Enzymatic Fluorination and Biotechnological Developments of the Fluorinase

被引:261
作者
O'Hagan, David [1 ]
Deng, Hai [2 ]
机构
[1] Univ St Andrews, EaStChem Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Aberdeen, Dept Chem, UK Marine Biodiscovery Ctr, Aberdeen AB24 3UE, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
C-F-18 BOND FORMATION; FLUOROMETABOLITE BIOSYNTHESIS; STREPTOMYCES-CATTLEYA; PROTEASOME INHIBITOR; HYDROXIDE ADENOSYLTRANSFERASE; SUBSTRATE-SPECIFICITY; FLUOROACETIC ACID; CRYSTAL-STRUCTURE; GENOME SEQUENCE; RGD PEPTIDES;
D O I
10.1021/cr500209t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There has been some exciting success in cloning the fluorinase gene (flA) gene to induce fluorometabolite production in a host organism. This was demonstrated in S. tropica where the marine organism was engineered to produce fluorosalinosporamide. The study points the way to preparing other fluorinated bioactives by microbial engineering, although it highlights the necessity for good pathway regulation and to engineer a host organisms that is tolerant to fluoride ion. The enzyme has proven to be a particularly useful catalyst for securing the fluorine-18 isotope from [18F]-fluoride ion, to prepare a range of molecules for positron emission tomography. Also the fluorinase offers a strategy to access a range of [18F]-nucleosides and [18F]-fluoroacetate as tracers for PET, as well as a last-step [18F]-labeling approach to peptides under ambient conditions.
引用
收藏
页码:634 / 649
页数:16
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