This review outlines the recent developments in uncovering the enzymes and intermediates involved in fluorometabolite biosynthesis in the bacterium Streptomyces cattleya. A particular emphasis is placed on the purification and characterisation of the fluorinase, the C-F bond forming enzyme which initiates the biosynthesis. Nature has hardly developed a biochemistry around fluorine, yet fluorinated organics are important commercial entities, therefore a biotransformation from inorganic to organic fluorine is novel and of contemporary interest.</p
SummaryA genomic library of Streptomyces cattleya was screened to isolate a gene cluster encoding en...
Nature has evolved the ability to form a C-F bond, as exemplified by the bacterium Streptomyces catt...
Fluorination has become a very useful tool in the design and optimization of bioactive small molecul...
Enzymatic fluorination of natural products is extremely rare. Of the 4000 halogenated natural produc...
Organofluorine compounds are rare in Nature, with only a handful known to be produced by some specie...
To date, only five fluorinated natural products have been identified. These were isolated from both...
Enzymatic halogenation occurs during the biosynthesis of more than 4,000 natural products. The pres...
In this paper, we report that fluoride ion is converted to the amino acid/antibiotic 4-fluorothreoni...
Fluorine is the thirteenth most abundant element in the earth's crust, but fluoride concentrations i...
Nature has hardly evolved a biochemistry of fluorine although there is a low-level occurrence of flu...
Streptomyces cattleya DSM 46488 is unusual in its ability to biosynthesise fluorine containing natur...
5'-Fluoro-5'-deoxy-D-ribose-1-phosphate (FDRP) is identified as a biosynthetic intermediate during f...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN029276 / BLDSC - British Library D...
Organofluorine compounds play an important role in medicinal chemistry, where they are responsible f...
Organofluorine compounds are widely prepared throughout the chemicals industry, but their preparario...
SummaryA genomic library of Streptomyces cattleya was screened to isolate a gene cluster encoding en...
Nature has evolved the ability to form a C-F bond, as exemplified by the bacterium Streptomyces catt...
Fluorination has become a very useful tool in the design and optimization of bioactive small molecul...
Enzymatic fluorination of natural products is extremely rare. Of the 4000 halogenated natural produc...
Organofluorine compounds are rare in Nature, with only a handful known to be produced by some specie...
To date, only five fluorinated natural products have been identified. These were isolated from both...
Enzymatic halogenation occurs during the biosynthesis of more than 4,000 natural products. The pres...
In this paper, we report that fluoride ion is converted to the amino acid/antibiotic 4-fluorothreoni...
Fluorine is the thirteenth most abundant element in the earth's crust, but fluoride concentrations i...
Nature has hardly evolved a biochemistry of fluorine although there is a low-level occurrence of flu...
Streptomyces cattleya DSM 46488 is unusual in its ability to biosynthesise fluorine containing natur...
5'-Fluoro-5'-deoxy-D-ribose-1-phosphate (FDRP) is identified as a biosynthetic intermediate during f...
SIGLEAvailable from British Library Document Supply Centre-DSC:DXN029276 / BLDSC - British Library D...
Organofluorine compounds play an important role in medicinal chemistry, where they are responsible f...
Organofluorine compounds are widely prepared throughout the chemicals industry, but their preparario...
SummaryA genomic library of Streptomyces cattleya was screened to isolate a gene cluster encoding en...
Nature has evolved the ability to form a C-F bond, as exemplified by the bacterium Streptomyces catt...
Fluorination has become a very useful tool in the design and optimization of bioactive small molecul...