Background: Citrus wine, a value-added product of citrus deep processing, often exhibits unwanted bitterness caused by naringin and limonin, along with an aroma, which limits consumer acceptance. This study investigated the potential of co-fermenting Saccharomyces cerevisiae with selected lactic acid bacteria (LAB) to reduce bitterness and enhance aromatic quality.
Results: Co-fermentation of Lactiplantibacillus plantarum and Saccharomyces cerevisiae increased α-rhamnosidase activity and reduced naringin concentration from 73.87 ± 0.15 to 39.21 ± 1.62 mg L⁻¹ (P < 0.01), limiting limonin accumulation to 15.32 ± 1.01 mg L⁻¹. This was a 50.79% reduction compared with fermentation using S. cerevisiae alone. A total of 150 volatile compounds were identified by headspace solid-phasemicroextraction coupled with gas chromatography-mass spectrometry (HS-SPME-GC-MS) among which the esters, including ethyl caproate, ethyl 9-decenoate and ethyl laurate were enhanced by co-fermentation. The process also increased the odor activity value (OAV) of isoamyl acetate, isoamyl formate, octanoic acid-2-phenylethanol ester, and nonanal, which contribute to fruity and floral aroma characteristics. Sensory evaluation confirmed reduced bitterness and astringency and improved overall flavor acceptance.
Conclusion: Co-fermentation of S. cerevisiae and L. plantarum improved citrus wine quality by degrading naringin and limonin to reduce bitterness, enriching key esters to improve aroma, achieving overall sensory optimization. This study provides a scientific basis for microbial synergy in fruit wine production, offering a practical approach to improving the organoleptic properties of citrus wine. © 2025 Society of Chemical Industry.
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| Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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| Site | Modification | Modifier | Source | Reference |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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| Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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| Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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