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Authordc.contributor.authorLetelier Parga, Juan 
Authordc.contributor.authorSoto Andrade, Jorge es_CL
Authordc.contributor.authorGuíñez Abarzúa, Flavio Ricardo es_CL
Authordc.contributor.authorCornish Bowden, Athel es_CL
Authordc.contributor.authorCárdenas, María Luz es_CL
Admission datedc.date.accessioned2011-03-23T17:15:13Z
Available datedc.date.available2011-03-23T17:15:13Z
Publication datedc.date.issued2005-08-24
Cita de ítemdc.identifier.citationJournal of Theoretical Biology 238 (2006) 949–961en_US
Identifierdc.identifier.issn0022-5193
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119103
Abstractdc.description.abstractThis article analyses the work of Robert Rosen on an interpretation of metabolic networks that he called ðM;RÞ systems. His main contribution was an attempt to prove that metabolic closure (or metabolic circularity) could be explained in purely formal terms, but his work remains very obscure and we try to clarify his line of thought. In particular, we clarify the algebraic formulation of ðM;RÞ systems in terms of mappings and sets of mappings, which is grounded in the metaphor of metabolism as a mathematical mapping. We define Rosen’s central result as the mathematical expression in which metabolism appears as a mapping f that is the solution to a fixed-point functional equation. Crucially, our analysis reveals the nature of the mapping, and shows that to have a solution the set of admissible functions representing a metabolism must be drastically smaller than Rosen’s own analysis suggested that it needed to be. For the first time, we provide a mathematical example of an ðM;RÞ system with organizational invariance, and we analyse a minimal (three-step) autocatalytic set in the context of ðM;RÞ systems. In addition, by extending Rosen’s construction, we show how one might generate self-referential objects f with the remarkable property f ðfÞ ¼ f , where f acts in turn as function, argument and result. We conclude that Rosen’s insight, although not yet in an easily workable form, represents a valuable tool for understanding metabolic networks.en_US
Patrocinadordc.description.sponsorshipThis work was supported by Fondecyt 1030371 (JCL), Fondecyt 1040444 (JSA) and the CNRS (AC-B, MLC).en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevier Ltd.en_US
Keywordsdc.subjectSistemas (M,R)en_US
Títulodc.titleOrganizational invariance and metabolic closure: Analysis in terms of M;R systemsen_US
Document typedc.typeArtículo de revista


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