Ohno S, Yokogawa T, Fujii I, Asahara H, Inokuchi H, Nishikawa K
Department of Biomolecular Science, Faculty of Engineering, Gifu University, Gifu, 501-1193, Japan.
J Biochem. 1998 Dec 1;124(6):1065-8. doi: 10.1093/oxfordjournals.jbchem.a022221.
An efficient system was developed for the co-expression of a yeast tRNATyr/tyrosyl-tRNA synthetase (TyrRS) pair in Escherichia coli. Analysis of suppression patterns using several sets of E. coli and lambda phage mutants indicated that the expressed yeast suppressor tRNATyr was aminoacylated only with tyrosine by its cognate yeast TyrRS and not by E. coli TyrRS or other aminoacyl-tRNA synthetases. This extra tRNA/TyrRS pair is expected to be a key bridgehead for developing an in vivo system for the site-directed incorporation of unnatural amino acids into proteins.
开发了一种高效系统,用于在大肠杆菌中共表达酵母tRNATyr/酪氨酰-tRNA合成酶(TyrRS)对。使用几组大肠杆菌和λ噬菌体突变体分析抑制模式表明,表达的酵母抑制性tRNATyr仅被其同源酵母TyrRS用酪氨酸进行氨酰化,而不被大肠杆菌TyrRS或其他氨酰-tRNA合成酶氨酰化。这种额外的tRNA/TyrRS对有望成为开发用于将非天然氨基酸定点掺入蛋白质的体内系统的关键桥头堡。