3.5.5.5: Arylacetonitrilase
This is an abbreviated version!
For detailed information about Arylacetonitrilase, go to the full flat file.
Word Map on EC 3.5.5.5
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3.5.5.5
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mandelonitrile
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enantioselectivity
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fluorescens
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arylacetonitriles
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enantiomeric
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s-mandelic
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phenylacetonitrile
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alcaligenes
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r,s-mandelonitrile
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benzaldehyde
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synthesis
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arylacetic
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esculenta
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enantiospecificity
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ultrafast
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psychrotolerans
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s-selectivity
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manihot
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biotechnology
- 3.5.5.5
- mandelonitrile
-
enantioselectivity
- fluorescens
- arylacetonitriles
-
enantiomeric
-
s-mandelic
- phenylacetonitrile
- alcaligenes
-
r,s-mandelonitrile
- benzaldehyde
- synthesis
-
arylacetic
- esculenta
-
enantiospecificity
-
ultrafast
- psychrotolerans
-
s-selectivity
-
manihot
- biotechnology
Reaction
Synonyms
Arylacetonitrilase, arylacetonitrile-hydrolyzing nitrilase, arylacetonitrile-specific nitrilase, blr3397, enantioselective arylacetonitrilase, GPnor51, NIT, NitA, NitAd, NitAk2, NitAn, NitMp, NitP, nitrilase, nitrilase PpL19, Nitrilase, arylaceto-, NitTv
ECTree
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Organic Solvent Stability
Organic Solvent Stability on EC 3.5.5.5 - Arylacetonitrilase
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dimethyl sulfoxide
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2.5 or 5%, up to 20% increase in activity, decrease above
Ethanol
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5%, 63% enhancement in activity probably due to increased availibaility of substrate. Above 10% ethanol, significant decrease in activity
Methanol
Methanol
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5%, 78% enhancement in activity probably due to increased availibaility of substrate. Above 10% methanol, significant decrease in activity