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Main conclusion <p><i>GbF3H</i> acts as a hierarchical switch that suppresses <i>NtFLS1</i> but activates <i>NtFLS2</i>, thereby diverting flavonoid flux away from flavonols and toward isoflavonoids in transgenic tobacco.</p> Abstract <p>Flavanone 3-hydroxylase (F3H) is a key branch-point enzyme in the flavonoid biosynthesis, catalyzing the hydroxylation of naringenin to dihydrokaempferol and thereby directing metabolic flux into distinct flavonoid branches. In this study, we employed an integrated approach combining bioinformatic, molecular characterization, and transgenic techniques to elucidate the function and regulatory role of F3H in <i>Ginkgo biloba</i>. The cloned <i>GbF3H</i> encodes a cytoplasm-localized hydrophobic acidic protein of 369 amino acids, containing the conserved DIOX_N and 2OG-FeII_Oxy domains characteristic of 2-oxoglutarate-dependent dioxygenases. Expression profiling revealed that <i>GbF3H</i> transcripts were most abundant in immature fruits, ovulate strobili, and juvenile leaves, and were significantly modulated by different nitrogen forms and abscisic acid (ABA). Heterologous overexpression of <i>GbF3H</i> in tobacco (<i>Nicotiana tabacum</i> cv. K326) substantially reshaped the flavonoid metabolome, characterized by the pronounced upregulation in isoflavonoids and concomitant downregulation in flavonols. Concurrent transcriptomic analysis demonstrated that <i>GbF3H</i> overexpression suppressed key flavonoid biosynthetic genes (<i>Nt4CL</i>, <i>NtFLS1</i>, and <i>NtUFGT</i>), while differentially regulating <i>NtFLS2</i>, indicating a hierarchical regulatory mechanism governing the flavonoid metabolic network. Collectively, these results establish <i>GbF3H</i> as a central switch of flavonoid metabolic flux partitioning in <i>G. biloba</i>, providing crucial mechanistic insights for understanding the regulation of flavonoid biosynthesis and providing a basis for future metabolic engineering strategies.</p>

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Heterologous expression of Ginkgo biloba flavanone 3-hydroxylase acts as a key metabolic switch partitioning flavonoid metabolic flux in transgenic tobacco

  • 期刊论文

  • 发表日期：

    2026年3月26日

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  • Jing Guo,
  • Xiaoxue Zhang,
  • Xinru Sun,
  • Yaqiong Wu,
  • Yuhua Liu,
  • Pengfei Yu,
  • Guibin Wang

摘要

Main conclusion

GbF3H acts as a hierarchical switch that suppresses NtFLS1 but activates NtFLS2, thereby diverting flavonoid flux away from flavonols and toward isoflavonoids in transgenic tobacco.

Abstract

Flavanone 3-hydroxylase (F3H) is a key branch-point enzyme in the flavonoid biosynthesis, catalyzing the hydroxylation of naringenin to dihydrokaempferol and thereby directing metabolic flux into distinct flavonoid branches. In this study, we employed an integrated approach combining bioinformatic, molecular characterization, and transgenic techniques to elucidate the function and regulatory role of F3H in Ginkgo biloba. The cloned GbF3H encodes a cytoplasm-localized hydrophobic acidic protein of 369 amino acids, containing the conserved DIOX_N and 2OG-FeII_Oxy domains characteristic of 2-oxoglutarate-dependent dioxygenases. Expression profiling revealed that GbF3H transcripts were most abundant in immature fruits, ovulate strobili, and juvenile leaves, and were significantly modulated by different nitrogen forms and abscisic acid (ABA). Heterologous overexpression of GbF3H in tobacco (Nicotiana tabacum cv. K326) substantially reshaped the flavonoid metabolome, characterized by the pronounced upregulation in isoflavonoids and concomitant downregulation in flavonols. Concurrent transcriptomic analysis demonstrated that GbF3H overexpression suppressed key flavonoid biosynthetic genes (Nt4CL, NtFLS1, and NtUFGT), while differentially regulating NtFLS2, indicating a hierarchical regulatory mechanism governing the flavonoid metabolic network. Collectively, these results establish GbF3H as a central switch of flavonoid metabolic flux partitioning in G. biloba, providing crucial mechanistic insights for understanding the regulation of flavonoid biosynthesis and providing a basis for future metabolic engineering strategies.