Chemical reaction network properties of S-systems and decompositions of reaction networks

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ID: 286886
2021
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Abstract
This thesis examined two models of the gene regulatory system of Mycobacterium Tuberculosis (Mtb) presented as S-system by Magombedze and Mulder (2013). The models are partitioned into three subsystems based on putative gene function and role in dormancy/latency development. This study investigated the chemical reaction network (CRN) representation of the Mtb models and each subsystem to obtain new mathematical results in Chemical Reaction Network Theory. The subsystems are represented as embedded networks (an arc connecting two vertices that represent genes from different subsystems is retained). For the embedded networks of S_system CRNs (with at least two species) are discordant. Analyzing the subsystems as subnetworks, we formed a digraph homomorphism from the corresponding subnetworks to the embedded networks and explored the modularity concepts of digraph. Further analysis of the Mtb S-systems led us to develop different classes of decomposition of reaction networks based on the approach of Feinberg (1987) in decomposing a CRN and were used to correct a deficiency formula of Arceo et al. (2015).
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persistent_1760659956_68f189f48bb66 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Farinas, Honeylou F.
Journal Malay Journal
Year 2021
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