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Unravelling metabolic cross‐feeding in a yeast–bacteria community using (13)C‐based proteomics

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 metabo...

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Detalles Bibliográficos
Autores principales: Gabrielli, Natalia, Maga‐Nteve, Christoniki, Kafkia, Eleni, Rettel, Mandy, Loeffler, Jakob, Kamrad, Stephan, Typas, Athanasios, Patil, Kiran Raosaheb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10090948/
https://www.ncbi.nlm.nih.gov/pubmed/36779294
http://dx.doi.org/10.15252/msb.202211501
Descripción
Sumario: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.