Biotransformation of 2,6-diaminopurine nucleosides by immobilized Geobacillus stearothermophilus

Biotechnol Prog. 2012 Sep-Oct;28(5):1251-6. doi: 10.1002/btpr.1602. Epub 2012 Aug 28.

Abstract

An efficient and green bioprocess to obtain 2,6-diaminopurine nucleosides using thermophilic bacteria is herein reported. Geobacillus stearothermophilus CECT 43 showed a conversion rate of 90 and 83% at 2 h to obtain 2,6-diaminopurine-2'-deoxyriboside and 2,6-diaminopurine riboside, respectively. The selected biocatalyst was successfully stabilized in an agarose matrix and used to produce up to 23.4 g of 2,6-diaminopurine-2'-deoxyriboside in 240 h of process. These nucleoside analogues can be used as prodrug precursors or in antisense oligonucleotide synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2-Aminopurine / analogs & derivatives*
  • 2-Aminopurine / metabolism
  • Biotransformation
  • Cells, Immobilized / metabolism
  • Geobacillus stearothermophilus / metabolism*
  • Nucleosides / metabolism*

Substances

  • Nucleosides
  • 2-Aminopurine
  • 2,6-diaminopurine