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spelling paper:paper_13811177_v39_n1-4_p40_Medici2023-06-08T16:12:20Z Microbial synthesis of 2,6-diaminopurine nucleosides 2,6-Diaminopurine nucleoside Microbial transglycosylation Nucleoside analogues Whole cells Bacteria Biocatalysts Derivatives Diseases Drug products Synthesis (chemical) Microbial transglycosylation Nucleoside analogues Nucleosides Whole cells Nitrogen compounds 2 aminoadenosine 2' deoxyriboside 2',3' dideoxyriboside arabinofuranoside nucleoside derivative unclassified drug Achromobacter Aeromonas Arthrobacter article Bacillus bacterial cell biocatalyst Brevibacterium Cellulomonas Citrobacter Corynebacterium drug synthesis Enterobacter Erwinia Escherichia coli glycosylation Klebsiella Micrococcus nonhuman Proteus Pseudomonas Rhizobium Serratia Staphylococcus whole cell Xanthomonas Achromobacter Aeromonas Arthrobacter Bacillus (bacterium) Bacteria (microorganisms) Brevibacterium Cellulomonas Citrobacter Corynebacterium Enterobacter Erwinia Escherichia coli Klebsiella Micrococcus Proteus (enterobacteria) Pseudomonas Rhizobium Serratia Staphylococcus Xanthomonas 2,6-Diaminopurine nucleosides are used as pharmaceutical drugs or prodrugs against cancer and viral diseases. The synthesis of 2,6-diaminopurine riboside, -2′-deoxyriboside, -2′,3′-dideoxyriboside and -arabinofuranoside was efficiently carried out by transglycosylation using bacterial whole cells as biocatalysts. The preparation of 2,6-diaminopurine-2′,3′-dideoxyriboside catalysed by whole cells is here reported for the first time. © 2006 Elsevier B.V. All rights reserved. 2006 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v39_n1-4_p40_Medici http://hdl.handle.net/20.500.12110/paper_13811177_v39_n1-4_p40_Medici
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 2,6-Diaminopurine nucleoside
Microbial transglycosylation
Nucleoside analogues
Whole cells
Bacteria
Biocatalysts
Derivatives
Diseases
Drug products
Synthesis (chemical)
Microbial transglycosylation
Nucleoside analogues
Nucleosides
Whole cells
Nitrogen compounds
2 aminoadenosine
2' deoxyriboside
2',3' dideoxyriboside
arabinofuranoside
nucleoside derivative
unclassified drug
Achromobacter
Aeromonas
Arthrobacter
article
Bacillus
bacterial cell
biocatalyst
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
drug synthesis
Enterobacter
Erwinia
Escherichia coli
glycosylation
Klebsiella
Micrococcus
nonhuman
Proteus
Pseudomonas
Rhizobium
Serratia
Staphylococcus
whole cell
Xanthomonas
Achromobacter
Aeromonas
Arthrobacter
Bacillus (bacterium)
Bacteria (microorganisms)
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
Enterobacter
Erwinia
Escherichia coli
Klebsiella
Micrococcus
Proteus (enterobacteria)
Pseudomonas
Rhizobium
Serratia
Staphylococcus
Xanthomonas
spellingShingle 2,6-Diaminopurine nucleoside
Microbial transglycosylation
Nucleoside analogues
Whole cells
Bacteria
Biocatalysts
Derivatives
Diseases
Drug products
Synthesis (chemical)
Microbial transglycosylation
Nucleoside analogues
Nucleosides
Whole cells
Nitrogen compounds
2 aminoadenosine
2' deoxyriboside
2',3' dideoxyriboside
arabinofuranoside
nucleoside derivative
unclassified drug
Achromobacter
Aeromonas
Arthrobacter
article
Bacillus
bacterial cell
biocatalyst
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
drug synthesis
Enterobacter
Erwinia
Escherichia coli
glycosylation
Klebsiella
Micrococcus
nonhuman
Proteus
Pseudomonas
Rhizobium
Serratia
Staphylococcus
whole cell
Xanthomonas
Achromobacter
Aeromonas
Arthrobacter
Bacillus (bacterium)
Bacteria (microorganisms)
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
Enterobacter
Erwinia
Escherichia coli
Klebsiella
Micrococcus
Proteus (enterobacteria)
Pseudomonas
Rhizobium
Serratia
Staphylococcus
Xanthomonas
Microbial synthesis of 2,6-diaminopurine nucleosides
topic_facet 2,6-Diaminopurine nucleoside
Microbial transglycosylation
Nucleoside analogues
Whole cells
Bacteria
Biocatalysts
Derivatives
Diseases
Drug products
Synthesis (chemical)
Microbial transglycosylation
Nucleoside analogues
Nucleosides
Whole cells
Nitrogen compounds
2 aminoadenosine
2' deoxyriboside
2',3' dideoxyriboside
arabinofuranoside
nucleoside derivative
unclassified drug
Achromobacter
Aeromonas
Arthrobacter
article
Bacillus
bacterial cell
biocatalyst
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
drug synthesis
Enterobacter
Erwinia
Escherichia coli
glycosylation
Klebsiella
Micrococcus
nonhuman
Proteus
Pseudomonas
Rhizobium
Serratia
Staphylococcus
whole cell
Xanthomonas
Achromobacter
Aeromonas
Arthrobacter
Bacillus (bacterium)
Bacteria (microorganisms)
Brevibacterium
Cellulomonas
Citrobacter
Corynebacterium
Enterobacter
Erwinia
Escherichia coli
Klebsiella
Micrococcus
Proteus (enterobacteria)
Pseudomonas
Rhizobium
Serratia
Staphylococcus
Xanthomonas
description 2,6-Diaminopurine nucleosides are used as pharmaceutical drugs or prodrugs against cancer and viral diseases. The synthesis of 2,6-diaminopurine riboside, -2′-deoxyriboside, -2′,3′-dideoxyriboside and -arabinofuranoside was efficiently carried out by transglycosylation using bacterial whole cells as biocatalysts. The preparation of 2,6-diaminopurine-2′,3′-dideoxyriboside catalysed by whole cells is here reported for the first time. © 2006 Elsevier B.V. All rights reserved.
title Microbial synthesis of 2,6-diaminopurine nucleosides
title_short Microbial synthesis of 2,6-diaminopurine nucleosides
title_full Microbial synthesis of 2,6-diaminopurine nucleosides
title_fullStr Microbial synthesis of 2,6-diaminopurine nucleosides
title_full_unstemmed Microbial synthesis of 2,6-diaminopurine nucleosides
title_sort microbial synthesis of 2,6-diaminopurine nucleosides
publishDate 2006
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v39_n1-4_p40_Medici
http://hdl.handle.net/20.500.12110/paper_13811177_v39_n1-4_p40_Medici
_version_ 1768544097502494720