Production of squalene by squalene synthases and their truncated mutants in Escherichia coli

J Biosci Bioeng. 2015 Feb;119(2):165-71. doi: 10.1016/j.jbiosc.2014.07.013. Epub 2014 Oct 2.

Abstract

Squalene is a precursor of thousands of bioactive triterpenoids and also has industrial value as a lubricant, health-promoting agent, and/or drop-in biofuel. To establish an efficient Escherichia coli-based system for squalene production, we tested two different squalene synthases and their mutants in combination with precursor pathways. By co-expressing a chimeric mevalonate pathway with human or Thermosynechococcus squalene synthase, E. coli accumulated squalene up to 230 mg/L or 55 mg/g-DCW in flask culture. We also determined that a significant truncation of squalene synthase at the C-terminus retains partial cellular activity. The squalene-producing strain described herein represents a convenient platform for gene discovery and the construction of the pathway toward natural and non-natural hopanoids/steroids.

Keywords: Bacterial production; Carotenoid; Mevalonate pathway; Squalene synthase; Triterpenoid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Cyanobacteria / enzymology
  • Cyanobacteria / genetics
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Farnesyl-Diphosphate Farnesyltransferase / chemistry
  • Farnesyl-Diphosphate Farnesyltransferase / genetics*
  • Farnesyl-Diphosphate Farnesyltransferase / metabolism*
  • Humans
  • Mevalonic Acid / metabolism
  • Mutant Proteins / chemistry*
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism*
  • Mutation / genetics*
  • Squalene / metabolism*
  • Temperature

Substances

  • Mutant Proteins
  • Squalene
  • Farnesyl-Diphosphate Farnesyltransferase
  • Mevalonic Acid