Title of article :
The identification of 5′-fluoro-5-deoxyinosine as a shunt product in cell free extracts of Streptomyces cattleya
Author/Authors :
Cobb، نويسنده , , Steven L. and Deng، نويسنده , , Hai and Hamilton، نويسنده , , John T.G. and McGlinchey، نويسنده , , Ryan P. and O’Hagan، نويسنده , , David and Schaffrath، نويسنده , , Christoph، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
9
From page :
393
To page :
401
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.
Keywords :
5?-Fluoro-5?-deoxyadenosine , Fluorometabolite , Fluorinase , 4-Fluorothreonine , Fluoroacetate , 5?-Fluoro?-deoxyinosine
Journal title :
Bioorganic Chemistry: an International Journal
Serial Year :
2005
Journal title :
Bioorganic Chemistry: an International Journal
Record number :
1385828
Link To Document :
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