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February 11, 2026Advanced Science2 citationsOpen Access

Bacteria and Fungi Synergistically Reprogram Flavonoid Metabolites in the Pericarp of Citrus Reticulata 'Chachi' During Storage

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JSJianmu SuSZSisheng ZhangLLLidi Liang

Key Points

  • This research aims to explore how microbes influence the flavonoid profile of Citrus reticulata during long-term storage.
  • Employed targeted metabolomics to analyze flavonoid profiles
  • Used microbial amplicon sequencing to characterize bacterial and fungal communities
  • Conducted solid-state and liquid-state fermentation assays to test microbial effects on flavonoids
  • Performed correlation analysis to connect microbial presence with flavonoid accumulation
  • Bacillus subtilis N18-1 increased specific polymethoxyflavones, while Aspergillus tubingensis P21-1 decreased them
  • During fermentation, A. tubingensis converted nobiletin into 3'-demethylnobiletin, which B. subtilis then converted to tangeretin
  • Identified candidate genes responsible for these conversions through genome sequencing and molecular docking

Abstract

ABSTRACT The mature pericarp of Citrus reticulata ' Chachi ' (PCRC) is a traditional Chinese medicine known for its enhanced efficacy through long‐term storage and processing. However, the specific mechanisms underlying these enhancements remain unclear. This study employed widely targeted metabolomics, microbial amplicon sequencing, and fermentation assays to investigate the microbiome 's influence on PCRC 's flavonoid profile over 0–19 years of storage. Correlation analysis revealed that the accumulation of polymethoxyflavones (PMFs) was closely linked to specific bacterial and fungal communities. Solid‐state fermentation showed that Bacillus subtilis N18‐1 enhanced the content of certain PMFs, while Aspergillus tubingensis P21‐1 reduced them. Liquid‐state assays confirmed that A. tubingensis P21‐1 converted nobiletin to 3 ' ‐demethylnobiletin, and B . subtilis N18‐1 further converted this to tangeretin. Combined with genome sequencing and molecular docking, four candidate genes were identified. The catalytic activity verification assays demonstrated that At21‐68 and At21‐21 catalyze the conversion of nobiletin to 3 '‐demethylnobiletin, while Bs18‐51 and Bs18‐84 catalyze the conversion of 3 ' ‐demethylnobiletin to tangeretin. These findings highlight the synergistic molecular mechanism by which microorganisms modulate PMFs during PCRC aging, providing insights for optimizing medicinal plant aging through microbial biotransformation.

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Cite This Study

Su et al. (2026) studied this question.

synapsesocial.com/papers/698c1cd3267fb587c655f84ehttps://doi.org/10.1002/advs.202500267
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