Related Experiment Video
Updated: Sep 29, 2026

Mapping Bacterial Functional Networks and Pathways in Escherichia Coli using Synthetic Genetic Arrays
Published on: November 12, 2012
A generalizable framework for genetic code expansion in bacterial systems beyond E. coli
Elise Van Fossen1, Molly Stephenson1, Andrew Frank1
1Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, USA.
Abstract:
Genetic code expansion (GCE) enables the site-specific incorporation of noncanonical amino acids into proteins, providing a powerful platform to investigate and engineer biological functions with molecular precision. While GCE has facilitated transformative studies in Escherichia coli, its utility in bacteria other than E. coli has been hindered by the lack of universal, high-efficiency methods for its implementation and optimization. To address this limitation, we introduce a modular, extensible platform for the generalizable implementation and optimization of GCE in phylogenetically diverse bacteria, based on the host-agnostic serine recombinase-assisted genome engineering toolkit. We apply this approach to five bacterial species and demonstrate robust incorporation of structurally diverse noncanonical amino acids, including a key bacterial post-translational modification. This work provides a generalizable and scalable strategy to deploy expanded genetic systems in bacteria, advancing programmable microbial engineering across diverse applications.IMPORTANCEExpanding the genetic code allows scientists to introduce new chemical functionalities into proteins, creating powerful opportunities to study and engineer biological systems. However, these technologies have remained largely confined to the laboratory bacterium Escherichia coli because adapting them to other bacterial species has been slow and organism-specific. We developed a general, chromosomally integrated framework that makes it easier to establish and optimize genetic code expansion across diverse bacteria. Using this approach, we identify practical design principles for improving performance, demonstrate transferability between distantly related species, and enable site-specific incorporation of modified amino acids into native bacterial proteins. This work expands access to advanced protein engineering technologies for studying bacterial post-translational regulation and developing engineered microbes for biotechnology, environmental applications, and synthetic biology.
More Related Videos
05:58Site-Specific Lysine Lactylation via Genetic Code Expansion in E. coli and Mammalian Cells
Published on: February 24, 2026
11:47Residue-specific Incorporation of Noncanonical Amino Acids into Model Proteins Using an Escherichia coli Cell-free Transcription-translation System
Published on: August 1, 2016
Related Concept Videos
The Central Dogma
The Central Dogma
RNA is the Missing Link Between DNA and Proteins
In the early 1900s, scientists discovered that DNA stores all the information needed for cellular functions and that proteins perform most of these functions. However, the mechanisms of converting genetic information into functional proteins remained unknown for many years. Initially, it was believed that a single gene is...
From DNA to Protein
Genome Size and the Evolution of New Genes
Genome Size and the Evolution of New Genes
Evolution of Microbial Genome