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