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Biotransformation of halogenated 2′-deoxyribosides by immobilized lactic acid bacteria

Authors :
Britos, Claudia N.
Cappa, Valeria A.
Rivero, Cintia W.
Sambeth, Jorge E.
Lozano, Mario E.
Trelles, Jorge A.
Source :
Journal of Molecular Catalysis B: Enzymatic. Jul2012, Vol. 79, p49-53. 5p.
Publication Year :
2012

Abstract

Abstract: An efficient and green bioprocess is herein reported to obtain halogenated nucleosides by transglycosylation using immobilized lactic acid bacteria (LAB). Lactobacillus animalis ATCC 35046 showed a yield of 95% at 0.5h to synthesize 5-fluorouracil-2′-deoxyriboside (floxuridine). Calcium alginate was the best matrix for whole-cell immobilization by entrapment. Its productivity was 87mg/Lh in a continuous bioprocess. When adsorption techniques were evaluated, DEAE-Sepharose was the support which showed higher microbial load, its productivity being 53mg/Lh. Additionally, this microorganism was able to produce 5-bromouracil-2′-deoxyriboside, 6-chloropurine-2′-deoxyriboside and 6-bromopurine-2′-deoxyriboside. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
13811177
Volume :
79
Database :
Academic Search Index
Journal :
Journal of Molecular Catalysis B: Enzymatic
Publication Type :
Academic Journal
Accession number :
75184813
Full Text :
https://doi.org/10.1016/j.molcatb.2012.04.004