<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-01T07:51:38Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/35328" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/35328</identifier><datestamp>2026-02-03T10:58:50Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>A bottom-up characterization of transfer functions for synthetic biology designs: lessons from enzymology</dc:title>
   <dc:creator>Carbonell-Ballesteros, Max</dc:creator>
   <dc:creator>Durán-Nebreda, Salva</dc:creator>
   <dc:creator>Montañez, Raúl</dc:creator>
   <dc:creator>Macía, Javier</dc:creator>
   <dc:creator>Rodríguez-Caso, Carlos Francisco</dc:creator>
   <dc:subject>Enzimología</dc:subject>
   <dcterms:abstract>Within the field of synthetic biology, a rational design of genetic parts should include a causal understanding of their input-output responses-the so-called transfer function-and how to tune them. However, a commonly adopted strategy is to fit data to Hill-shaped curves without considering the underlying molecular mechanisms. Here we provide a novel mathematical formalization that allows prediction of the global behavior of a synthetic device by considering the actual information from the involved biological parts. This is achieved by adopting an enzymology-like framework, where transfer functions are described in terms of their input affinity constant and maximal response. As a proof of concept, we characterize a set of Lux homoserine-lactone-inducible genetic devices with different levels of Lux receptor and signal molecule. Our model fits the experimental results and predicts the impact of the receptor's ribosome-binding site strength, as a tunable parameter that affects gene expression. The evolutionary implications are outlined.</dcterms:abstract>
   <dcterms:dateAccepted>2024-11-26T12:30:07Z</dcterms:dateAccepted>
   <dcterms:available>2024-11-26T12:30:07Z</dcterms:available>
   <dcterms:created>2024-11-26T12:30:07Z</dcterms:created>
   <dcterms:issued>2014-12-16</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Max Carbonell-Ballestero, Salva Duran-Nebreda, Raúl Montañez, Ricard Solé, Javier Macía, Carlos Rodríguez-Caso, A bottom-up characterization of transfer functions for synthetic biology designs: lessons from enzymology, Nucleic Acids Research, Volume 42, Issue 22, 16 December 2014, Pages 14060–14069, https://doi.org/10.1093/nar/gku964</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/35328</dc:identifier>
   <dc:identifier>10.1093/nar/gku964</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>Oxfrod University Press</dc:publisher>
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