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The leaving group abilities (nucleofugalities) of a series of aliphatic carboxylates have been obtained by determining the nucleofuge-specific parameters (Nf and sf) from solvolysis rate constants of X,Y-substituted benzhydryl carboxylates in a series of aqueous ethanol mixtures by applyication of the linear free energy relationship (LFER) equation: log k = sf (Ef + Nf). These values can be employed to compare reactivities of carboxylates with those of other leaving groups previously included in the nucleofugality scale, and also to estimate the solvolysis rates of various carboxylates. It is confirmed that the inductive effect is the most important variable governing the reactivities of halogenated carboxylates in solution. Moreover, both the Hammett correlation and the solvolytic activation parameters have revealed a strong influence of the inductive effect on the nucleofugality of alkyl-substituted carboxylates. The reaction constants (sf) indicate that carboxylate substrates with weaker leaving groups solvolyze via later, more carbocation-like, transition states, which is in accord with the Hammond postulate. In addition, due to the weaker demand for solvation of transition states that produce more strongly stabilized benzhydrylium ions, in which more efficient charge delocalization occurs, the reaction constants (sf) obtained with most of the leaving groups investigated here increase as the polarity of the solvent decreases.

The fluorinase is an enzyme that catalyses the combination of S-adenosyl-L-methionine (SAM) and a fluoride ion to generate 5′-fluorodeoxy adenosine (FDA) and L-methionine through a nucleophilic substitution reaction with a fluoride ion as the nucleophile. It is the only native fluorination enzyme that has been characterised. The fluorinase was isolated in 2002 from Streptomyces cattleya, and, to date, this has been the only source of the fluorinase enzyme. Herein, we report three new fluorinase isolates that have been identified by genome mining. The novel fluorinases from Streptomyces sp. MA37, Nocardia brasiliensis, and an Actinoplanes sp. have high homology (80-87 % identity) to the original S. cattleya enzyme. They all possess a characteristic 21-residue loop. The three newly identified genes were overexpressed in E. coli and shown to be fluorination enzymes. An X-ray crystallographic study of the Streptomyces sp. MA37 enzyme demonstrated that it is almost identical in structure to the original fluorinase. Culturing of the Streptomyces sp. MA37 strain demonstrated that it not only also elaborates the fluorometabolites, fluoroacetate and 4-fluorothreonine, similar to S. cattleya, but this strain also produces a range of unidentified fluorometabolites. These are the first new fluorinases to be reported since the first isolate, over a decade ago, and their identification extends the range of fluorination genes available for fluorination biotechnology. Get on the fluor! The fluorinase enzyme from Streptomyces cattleya was identified in 2002 as the only fluorination enzyme known in biochemistry. Three additional fluorinases expressed through bacterial genome mining are now reported. These new fluorinases extend the range of genes available for developing fluorination biotechnology. Copyright

The recycle of fluoride ion generated from the degradation of 1-methyl-3-butylimidazolium tetrafluoroborate, diethyl methyl methoxyethylammonium tetrafluoroborate in the presence of Tris-HCl buffer solution and/or the biodegradation of fluorobenzene and b