4.8 Article

Chemical Evolution of a Bacterial Proteome

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 34, Pages 10030-10034

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201502868

Keywords

continuous evolution; Escherichia coli; genetic code translation; synthetic biology; tryptophan analogues

Funding

  1. Einstein Foundation
  2. FP7 EU
  3. UniCat Excellence Cluster of TU Berlin
  4. graduate school Fluorine as a key element of DFG [GRK1582]
  5. National Institute for General Medical Sciences
  6. Defense Advanced Research Projects Agency [N66001-12-C-4020, N66001-12-C-4211]
  7. DFG [Forschergruppe 1805]

Ask authors/readers for more resources

We have changed the amino acid set of the genetic code of Escherichia coli by evolving cultures capable of growing on the synthetic noncanonical amino acid L-beta-(thieno[3,2-b]pyrrolyl)alanine ([3,2]Tpa) as a sole surrogate for the canonical amino acid L-tryptophan (Trp). A long-term cultivation experiment in defined synthetic media resulted in the evolution of cells capable of surviving Trp![3,2] Tpa substitutions in their proteomes in response to the 20899 TGG codons of the E. coli W3110 genome. These evolved bacteria with new-to-nature amino acid composition showed robust growth in the complete absence of Trp. Our experimental results illustrate an approach for the evolution of synthetic cells with alternative biochemical building blocks.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available