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Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift
Timely adaptation to nutrient downshift is crucial for bacteria to maintain fitness during feast and famine cycle in the natural niche. However, the molecular mechanism that ensures the timely adaption of bacterial growth to nutrient downshift remains poorly understood. Here, we quantitatively inves...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884231/ https://www.ncbi.nlm.nih.gov/pubmed/36709335 http://dx.doi.org/10.1038/s41467-023-36254-0 |
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author | Zhu, Manlu Dai, Xiongfeng |
author_facet | Zhu, Manlu Dai, Xiongfeng |
author_sort | Zhu, Manlu |
collection | PubMed |
description | Timely adaptation to nutrient downshift is crucial for bacteria to maintain fitness during feast and famine cycle in the natural niche. However, the molecular mechanism that ensures the timely adaption of bacterial growth to nutrient downshift remains poorly understood. Here, we quantitatively investigated the adaptation of Escherichia coli to various kinds of nutrient downshift. We found that relA deficient strain, which is devoid of stringent response, exhibits a significantly longer growth lag than wild type strain during adapting to both amino acid downshift and carbon downshift. Quantitative proteomics show that increased (p)ppGpp level promotes the growth adaption of bacteria to amino acid downshift via triggering the proteome resource re-allocation from ribosome synthesis to amino acid biosynthesis. Such type of proteome re-allocation is significantly delayed in the relA-deficient strain, which underlies its longer lag than wild type strain during amino acid downshift. During carbon downshift, a lack of stringent response in relA deficient strain leads to disruption of the transcription-translation coordination, thus compromising the transcription processivity and further the timely expression of related catabolic operons for utilizing secondary carbon sources. Our studies shed light on the fundamental strategy of bacteria to maintain fitness under nutrient-fluctuating environments. |
format | Online Article Text |
id | pubmed-9884231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98842312023-01-30 Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift Zhu, Manlu Dai, Xiongfeng Nat Commun Article Timely adaptation to nutrient downshift is crucial for bacteria to maintain fitness during feast and famine cycle in the natural niche. However, the molecular mechanism that ensures the timely adaption of bacterial growth to nutrient downshift remains poorly understood. Here, we quantitatively investigated the adaptation of Escherichia coli to various kinds of nutrient downshift. We found that relA deficient strain, which is devoid of stringent response, exhibits a significantly longer growth lag than wild type strain during adapting to both amino acid downshift and carbon downshift. Quantitative proteomics show that increased (p)ppGpp level promotes the growth adaption of bacteria to amino acid downshift via triggering the proteome resource re-allocation from ribosome synthesis to amino acid biosynthesis. Such type of proteome re-allocation is significantly delayed in the relA-deficient strain, which underlies its longer lag than wild type strain during amino acid downshift. During carbon downshift, a lack of stringent response in relA deficient strain leads to disruption of the transcription-translation coordination, thus compromising the transcription processivity and further the timely expression of related catabolic operons for utilizing secondary carbon sources. Our studies shed light on the fundamental strategy of bacteria to maintain fitness under nutrient-fluctuating environments. Nature Publishing Group UK 2023-01-28 /pmc/articles/PMC9884231/ /pubmed/36709335 http://dx.doi.org/10.1038/s41467-023-36254-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhu, Manlu Dai, Xiongfeng Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title | Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title_full | Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title_fullStr | Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title_full_unstemmed | Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title_short | Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
title_sort | stringent response ensures the timely adaptation of bacterial growth to nutrient downshift |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884231/ https://www.ncbi.nlm.nih.gov/pubmed/36709335 http://dx.doi.org/10.1038/s41467-023-36254-0 |
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