<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hoesl MG</submitter><funding>Defense Advanced Research Projects Agency</funding><funding>EU</funding><funding>Einstein Foundation</funding><funding>DFG</funding><funding>Wellcome Trust</funding><funding>National Institute for General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>10030-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4782924</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(34)</volume><pubmed_abstract>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-β-(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 20,899 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.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Chemical Evolution of a Bacterial Proteome.</pubmed_title><pmcid>PMC4782924</pmcid><funding_grant_id>GRK1582</funding_grant_id><funding_grant_id>R01 GM022854</funding_grant_id><funding_grant_id>103139/Z/13/Z</funding_grant_id><funding_grant_id>N66001-12-C-4020</funding_grant_id><funding_grant_id>092076</funding_grant_id><funding_grant_id>103139</funding_grant_id><funding_grant_id>N66001-12-C-4211</funding_grant_id><pubmed_authors>Peil L</pubmed_authors><pubmed_authors>Oehm S</pubmed_authors><pubmed_authors>Rinehart J</pubmed_authors><pubmed_authors>Soll D</pubmed_authors><pubmed_authors>Hoesl MG</pubmed_authors><pubmed_authors>Darmon E</pubmed_authors><pubmed_authors>Rappsilber J</pubmed_authors><pubmed_authors>Durkin P</pubmed_authors><pubmed_authors>Aerni HR</pubmed_authors><pubmed_authors>Leach D</pubmed_authors><pubmed_authors>Budisa N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemical Evolution of a Bacterial Proteome.</name><description>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-β-(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 20,899 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.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Aug</publication><modification>2025-04-05T11:57:04.38Z</modification><creation>2019-03-27T02:10:40Z</creation></dates><accession>S-EPMC4782924</accession><cross_references><pubmed>26136259</pubmed><doi>10.1002/anie.201502868</doi></cross_references></HashMap>