Microbial synthesis of m-tyrosine via whole-cell biocatalysis

Enzyme Microb Technol. 2025 Apr:185:110590. doi: 10.1016/j.enzmictec.2025.110590. Epub 2025 Jan 22.

Abstract

Meta-tyrosine (m-tyrosine), a nonproteinogenic amino acid, has shown significant potential for applications as an herbicide in agriculture and for various medical uses. However, the natural abundance of m-tyrosine is very low, limiting its widespread use. In this study, we successfully achieved microbial production of m-tyrosine by establishing the in vivo enzyme activity of phenylalanine 3-hydroxylase (PacX from Streptomyces coeruleoribudus) in E. coli, which catalyzes the meta-hydroxylation of phenylalanine to produce m-tyrosine. Remarkably, PacX is capable of utilizing the native E. coli cofactor tetrahydromonapterin (MH4) for its hydroxylation activity. The integration of a non-native MH4 regeneration system significantly improved the bioconversion efficiency, resulting in the accumulation of m-tyrosine at a concentration of up to 368 mg/L. Additionally, we attempted to modify a well-characterized phenylalanine 4-hydroxylase (P4H) from Xanthomonas campestris to alter its regioselectivity through protein engineering. Remarkably, a double mutant (F184C/G199T) successfully shifted the enzyme's hydroxylation specificity from the para- to the meta-position, demonstrating the feasibility of altering the regioselectivity of aromatic amino acid hydroxylases (AAAHs). To the best of our knowledge, this is the first report of microbial production of m-tyrosine through whole-cell biocatalysis.

Keywords: Bioconversion; Microbial Production; Phenylalanine hydroxylase; Protein Engineering; m-Tyrosine.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Biocatalysis*
  • Escherichia coli* / genetics
  • Escherichia coli* / metabolism
  • Hydroxylation
  • Phenylalanine / metabolism
  • Protein Engineering
  • Streptomyces* / enzymology
  • Streptomyces* / genetics
  • Streptomyces* / metabolism
  • Substrate Specificity
  • Tyrosine* / metabolism
  • Xanthomonas campestris / enzymology
  • Xanthomonas campestris / genetics
  • Xanthomonas campestris / metabolism

Substances

  • Tyrosine
  • 3-tyrosine
  • Bacterial Proteins
  • Phenylalanine