2001
DOI: 10.1081/ncn-100002472
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Recombinant Bacterial Cells as Efficient Biocatalysts for the Production of Nucleosides

Abstract: The preparation of nucleosides as well as their base-modified analogues using purified nucleoside phosphorylase enzymes or, more conveniently, using whole bacterial cells is described. The development of genetically modified strains of Escherichia coli, able to over-produce Uridine-phosphorylase and Purine-nucleoside-phosphorylase in the same cells, improves the specific biocatalytic activity and the consequent industrial scale approach.

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Cited by 11 publications
(2 citation statements)
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“…In cases were industrial application has been hampered by the low specific activity associated with the wild type microorganisms, genetically modified strains that co-express NPs at very high level were developed [97]. This strategy enables the optimization of nucleosides preparation in terms of productivity and cost as well as the direct implementation of the process at preparative scale.…”
Section: Screening and Immobilisationmentioning
confidence: 99%
See 1 more Smart Citation
“…In cases were industrial application has been hampered by the low specific activity associated with the wild type microorganisms, genetically modified strains that co-express NPs at very high level were developed [97]. This strategy enables the optimization of nucleosides preparation in terms of productivity and cost as well as the direct implementation of the process at preparative scale.…”
Section: Screening and Immobilisationmentioning
confidence: 99%
“…More recently, the construction of genetically modified bacteria that express high levels of NPs recombinant forms, were advantageously applied to both the production of isolated enzymes and the direct use of the whole cells as biocatalysts [97,138].…”
Section: B Nucleoside Synthesismentioning
confidence: 99%