Evaluation of Brachypodium distachyon L-Tyrosine Decarboxylase Using L-Tyrosine Over-Producing Saccharomyces cerevisiae

PLoS One. 2015 May 21;10(5):e0125488. doi: 10.1371/journal.pone.0125488. eCollection 2015.

Abstract

To demonstrate that herbaceous biomass is a versatile gene resource, we focused on the model plant Brachypodium distachyon, and screened the B. distachyon for homologs of tyrosine decarboxylase (TDC), which is involved in the modification of aromatic compounds. A total of 5 candidate genes were identified in cDNA libraries of B. distachyon and were introduced into Saccharomyces cerevisiae to evaluate TDC expression and tyramine production. It is suggested that two TDCs encoded in the transcripts Bradi2g51120.1 and Bradi2g51170.1 have L-tyrosine decarboxylation activity. Bradi2g51170.1 was introduced into the L-tyrosine over-producing strain of S. cerevisiae that was constructed by the introduction of mutant genes that promote deregulated feedback inhibition. The amount of tyramine produced by the resulting transformant was 6.6-fold higher (approximately 200 mg/L) than the control strain, indicating that B. distachyon TDC effectively converts L-tyrosine to tyramine. Our results suggest that B. distachyon possesses enzymes that are capable of modifying aromatic residues, and that S. cerevisiae is a suitable host for the production of L-tyrosine derivatives.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brachypodium / genetics
  • Brachypodium / metabolism*
  • Cloning, Molecular
  • Gene Expression
  • Genes, Plant
  • Saccharomyces cerevisiae / metabolism*
  • Tyramine / biosynthesis
  • Tyrosine / biosynthesis*
  • Tyrosine Decarboxylase / genetics
  • Tyrosine Decarboxylase / metabolism*

Substances

  • Tyrosine
  • Tyrosine Decarboxylase
  • Tyramine

Grants and funding

The authors were supported by the RIKEN Biomass Engineering Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.