Biotransformation of halogenated 2′-deoxyribosides by immobilized lactic acid bacteria
; Cappa, Valeria Alejandra
; Rivero, Cintia Wanda
; Sambeth, Jorge Enrique
; Lozano, Mario Enrique
; Trelles, Jorge Abel 
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Fecha
2012-04-11
Editorial
Elsevier Science
Revista
Journal of Molecular Catalysis B: Enzymatic
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1381-1177
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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 0.5 h to synthesize 5-fluorouracil-2-deoxyriboside (floxuridine). Calcium alginate was the best matrix
for whole-cell immobilization by entrapment. Its productivity was 87 mg/L h in a continuous bioprocess. When adsorption techniques were evaluated, DEAE-Sepharose was the support which showed higher microbial load, its productivity being 53 mg/L h. Additionally, this microorganism was able to produce 5-bromouracil-2-deoxyriboside, 6-chloropurine-2-deoxyriboside and 6-bromopurine-2
-deoxyriboside.© 2
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