Abstract

Fungal secondary metabolites (FSMs) represent a remarkable array of bioactive compounds, with potential applications as pharmaceuticals, nutraceuticals, and agrochemicals. However, these molecules are typically produced only in limited amounts by their native hosts. The native organisms may also be difficult to cultivate and genetically engineer, and some can produce undesirable toxic side-products. Alternatively, recombinant production of fungal bioactives can be engineered into industrial cell factories, such as aspergilli or yeasts, which are well amenable for large-scale manufacturing in submerged fermentations. In this review, we summarize the development of baker’s yeast Saccharomyces cerevisiae to produce compounds derived from filamentous fungi and mushrooms. These compounds mainly include polyketides, terpenoids, and amino acid derivatives. We also describe how native biosynthetic pathways can be combined or expanded to produce novel derivatives and new-to-nature compounds. We describe some new approaches for cell factory engineering, such as genome-scale engineering, biosensor-based high-throughput screening, and machine learning, and how these tools have been applied for S. cerevisiae strain improvement. Finally, we prospect the challenges and solutions in further development of yeast cell factories to more efficiently produce FSMs.

Highlights

  • We describe some new approaches for cell factory engineering, such as genome-scale engineering, biosensor-based high-throughput screening, and machine learning, and how these tools have been applied for S. cerevisiae strain improvement

  • Its production (252 μg/l) in yeast was achieved in a S. cerevisiae strain expressing genes that encode for trichodiene synthase (FgTRI5) from Fusarium graminearum and cytochrome P450 monooxygenase from Trichoderma harzianum (TaTRI4 and TaTRI11), as well as overexpression of the native tHMGR1 and UPC2-1 enzymes [41]

  • Much progress has been made, challenges still exist in developing yeast as a universal chassis strain for fungal secondary metabolite (FSM)

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Summary

Introduction

Once the pathway genes are functionally expressed, the relevant FSMs are produced from the native yeast primary metabolites, precursors. Zhou et al co-expressed two iterative polyketide synthase (IPKS) genes, Rdc5 and Rdc1 from Pochonia chlamydosporia, in S. cerevisiae strain BJ5464-NpgA, and achieved the production of (R)-monocillin II

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