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
Biblioteca Digital (UBA-FCEN)
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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oai_identifier_str paperaa:paper_00992240_v78_n24_p8784_Bidart
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling 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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