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Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
Heme is an essential cofactor and alternative iron source for almost all bacterial species but may cause severe toxicity upon elevated levels and consequently, regulatory mechanisms coordinating heme homeostasis represent an important fitness trait. A remarkable scenario is found in several coryneba...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850329/ https://www.ncbi.nlm.nih.gov/pubmed/30767351 http://dx.doi.org/10.1111/mmi.14226 |
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author | Keppel, Marc Piepenbreier, Hannah Gätgens, Cornelia Fritz, Georg Frunzke, Julia |
author_facet | Keppel, Marc Piepenbreier, Hannah Gätgens, Cornelia Fritz, Georg Frunzke, Julia |
author_sort | Keppel, Marc |
collection | PubMed |
description | Heme is an essential cofactor and alternative iron source for almost all bacterial species but may cause severe toxicity upon elevated levels and consequently, regulatory mechanisms coordinating heme homeostasis represent an important fitness trait. A remarkable scenario is found in several corynebacterial species, e.g. Corynebacterium glutamicum and Corynebacterium diphtheriae, which dedicate two paralogous, heme‐responsive two‐component systems, HrrSA and ChrSA, to cope with the Janus nature of heme. Here, we combined experimental reporter profiling with a quantitative mathematical model to understand how this particular regulatory network architecture shapes the dynamic response to heme. Our data revealed an instantaneous activation of the detoxification response (hrtBA) upon stimulus perception and we found that kinase activity of both kinases contribute to this fast onset. Furthermore, instant deactivation of the P(hrtBA) promoter is achieved by a strong ChrS phosphatase activity upon stimulus decline. While the activation of detoxification response is uncoupled from further factors, heme utilization is additionally governed by the global iron regulator DtxR integrating information on iron availability into the regulatory network. Altogether, our data provide comprehensive insights how TCS cross‐regulation and network hierarchy shape the temporal dynamics of detoxification (hrtBA) and utilization (hmuO) as part of a global homeostatic response to heme. |
format | Online Article Text |
id | pubmed-6850329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68503292019-11-18 Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum Keppel, Marc Piepenbreier, Hannah Gätgens, Cornelia Fritz, Georg Frunzke, Julia Mol Microbiol Research Articles Heme is an essential cofactor and alternative iron source for almost all bacterial species but may cause severe toxicity upon elevated levels and consequently, regulatory mechanisms coordinating heme homeostasis represent an important fitness trait. A remarkable scenario is found in several corynebacterial species, e.g. Corynebacterium glutamicum and Corynebacterium diphtheriae, which dedicate two paralogous, heme‐responsive two‐component systems, HrrSA and ChrSA, to cope with the Janus nature of heme. Here, we combined experimental reporter profiling with a quantitative mathematical model to understand how this particular regulatory network architecture shapes the dynamic response to heme. Our data revealed an instantaneous activation of the detoxification response (hrtBA) upon stimulus perception and we found that kinase activity of both kinases contribute to this fast onset. Furthermore, instant deactivation of the P(hrtBA) promoter is achieved by a strong ChrS phosphatase activity upon stimulus decline. While the activation of detoxification response is uncoupled from further factors, heme utilization is additionally governed by the global iron regulator DtxR integrating information on iron availability into the regulatory network. Altogether, our data provide comprehensive insights how TCS cross‐regulation and network hierarchy shape the temporal dynamics of detoxification (hrtBA) and utilization (hmuO) as part of a global homeostatic response to heme. John Wiley and Sons Inc. 2019-03-22 2019-05 /pmc/articles/PMC6850329/ /pubmed/30767351 http://dx.doi.org/10.1111/mmi.14226 Text en © 2019 The Authors. Molecular Microbiology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Keppel, Marc Piepenbreier, Hannah Gätgens, Cornelia Fritz, Georg Frunzke, Julia Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum |
title | Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
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title_full | Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
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title_fullStr | Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
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title_full_unstemmed | Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
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title_short | Toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in Corynebacterium glutamicum
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title_sort | toxic but tasty – temporal dynamics and network architecture of heme‐responsive two‐component signaling in corynebacterium glutamicum |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850329/ https://www.ncbi.nlm.nih.gov/pubmed/30767351 http://dx.doi.org/10.1111/mmi.14226 |
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