Adaptive laboratory evolution of native methanol assimilation in Saccharomyces cerevisiae

Nat Commun. 2020 Nov 4;11(1):5564. doi: 10.1038/s41467-020-19390-9.

Abstract

Utilising one-carbon substrates such as carbon dioxide, methane, and methanol is vital to address the current climate crisis. Methylotrophic metabolism enables growth and energy generation from methanol, providing an alternative to sugar fermentation. Saccharomyces cerevisiae is an important industrial microorganism for which growth on one-carbon substrates would be relevant. However, its ability to metabolize methanol has been poorly characterised. Here, using adaptive laboratory evolution and 13C-tracer analysis, we discover that S. cerevisiae has a native capacity for methylotrophy. A systems biology approach reveals that global rearrangements in central carbon metabolism fluxes, gene expression changes, and a truncation of the uncharacterized transcriptional regulator Ygr067cp supports improved methylotrophy in laboratory evolved S. cerevisiae. This research paves the way for further biotechnological development and fundamental understanding of methylotrophy in the preeminent eukaryotic model organism and industrial workhorse, S. cerevisiae.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Alcohol Dehydrogenase / genetics
  • Alcohol Dehydrogenase / metabolism
  • Carbon Isotopes
  • Directed Molecular Evolution / methods*
  • Fermentation / genetics*
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / metabolism
  • Industrial Microbiology / methods*
  • Mass Spectrometry
  • Metabolic Engineering
  • Metabolomics
  • Methanol / metabolism*
  • Proteome / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Systems Biology / methods*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcriptome / genetics
  • Whole Genome Sequencing

Substances

  • ASC1 protein, S cerevisiae
  • Adaptor Proteins, Signal Transducing
  • Carbon Isotopes
  • Proteome
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • ADH2 protein, S cerevisiae
  • Alcohol Dehydrogenase
  • GTP-Binding Proteins
  • Methanol