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Literature summary for 3.5.5.5 extracted from

  • Mateo, C.; Chmura, A.; Rustler, S.; van Rantwijk, F.; Stolz, A.; Sheldon, R.A.
    Synthesis of enantiomerically pure (S)-mandelic acid using anoxynitrilasenitrilase bienzymatic cascade: a nitrilase surprisingly shows nitrile hydratase activity (2006), Tetrahedron Asymmetry, 17, 320-323.
No PubMed abstract available
Search for more literature for 3.5.5.5

Organism

Organism UniProt Comment Textmining
Pseudomonas fluorescens Q5EG61
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Pseudomonas fluorescens EBC191 Q5EG61
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(S)-mandelonitrile + 2 H2O
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 Pseudomonas fluorescens (S)-mandelic acid + NH3 the product is 94% enantiomeric pure (S)-isomer, the formation of ca 50% (S)-mandeloamide is observed ?
(S)-mandelonitrile + 2 H2O
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 Pseudomonas fluorescens EBC191 (S)-mandelic acid + NH3 the product is 94% enantiomeric pure (S)-isomer, the formation of ca 50% (S)-mandeloamide is observed ?

General Information

General Information Comment Organism
metabolism involved in the biosynthesis of adenosylcobalamin Pseudomonas fluorescens