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Jian-Hua Ju

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Sep 2026

Identification of Cembrene Synthases Uncovers Polyphyletic Origins of 14-Membered Carbocyclic Cembranoids Biosynthesis in Corals

Genome mining is an efficient strategy for natural product discovery, yet its application to terpene synthases frequently results in the repeated identification of identical products. Cembranoids, a class of coral-derived natural products featuring 14-membered carbocyclic scaffolds, present formidable challenges for chemical synthesis. To date, only two biosynthetic precursors have been synthesized across fifteen coral enzymes from six independent studies. To address these limitations, we developed Ariadne, an integrated platform for genome-wide targeted mining of terpene synthases from corals. Using this platform, we identified five cembrene synthases, including two with high sequence similarity to known cembrene B synthases and three low-similarity enzymes experimentally validated through heterologous expression in yeast, achieving a prediction accuracy of 80% from ninety terpene synthase homologs. Leveraging the rapid identification of novel cembrene synthases, phylogenetic analysis further uncovered the evolutionary trajectory of this enzyme family from coral, providing valuable guidance for the engineering of an early-diverging enzyme, which is capable of synthesizing an unreported cembrene scaffold by the coral enzyme. Collectively, this work establishes a new paradigm for terpene synthase discovery and substantially advances the genome mining in marine animals as well as the combinatorial biosynthesis of marine-derived natural products.

Yin-Hao Wang, Meng-Meng Yu, Zhao-Rui Jiang et al. · 0 citations
Sep 2026

An Enzyme from a Single P450 Monooxygenase Clade Orchestrates Six‑Electron Oxidation for Cyclopeptide Modification

The oxidative modification of complex natural products is critical for their biological activity. However, the enzymatic mechanisms that facilitate three-step, six-electron transfer reactions, such as the conversion of a methyl group to a carboxylic acid, on cyclopeptide scaffolds remain poorly understood. This study characterizes IlaL, a cytochrome P450 monooxygenase from Streptomyces atratus, which catalyzes a six‑electron methyl‑to‑carboxylic acid conversion during the biosynthesis of the potent antimycobacterial cyclopeptide ilamycins. IlaL possesses a noncanonical “Asp-Asn (DN)” dioxygen activation dyad and an extended, flexible BC-loop, which together enable sequential three-step oxidation. The high-resolution co-crystal structure of IlaL bound to the substrate ilamycin B2 reveals an enlarged cavity and dynamic gating conferring precise regioselectivity and broad substrate tolerance. Biochemical and phylogenetic analyses confirm the essential role of the DN dyad and show that DN‑type cytochrome P450 monooxygenases occupy a distinct, recently emerged phylogenetic clade. These findings provide structural and mechanistic insights into six‑electron oxidative modification and establish design principles for versatile biocatalysts enabling late‑stage natural product diversification.

Ming Peng, Qiao-Ling Wu, Ying-Ying Chen et al. · 0 citations

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