Green biosynthesis of floxuridine by immobilized microorganisms
This work describes an efficient, simple, and green bioprocess for obtaining 5-halogenated pyrimidine nucleosides from thymidine by transglycosylation using whole cells. Biosynthesis of 5-fluoro-2′-deoxyuridine (floxuridine) was achieved by free and immobilized Aeromonas salmonicida ATCC 27013 with...
| Authors: | , , , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2012 |
| Country: | Argentina |
| Institution: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repository: | CONICET Digital (CONICET) |
| Language: | English |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/189232 |
| Online Access: | http://hdl.handle.net/11336/189232 |
| Access Level: | Open access |
| Keyword: | 5-HALOGENATED 2′-DEOXYNUCLEOSIDES AEROMONAS SALMONICIDA ENTRAPMENT IMMOBILIZATION GREEN CHEMISTRY PYRIMIDINE NUCLEOSIDE PHOSPHORYLASE https://purl.org/becyt/ford/2.9 https://purl.org/becyt/ford/2 |
| Summary: | This work describes an efficient, simple, and green bioprocess for obtaining 5-halogenated pyrimidine nucleosides from thymidine by transglycosylation using whole cells. Biosynthesis of 5-fluoro-2′-deoxyuridine (floxuridine) was achieved by free and immobilized Aeromonas salmonicida ATCC 27013 with an 80% and 65% conversion occurring in 1 h, respectively. The immobilized biocatalyst was stable for more than 4 months in storage conditions (4 °C) and could be reused at least 30 times without loss of its activity. This microorganism was able to biosynthesize 2.0 mg L -1 min -1 (60%) of 5-chloro-2′-deoxyuridine in 3 h. These halogenated pyrimidine 2′-deoxynucleosides are used as antitumoral agents. |
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