Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitrilase activity utilization

Nitrilases have been utilized successfully for the desymmetrisation of symmetric starting materials. At Diversa it was demonstrated that mutagenesis could create a highly selective nitrilase that was active at high substrate concentrations [105]. For their enzymatic route towards the atorvastatin (lipitor) side-chain this nitrilase now converts a symmetric precursor with 600 g IT1 d-1 into the enan-tiopure (R)-4-cyano-3-hydroxybutyric acid (ee=98.5%, Scheme 6.34). [Pg.287]

Plant nitrilases and related enzymes in some plant-associated bacteria preferentially utilize arylaliphatic nitriles such as 3-phenylpropionitrile or 3-phenylbutyronitrile. These enz3unes also exhibit remarkable activities for aliphatic nitriles (Table 12.4). [Pg.339]


See other pages where Nitrilase activity utilization is mentioned: [Pg.51]    [Pg.630]    [Pg.631]    [Pg.631]    [Pg.634]    [Pg.178]    [Pg.21]    [Pg.237]    [Pg.238]    [Pg.238]    [Pg.21]    [Pg.637]   
See also in sourсe #XX -- [ Pg.288 , Pg.289 ]




SEARCH



Nitrilase activity

Nitrilases

© 2024 chempedia.info