Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model

Metabolic control of glutamine and glutamate synthesis from ammonia and oxoglutarate in Escherichia coli is tight and complex. In this work, the role of glutamine synthetase (GS) and glutamate dehydrogenase (GDH) regulation in this control was studied. Both enzymes form a linear pathway, which can a...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Lodeiro, Aníbal Roberto, Melgarejo, Augusto Argentino
Formato: Articulo
Lenguaje:Español
Publicado: 2008
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/107234
http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC2577740&blobtype=pdf
Aporte de:
id I19-R120-10915-107234
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Español
topic Ciencias Exactas
Glutamine synthetase
Pathway topology
Regulation
Kinetic model
Metabolic control
spellingShingle Ciencias Exactas
Glutamine synthetase
Pathway topology
Regulation
Kinetic model
Metabolic control
Lodeiro, Aníbal Roberto
Melgarejo, Augusto Argentino
Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
topic_facet Ciencias Exactas
Glutamine synthetase
Pathway topology
Regulation
Kinetic model
Metabolic control
description Metabolic control of glutamine and glutamate synthesis from ammonia and oxoglutarate in Escherichia coli is tight and complex. In this work, the role of glutamine synthetase (GS) and glutamate dehydrogenase (GDH) regulation in this control was studied. Both enzymes form a linear pathway, which can also have a cyclic topology if glutamate–oxoglutarate amino transferase (GOGAT) activity is included. We modelled the metabolic pathways in the linear or cyclic topologies using a coupled nonlinear differential equations system. To simulate GS regulation by covalent modification, we introduced a relationship that took into account the levels of oxoglutarate and glutamine as signal inputs, as well as the ultrasensitive response of enzyme adenylylation. Thus, by including this relationship or not, we were able to model the system with or without GS regulation. In addition, GS and GDH activities were changed manually. The response of the model in different stationary states, or under the influence of N-input exhaustion or oscillation, was analyzed in both pathway topologies. Our results indicate a metabolic control coefficient for GDH ranging from 0.94 in the linear pathway with GS regulation to 0.24 in the cyclic pathway without regulation, employing a default GDH concentration of 8 μM. Thus, in these conditions, GDH seemed to have a high degree of control in the linear pathway while having limited influence in the cyclic one. When GS was regulated, system responses to N-input perturbations were more sensitive, especially in the cyclic pathway. Furthermore, we found that effects of regulation against perturbations depended on the relative values of the glutamine and glutamate output first-order kinetic constants, which we named k6 and k7, respectively. Effects of regulation grew exponentially with a factor around 2, with linear increases of (k7 − k6). These trends were sustained but with lower differences at higher GS concentration. Hence, GS regulation seemed important for metabolic stability in a changing environment, depending on the cell’s metabolic status.
format Articulo
Articulo
author Lodeiro, Aníbal Roberto
Melgarejo, Augusto Argentino
author_facet Lodeiro, Aníbal Roberto
Melgarejo, Augusto Argentino
author_sort Lodeiro, Aníbal Roberto
title Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
title_short Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
title_full Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
title_fullStr Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
title_full_unstemmed Robustness in <i>Escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
title_sort robustness in <i>escherichia coli</i> glutamate and glutamine synthesis studied by a kinetic model
publishDate 2008
url http://sedici.unlp.edu.ar/handle/10915/107234
http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC2577740&blobtype=pdf
work_keys_str_mv AT lodeiroanibalroberto robustnessiniescherichiacoliiglutamateandglutaminesynthesisstudiedbyakineticmodel
AT melgarejoaugustoargentino robustnessiniescherichiacoliiglutamateandglutaminesynthesisstudiedbyakineticmodel
bdutipo_str Repositorios
_version_ 1764820443816001536