O'Hagan David, Schaffrath Christoph, Cobb Steven L, Hamilton John T G, Murphy Cormac D
School of Chemistry and Centre for Biomolecular Sciences, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, UK.
Nature. 2002 Mar 21;416(6878):279. doi: 10.1038/416279a.
Although fluorine in the form of fluoride minerals is the most abundant halogen in the Earth's crust, only 12 naturally occurring organofluorine compounds have so far been found, and how these are biosynthesized remains a mystery. Here we describe an enzymatic reaction that occurs in the bacterium Streptomyces cattleya and which catalyses the conversion of fluoride ion and S-adenosylmethionine (SAM) to 5'-fluoro-5'-deoxyfluoroadenosine (5'-FDA). To our knowledge, this is the first fluorinase enzyme to be identified, a discovery that opens up a new biotechnological opportunity for the preparation of organofluorine compounds.
尽管以氟化物矿物形式存在的氟是地壳中含量最丰富的卤素,但迄今为止仅发现了12种天然存在的有机氟化合物,其生物合成方式仍是个谜。在此,我们描述了一种发生在卡特利链霉菌中的酶促反应,该反应催化氟离子和S-腺苷甲硫氨酸(SAM)转化为5'-氟-5'-脱氧氟腺苷(5'-FDA)。据我们所知,这是首个被鉴定出的氟化酶,这一发现为有机氟化合物的制备开辟了新的生物技术机遇。