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All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12
The electron transport chain of E. coli contains three different quinone species, ubiquinone (UQ), menaquinone (MK) and demethylmenaquinone (DMK). The content and ratio of the different quinone species vary depending on the external conditions. To study the function of the different quinone species...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882134/ https://www.ncbi.nlm.nih.gov/pubmed/29614086 http://dx.doi.org/10.1371/journal.pone.0194699 |
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author | Nitzschke, Annika Bettenbrock, Katja |
author_facet | Nitzschke, Annika Bettenbrock, Katja |
author_sort | Nitzschke, Annika |
collection | PubMed |
description | The electron transport chain of E. coli contains three different quinone species, ubiquinone (UQ), menaquinone (MK) and demethylmenaquinone (DMK). The content and ratio of the different quinone species vary depending on the external conditions. To study the function of the different quinone species in more detail, strains with deletions preventing UQ synthesis, as well as MK and/or DMK synthesis were cultured under aerobic and anaerobic conditions. The strains were characterized with respect to growth and product synthesis. As quinones are also involved in the control of ArcB/A activity, we analyzed the phosphorylation state of the response regulator as well as the expression of selected genes.The data show reduced aerobic growth coupled to lactate production in the mutants defective in ubiquinone synthesis. This confirms the current assumption that ubiquinone is the main quinone under aerobic growth conditions. In the UQ mutant strains the amount of MK and DMK is significantly elevated. The strain synthesizing only DMK is less affected in growth than the strain synthesizing MK as well as DMK. An inhibitory effect of MK on aerobic growth due to increased oxidative stress is postulated.Under fermentative growth conditions the mutant synthesizing only UQ is severely impaired in growth. Obviously, UQ is not able to replace MK and DMK during anaerobic growth. Mutations affecting quinone synthesis have an impact on ArcA phosphorylation only under anaerobic conditions. ArcA phosphorylation is reduced in strains synthesizing only MK or MK plus DMK. |
format | Online Article Text |
id | pubmed-5882134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58821342018-04-13 All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 Nitzschke, Annika Bettenbrock, Katja PLoS One Research Article The electron transport chain of E. coli contains three different quinone species, ubiquinone (UQ), menaquinone (MK) and demethylmenaquinone (DMK). The content and ratio of the different quinone species vary depending on the external conditions. To study the function of the different quinone species in more detail, strains with deletions preventing UQ synthesis, as well as MK and/or DMK synthesis were cultured under aerobic and anaerobic conditions. The strains were characterized with respect to growth and product synthesis. As quinones are also involved in the control of ArcB/A activity, we analyzed the phosphorylation state of the response regulator as well as the expression of selected genes.The data show reduced aerobic growth coupled to lactate production in the mutants defective in ubiquinone synthesis. This confirms the current assumption that ubiquinone is the main quinone under aerobic growth conditions. In the UQ mutant strains the amount of MK and DMK is significantly elevated. The strain synthesizing only DMK is less affected in growth than the strain synthesizing MK as well as DMK. An inhibitory effect of MK on aerobic growth due to increased oxidative stress is postulated.Under fermentative growth conditions the mutant synthesizing only UQ is severely impaired in growth. Obviously, UQ is not able to replace MK and DMK during anaerobic growth. Mutations affecting quinone synthesis have an impact on ArcA phosphorylation only under anaerobic conditions. ArcA phosphorylation is reduced in strains synthesizing only MK or MK plus DMK. Public Library of Science 2018-04-03 /pmc/articles/PMC5882134/ /pubmed/29614086 http://dx.doi.org/10.1371/journal.pone.0194699 Text en © 2018 Nitzschke, Bettenbrock http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Nitzschke, Annika Bettenbrock, Katja All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title | All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title_full | All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title_fullStr | All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title_full_unstemmed | All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title_short | All three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in E. coli K12 |
title_sort | all three quinone species play distinct roles in ensuring optimal growth under aerobic and fermentative conditions in e. coli k12 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882134/ https://www.ncbi.nlm.nih.gov/pubmed/29614086 http://dx.doi.org/10.1371/journal.pone.0194699 |
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