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Li-dan Ye

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Review Open access Sep 2026

Genome-wide analysis of TPS family reveals kaurene synthase-like genes in Isodon rubescens f. lushanensis

Isodon rubescens f. lushanensis, a typical form of I. rubescens , is characterized by its natural deficiency in oridonin and the presence of a unique ent-kaurane diterpenoid, lushanrubescensin. To elucidate the molecular basis underlying the distinct chemical profiles between I. rubescens f. lushanensis and I. rubescens (Hemsl.) Hara, we conducted a comprehensive analysis utilizing high-quality genomic and transcriptomic data of I. rubescens f. lushanensis. Through a genome-wide survey, our study identified 83 terpene synthase ( TPS ) genes, including 13 TPS -C and 9 TPS-e /f subfamily genes, which are implicated in diterpenoid biosynthesis. By integrating conserved motif analysis, differential expression profiling (FPKM), and RT-qPCR validation, we successfully screened key candidate genes. Subsequent heterologous expression in Saccharomyces cerevisiae enabled the functional characterization of five diterpene synthase genes, specifically CPS and KSL enzymes, involved in the central modules of diterpenoid synthesis. These findings not only expand the repertoire of known biosynthetic genes in I. rubescens but also offer valuable insights into the divergent biosynthetic pathways of oridonin and lushanrubescensin, paving the way for future metabolic engineering and synthetic biology studies.

Hao Yang, Jin-Lu Liu, Conglong Lian et al. · 0 citations
Jul 2026

Metabolic Engineering of Yarrowia lipolytica for High-Level de novo Biosynthesis of Xylitol from Glucose.

Xylitol is a highly functional sweetener with extensive applications. Sustainable biosynthesis from glucose is desirable yet metabolically challenging. Here, we engineered Yarrowia lipolytica as a cell factory by constructing a core biosynthetic route via combinatorial screening and multicopy integration of d-arabitol dehydrogenases (ArDH) and an NADPH-dependent xylitol dehydrogenase (XDH) in the robust chassis NBRC1631. To further drive the metabolic flux and alleviate bottlenecks, we employed a synergistic push-and-pull strategy: overexpressing glucose transporters (YH3 and YH4), while upregulating pentose phosphate pathway enzymes (ZWF1 and GND1) to enhance NADPH regeneration, matching the redox demand of the synthetic cascade. Following two-stage pH-controlled fed-batch fermentation in a 3 L bioreactor, the final engineered strain achieved a record-high xylitol titer of 39.0 g/L with a yield of 0.09 g/g glucose. This study establishes a productive platform for microbial de novo xylitol biosynthesis from glucose, offering a green and economically viable route for industrial production.

Bingbing Liu, Xi Yao, Jianping Lin et al. · 0 citations

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