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dc.contributor.authorGuil Asensio, Francisco-
dc.contributor.authorSánchez-Cid, Guillermo-
dc.contributor.authorGarcía Carrasco, José Manuel-
dc.contributor.otherFacultades, Departamentos, Servicios y Escuelas::Departamentos de la UMU::Ingeniería y Tecnología de Computadoreses
dc.date.accessioned2024-02-08T12:21:39Z-
dc.date.available2024-02-08T12:21:39Z-
dc.date.issued2022-08-28-
dc.identifier.citationMetaboliteses
dc.identifier.issn2218-1989-
dc.identifier.urihttp://hdl.handle.net/10201/139004-
dc.description©2022. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by /4.0/ This document is the Published, version of a Published Work that appeared in final form in Metabolites. To access the final edited and published work see https://doi.org/10.3390/ metabo12090808es
dc.description.abstractIncreasingly, systems biology is gaining relevance in basic and applied research. The combination of computational biology with wet laboratory methods produces synergy that results in an exponential increase in knowledge of biological systems. The study of microorganisms such as Staphylococcus epidermidis RP62A enables the researcher to understand better their metabolic networks, which allows the design of effective strategies to treat infections caused by this species or others. S. epidermidis is the second most commoncause of infection in patients with joint implants, so treating its proliferation seems vital for public health. There are different approaches to the analysis of metabolic networks. Flux balance analysis (FBA) is one of the most widespread streams of research. It allows the study of large metabolic networks, the study their structural properties, the optimization of metabolic flux, and the search for intervention strategies to modify the state of the metabolic network. This work presents the validation of the Staphylococcus epidermidis RP62A metabolic network model elaborated by Díaz Calvo et al. Then, we elaborate further on the network analysis’s essential reactions. The full set of essential reactions (including a previously unobserved one) was computed, and we classified them into equivalence classes. Some proposals to intervene in the network and design knock-outs by studying minimal cut sets of small length are also introduced. In particular, minimal cut sets related to the medium (including exchange reactions associated with medium metabolites) have been computed. In this sense, the unique external MCS (composed of cysteine and sulfate ion) has been found, and all hybrid MCS (based on knocking out both internal and exchange reactions) of length two have also been computed. The paper also points out the possible importance of these new intervention strategieses
dc.formatapplication/pdfes
dc.format.extent14es
dc.languageenges
dc.publisherMDPIes
dc.relationThis work has been partially funded by the AEI (State Research Agency, Spain) and the ERDF (European Regional Development Fund, EU) under the Contracts RTI2018-098156-B-C53 and TED2021-129221B-I00 (MCI/AEI/FEDER, UE).es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectStaphylococcus epidermidises
dc.subjectMetabolic network validationes
dc.subjectMinimal cut setses
dc.subjectKnock-outses
dc.subjectSystems biologyes
dc.titleStaphylococcus epidermidis RP62A’s Metabolic Network: Validation and Intervention Strategieses
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.3390/ metabo12090808-
Aparece en las colecciones:Artículos: Ingeniería y Tecnología de Computadores

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