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Nucleoside Phosphorylases make N7-xanthosine

Westarp, Sarah;
GND
1184331677
ORCID
0000-0003-2200-5649
Affiliation/Institute
Institut für Physikalische und Theoretische Chemie
Brandt, Felix; Neumair, Lena; Betz, Christina; Dagane, Amin; Kemper, Sebastian;
GND
1184339031
ORCID
0000-0002-6227-8476
Affiliation/Institute
Institut für Physikalische und Theoretische Chemie
Jacob, Christoph R.; Neubauer, Peter; Kurreck, Anke;
GND
1235845788
ORCID
0000-0001-6391-043X
Affiliation/Institute
Institut für Biochemie, Biotechnologie und Bioinformatik
Kaspar, Felix

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.

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