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. (c) 2005 Elsevier Inc. All rights reserved.
Original language | English |
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Pages (from-to) | 393-401 |
Number of pages | 9 |
Journal | Bioorganic Chemistry |
Volume | 33 |
DOIs | |
Publication status | Published - Oct 2005 |
Keywords
- fluoroacetate
- 4-fluorothreonine
- 5 '-fluoro-5 '-deoxyadenosine
- 5 '-fluoro '-deoxyinosine
- fluorometabolite
- fluorinase
- FLUOROMETABOLITE BIOSYNTHESIS
- BOND FORMATION
- FLUOROACETATE
- 4-FLUOROTHREONINE
- FLUORINASE
- ENZYME