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De novo biosynthesis of Asperosaponin VI in <i>Saccharomyces cerevisiae</i>.


ABSTRACT: Asperosaponin VI (ASA VI), the primary bioactive triterpenoid saponin marker of Dipsacus asper Wall. (Chinese Pharmacopoeia 2020), possesses significant neuroprotective, anti-inflammatory, and osteogenic activities. However, its low natural abundance limits large-scale production. In this study, we reported the first complete biosynthetic reconstruction of ASA VI in Saccharomyces cerevisiae using a modular synthetic biology strategy. The pathway included in situ UDP-arabinose (UDP-Ara) biosynthesis via heterologous expression of AtUGDH3, GuUXS2, and GuUXE1; triterpenoid scaffold generation through ERG9, ERG1, CqBAS1, and CqCYP716A78 for oleanolic acid (OA) production; and downstream modifications including C-23 hydroxylation by multicopy-expressed CaCYP714E19, stepwise glucosylation at C-28 by CaUGT73AD1 and CaUGT73C8, and C-3 arabinosylation by AsUGT99D1 to yield ASA VI. LC-MS analysis confirmed ASA VI biosynthesis and the accumulation of key intermediates (OA, HED, HED-28-Glc, and HED-28-Glc-Glc). Although production remained at trace levels (395 ng/L), pathway analysis suggested that the downstream glycosylation steps and UDP-Ara supply could be the major rate-limiting factors. This work established a microbial chassis for the sustainable synthesis of ASA VI and related arabinosylated saponins.

SUBMITTER: Hao L 

PROVIDER: S-EPMC12423682 | biostudies-literature | 2025 Dec

REPOSITORIES: biostudies-literature

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De novo biosynthesis of Asperosaponin VI in &lt;i&gt;Saccharomyces cerevisiae&lt;/i&gt;.

Hao Lin L   Dong Guiru G   Sun Tianzhen T   Liu Jingyan J   Wu Hui H   Li Fahui F   Song Weiguo W   Luo Xiaozhou X   Zhang Jian J   Qiao Yanan Y  

Synthetic and systems biotechnology 20250819 4


Asperosaponin VI (ASA VI), the primary bioactive triterpenoid saponin marker of <i>Dipsacus asper</i> Wall. (Chinese Pharmacopoeia 2020), possesses significant neuroprotective, anti-inflammatory, and osteogenic activities. However, its low natural abundance limits large-scale production. In this study, we reported the first complete biosynthetic reconstruction of ASA VI in <i>Saccharomyces cerevisiae</i> using a modular synthetic biology strategy. The pathway included in situ UDP-arabinose (UDP-  ...[more]

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