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Unravelling metabolic cross-feeding in a yeast-bacteria community using 13 C-based proteomics.
Gabrielli, Natalia; Maga-Nteve, Christoniki; Kafkia, Eleni; Rettel, Mandy; Loeffler, Jakob; Kamrad, Stephan; Typas, Athanasios; Patil, Kiran Raosaheb.
Afiliación
  • Gabrielli N; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Maga-Nteve C; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Kafkia E; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Rettel M; Medical Research Council Toxicology Unit, University of Cambridge, Cambridge, UK.
  • Loeffler J; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Kamrad S; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Typas A; Medical Research Council Toxicology Unit, University of Cambridge, Cambridge, UK.
  • Patil KR; European Molecular Biology Laboratory, Heidelberg, Germany.
Mol Syst Biol ; 19(4): e11501, 2023 04 12.
Article en En | MEDLINE | ID: mdl-36779294
Cross-feeding is fundamental to the diversity and function of microbial communities. However, identification of cross-fed metabolites is often challenging due to the universality of metabolic and biosynthetic intermediates. Here, we use 13 C isotope tracing in peptides to elucidate cross-fed metabolites in co-cultures of Saccharomyces cerevisiae and Lactococcus lactis. The community was grown on lactose as the main carbon source with either glucose or galactose fraction of the molecule labelled with 13 C. Data analysis allowing for the possible mass-shifts yielded hundreds of peptides for which we could assign both species identity and labelling degree. The labelling pattern showed that the yeast utilized galactose and, to a lesser extent, lactic acid shared by L. lactis as carbon sources. While the yeast provided essential amino acids to the bacterium as expected, the data also uncovered a complex pattern of amino acid exchange. The identity of the cross-fed metabolites was further supported by metabolite labelling in the co-culture supernatant, and by diminished fitness of a galactose-negative yeast mutant in the community. Together, our results demonstrate the utility of 13 C-based proteomics for uncovering microbial interactions.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Galactosa Idioma: En Revista: Mol Syst Biol Asunto de la revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Galactosa Idioma: En Revista: Mol Syst Biol Asunto de la revista: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Alemania