbon sources reveals a novel layer of regulation for the malt regulon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161199/
https://www.ncbi.nlm.nih.gov/pubmed/21912549
http://dx.doi.org/10.1155/2011/107023
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