Cross-linked amorphous nitrilase aggregates for enantioselective nitrile hydrolysis

A recombinant Escherichia coli strain was constructed which efficiently expressed the enantio-selective nitrilase from Alcaligenes faecalis DSMZ 30030 as a hisitidine-tagged enzyme variant under the control of a rhamnose inducible promoter. ne enzyme was purified from cell extracts and used for the preparation of cross-linked enzyme aggregates (CLEAs). The conditions for the preparation of the CLEAs were optimized using various organic solvents and cross-linking agents and a procedure was developed which combined a precipitation with 85% (v/v) isopropyl alcohol and a cross-linking with 30 mM glutaraldehyde. Thus, about 80% of the initial nitrilase activity could be incorporated into the CLEAs. The hydrolysis of racemic mandelonitrile to (R)-mandelic acid was compared between the soluble nitrilase preparations and their CLEAs (nit-CLEAs). The nitrilase activity in the CLEAs was at 30 degrees C and 60 degrees C about 5 times more stable than in the soluble preparations. The CLEAs could be reused 5 times with only about 10% reduction in activity. The enantioselectivity of the nitrilase for the formation of (R)-mandelic acid from racemic mandelonitrile decreased for both preparations with increasing temperatures (10 degrees C to 50 degrees C), but this effect was significantly less pronounced for the CLEAs. A detailed analysis of solvent effects on nitrilase enantioselectivity allowed thermodynamic insights into contributions from free energy component (activation enthalpy and entropy) to chiral preference of nitrilase in such non conventional media.