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Palabras clave – provistas por la editorial

growth effect; lysine acetylation; Escherichia coli; posttranslational modification; class II aminoacyl-tRNA synthetase; amber stop codon suppression; genetic code expansion; yeasts; phosphoseryl-tRNA synthetase; M. jannaschii orthogonal pair; gene ontology; selenocysteine; genetic firewall; indirect tRNA aminoacylation; tRNA editing; unnatural nucleotides; reverse polymerization; RNA metabolism; genome editing; tRNA; tRNASer; alternative amino acid and nucleotide repertoires; biocontainment; fluorescent reporter; optogenetics; tRNASep; GluRS-like; genetic isolation; live cell imaging; alternative core cellular chemistries; fluorescence-based screen; phosphoinositide dependent kinase 1; synthetic biology; mistranslation; tRNA repair; synthetic life; CUG-Ser; unnatural amino acids; recombinant protein production; biopharmaceuticals; protein modification; functional conservation; branched-chain amino acids; alanyl-tRNA synthetase; release factor 1; cyclic peptides; AspRS; xenobiology; DNA delivery; gene overexpression; non-canonical amino acids; ASKA collection; protein kinase B; codon bias; microRNA quantification; anticodon; small molecule drug screening; mRNA display; genetic tools; protein engineering; misacylation; transfer RNA; Metschnikowia; genome synthesis; expanded genetic code; yeast two hybrid; orthogonal central dogma of molecular biology; microRNA; genome engineering