The identification of 5'-fluoro-5-deoxyinosine as a shunt product in cell free extracts of Streptomyces cattleya |
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Authors: | Cobb Steven L Deng Hai Hamilton John T G McGlinchey Ryan P O'Hagan David Schaffrath Christoph |
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Affiliation: | School of Chemistry and Centre for Biomolecular Sciences, University of St. Andrews, St. Andrews, Fife, UK. |
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Abstract: | 5'-Fluoro-5'-deoxyinosine (5'-FDI) is identified as an adventitious side product that accumulates in cell free incubations of SAM and fluoride ion in Streptomyces cattleya. 5'-FDI was identified by a combination of isotopic labelling studies and co-synthesis studies as well as enzymatic degradation. Although it is an efficiently generated end product of the cell free incubations, 5'-FDI is not a biosynthetic intermediate and it does not accumulate as a fluorometabolite with fluoroacetate and 4-fluorothreonine in whole cell incubations of S. cattleya. Clearly the purine deaminase which converts 5'-fluoro-5'-deoxyadenosine (5'-FDA) to 5'-FDI in the cell free extract does not come into contact with 5'-FDA in whole cells, suggesting some level of compartmentalisation in cells of S. cattleya. The biotransformation of 5'-FDI from fluoride ion extends the range of organofluorine products, beyond biosynthetic intermediates, that can be generated by this system, for applications such as enzymatic labelling with fluorine-18 for positron emission tomography applications. |
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Keywords: | Fluoroacetate 4-Fluorothreonine 5′-Fluoro-5′-deoxyadenosine 5′-Fluoro′-deoxyinosine Fluorometabolite Fluorinase |
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