A delayed mass-action model for the transcriptional control of Hmp, an NO detoxifying enzyme, by the iron-sulfur protein FNR

dc.contributor.authorRoussel, Marc R.
dc.date.accessioned2019-12-20T18:20:12Z
dc.date.available2019-12-20T18:20:12Z
dc.date.issued2019
dc.descriptionPermission to archive accepted author manuscript.en_US
dc.description.abstractIn Escherichia coli, an enzyme called Hmp is a key contributor to the detoxification of nitric oxide (NO). In the absence of NO, the transcription of the hmp gene is repressed by an iron-sulfur protein called FNR. NO damages the iron-sulfur cluster of FNR, weakening the repression of hmp and allowing expression of Hmp to high levels. A delayed mass-action model for the Hmp-FNR network has been developed. This model has 33 parameters, all but three of which were estimated. One of the unknown parameters, the rate of NO inflow into the cell’s cytoplasm, was used as a control parameter in a study of the steady-state structure of this model. This study revealed bistability across a wide range of inflow rates, oxygen concentrations, and values of the unknown parameters. The bistability is caused by substrate inhibition of Hmp by NO, which allows for a high-NO steady state, which would likely be lethal, to coexist with a biologically desirable low-NO steady state.
dc.identifier.citationRoussel, M. R. (2019). A delayed mass-action model for the transcriptional control of Hmp, an NO detoxifying enzyme, by the iron-sulfur protein FNR. In G. Valmorbida, A. Seuret, I. Boussaada, & R. Sipahi (Eds.), Advances in delays and dynamics: Vol. 10: Delays and interconnections: Methodology, algorithms and applications (pp. 215-230). Basel: Springer.en_US
dc.identifier.urihttps://hdl.handle.net/10133/5646
dc.language.isoen_USen_US
dc.publisherSpringeren_US
dc.publisher.departmentDepartment of Chemistry and Biochemistryen_US
dc.publisher.facultyArts and Scienceen_US
dc.publisher.institutionUniversity of Lethbridgeen_US
dc.publisher.urlhttps://doi.org/10.1007/978-3-030-11554-8_14
dc.titleA delayed mass-action model for the transcriptional control of Hmp, an NO detoxifying enzyme, by the iron-sulfur protein FNRen_US
dc.typeBook Chapteren_US
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