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March 15, 2026ACS Synthetic Biology3 citations

Reprogramming Carbon Partition for Salidroside Overproduction in Saccharomyces cerevisiae

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JLJian LiTianjin UniversityHLHonghao LiTianjin UniversityXDX DaiTianjin University

Key Points

  • The study aims to enhance salidroside production in Saccharomyces cerevisiae by addressing competition for UDP-glucose between cell wall construction and glycoside synthesis.
  • Constructed a high-yielding microbial cell factory through systematic metabolic engineering.
  • Rewired central metabolism with a thiamine diphosphate regeneration strategy to increase tyrosol production.
  • Introduced glycosyltransferase RrU8GT33 to convert tyrosol into salidroside.
  • Enhanced UDP-glucose availability by overexpressing UGP1 and PGM1.
  • Implemented cell wall engineering to redirect carbon flux from biomass to salidroside synthesis.
  • Achieved a salidroside titer of 40.46 g/L in bioreactor fermentation.
  • Reported a productivity of 0.24 g/(L h) and a yield of 0.27 g/g glucose.
  • Demonstrated successful decoupling of growth pressure from salidroside synthesis demand.

Abstract

Salidroside, a valuable plant-derived glycoside, holds great promise for nutraceutical and pharmaceutical applications. Although microbial biosynthesis has been established, further enhancement of its production faces a universal bottleneck in glycoside synthesis: the competition for the glycosyl donor UDP-glucose (UDPG) between essential cell wall construction and target product formation. To overcome this fundamental conflict, we constructed a high-yielding microbial cell factory through a systematic engineering strategy. We first rewired central metabolism via a thiamine diphosphate (ThDP) regeneration strategy to secure a high-level production of the precursor tyrosol. Subsequently, the introduction of a glycosyltransferase RrU8GT33 from Rhodiola rosea enabled the conversion of tyrosol to salidroside. To address the key limitation, we enhanced UDP-glucose availability by overexpressing UDP-glucose pyrophosphorylase (UGP1) and phosphoglucose mutase (PGM1), and most critically implemented cell wall engineering to dynamically redirect carbon flux from biomass synthesis toward salidroside production by regulating β-1,3-glucan synthase (FKS1) expression. This approach effectively decouples growth pressure from the synthesis demand. Subsequent engineering steps alleviated physiological constraints, yielding a robust production host. In a bioreactor fermentation, the final strain achieved a record-breaking salidroside titer of 40.46 g/L, with a productivity of 0.24 g/(L h) and a yield of 0.27 g/g glucose. This work demonstrates the efficacy of cofactor and cell wall engineering in optimizing glycoside production and provides a scalable strategy for the microbial manufacturing of high-value natural glycosides.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69b64d48b42794e3e660e0c6https://doi.org/10.1021/acssynbio.5c00805
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