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Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”

Studying the toxicity of chemical compounds using isothermal microcalorimetry (IMC), which monitors the metabolic heat from living microorganisms, is a rapidly expanding field. The unprecedented sensitivity of IMC is particularly attractive for studies at low levels of stressors, where lethality-bas...

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Autores principales: Oertel, Jana, Sachs, Susanne, Flemming, Katrin, Obeid, Muhammad Hassan, Fahmy, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056173/
https://www.ncbi.nlm.nih.gov/pubmed/36985158
http://dx.doi.org/10.3390/microorganisms11030584
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author Oertel, Jana
Sachs, Susanne
Flemming, Katrin
Obeid, Muhammad Hassan
Fahmy, Karim
author_facet Oertel, Jana
Sachs, Susanne
Flemming, Katrin
Obeid, Muhammad Hassan
Fahmy, Karim
author_sort Oertel, Jana
collection PubMed
description Studying the toxicity of chemical compounds using isothermal microcalorimetry (IMC), which monitors the metabolic heat from living microorganisms, is a rapidly expanding field. The unprecedented sensitivity of IMC is particularly attractive for studies at low levels of stressors, where lethality-based data are inadequate. We have revealed via IMC the effect of low dose rates from radioactive β(−)-decay on bacterial metabolism. The low dose rate regime (<400 µGyh(−1)) is typical of radioactively contaminated environmental sites, where chemical toxicity and radioactivity-mediated effects coexist without a predominance or specific characteristic of either of them. We found that IMC allows distinguishing the two sources of metabolic interference on the basis of “isotope-editing” and advanced thermogram analyses. The stable and radioactive europium isotopes (153)Eu and (152)Eu, respectively, were employed in monitoring Lactococcus lactis cultures via IMC. β(−)-emission (electrons) was found to increase initial culture growth by increased nutrient uptake efficiency, which compensates for a reduced maximal cell division rate. Direct adsorption of the radionuclide to the biomass, revealed by mass spectrometry, is critical for both the initial stress response and the “dilution” of radioactivity-mediated damage at later culture stages, which are dominated by the chemical toxicity of Eu.
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spelling pubmed-100561732023-03-30 Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing” Oertel, Jana Sachs, Susanne Flemming, Katrin Obeid, Muhammad Hassan Fahmy, Karim Microorganisms Article Studying the toxicity of chemical compounds using isothermal microcalorimetry (IMC), which monitors the metabolic heat from living microorganisms, is a rapidly expanding field. The unprecedented sensitivity of IMC is particularly attractive for studies at low levels of stressors, where lethality-based data are inadequate. We have revealed via IMC the effect of low dose rates from radioactive β(−)-decay on bacterial metabolism. The low dose rate regime (<400 µGyh(−1)) is typical of radioactively contaminated environmental sites, where chemical toxicity and radioactivity-mediated effects coexist without a predominance or specific characteristic of either of them. We found that IMC allows distinguishing the two sources of metabolic interference on the basis of “isotope-editing” and advanced thermogram analyses. The stable and radioactive europium isotopes (153)Eu and (152)Eu, respectively, were employed in monitoring Lactococcus lactis cultures via IMC. β(−)-emission (electrons) was found to increase initial culture growth by increased nutrient uptake efficiency, which compensates for a reduced maximal cell division rate. Direct adsorption of the radionuclide to the biomass, revealed by mass spectrometry, is critical for both the initial stress response and the “dilution” of radioactivity-mediated damage at later culture stages, which are dominated by the chemical toxicity of Eu. MDPI 2023-02-25 /pmc/articles/PMC10056173/ /pubmed/36985158 http://dx.doi.org/10.3390/microorganisms11030584 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Oertel, Jana
Sachs, Susanne
Flemming, Katrin
Obeid, Muhammad Hassan
Fahmy, Karim
Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title_full Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title_fullStr Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title_full_unstemmed Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title_short Distinct Effects of Chemical Toxicity and Radioactivity on Metabolic Heat of Cultured Cells Revealed by “Isotope-Editing”
title_sort distinct effects of chemical toxicity and radioactivity on metabolic heat of cultured cells revealed by “isotope-editing”
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056173/
https://www.ncbi.nlm.nih.gov/pubmed/36985158
http://dx.doi.org/10.3390/microorganisms11030584
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