Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress

<p>Abstract</p> <p>Background</p> <p><it>E. coli </it>cells are rich in thiamine, most of it in the form of the cofactor thiamine diphosphate (ThDP). Free ThDP is the precursor for two triphosphorylated derivatives, thiamine triphosphate (ThTP) and the newly...

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Main Authors: Zorzi Willy, El Moualij Benaïssa, Wins Pierre, Lakaye Bernard, Gigliobianco Tiziana, Bettendorff Lucien
Format: Article
Language:English
Published: BMC 2010-05-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/10/148
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spelling doaj-e6ea3e4c566042b891f36edb6749b70d2020-11-25T00:27:21ZengBMCBMC Microbiology1471-21802010-05-0110114810.1186/1471-2180-10-148Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stressZorzi WillyEl Moualij BenaïssaWins PierreLakaye BernardGigliobianco TizianaBettendorff Lucien<p>Abstract</p> <p>Background</p> <p><it>E. coli </it>cells are rich in thiamine, most of it in the form of the cofactor thiamine diphosphate (ThDP). Free ThDP is the precursor for two triphosphorylated derivatives, thiamine triphosphate (ThTP) and the newly discovered adenosine thiamine triphosphate (AThTP). While, ThTP accumulation requires oxidation of a carbon source, AThTP slowly accumulates in response to carbon starvation, reaching ~15% of total thiamine. Here, we address the question whether AThTP accumulation in <it>E. coli </it>is triggered by the absence of a carbon source in the medium, the resulting drop in energy charge or other forms of metabolic stress.</p> <p>Results</p> <p>In minimal M9 medium, <it>E. coli </it>cells produce AThTP not only when energy substrates are lacking but also when their metabolization is inhibited. Thus AThTP accumulates in the presence of glucose, when glycolysis is blocked by iodoacetate, or in the presence lactate, when respiration is blocked by cyanide or anoxia. In both cases, ATP synthesis is impaired, but AThTP accumulation does not appear to be a direct consequence of reduced ATP levels. Indeed, in the CV2 <it>E. coli </it>strain (containing a thermolabile adenylate kinase), the ATP content is very low at 37°C, even in the presence of metabolizable substrates (glucose or lactate) and under these conditions, the cells produce ThTP but not AThTP. Furthermore, we show that ThTP inhibits AThTP accumulation. Therefore, we conclude that a low energy charge is not sufficient to trigger AThTP accumulation and the latter can only accumulate under conditions where no ThTP is synthesized. We further show that AThTP production can also be induced by the uncoupler CCCP but, unexpectedly, this requires the presence of pyruvate or a substrate yielding pyruvate (such a D-glucose or L-lactate). Under the conditions described, AThTP production is not different when RelA or SpoT mutants are used.</p> <p>Conclusions</p> <p>In <it>E. coli</it>, AThTP accumulates in response to two different conditions of metabolic stress: lack of energy substrates (or inhibition of their metabolization) and uncoupled pyruvate oxidation. Both conditions prevent bacterial growth. There is no obvious link with the stringent response or catabolite repression.</p> http://www.biomedcentral.com/1471-2180/10/148
collection DOAJ
language English
format Article
sources DOAJ
author Zorzi Willy
El Moualij Benaïssa
Wins Pierre
Lakaye Bernard
Gigliobianco Tiziana
Bettendorff Lucien
spellingShingle Zorzi Willy
El Moualij Benaïssa
Wins Pierre
Lakaye Bernard
Gigliobianco Tiziana
Bettendorff Lucien
Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
BMC Microbiology
author_facet Zorzi Willy
El Moualij Benaïssa
Wins Pierre
Lakaye Bernard
Gigliobianco Tiziana
Bettendorff Lucien
author_sort Zorzi Willy
title Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
title_short Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
title_full Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
title_fullStr Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
title_full_unstemmed Adenosine thiamine triphosphate accumulates in <it>Escherichia coli </it>cells in response to specific conditions of metabolic stress
title_sort adenosine thiamine triphosphate accumulates in <it>escherichia coli </it>cells in response to specific conditions of metabolic stress
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2010-05-01
description <p>Abstract</p> <p>Background</p> <p><it>E. coli </it>cells are rich in thiamine, most of it in the form of the cofactor thiamine diphosphate (ThDP). Free ThDP is the precursor for two triphosphorylated derivatives, thiamine triphosphate (ThTP) and the newly discovered adenosine thiamine triphosphate (AThTP). While, ThTP accumulation requires oxidation of a carbon source, AThTP slowly accumulates in response to carbon starvation, reaching ~15% of total thiamine. Here, we address the question whether AThTP accumulation in <it>E. coli </it>is triggered by the absence of a carbon source in the medium, the resulting drop in energy charge or other forms of metabolic stress.</p> <p>Results</p> <p>In minimal M9 medium, <it>E. coli </it>cells produce AThTP not only when energy substrates are lacking but also when their metabolization is inhibited. Thus AThTP accumulates in the presence of glucose, when glycolysis is blocked by iodoacetate, or in the presence lactate, when respiration is blocked by cyanide or anoxia. In both cases, ATP synthesis is impaired, but AThTP accumulation does not appear to be a direct consequence of reduced ATP levels. Indeed, in the CV2 <it>E. coli </it>strain (containing a thermolabile adenylate kinase), the ATP content is very low at 37°C, even in the presence of metabolizable substrates (glucose or lactate) and under these conditions, the cells produce ThTP but not AThTP. Furthermore, we show that ThTP inhibits AThTP accumulation. Therefore, we conclude that a low energy charge is not sufficient to trigger AThTP accumulation and the latter can only accumulate under conditions where no ThTP is synthesized. We further show that AThTP production can also be induced by the uncoupler CCCP but, unexpectedly, this requires the presence of pyruvate or a substrate yielding pyruvate (such a D-glucose or L-lactate). Under the conditions described, AThTP production is not different when RelA or SpoT mutants are used.</p> <p>Conclusions</p> <p>In <it>E. coli</it>, AThTP accumulates in response to two different conditions of metabolic stress: lack of energy substrates (or inhibition of their metabolization) and uncoupled pyruvate oxidation. Both conditions prevent bacterial growth. There is no obvious link with the stringent response or catabolite repression.</p>
url http://www.biomedcentral.com/1471-2180/10/148
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