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Nucleoside Phosphorylases make N7-xanthosine

  • Sarah Westarp,
  • Felix Brandt,
  • Lena Neumair,
  • Christina Betz,
  • Amin Dagane,
  • Sebastian Kemper,
  • Christoph R. Jacob,
  • Peter Neubauer,
  • Anke Kurreck,
  • Felix Kaspar

摘要

Modern, highly evolved nucleoside-processing enzymes are known to exhibit perfect regioselectivity over the glycosylation of purine nucleobases at N9. We herein report an exception to this paradigm. Wild-type nucleoside phosphorylases also furnish N7-xanthosine, a “non-native” ribosylation regioisomer of xanthosine. This unusual nucleoside possesses several atypical physicochemical properties such as redshifted absorption spectra, a high equilibrium constant of phosphorolysis and low acidity. Ultimately, the biosynthesis of this previously unknown natural product illustrates how even highly evolved, essential enzymes from primary metabolism are imperfect catalysts.