Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system
- Autores
- Bidart, G.N.; Ruiz, J.A.; de Almeida, A.; Méndez, B.S.; Nikel, P.I.
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Bioprocesses conducted under conditions with restricted O2 supply are increasingly exploited for the synthesis of reduced biochemicals using different biocatalysts. The model facultative anaerobe Escherichia coli has elaborate sensing and signal transduction mechanisms for redox control in response to the availability of O2 and other electron acceptors. The ArcBA two-component system consists of ArcB, a membrane-associated sensor kinase, and ArcA, the cognate response regulator. The tripartite hybrid kinase ArcB possesses a transmembrane, a PAS, a primary transmitter (H1), a receiver (D1), and a phosphotransfer (H2) domain. Metabolic fluxes were compared under anoxic conditions in a wild-type E. coli strain, its ΔarcB derivative, and two partial arcB deletion mutants in which ArcB lacked either the H1 domain or the PAS-H1-D1 domains. These analyses revealed that elimination of different segments in ArcB determines a distinctive distribution of D-glucose catabolic fluxes, different from that observed in the ΔarcB background. Metabolite profiles, enzyme activity levels, and gene expression patterns were also investigated in these strains. Relevant alterations were observed at the P-enol-pyruvate/pyruvate and acetyl coenzyme A metabolic nodes, and the formation of reduced fermentation metabolites, such as succinate, D-lactate, and ethanol, was favored in the mutant strains to different extents compared to the wild-type strain. These phenotypic traits were associated with altered levels of the enzymatic activities operating at these nodes, as well as with elevated NADH/NAD+ ratios. Thus, targeted modification of global regulators to obtain different metabolic flux distributions under anoxic conditions is emerging as an attractive tool for metabolic engineering purposes. © 2012, American Society for Microbiology.
Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:de Almeida, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Méndez, B.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. - Fuente
- Appl. Environ. Microbiol. 2012;78(24):8784-8794
- Materia
-
Acetyl coenzyme A
Anoxic conditions
Bioprocesses
D-glucose
D-lactate
Deletion mutants
Deletion variants
E. coli
Electron acceptor
Enzymatic activities
Facultative anaerobes
Gene expression patterns
Metabolic flux
Metabolic flux distribution
Metabolite profiles
Mutant strain
Phenotypic traits
Phospho-transfer
Response regulators
Sensor kinase
Signal transduction mechanism
Transmembranes
Two component systems
Wild types
Wild-type strain
Enzymes
Escherichia coli
Ethanol
Gene expression
Glucose
Metabolites
Plants (botany)
Signal transduction
Metabolism
alcohol
arcA protein, E coli
arcB protein, E coli
Escherichia coli protein
glucose
lactic acid
membrane protein
nicotinamide adenine dinucleotide
outer membrane protein
protein kinase
repressor protein
succinic acid
anoxic conditions
biochemical composition
catalyst
coliform bacterium
metabolism
mutation
oxygen
redox conditions
anaerobic growth
article
enzymology
Escherichia coli
fermentation
gene deletion
genetics
metabolism
Anaerobiosis
Bacterial Outer Membrane Proteins
Escherichia coli
Escherichia coli Proteins
Ethanol
Fermentation
Glucose
Lactic Acid
Membrane Proteins
Metabolic Networks and Pathways
NAD
Protein Kinases
Repressor Proteins
Sequence Deletion
Succinic Acid
Arca
Escherichia coli - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/2.5/ar
- Repositorio
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_00992240_v78_n24_p8784_Bidart
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Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component systemBidart, G.N.Ruiz, J.A.de Almeida, A.Méndez, B.S.Nikel, P.I.Acetyl coenzyme AAnoxic conditionsBioprocessesD-glucoseD-lactateDeletion mutantsDeletion variantsE. coliElectron acceptorEnzymatic activitiesFacultative anaerobesGene expression patternsMetabolic fluxMetabolic flux distributionMetabolite profilesMutant strainPhenotypic traitsPhospho-transferResponse regulatorsSensor kinaseSignal transduction mechanismTransmembranesTwo component systemsWild typesWild-type strainEnzymesEscherichia coliEthanolGene expressionGlucoseMetabolitesPlants (botany)Signal transductionMetabolismalcoholarcA protein, E coliarcB protein, E coliEscherichia coli proteinglucoselactic acidmembrane proteinnicotinamide adenine dinucleotideouter membrane proteinprotein kinaserepressor proteinsuccinic acidanoxic conditionsbiochemical compositioncatalystcoliform bacteriummetabolismmutationoxygenredox conditionsanaerobic growtharticleenzymologyEscherichia colifermentationgene deletiongeneticsmetabolismAnaerobiosisBacterial Outer Membrane ProteinsEscherichia coliEscherichia coli ProteinsEthanolFermentationGlucoseLactic AcidMembrane ProteinsMetabolic Networks and PathwaysNADProtein KinasesRepressor ProteinsSequence DeletionSuccinic AcidArcaEscherichia coliBioprocesses conducted under conditions with restricted O2 supply are increasingly exploited for the synthesis of reduced biochemicals using different biocatalysts. The model facultative anaerobe Escherichia coli has elaborate sensing and signal transduction mechanisms for redox control in response to the availability of O2 and other electron acceptors. The ArcBA two-component system consists of ArcB, a membrane-associated sensor kinase, and ArcA, the cognate response regulator. The tripartite hybrid kinase ArcB possesses a transmembrane, a PAS, a primary transmitter (H1), a receiver (D1), and a phosphotransfer (H2) domain. Metabolic fluxes were compared under anoxic conditions in a wild-type E. coli strain, its ΔarcB derivative, and two partial arcB deletion mutants in which ArcB lacked either the H1 domain or the PAS-H1-D1 domains. These analyses revealed that elimination of different segments in ArcB determines a distinctive distribution of D-glucose catabolic fluxes, different from that observed in the ΔarcB background. Metabolite profiles, enzyme activity levels, and gene expression patterns were also investigated in these strains. Relevant alterations were observed at the P-enol-pyruvate/pyruvate and acetyl coenzyme A metabolic nodes, and the formation of reduced fermentation metabolites, such as succinate, D-lactate, and ethanol, was favored in the mutant strains to different extents compared to the wild-type strain. These phenotypic traits were associated with altered levels of the enzymatic activities operating at these nodes, as well as with elevated NADH/NAD+ ratios. Thus, targeted modification of global regulators to obtain different metabolic flux distributions under anoxic conditions is emerging as an attractive tool for metabolic engineering purposes. © 2012, American Society for Microbiology.Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:de Almeida, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Méndez, B.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2012info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_00992240_v78_n24_p8784_BidartAppl. Environ. Microbiol. 2012;78(24):8784-8794reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-04T09:48:24Zpaperaa:paper_00992240_v78_n24_p8784_BidartInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-04 09:48:25.742Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse |
dc.title.none.fl_str_mv |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
title |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
spellingShingle |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system Bidart, G.N. Acetyl coenzyme A Anoxic conditions Bioprocesses D-glucose D-lactate Deletion mutants Deletion variants E. coli Electron acceptor Enzymatic activities Facultative anaerobes Gene expression patterns Metabolic flux Metabolic flux distribution Metabolite profiles Mutant strain Phenotypic traits Phospho-transfer Response regulators Sensor kinase Signal transduction mechanism Transmembranes Two component systems Wild types Wild-type strain Enzymes Escherichia coli Ethanol Gene expression Glucose Metabolites Plants (botany) Signal transduction Metabolism alcohol arcA protein, E coli arcB protein, E coli Escherichia coli protein glucose lactic acid membrane protein nicotinamide adenine dinucleotide outer membrane protein protein kinase repressor protein succinic acid anoxic conditions biochemical composition catalyst coliform bacterium metabolism mutation oxygen redox conditions anaerobic growth article enzymology Escherichia coli fermentation gene deletion genetics metabolism Anaerobiosis Bacterial Outer Membrane Proteins Escherichia coli Escherichia coli Proteins Ethanol Fermentation Glucose Lactic Acid Membrane Proteins Metabolic Networks and Pathways NAD Protein Kinases Repressor Proteins Sequence Deletion Succinic Acid Arca Escherichia coli |
title_short |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
title_full |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
title_fullStr |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
title_full_unstemmed |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
title_sort |
Manipulation of the anoxic metabolism in escherichia coli by ArcB deletion variants in the ArcBA two-component system |
dc.creator.none.fl_str_mv |
Bidart, G.N. Ruiz, J.A. de Almeida, A. Méndez, B.S. Nikel, P.I. |
author |
Bidart, G.N. |
author_facet |
Bidart, G.N. Ruiz, J.A. de Almeida, A. Méndez, B.S. Nikel, P.I. |
author_role |
author |
author2 |
Ruiz, J.A. de Almeida, A. Méndez, B.S. Nikel, P.I. |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
Acetyl coenzyme A Anoxic conditions Bioprocesses D-glucose D-lactate Deletion mutants Deletion variants E. coli Electron acceptor Enzymatic activities Facultative anaerobes Gene expression patterns Metabolic flux Metabolic flux distribution Metabolite profiles Mutant strain Phenotypic traits Phospho-transfer Response regulators Sensor kinase Signal transduction mechanism Transmembranes Two component systems Wild types Wild-type strain Enzymes Escherichia coli Ethanol Gene expression Glucose Metabolites Plants (botany) Signal transduction Metabolism alcohol arcA protein, E coli arcB protein, E coli Escherichia coli protein glucose lactic acid membrane protein nicotinamide adenine dinucleotide outer membrane protein protein kinase repressor protein succinic acid anoxic conditions biochemical composition catalyst coliform bacterium metabolism mutation oxygen redox conditions anaerobic growth article enzymology Escherichia coli fermentation gene deletion genetics metabolism Anaerobiosis Bacterial Outer Membrane Proteins Escherichia coli Escherichia coli Proteins Ethanol Fermentation Glucose Lactic Acid Membrane Proteins Metabolic Networks and Pathways NAD Protein Kinases Repressor Proteins Sequence Deletion Succinic Acid Arca Escherichia coli |
topic |
Acetyl coenzyme A Anoxic conditions Bioprocesses D-glucose D-lactate Deletion mutants Deletion variants E. coli Electron acceptor Enzymatic activities Facultative anaerobes Gene expression patterns Metabolic flux Metabolic flux distribution Metabolite profiles Mutant strain Phenotypic traits Phospho-transfer Response regulators Sensor kinase Signal transduction mechanism Transmembranes Two component systems Wild types Wild-type strain Enzymes Escherichia coli Ethanol Gene expression Glucose Metabolites Plants (botany) Signal transduction Metabolism alcohol arcA protein, E coli arcB protein, E coli Escherichia coli protein glucose lactic acid membrane protein nicotinamide adenine dinucleotide outer membrane protein protein kinase repressor protein succinic acid anoxic conditions biochemical composition catalyst coliform bacterium metabolism mutation oxygen redox conditions anaerobic growth article enzymology Escherichia coli fermentation gene deletion genetics metabolism Anaerobiosis Bacterial Outer Membrane Proteins Escherichia coli Escherichia coli Proteins Ethanol Fermentation Glucose Lactic Acid Membrane Proteins Metabolic Networks and Pathways NAD Protein Kinases Repressor Proteins Sequence Deletion Succinic Acid Arca Escherichia coli |
dc.description.none.fl_txt_mv |
Bioprocesses conducted under conditions with restricted O2 supply are increasingly exploited for the synthesis of reduced biochemicals using different biocatalysts. The model facultative anaerobe Escherichia coli has elaborate sensing and signal transduction mechanisms for redox control in response to the availability of O2 and other electron acceptors. The ArcBA two-component system consists of ArcB, a membrane-associated sensor kinase, and ArcA, the cognate response regulator. The tripartite hybrid kinase ArcB possesses a transmembrane, a PAS, a primary transmitter (H1), a receiver (D1), and a phosphotransfer (H2) domain. Metabolic fluxes were compared under anoxic conditions in a wild-type E. coli strain, its ΔarcB derivative, and two partial arcB deletion mutants in which ArcB lacked either the H1 domain or the PAS-H1-D1 domains. These analyses revealed that elimination of different segments in ArcB determines a distinctive distribution of D-glucose catabolic fluxes, different from that observed in the ΔarcB background. Metabolite profiles, enzyme activity levels, and gene expression patterns were also investigated in these strains. Relevant alterations were observed at the P-enol-pyruvate/pyruvate and acetyl coenzyme A metabolic nodes, and the formation of reduced fermentation metabolites, such as succinate, D-lactate, and ethanol, was favored in the mutant strains to different extents compared to the wild-type strain. These phenotypic traits were associated with altered levels of the enzymatic activities operating at these nodes, as well as with elevated NADH/NAD+ ratios. Thus, targeted modification of global regulators to obtain different metabolic flux distributions under anoxic conditions is emerging as an attractive tool for metabolic engineering purposes. © 2012, American Society for Microbiology. Fil:Ruiz, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:de Almeida, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Méndez, B.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. |
description |
Bioprocesses conducted under conditions with restricted O2 supply are increasingly exploited for the synthesis of reduced biochemicals using different biocatalysts. The model facultative anaerobe Escherichia coli has elaborate sensing and signal transduction mechanisms for redox control in response to the availability of O2 and other electron acceptors. The ArcBA two-component system consists of ArcB, a membrane-associated sensor kinase, and ArcA, the cognate response regulator. The tripartite hybrid kinase ArcB possesses a transmembrane, a PAS, a primary transmitter (H1), a receiver (D1), and a phosphotransfer (H2) domain. Metabolic fluxes were compared under anoxic conditions in a wild-type E. coli strain, its ΔarcB derivative, and two partial arcB deletion mutants in which ArcB lacked either the H1 domain or the PAS-H1-D1 domains. These analyses revealed that elimination of different segments in ArcB determines a distinctive distribution of D-glucose catabolic fluxes, different from that observed in the ΔarcB background. Metabolite profiles, enzyme activity levels, and gene expression patterns were also investigated in these strains. Relevant alterations were observed at the P-enol-pyruvate/pyruvate and acetyl coenzyme A metabolic nodes, and the formation of reduced fermentation metabolites, such as succinate, D-lactate, and ethanol, was favored in the mutant strains to different extents compared to the wild-type strain. These phenotypic traits were associated with altered levels of the enzymatic activities operating at these nodes, as well as with elevated NADH/NAD+ ratios. Thus, targeted modification of global regulators to obtain different metabolic flux distributions under anoxic conditions is emerging as an attractive tool for metabolic engineering purposes. © 2012, American Society for Microbiology. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/20.500.12110/paper_00992240_v78_n24_p8784_Bidart |
url |
http://hdl.handle.net/20.500.12110/paper_00992240_v78_n24_p8784_Bidart |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/2.5/ar |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Appl. Environ. Microbiol. 2012;78(24):8784-8794 reponame:Biblioteca Digital (UBA-FCEN) instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales instacron:UBA-FCEN |
reponame_str |
Biblioteca Digital (UBA-FCEN) |
collection |
Biblioteca Digital (UBA-FCEN) |
instname_str |
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
instacron_str |
UBA-FCEN |
institution |
UBA-FCEN |
repository.name.fl_str_mv |
Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
repository.mail.fl_str_mv |
ana@bl.fcen.uba.ar |
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