Immobilized Drosophila melanogaster Deoxyribonucleoside Kinase (DmdNK) as a High Performing Biocatalyst for the Synthesis of Purine Arabinonucleotides

Serra, Immacolata; Conti, Silvia; Piskur, Jure; Clausen, Anders Ranegaard, et al. (2014). Immobilized Drosophila melanogaster Deoxyribonucleoside Kinase (DmdNK) as a High Performing Biocatalyst for the Synthesis of Purine Arabinonucleotides. Advanced Synthesis & Catalysis, 356, (2-3), 563 - 570
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DOI:
| Published | English
Authors:
Serra, Immacolata ; Conti, Silvia ; Piskur, Jure ; Clausen, Anders Ranegaard , et al.
Department:
Molecular Cell Biology
Department of Biology
Abstract:
Fruit fly (Drosophila melanogaster) deoxyribonucleoside kinase (DmdNK; EC: 2.7.1.145) was characterized for its substrate specificity towards natural and non-natural nucleosides, confirming its potential in the enzymatic synthesis of modified nucleotides. DmdNK was adsorbed on a solid ion exchange support (bearing primary amino groups) achieving an expressed activity >98%. Upon cross-linking with aldehyde dextran, expressed activity was 30-40%. Both biocatalysts (adsorbed or cross-linked) were stable at pH10 and room temperature for 24h (about 70% of retained activity). The cross-linked DmdNK preparation was used for the preparative synthesis of arabinosyladenine monophosphate (araA-MP) and fludarabine monophosphate (FaraA-MP). Upon optimization of the reaction conditions (50mM ammonium acetate, substrate/ATP ratio=1:1.25, 2mM MgCl2, 37 degrees C, pH8) immobilized DmdNK afforded the title nucleotides with high conversion (>90%), whereas with the soluble enzyme lower conversions were achieved (78-87%). Arabinosyladenine monophosphate was isolated in 95% yield and high purity (96.5%).
Keywords:
biocatalysis ; deoxyribonucleoside kinase ; immobilization ; nucleotides ; phosphorylation
ISSN:
1615-4150

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