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http://purl.uniprot.org/citations/20159998http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20159998http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20159998http://www.w3.org/2000/01/rdf-schema#comment"Non-natural amino acids have been genetically encoded in living cells, using aminoacyl-tRNA synthetase-tRNA pairs orthogonal to the host translation system. In the present study, we engineered Escherichia coli cells with a translation system orthogonal to the E. coli tyrosyl-tRNA synthetase (TyrRS)-tRNA(Tyr) pair, to use E. coli TyrRS variants for non-natural amino acids in the cells without interfering with tyrosine incorporation. We showed that the E. coli TyrRS-tRNA(Tyr) pair can be functionally replaced by the Methanocaldococcus jannaschii and Saccharomyces cerevisiae tyrosine pairs, which do not cross-react with E. coli TyrRS or tRNA(Tyr). The endogenous TyrRS and tRNA(Tyr) genes were then removed from the chromosome of the E. coli cells expressing the archaeal TyrRS-tRNA(Tyr) pair. In this engineered strain, 3-iodo-L-tyrosine and 3-azido-L-tyrosine were each successfully encoded with the amber codon, using the E. coli amber suppressor tRNATyr and a TyrRS variant, which was previously developed for 3-iodo-L-tyrosine and was also found to recognize 3-azido-L-tyrosine. The structural basis for the 3-azido-L-tyrosine recognition was revealed by X-ray crystallography. The present engineering allows E. coli TyrRS variants for non-natural amino acids to be developed in E. coli, for use in both eukaryotic and bacterial cells for genetic code expansion."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.org/dc/terms/identifier"doi:10.1093/nar/gkq080"xsd:string
http://purl.uniprot.org/citations/20159998http://purl.org/dc/terms/identifier"doi:10.1093/nar/gkq080"xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Kobayashi T."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Kobayashi T."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Sakamoto K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Sakamoto K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Ohno S."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Ohno S."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Yokoyama S."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Yokoyama S."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Yokogawa T."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Yokogawa T."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Nishikawa K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Nishikawa K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Oki K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Oki K."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Iraha F."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/author"Iraha F."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/name"Nucleic Acids Res."xsd:string
http://purl.uniprot.org/citations/20159998http://purl.uniprot.org/core/name"Nucleic Acids Res."xsd:string