Metabolic Engineering of Saccharomyces cerevisiae to Improve Glucan Biosynthesis

J Microbiol Biotechnol. 2019 May 28;29(5):758-764. doi: 10.4014/jmb.1812.12049.

Abstract

β-Glucan is a chief structural polymer in the cell wall of yeast. β-Glucan has attracted intensive attention because of its wide applications in health protection and cosmetic areas. In the present study, the β-glucan biosynthesis pathway in S. Cerevisiae was engineered to enhance β-glucan accumulation. A newly identified bacterial β-1, 6-glucan synthase GsmA from Mycoplasma agalactiae was expressed, and increased β-glucan content by 43%. In addition, other pathway enzymes were investigated to direct more metabolic flux towards the building of β-glucan chains. We found that overexpression of Pgm2 (phosphoglucomutase) and Rho1 (a GTPase for activating glucan synthesis) significantly increased β-glucan accumulation. After further optimization of culture conditions, the β-glucan content was increased by 53.1%. This study provides a new approach to enhance β-glucan biosynthesis in Saccharomyces cerevisiae.

Keywords: Saccharomyces cerevisiae; cell resistance; enzyme overexpression; synthase; β-glucan.

MeSH terms

  • Biosynthetic Pathways / genetics*
  • Carbohydrate Metabolism / genetics
  • Cell Wall / chemistry
  • Culture Media / chemistry
  • Glucans / biosynthesis*
  • Glucans / genetics*
  • Glucosyltransferases / genetics
  • Metabolic Engineering / methods*
  • Mycoplasma agalactiae / enzymology
  • Mycoplasma agalactiae / genetics
  • Phosphoglucomutase / metabolism
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism
  • beta-Glucans / metabolism
  • rho GTP-Binding Proteins / metabolism

Substances

  • Culture Media
  • Glucans
  • Saccharomyces cerevisiae Proteins
  • beta-Glucans
  • Glucosyltransferases
  • glucan synthase
  • RHO1 protein, S cerevisiae
  • rho GTP-Binding Proteins
  • Phosphoglucomutase