Artículo

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

Britos, Claudia Noelia Icon; Cappa, Valeria Alejandra Icon; Rivero, Cintia Wanda Icon; Sambeth, Jorge Enrique Icon; Lozano, Mario Enrique Icon; Trelles, Jorge Abel Icon

Otros responsables

Fecha

2012-04-11

Editorial

Elsevier Science

Revista

Journal of Molecular Catalysis B: Enzymatic

Título del libro

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Institución organizadora

ISSN

1381-1177

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

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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