<?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>2026-06-07T19:16:00Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/124626" metadataPrefix="rdf">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/124626</identifier><datestamp>2025-10-07T23:57:03Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><rdf:RDF xmlns:rdf="http://www.openarchives.org/OAI/2.0/rdf/" xmlns:ow="http://www.ontoweb.org/ontology/1#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:ds="http://dspace.org/ds/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/rdf/ http://www.openarchives.org/OAI/2.0/rdf.xsd">
   <ow:Publication rdf:about="oai:docta.ucm.es:20.500.14352/124626">
      <dc:title>Metabolic-inhibitor profiling links phenotype and transcriptome of Lachancea thermotolerans to wine fermentation chemistry</dc:title>
      <dc:creator>Jimena López, Samuel</dc:creator>
      <dc:creator>Vicente Sánchez, Javier</dc:creator>
      <dc:creator>Benito Sáez, Santiago</dc:creator>
      <dc:creator>Marquina Díaz, Domingo</dc:creator>
      <dc:creator>Santos de la Sen, Antonio</dc:creator>
      <dc:description>Acknowledgements
Funding for this research was provided by the LowpHWine Companies Consortia through the CDTI project LowpHWine (IDI-20210391) and the Spanish Ministry of Science and Innovation under the VinSegCalClim project (PID2020-119008RB-I00). Javier Vicente conducted this research under a fellowship from Complutense University of Madrid (CT58/21-CT59/21). Samuel Jimena conducted this research under an INVESTIGO (CT19/23-INVM-18) contract from the Spanish Ministry of Labour and Social Economy.</dc:description>
      <dc:description>We applied targeted metabolic inhibitors to 145 Lachancea thermotolerans strains to uncover fermentation traits with direct relevance to wine quality. Oxamate, a lactate dehydrogenase inhibitor, reduced lactic acid and total
titratable acidity by 21% and 26%, respectively, while increasing succinic acid and pH without affecting ethanol levels, offering a promising strategy to fine-tune wine freshness and balance. Notably, industrial grape-associated
strains (clusters C4–C6) maintained robust growth under oxamate stress, unlike wild strains, positioning oxamate resistance as a practical marker for selecting high-performing, acidifying yeasts for winemaking. Additional
inhibitors such as metformin shifted redox metabolism, significantly enhancing glycerol (+25%) and acetic acid (+319%) production. Transcriptomic analyses showed that OXA alone, and even more so the DSF + OXA
combination, repressed LDH2 and upregulated GPD1 and oxidative phosphorylation genes, whereas MET caused only moderate changes. This integrated phenomic-transcriptomic approach not only provides valuable tools for
yeast screening but also defines a roadmap for optimizing wine composition through the precision selection of L. thermotolerans strains.</dc:description>
      <dc:date>2025-10-07T17:26:52Z</dc:date>
      <dc:date>2025-10-07T17:26:52Z</dc:date>
      <dc:date>2025-09</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Jimena-López S, Vicente J, Benito S, Marquina D, Santos A. Metabolic-inhibitor profiling links phenotype and transcriptome of Lachancea thermotolerans to wine fermentation chemistry. Food Chemistry: Molecular Sciences 2025;11:100301. https://doi.org/10.1016/j.fochms.2025.100301.</dc:identifier>
      <dc:identifier>10.1016/j.fochms.2025.100301</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/124626</dc:identifier>
      <dc:identifier>2666-5662</dc:identifier>
      <dc:identifier>https://doi.org/10.1016/j.fochms.2025.100301</dc:identifier>
      <dc:identifier>https://www.sciencedirect.com/science/article/pii/S2666566225000620</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>PID2020-119008RB-I00</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
      <dc:publisher>Elsevier</dc:publisher>
   </ow:Publication>
</rdf:RDF></metadata></record></GetRecord></OAI-PMH>