Efficient aspartic acid production by a psychrophile-based simple biocatalyst

J Ind Microbiol Biotechnol. 2015 Oct;42(10):1319-24. doi: 10.1007/s10295-015-1669-7. Epub 2015 Aug 8.

Abstract

We previously constructed a Psychrophile-based Simple bioCatalyst (PSCat) reaction system, in which psychrophilic metabolic enzymes are inactivated by heat treatment, and used it here to study the conversion of aspartic acid from fumaric acid mediated by the activity of aspartate ammonia-lyase (aspartase). In Escherichia coli, the biosynthesis of aspartic acid competes with that of L-malic acid produced from fumaric acid by fumarase. In this study, E. coli aspartase was expressed in psychrophilic Shewanella livingstonensis Ac10 heat treated at 50 °C for 15 min. The resultant PSCat could convert fumaric acid to aspartic acid without the formation of L-malic acid because of heat inactivation of psychrophilic fumarase activity. Furthermore, alginate-immobilized PSCat produced high yields of aspartic acid and could be re-used nine times. The results of our study suggest that PSCat can be applied in biotechnological production as a new approach to increase the yield of target compounds.

Keywords: Alginate; Aspartic acid; Biomass; Immobilization; Psychrophilic bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspartate Ammonia-Lyase / metabolism
  • Aspartic Acid / biosynthesis*
  • Biocatalysis*
  • Biotechnology / methods
  • Enzyme Stability
  • Equipment Reuse
  • Escherichia coli / enzymology
  • Escherichia coli / metabolism
  • Fumarate Hydratase / metabolism
  • Fumarates / metabolism
  • Hot Temperature
  • Malates / metabolism
  • Shewanella / enzymology
  • Shewanella / genetics
  • Shewanella / metabolism*

Substances

  • Fumarates
  • Malates
  • Aspartic Acid
  • malic acid
  • fumaric acid
  • Fumarate Hydratase
  • Aspartate Ammonia-Lyase