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
Link To Document :
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