Title of article :
On the substrate preference of glutaryl acylases
Author/Authors :
Rosini، نويسنده , , Elena and Monelli، نويسنده , , Claudia Stella and Pollegioni، نويسنده , , Loredano and Riva، نويسنده , , Sergio and Monti، نويسنده , , Daniela، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
7
From page :
52
To page :
58
Abstract :
The substrate preferences of three acylases – two wild-type enzymes and an evolved variant obtained by directed evolution – which are prototypical enzymes for glutaryl-7-ACA acylase and cephalosporin C acylase subfamilies, have been investigated. A preliminary screening of enzymes’ performances on a large set of substrates has been carried out by a colorimetric assay performed in 96-well plates and by a pH-Stat monitoring the hydrolytic activities. Subsequently, kinetic data for selected substrates have been determined, thus elucidating the substrate preference of members of glutaryl-7-ACA acylase vs. cephalosporin C acylase subfamilies. These achievements pave the way to the ability of choosing the best enzyme for the hydrolysis of different compounds of industrial importance.
Keywords :
Acylases , bioconversion , Substrate Specificity , substrate promiscuity , cephalosporin C
Journal title :
Journal of Molecular Catalysis B Enzymatic
Serial Year :
2012
Journal title :
Journal of Molecular Catalysis B Enzymatic
Record number :
1717055
Link To Document :
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