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      Misacylation of pyrrolysine tRNA in vitro and in vivo.

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          Abstract

          Methanosarcina barkeri inserts pyrrolysine (Pyl) at an in-frame UAG codon in its monomethylamine methyltransferase gene. Pyrrolysyl-tRNA synthetase acylates Pyl onto tRNAPyl, the amber suppressor pyrrolysine Pyl tRNA. Here we show that M. barkeri Fusaro tRNAPyl can be misacylated with serine by the M. barkeri bacterial-type seryl-tRNA synthetase in vitro and in vivo in Escherichia coli. Compared to the M. barkeri Fusaro tRNA, the M. barkeri MS tRNAPyl contains two base changes; a G3:U70 pair, the known identity element for E. coli alanyl-tRNA synthetase (AlaRS). While M. barkeri MS tRNAPyl cannot be alanylated by E. coli AlaRS, mutation of the MS tRNAPyl A4:U69 pair into C4:G69 allows aminoacylation by E. coli AlaRS both in vitro and in vivo.

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          Author and article information

          Journal
          FEBS Lett
          FEBS letters
          Elsevier BV
          0014-5793
          0014-5793
          Oct 15 2008
          : 582
          : 23-24
          Affiliations
          [1 ] Departments of Molecular Biophysics and Biochemistry, Yale University, P.O. Box 208114, 266 Whitney Avenue, New Haven, CT 06520-8114, USA.
          Article
          S0014-5793(08)00714-X NIHMS74221
          10.1016/j.febslet.2008.08.027
          2577721
          18775710
          b1946655-221c-4c6a-bbe1-efab40609aed
          History

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