Recoded organisms engineered to depend on synthetic amino acids

Nature. 2015 Feb 5;518(7537):89-93. doi: 10.1038/nature14095. Epub 2015 Jan 21.

Abstract

Genetically modified organisms (GMOs) are increasingly used in research and industrial systems to produce high-value pharmaceuticals, fuels and chemicals. Genetic isolation and intrinsic biocontainment would provide essential biosafety measures to secure these closed systems and enable safe applications of GMOs in open systems, which include bioremediation and probiotics. Although safeguards have been designed to control cell growth by essential gene regulation, inducible toxin switches and engineered auxotrophies, these approaches are compromised by cross-feeding of essential metabolites, leaked expression of essential genes, or genetic mutations. Here we describe the construction of a series of genomically recoded organisms (GROs) whose growth is restricted by the expression of multiple essential genes that depend on exogenously supplied synthetic amino acids (sAAs). We introduced a Methanocaldococcus jannaschii tRNA:aminoacyl-tRNA synthetase pair into the chromosome of a GRO derived from Escherichia coli that lacks all TAG codons and release factor 1, endowing this organism with the orthogonal translational components to convert TAG into a dedicated sense codon for sAAs. Using multiplex automated genome engineering, we introduced in-frame TAG codons into 22 essential genes, linking their expression to the incorporation of synthetic phenylalanine-derived amino acids. Of the 60 sAA-dependent variants isolated, a notable strain harbouring three TAG codons in conserved functional residues of MurG, DnaA and SerS and containing targeted tRNA deletions maintained robust growth and exhibited undetectable escape frequencies upon culturing ∼10(11) cells on solid media for 7 days or in liquid media for 20 days. This is a significant improvement over existing biocontainment approaches. We constructed synthetic auxotrophs dependent on sAAs that were not rescued by cross-feeding in environmental growth assays. These auxotrophic GROs possess alternative genetic codes that impart genetic isolation by impeding horizontal gene transfer and now depend on the use of synthetic biochemical building blocks, advancing orthogonal barriers between engineered organisms and the environment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry
  • Amino Acids / metabolism
  • Amino Acids / pharmacology*
  • Amino Acyl-tRNA Synthetases / genetics
  • Amino Acyl-tRNA Synthetases / metabolism
  • Catalytic Domain / genetics
  • Codon / genetics
  • Containment of Biohazards / methods*
  • Culture Media / chemistry
  • Culture Media / pharmacology
  • Environment
  • Escherichia coli / cytology
  • Escherichia coli / drug effects*
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism
  • Escherichia coli Proteins / biosynthesis
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / genetics
  • Escherichia coli Proteins / metabolism
  • Evolution, Molecular
  • Gene Transfer, Horizontal / genetics
  • Genes, Essential / genetics
  • Genetic Code / genetics
  • Genetic Engineering / methods
  • Genome, Bacterial / genetics
  • Microbial Viability / drug effects*
  • Microbial Viability / genetics
  • Molecular Sequence Data
  • Organisms, Genetically Modified / genetics
  • Organisms, Genetically Modified / growth & development
  • Organisms, Genetically Modified / metabolism
  • Peptide Termination Factors / genetics
  • Phenylalanine / chemistry
  • Phenylalanine / metabolism
  • Protein Multimerization / genetics
  • RNA, Transfer / genetics
  • Synthetic Biology / methods*

Substances

  • Amino Acids
  • Codon
  • Culture Media
  • Escherichia coli Proteins
  • Peptide Termination Factors
  • prfA protein, E coli
  • Phenylalanine
  • RNA, Transfer
  • Amino Acyl-tRNA Synthetases

Associated data

  • GENBANK/CP010455
  • GENBANK/CP010456