Abstract

Sesquiterpenoids are important secondary metabolites with various pharma- and nutraceutical properties. In particular, higher basidiomycetes possess a versatile biosynthetic repertoire for these bioactive compounds. To date, only a few microbial production systems for fungal sesquiterpenoids have been established. Here, we introduce Ustilago maydis as a novel production host. This model fungus is a close relative of higher basidiomycetes. It offers the advantage of metabolic compatibility and potential tolerance for substances toxic to other microorganisms. We successfully implemented a heterologous pathway to produce the carotenoid lycopene that served as a straightforward read-out for precursor pathway engineering. Overexpressing genes encoding enzymes of the mevalonate pathway resulted in increased lycopene levels. Verifying the subcellular localization of the relevant enzymes revealed that initial metabolic reactions might take place in peroxisomes: despite the absence of a canonical peroxisomal targeting sequence, acetyl-CoA C-acetyltransferase Aat1 localized to peroxisomes. By expressing the plant (+)-valencene synthase CnVS and the basidiomycete sesquiterpenoid synthase Cop6, we succeeded in producing (+)-valencene and α-cuprenene, respectively. Importantly, the fungal compound yielded about tenfold higher titers in comparison to the plant substance. This proof of principle demonstrates that U. maydis can serve as promising novel chassis for the production of terpenoids.

Highlights

  • Terpenoids constitute an important class of secondary metabolites found mainly in plants and fungi

  • We used the detailed knowledge on S. cerevisiae, H. sapiens, and A. thaliana as a blueprint (Figure 1, Table 1, and Supplementary Figure S1; Nielsen and Keasling, 2016; Ye et al, 2016)

  • Loss of retinal biosynthesis does not affect the growth of cells and currently, no light-regulated biological function could be assigned to retinal-dependent opsins (Estrada et al, 2009)

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Summary

Introduction

Terpenoids (isoprenoids) constitute an important class of secondary metabolites found mainly in plants and fungi They are classified according to the number of C5 scaffold isopentenyl diphosphate (IPP) building blocks. Terpenoids exhibit a plethora of biological functions like photoprotection, hormone signaling and defense against pathogens (Schmidt-Dannert, 2015; Moser and Pichler, 2019; Troost et al, 2019). Because of these diverse bioactivities they are of interest for biotechnology. The latter serves as precursor for the synthesis of the highly valuable aromatic substance nootkatone (Schempp et al, 2018; Moser and Pichler, 2019)

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