Relationship of trehalose accumulation with ethanol fermentation in industrial Saccharomyces cerevisiae yeast strains

Bioresour Technol. 2014:152:371-6. doi: 10.1016/j.biortech.2013.11.033. Epub 2013 Nov 21.

Abstract

The protective effect and the mechanisms of trehalose accumulation in industrial Saccharomyces cerevisiae strains were investigated during ethanol fermentation. The engineered strains with more intercellular trehalose achieved significantly higher fermentation rates and ethanol yields than their wild strain ZS during very high gravity (VHG) fermentation, while their performances were not different during regular fermentation. The VHG fermentation performances of these strains were consistent with their growth capacity under osmotic stress and ethanol stress, the key stress factors during VHG fermentation. These results suggest that trehalose accumulation is more important for VHG fermentation of industrial yeast strains than regular one. The differences in membrane integrity and antioxidative capacity of these strains indicated the possible mechanisms of trehalose as a protectant under VHG condition. Therefore, trehalose metabolic engineering may be a useful strategy for improving the VHG fermentation performance of industrial yeast strains.

Keywords: Ethanol; Osmotic stress; Saccharomyces cerevisiae; Trehalose; Very high gravity fermentation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / metabolism
  • Catalase / metabolism
  • Cell Membrane / metabolism
  • Ethanol / metabolism*
  • Fermentation*
  • Gene Deletion
  • Industrial Microbiology*
  • Intracellular Space / metabolism
  • Metabolic Engineering
  • Microbial Viability
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Stress, Physiological
  • Superoxide Dismutase / metabolism
  • Trehalose / metabolism*

Substances

  • Antioxidants
  • Saccharomyces cerevisiae Proteins
  • Ethanol
  • Trehalose
  • Catalase
  • Superoxide Dismutase