EC Number   |
Application |
Reference |
|---|
   3.5.5.1 | analysis |
tools in the biodegradation and biodetection of cyanide |
746898 |
| 3.5.5.1 | industry |
spore surface display of nitrilases is an effective approach for enzyme immobilization in biochemical engineering on an industrial scale |
757454 |
| 3.5.5.1 | industry |
the high chemical specificity and frequent enantioselectivity of nitrilases makes them attractive biocatalysts for the production of fine chemicals and pharmaceutical intermediates. Nitrilases are also used in the treatment of toxic industrial effluent and cyanide remediation |
-, 712260 |
| 3.5.5.1 | industry |
the high-level production of Arthrobacter aurescens CYC705 nitrilase will meet the need of industrial biosynthesis of iminodiacetic acid |
-, 756238 |
| 3.5.5.1 | industry |
the purified enzyme reveales its selectivity towards dinitriles, which suggests a possible industrial application in the synthesis of cyanocarboxylic acids |
756289 |
| 3.5.5.1 | synthesis |
a cascade reaction for the synthesis of optically pure (S)-beta-phenylalanine from benzoylacetonitrile was developed by coupling HpN with an omega-transaminase from Polaromonas sp. JS666 in toluene-water biphasic reaction system using beta-alanine as an amino donor. Various (S)-beta-amino acids can be produced from benzoylacetonitrile derivatives with moderate to high conversions (73-99%) and excellent enantioselectivity (above 99% enantiomeric exess). Great potential of this cascade reaction for the practical synthesis of (S)-beta-phenylalanine |
-, 755874 |
| 3.5.5.1 | synthesis |
attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives |
-, 686039 |
| 3.5.5.1 | synthesis |
biotransformation of benzonitrile to benzoic acid. The effect of whole cell immobilisation on the biotransformation of benzonitrile and the use of direct electric current for enhanced product removal |
668039 |
| 3.5.5.1 | synthesis |
biotransformation of trans-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]-acrylonitrile to trans-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]-acrylic acid with isolated enzyme, immobilized enzyme and with recombinant cells containing AtNIT1 |
669903 |
| 3.5.5.1 | synthesis |
enzyme can be used as a biocatalyst for the synthesis of a range of alpha-hydroxy carboxylic acids or amides from aldehydes in presence of cyanide, halting of the reaction at the amide intermediate by use of specific inhibitors is possible |
-, 654314 |
