Abstract

The ability of the yeast Saccharomyces cerevisiae to convert glucose, even in the presence of oxygen, via glycolysis and the fermentative pathway to ethanol has played an important role in its domestication. Despite the extensive knowledge on these pathways in S. cerevisiae, relatively little is known about their genetic makeup in other industrially relevant Saccharomyces yeast species. In this study we explore the diversity of the glycolytic and fermentative pathways within the Saccharomyces genus using S. cerevisiae, Saccharomyces kudriavzevii, and Saccharomyces eubayanus as paradigms. Sequencing data revealed a highly conserved genetic makeup of the glycolytic and fermentative pathways in the three species in terms of number of paralogous genes. Although promoter regions were less conserved between the three species as compared to coding sequences, binding sites for Rap1, Gcr1 and Abf1, main transcriptional regulators of glycolytic and fermentative genes, were highly conserved. Transcriptome profiling of these three strains grown in aerobic batch cultivation in chemically defined medium with glucose as carbon source, revealed a remarkably similar expression of the glycolytic and fermentative genes across species, and the conserved classification of genes into major and minor paralogs. Furthermore, transplantation of the promoters of major paralogs of S. kudriavzevii and S. eubayanus into S. cerevisiae demonstrated not only the transferability of these promoters, but also the similarity of their strength and response to various environmental stimuli. The relatively low homology of S. kudriavzevii and S. eubayanus promoters to their S. cerevisiae relatives makes them very attractive alternatives for strain construction in S. cerevisiae, thereby expanding the S. cerevisiae molecular toolbox.

Highlights

  • The yeast Saccharomyces cerevisiae is known for its fast fermentative metabolism, which has played an important role in its domestication (Sicard and Legras, 2011)

  • The genetic makeup of pathways involved in central carbon metabolism in S. cerevisiae has already been well characterized, and more for glycolysis and alcoholic fermentation

  • S. cerevisiae’s high genetic redundancy and the locations of the genes were fully mirrored in S. kudriavzevii and S. eubayanus genomes (Figure 1)

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Summary

Introduction

The yeast Saccharomyces cerevisiae is known for its fast fermentative metabolism, which has played an important role in its domestication (Sicard and Legras, 2011). To sustain the energy demand for growth and maintenance despite the low ATP yield of alcoholic fermentation (2 moles of ATP per glucose molecule), the glycolytic flux in S. cerevisiae can reach fluxes of 20–25 mmoles ethanol per gram dry weight per hour (SolisEscalante et al, 2015). This high activity of the glycolytic pathway is reflected in the remarkably high concentration of glycolytic enzymes in the cell, which can represent up to 30% of the total amount of soluble protein (Fraenkel, 2003; Carroll et al, 2011)

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