A NOVEL THERMOSTABLE NITRILE HYDRATASE

A novel, nitrile-degrading, thermophilic microorganism belonging to th e genus Bacillus and most closely related to strain DSM 2349 has been isolated. The strain grew optimally at 65 degrees C with the constitut ive expression of a thermostable intracellular nitrile hydratase. No a romatic-specific ''benzonitrilase'' activity was detected under any co nditions. The enzyme, an alpha(2)beta(2) heterotetramer with a native molecular weight of 110kDa, was purified to homogeneity, N-terminal se quence data showed no homology to known bacterial ct subunit sequences but had a high level of identity with other bacterial N-terminal beta subunit sequences. The purified enzyme had a broad pH-activity range (50% activity limits were pH 5.1 and 8.7) and was stable in aqueous so lution up to 60 degrees C in the absence of either substrates or subst rate analogues, Substrate specificity was restricted to aliphatic nitr iles, but an unusual preference for branched and cyclic aliphatic nitr iles was noted. Turnover rates under optimum reaction conditions were 746 and 4580 sec(-1) for acetonitrile and valeronitrile, respectively.