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Optimization of Medium and Transcriptomic Analysis for Converting Ellagic Acid to Urolithin A by Limosilactobacillus fermentum FUA033
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Gewen ZHANG1, Liangliang QIAN2, Wenmei ZHOU3, Yanyan GONG3, Tao CHEN4, Yingling LIU1, Yaowei FANG1, Shu LIU1, *
Science and Technology of Food Industry | 2026, 47(1) : 197 - 205
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Science and Technology of Food Industry | 2026, 47(1): 197-205
• Bioengineering •
Optimization of Medium and Transcriptomic Analysis for Converting Ellagic Acid to Urolithin A by Limosilactobacillus fermentum FUA033
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Gewen ZHANG1, Liangliang QIAN2, Wenmei ZHOU3, Yanyan GONG3, Tao CHEN4, Yingling LIU1, Yaowei FANG1, Shu LIU1, *
Affiliations
  • 1College of Marine Food and Bioengineering, Jiangsu Ocean University, Lianyungang 222005, China
  • 2Lianyungang Quality and Technology Comprehensive Inspection and Testing Center, Lianyungang 222005, China
  • 3Lianyungang Food and Drug Inspection and Testing Center, Lianyungang 222005, China
  • 4Suqian Product Quality Supervision and Testing Institute, Suqian 223814, China
Published: 2026-01-01 doi: 10.13386/j.issn1002-0306.2024110318
Outline
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This study aimed to establish a systematic framework for enhancing the bioconversion efficiency of ellagic acid to urolithin A by Limosilactobacillus fermentum FUA033 through rational medium engineering, while deciphering the molecular orchestration underlying this metabolic process. Single factor and response surface methodology were used to optimize the culture medium. Transcriptome sequencing technology was utilized to analyze L. fermentum FUA033 before and after ellagic acid supplementation in media, and predict the molecular mechanisms involved in the biotransformation of ellagic acid into urolithin A. The optimized medium was determined to be Wilkins-Chalgren Anaerobe Broth (WAM) supplemented with 0.16% trace element solution, 0.16 mmol/L methyl viologen, and 0.21% vitamin solution. The optimization resulted in biotransformation rate of 74.91%, 20.83% improved as compared to the unoptimized condition. Following the addition of ellagic acid, 64 significantly up-regulated genes, and 123 differentially down-regulated genes. GO enrichment analysis demonstrated that the differentially expressed genes were significantly enriched in molecular functions including transporter activity, membrane, and ion transport. The KEGG pathway enrichment analysis demonstrated significant alterations in oxidative phosphorylation (P<0.05), with substantial enrichment of functional genes related to metabolic pathways and the biosynthesis of secondary metabolites. Notably, two lactonase-encoding genes exhibited significant upregulation, strongly suggesting their catalytic role in hydrolyzing ellagic acid's lactone rings to generate the urolithin A precursor. These findings establish a mechanistic foundation for microbial biosynthesis of urolithin A through fermentation, while systematically delineating the enzymatic determinants governing the bacterial-mediated biotransformation of ellagic acid into urolithin A.

Limosilactobacillus fermentum FUA033  /  ellagic acid  /  urolithin A  /  fermentation optimization  /  transcriptome analysis
张格文, 钱亮亮, 周文梅, 宫艳艳, 陈涛, 刘莹呤, 房耀维, 刘姝. Limosilactobacillus fermentum FUA033转化鞣花酸生成尿石素A的培养基优化及转录组学分析. 食品工业科技, 2026 , 47 (1) : 197 -205 . DOI: 10.13386/j.issn1002-0306.2024110318
Gewen ZHANG, Liangliang QIAN, Wenmei ZHOU, Yanyan GONG, Tao CHEN, Yingling LIU, Yaowei FANG, Shu LIU. Optimization of Medium and Transcriptomic Analysis for Converting Ellagic Acid to Urolithin A by Limosilactobacillus fermentum FUA033[J]. Science and Technology of Food Industry, 2026 , 47 (1) : 197 -205 . DOI: 10.13386/j.issn1002-0306.2024110318
Year 2026 volume 47 Issue 1
102
44
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doi: 10.13386/j.issn1002-0306.2024110318
  • Receive Date:2024-11-25
  • Online Date:2026-10-24
  • Published:2026-01-01
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  • Received:2024-11-25
Affiliations
    1College of Marine Food and Bioengineering, Jiangsu Ocean University, Lianyungang 222005, China
    2Lianyungang Quality and Technology Comprehensive Inspection and Testing Center, Lianyungang 222005, China
    3Lianyungang Food and Drug Inspection and Testing Center, Lianyungang 222005, China
    4Suqian Product Quality Supervision and Testing Institute, Suqian 223814, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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