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• W2793232695 abstract "The effect of ethanol on the metabolism of Oenococcus oeni, the bacterium responsible for the malolactic fermentation of wine, is still scarcely understood. Here, we characterized the global metabolic response in O. oeni to increasing ethanol contents, ranging from 0 to 12% (v/v). We first optimized a wine-like, defined culture medium, MaxOeno, to allow sufficient bacterial growth to be able to quantitate different metabolites in batch cultures of O. oeni. Then, taking advantage of the recently reconstructed genome-scale metabolic model iSM454 for O. oeni PSU-1 and the resulting experimental data, we determined the redistribution of intracellular metabolic fluxes, under the different ethanol conditions. Four growth phases were clearly identified during the batch cultivation of O. oeni PSU-1 strain, according to the temporal consumption of malic and citric acids, sugar and aminoacids uptake, and biosynthesis rates of metabolic products – biomass, erythritol, mannitol and acetic acid, among others. We showed that, under increasing ethanol conditions, O. oeni favors anabolic reactions related with cell maintenance, as the requirements of NAD(P)+ and ATP increased with ethanol content. Specifically, cultures containing 9 and 12% ethanol required 10 and 17 times more NGAM (non-growth associated maintenance ATP) during phase I, respectively, than cultures without ethanol. Malolactic fermentation and citric acid consumption are vital at high ethanol concentrations, as they are the main source for proton extrusion, allowing higher ATP production by F0F1-ATPase, the main route of ATP synthesis under these conditions. Mannitol and erythritol synthesis are the main sources of NAD(P)+, countervailing for 51-57% of its usage, as predicted by the model. Finally, cysteine shows the fastest specific consumption rate among the amino acids, confirming its key role for bacterial survival under ethanol stress. As a whole, this study provides a global insight into how ethanol content exerts a differential physiological response in O. oeni PSU-1 strain. It will help to design better strategies of nutrient addition to achieve a successful malolactic fermentation of wine." @default.
• W2793232695 created "2018-03-29" @default.
• W2793232695 creator A5007554807 @default.
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• W2793232695 date "2018-03-01" @default.
• W2793232695 modified "2023-09-26" @default.
• W2793232695 title "Mapping the Physiological Response of Oenococcus oeni to Ethanol Stress Using an Extended Genome-Scale Metabolic Model" @default.
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• W2793232695 doi "https://doi.org/10.3389/fmicb.2018.00291" @default.
• W2793232695 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5838312" @default.
• W2793232695 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29545779" @default.
• W2793232695 hasPublicationYear "2018" @default.
• W2793232695 type Work @default.

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