Abstract

AbstractMultimeric uridine phosphorylase (UP) and purine nucleoside phosphorylase (PNP) of Bacillus subtilis have been expressed from genes cloned in Escherichia coli, purified, characterized, immobilized and stabilized on solid support. A new immobilization strategy has been developed for UP onto Sepabeads coated with polyethyleneamine followed by cross‐linking with aldehyde‐dextran. PNP has been immobilized onto glyoxyl‐agarose. At pH 10 and 45 °C these derivatives catalyzed the transglycosylation of 2′‐deoxyuridine to 2′‐deoxyguanosine in high yield (92%). Under the same conditions the not immobilized enzymes were promptly inactivated.

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