The identification of 5′-fluoro-5-deoxyino sine as a shunt product in cell free extracts of Streptomyces cattleya

被引:11
作者
Cobb, SL
Deng, H
Hamilton, JTG
McGlinchey, RP
O'Hagan, D [1 ]
Schaffrath, C
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ St Andrews, Ctr Biomol Sci, St Andrews KY16 9ST, Fife, Scotland
[3] Queens Univ Belfast, Dept Food Sci, Microbial Biochem Sect, Belfast BT9 SPX, Antrim, North Ireland
基金
英国工程与自然科学研究理事会;
关键词
fluoroacetate; 4-fluorothreonine; 5 '-fluoro-5 '-deoxyadenosine; 5 '-fluoro '-deoxyinosine; fluorometabolite; fluorinase;
D O I
10.1016/j.bioorg.2005.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:393 / 401
页数:9
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