bioRxivMolecular BiologyPreprint
Mining Yeast Diversity Unveils Novel Targets for Improved Heterologous Laccase Production in Saccharomyces cerevisiae
Ryan Wei Kwan WongiD, Marissa FooiD, Jasmine R. S. Lay, Tiffany L. T. Wai, Jackson MooreiD, Fabien DutreuxiD, Cristen M. MolzahniD, Corey NislowiD, Vivien MeasdayiD, Joseph SchachereriD, Thibault MayoriD
Abstract
The budding yeast Saccharomyces cerevisiae is a widely utilized host cell for recombinant protein production due to its well studied and annotated genome, its ability to secrete large and post-translationally modified proteins, fast growth and cost-effective culturing. However, recombinant protein yields from S. cerevisiae often fall behind that of other host systems. To address this, we developed a high throughput screen of wild, industrial and laboratory S. cerevisiae isolates to identify strains with a natural propensity for greater recombinant protein production, specifically focussing on laccase multicopper oxidases from the fungi Trametes trogii and Myceliophthora thermophila. Using this method, we identified 20 non-laboratory strains with higher capacity to produce active laccase. Interestingly, lower levels of laccase mRNA were measured in most cases, indicating that the drivers of elevated protein production capacity lie beyond the regulation of recombinant gene expression. We characterized the identified strains using complementary genomic and proteomic approaches to reveal several potential pathways driving the improved expression phenotype. Gene ontology analysis suggests broad changes in cellular metabolism, specifically in genes/proteins involved in carbohydrate catabolism, thiamine biosynthesis, transmembrane transport and vacuolar degradation. Targeted deletions of the hexose transporter HXT11 and the Coat protein complex II interacting paralogs PRM8 and 9, involved in ER to Golgi transport, resulted in significantly improved laccase production from the S288C laboratory strain. Whereas the deletion of the Hsp110 SSE1 gene, guided by our proteomic analysis, also led to higher laccase activity, we did not observe major changes of the protein homeostasis network within the strains with higher laccase activity. This study opens new avenues to leverage the vast diversity of Saccharomyces cerevisiae for recombinant protein production, as well as offers new strategies and insights to enhance recombinant protein yields of current strains.
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Genome-wide screen identifies new set of genes for improved heterologous laccase expression in Saccharomyces cerevisiae
- Recombinant Laccase Production Causes Alterations of the S. cerevisiae Proteome that are Dependent on the Strain Origins
Ryan Wei Kwan Wong, Sahil Chandhok, … Thibault Mayor·bioRxiv·Dec 23, 2025
- Deletion of two genes improves heterologous secretion of fungal lignin-degrading heme peroxidases in S. cerevisiae
N. A. Khlystov·bioRxiv·Nov 27, 2021
- CRISPRi screens reveal genes modulating yeast growth in lignocellulose hydrolysate
F. Gutmann, C. Jann, … K. R. Patil·bioRxiv·Sep 17, 2020
- Genome scale modeling of the protein secretory pathway reveals novel targets for improved recombinant protein production in yeast
Feiran Li, Yu Chen, … Jens Nielsen·Nature CommunicationsPeer-reviewed·May 27, 2022
- Hemicellulose Degradation and Utilization by a Synthetic Saccharomyces cerevisiae Consortium
Ian Dominic F. Tabañag, Shen-Long Tsai·bioRxiv·Jan 7, 2018