open access publication

Article, 2024

First-class – biosynthesis of 6-MSA and bostrycoidin type I polyketides in Yarrowia lipolytica

Frontiers in Fungal Biology, ISSN 2673-6128, Volume 5, Page 1327777, 10.3389/ffunb.2024.1327777

Contributors

Bejenari, Mihaela (Corresponding author) [1] Spedtsberg, Eva Mie Lang [1] Mathiesen, Julie [1] Jeppesen, Alexandra Claire [1] Cernat, Lucia [1] Toussaint, Aouregane [2] Apostol, Cristina [1] Stoianov, Victor [1] Pedersen, Tobias Bruun 0000-0002-8166-9704 [1] Nielsen, Mikkel Rank 0000-0003-2408-9444 [1] Sørensen, Jens Laurids 0000-0002-2392-5343 (Corresponding author) [1]

Affiliations

  1. [1] Aalborg University
  2. [NORA names: AAU Aalborg University; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Laboratoire Physiologie Cellulaire & Végétale
  4. [NORA names: France; Europe, EU; OECD]

Abstract

Fungal polyketides are a large group of secondary metabolites, valuable due to their diverse spectrum of pharmacological activities. Polyketide biosynthesis in filamentous fungi presents some challenges: small yield and low-purity titers. To tackle these issues, we switched to the yeast Yarrowia lipolytica, an easily cultivable heterologous host. As an oleaginous yeast, Y. lipolytica displays a high flux of acetyl- and malonyl-CoA precursors used in lipid synthesis. Likewise, acetyl- and malonyl-CoA are the building blocks of many natural polyketides, and we explored the possibility of redirecting this flux toward polyketide production. Despite its promising prospect, Y. lipolytica has so far only been used for heterologous expression of simple type III polyketide synthases (PKSs) from plants. Therefore, we decided to evaluate the potential of Y. lipolytica by targeting the more complex fungal polyketides synthesized by type I PKSs. We employed a CRISPR-Cas9-mediated genome editing method to achieve markerless gene integration of the genes responsible for bostrycoidin biosynthesis in Fusarium solani (fsr1, fsr2, and fsr3) and 6-methylsalicylic acid (6-MSA) biosynthesis in Aspergillus hancockii (6MSAS). Moreover, we attempted titer optimization through metabolic engineering by overexpressing two enzymes, TGL4 and AOX2, involved in lipid β-oxidation, but we did not observe an effect on polyketide production. With maximum titers of 403 mg/L 6-MSA and 35 mg/L bostrycoidin, the latter being substantially higher than our previous results in Saccharomyces cerevisiae (2.2 mg/L), this work demonstrates the potential of Y. lipolytica as a platform for heterologous production of complex fungal polyketides.

Keywords

AOX2, Aspergillus, B oxidation, Fusarium, Fusarium solani, Saccharomyces cerevisiae</i> , Tgl4, Yarrowia lipolytica, acetylation, acid, activity, biosynthesis, block, building, building blocks, diverse spectrum, editing methods, effect, engineering, enzyme, filamentous fungi, flux, fungal polyketides, fungi, gene integration, genes, genome editing methods, group, group of secondary metabolites, heterologous expression, heterologous host, heterologous production, host, integration, issues, lipid, lipid synthesis, malonyl-CoA, malonyl-CoA precursors, maximum titer, metabolic engineering, metabolites, method, natural polyketides, oleaginous yeasts, optimization, pharmacological activities, plants, platform, polyketide, polyketide biosynthesis, polyketide products, polyketide synthase, potential, precursor, production, results, secondary metabolites, small yields, solani, spectrum of pharmacological activities, synthase, synthesis, titers, type, type I PKSs, type I polyketide, type III polyketide synthase, yeast, yield

Funders

  • Novo Nordisk Foundation

Data Provider: Digital Science