Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset

During Escherichia coli growth on glucose, uptake exceeds the requirement of flux to precursors and the surplus is excreted as acetate. Beside the loss of carbon source, the excretion of a weak acid may result in increased energetic demands and hence a decreased yield. The deletion of ptsG, the gene coding for one of the components (IICB(Glc)) of the glucose-phosphoenolpyruvate phosphotransferase system (Glc-PTS) reduced glucose consumption and acetate excretion. Induction of protein production at the onset of cultivation decreased growth rate and glucose consumption rate for both the WT and the mutant strains. The mutant strain produced beta-galactosidase at higher rates than the wild-type strain while directing more carbon into biomass and CO(2) and less into acetate.

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Bibliographic Details
Main Authors: Picón Gálvez, Antonia María, de Mattos, M. J., Postma, P. W.
Format: journal article biblioteca
Language:English
Published: Oxford University Press 2008
Subjects:E. coli, ptsG deletion, Protein production, Batch-cultivation, Induction, Carbon-Xux, Acetic acid formation,
Online Access:http://hdl.handle.net/20.500.12792/3503
http://hdl.handle.net/10261/293372
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spelling dig-inia-es-10261-2933722023-02-20T10:27:52Z Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset Picón Gálvez, Antonia María de Mattos, M. J. Postma, P. W. E. coli ptsG deletion Protein production Batch-cultivation Induction Carbon-Xux Acetic acid formation During Escherichia coli growth on glucose, uptake exceeds the requirement of flux to precursors and the surplus is excreted as acetate. Beside the loss of carbon source, the excretion of a weak acid may result in increased energetic demands and hence a decreased yield. The deletion of ptsG, the gene coding for one of the components (IICB(Glc)) of the glucose-phosphoenolpyruvate phosphotransferase system (Glc-PTS) reduced glucose consumption and acetate excretion. Induction of protein production at the onset of cultivation decreased growth rate and glucose consumption rate for both the WT and the mutant strains. The mutant strain produced beta-galactosidase at higher rates than the wild-type strain while directing more carbon into biomass and CO(2) and less into acetate. 2023-02-20T10:27:52Z 2023-02-20T10:27:52Z 2008 journal article Journal of Industrial Microbiology and Biotechnology 35(4): 213-218 (2008) 1367-5435 http://hdl.handle.net/20.500.12792/3503 http://hdl.handle.net/10261/293372 10.1007/s10295-007-0285-6 1476-5535 en none Oxford University Press
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic E. coli
ptsG deletion
Protein production
Batch-cultivation
Induction
Carbon-Xux
Acetic acid formation
E. coli
ptsG deletion
Protein production
Batch-cultivation
Induction
Carbon-Xux
Acetic acid formation
spellingShingle E. coli
ptsG deletion
Protein production
Batch-cultivation
Induction
Carbon-Xux
Acetic acid formation
E. coli
ptsG deletion
Protein production
Batch-cultivation
Induction
Carbon-Xux
Acetic acid formation
Picón Gálvez, Antonia María
de Mattos, M. J.
Postma, P. W.
Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
description During Escherichia coli growth on glucose, uptake exceeds the requirement of flux to precursors and the surplus is excreted as acetate. Beside the loss of carbon source, the excretion of a weak acid may result in increased energetic demands and hence a decreased yield. The deletion of ptsG, the gene coding for one of the components (IICB(Glc)) of the glucose-phosphoenolpyruvate phosphotransferase system (Glc-PTS) reduced glucose consumption and acetate excretion. Induction of protein production at the onset of cultivation decreased growth rate and glucose consumption rate for both the WT and the mutant strains. The mutant strain produced beta-galactosidase at higher rates than the wild-type strain while directing more carbon into biomass and CO(2) and less into acetate.
format journal article
topic_facet E. coli
ptsG deletion
Protein production
Batch-cultivation
Induction
Carbon-Xux
Acetic acid formation
author Picón Gálvez, Antonia María
de Mattos, M. J.
Postma, P. W.
author_facet Picón Gálvez, Antonia María
de Mattos, M. J.
Postma, P. W.
author_sort Picón Gálvez, Antonia María
title Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
title_short Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
title_full Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
title_fullStr Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
title_full_unstemmed Protein production by Escherichia coli wild-type and DeltaptsG mutant strains with IPTG induction at the onset
title_sort protein production by escherichia coli wild-type and deltaptsg mutant strains with iptg induction at the onset
publisher Oxford University Press
publishDate 2008
url http://hdl.handle.net/20.500.12792/3503
http://hdl.handle.net/10261/293372
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AT demattosmj proteinproductionbyescherichiacoliwildtypeanddeltaptsgmutantstrainswithiptginductionattheonset
AT postmapw proteinproductionbyescherichiacoliwildtypeanddeltaptsgmutantstrainswithiptginductionattheonset
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