Precursor-directed biosynthesis of 5-hydroxytryptophan using metabolically engineered E. coli

ACS Synth Biol. 2015 May 15;4(5):554-8. doi: 10.1021/sb500303q. Epub 2014 Oct 10.

Abstract

A novel biosynthetic pathway was designed and verified reversely leading to the production of 5-hydroxytryptophan (5-HTP) from glucose. This pathway takes advantage of the relaxed substrate selectivities of relevant enzymes without employing the unstable tryptophan 5-hydroxylase. First, high-titer of 5-HTP was produced from 5-hydroxyanthranilate (5-HI) by the catalysis of E. coli TrpDCBA. Then, a novel salicylate 5-hydroxylase was used to convert the non-natural substrate anthranilate to 5-HI. After that, the production of 5-HI from glucose was achieved and optimized with modular optimization. In the end, we combined the full pathway and adopted a two-stage strategy to realize the de novo production of 5-HTP. This work demonstrated the application of enzyme promiscuity in non-natural pathway design.

Keywords: 5-hydroxyanthranilate; 5-hydroxytryptophan; precursor-directed biosynthesis; salicylate 5-hydroxylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5-Hydroxytryptophan / biosynthesis*
  • 5-Hydroxytryptophan / genetics*
  • Biosynthetic Pathways / genetics*
  • Escherichia coli / genetics*
  • Glucose / genetics
  • Metabolic Engineering / methods
  • Mixed Function Oxygenases / genetics
  • Tryptophan / genetics

Substances

  • Tryptophan
  • 5-Hydroxytryptophan
  • Mixed Function Oxygenases
  • salicylic acid 5-hydroxylase
  • Glucose