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Understanding the Stringent Response: Experimental Context Matters

As rapidly growing bacteria begin to exhaust essential nutrients, they enter a state of reduced growth, ultimately leading to stasis or quiescence. Investigation of the response to nutrient limitation has focused largely on the consequences of amino acid starvation, known as the “stringent response....

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Detalles Bibliográficos
Autor principal: Dworkin, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973329/
https://www.ncbi.nlm.nih.gov/pubmed/36625599
http://dx.doi.org/10.1128/mbio.03404-22
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author Dworkin, Jonathan
author_facet Dworkin, Jonathan
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description As rapidly growing bacteria begin to exhaust essential nutrients, they enter a state of reduced growth, ultimately leading to stasis or quiescence. Investigation of the response to nutrient limitation has focused largely on the consequences of amino acid starvation, known as the “stringent response.” Here, an uncharged tRNA in the A-site of the ribosome stimulates the ribosome-associated protein RelA to synthesize the hyperphosphorylated guanosine nucleotides (p)ppGpp that mediate a global slowdown of growth and biosynthesis. Investigations of the stringent response typically employ experimental methodologies that rapidly stimulate (p)ppGpp synthesis by abruptly increasing the fraction of uncharged tRNAs, either by explicit amino starvation or by inhibition of tRNA charging. Consequently, these methodologies inhibit protein translation, thereby interfering with the cellular pathways that respond to nutrient limitation. Thus, complete and/or rapid starvation is a problematic experimental paradigm for investigating bacterial responses to physiologically relevant nutrient-limited states.
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spelling pubmed-99733292023-03-01 Understanding the Stringent Response: Experimental Context Matters Dworkin, Jonathan mBio Minireview As rapidly growing bacteria begin to exhaust essential nutrients, they enter a state of reduced growth, ultimately leading to stasis or quiescence. Investigation of the response to nutrient limitation has focused largely on the consequences of amino acid starvation, known as the “stringent response.” Here, an uncharged tRNA in the A-site of the ribosome stimulates the ribosome-associated protein RelA to synthesize the hyperphosphorylated guanosine nucleotides (p)ppGpp that mediate a global slowdown of growth and biosynthesis. Investigations of the stringent response typically employ experimental methodologies that rapidly stimulate (p)ppGpp synthesis by abruptly increasing the fraction of uncharged tRNAs, either by explicit amino starvation or by inhibition of tRNA charging. Consequently, these methodologies inhibit protein translation, thereby interfering with the cellular pathways that respond to nutrient limitation. Thus, complete and/or rapid starvation is a problematic experimental paradigm for investigating bacterial responses to physiologically relevant nutrient-limited states. American Society for Microbiology 2023-01-10 /pmc/articles/PMC9973329/ /pubmed/36625599 http://dx.doi.org/10.1128/mbio.03404-22 Text en Copyright © 2023 Dworkin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Minireview
Dworkin, Jonathan
Understanding the Stringent Response: Experimental Context Matters
title Understanding the Stringent Response: Experimental Context Matters
title_full Understanding the Stringent Response: Experimental Context Matters
title_fullStr Understanding the Stringent Response: Experimental Context Matters
title_full_unstemmed Understanding the Stringent Response: Experimental Context Matters
title_short Understanding the Stringent Response: Experimental Context Matters
title_sort understanding the stringent response: experimental context matters
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973329/
https://www.ncbi.nlm.nih.gov/pubmed/36625599
http://dx.doi.org/10.1128/mbio.03404-22
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