Title of article
Biotransformation of halogenated 2′-deoxyribosides by immobilized lactic acid bacteria
Author/Authors
Medina-Britos، M. A. نويسنده , , Claudia N. and Cappa، نويسنده , , Valeria A. and Rivero، نويسنده , , Cintia W. and Sambeth، نويسنده , , Jorge E. and Lozano، نويسنده , , Mario E. and Trelles، نويسنده , , Jorge A.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2012
Pages
5
From page
49
To page
53
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 0.5 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.
Keywords
lactic acid bacteria , Whole-cell immobilization , antitumoral compounds , 2?-N-deoxyribosyltransferase
Journal title
Journal of Molecular Catalysis B Enzymatic
Serial Year
2012
Journal title
Journal of Molecular Catalysis B Enzymatic
Record number
1717241
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