Metabolic engineering of Escherichia coli for the synthesis of polyhydroxyalkanoates using acetate as a main carbon source

Microb Cell Fact. 2018 Jul 3;17(1):102. doi: 10.1186/s12934-018-0949-0.

Abstract

Background: High production cost of bioplastics polyhydroxyalkanoates (PHA) is a major obstacle to replace traditional petro-based plastics. To address the challenges, strategies towards upstream metabolic engineering and downstream fermentation optimizations have been continuously pursued. Given that the feedstocks especially carbon sources account up to a large portion of the production cost, it is of great importance to explore low cost substrates to manufacture PHA economically.

Results: Escherichia coli was metabolically engineered to synthesize poly-3-hydroxybutyrate (P3HB), poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P3HB4HB), and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) using acetate as a main carbon source. Overexpression of phosphotransacetylase/acetate kinase pathway was shown to be an effective strategy for improving acetate assimilation and biopolymer production. The recombinant strain overexpressing phosphotransacetylase/acetate kinase and P3HB synthesis operon produced 1.27 g/L P3HB when grown on minimal medium supplemented with 10 g/L yeast extract and 5 g/L acetate in shake flask cultures. Further introduction succinate semialdehyde dehydrogenase, 4-hydroxybutyrate dehydrogenase, and CoA transferase lead to the accumulation of P3HB4HB, reaching a titer of 1.71 g/L with a 4-hydroxybutyrate monomer content of 5.79 mol%. When 1 g/L of α-ketoglutarate or citrate was added to the medium, P3HB4HB titer increased to 1.99 and 2.15 g/L, respectively. To achieve PHBV synthesis, acetate and propionate were simultaneously supplied and propionyl-CoA transferase was overexpressed to provide 3-hydroxyvalerate precursor. The resulting strain produced 0.33 g/L PHBV with a 3-hydroxyvalerate monomer content of 6.58 mol%. Further overexpression of propionate permease improved PHBV titer and 3-hydroxyvalerate monomer content to 1.09 g/L and 10.37 mol%, respectively.

Conclusions: The application of acetate as carbon source for microbial fermentation could reduce the consumption of food and agro-based renewable bioresources for biorefineries. Our proposed metabolic engineering strategies illustrate the feasibility for producing polyhydroxyalkanoates using acetate as a main carbon source. Overall, as an abundant and renewable resource, acetate would be developed into a cost-effective feedstock to achieve low cost production of chemicals, materials, and biofuels.

Keywords: Acetate; Escherichia coli; Poly(3-hydroxybutyrate-co-3-hydroxyvalerate); Poly(3-hydroxybutyrate-co-4-hydroxybutyrate); Poly-3-hydroxybutyrate.

MeSH terms

  • 3-Hydroxybutyric Acid / biosynthesis
  • Acetate Kinase / genetics
  • Acetates / metabolism*
  • Batch Cell Culture Techniques
  • Biopolymers / biosynthesis
  • Carbon / metabolism
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Fermentation
  • Metabolic Engineering*
  • Phosphate Acetyltransferase / genetics
  • Plastics
  • Polyhydroxyalkanoates / biosynthesis*

Substances

  • Acetates
  • Biopolymers
  • Plastics
  • Polyhydroxyalkanoates
  • Carbon
  • Phosphate Acetyltransferase
  • Acetate Kinase
  • 3-Hydroxybutyric Acid