Improving Industrially Relevant Phenotypic Traits by Engineering Chromosome Copy Number in Saccharomyces pastorianus

Journal Article (2020)
Authors

A.R. de Vries (TU Delft - BT/Industriele Microbiologie)

Ewout Knibbe (TU Delft - BT/Industriele Microbiologie)

Roderick van Roosmalen (Student TU Delft)

Marcel van den Broek (TU Delft - BT/Industriele Microbiologie)

Pilar de la Torre (TU Delft - BT/Industriele Microbiologie)

Stephanie F. O’Herne (Student TU Delft)

Pascal A. Vijverberg (Student TU Delft)

Anissa El Masoudi (Student TU Delft)

N. Brouwers (TU Delft - BT/Industriele Microbiologie)

J.T. Pronk (TU Delft - BT/Biotechnologie)

Jean-Marc Daran (TU Delft - BT/Industriele Microbiologie)

Research Group
BT/Industriele Microbiologie
Copyright
© 2020 A.R. Gorter de Vries, E. Knibbe, Roderick van Roosmalen, M.A. van den Broek, P. de la Torre, Stephanie F. O’Herne, Pascal A. Vijverberg, Anissa el Masoudi, N. Brouwers, J.T. Pronk, J.G. Daran
To reference this document use:
https://doi.org/10.3389/fgene.2020.00518
More Info
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Publication Year
2020
Language
English
Copyright
© 2020 A.R. Gorter de Vries, E. Knibbe, Roderick van Roosmalen, M.A. van den Broek, P. de la Torre, Stephanie F. O’Herne, Pascal A. Vijverberg, Anissa el Masoudi, N. Brouwers, J.T. Pronk, J.G. Daran
Research Group
BT/Industriele Microbiologie
Volume number
11
DOI:
https://doi.org/10.3389/fgene.2020.00518
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Abstract

The lager-brewing yeast Saccharomyces pastorianus is a hybrid between S. cerevisiae and S. eubayanus with an exceptional degree of aneuploidy. While chromosome copy number variation (CCNV) is present in many industrial Saccharomyces strains and has been linked to various industrially-relevant traits, its impact on the brewing performance of S. pastorianus remains elusive. Here we attempt to delete single copies of chromosomes which are relevant for the production of off-flavor compound diacetyl by centromere silencing. However, the engineered strains display CNV of multiple non-targeted chromosomes. We attribute this unintended CCNV to inherent instability and to a mutagenic effect of electroporation and of centromere-silencing. Regardless, the resulting strains displayed large phenotypic diversity. By growing centromere-silenced cells in repeated sequential batches in medium containing 10% ethanol, mutants with increased ethanol tolerance were obtained. By using CCNV mutagenesis by exposure to the mitotic inhibitor MBC, selection in the same set-up yielded even more tolerant mutants that would not classify as genetically modified organisms. These results show that CCNV of alloaneuploid S. pastorianus genomes is highly unstable, and that CCNV mutagenesis can generate broad diversity. Coupled to effective selection or screening, CCNV mutagenesis presents a potent tool for strain improvement.