Title of article :
Nitroalkane oxidase, a carbanion-forming flavoprotein homologous to acyl-CoA dehydrogenase
Author/Authors :
Fitzpatrick، نويسنده , , Paul F. and Orville، نويسنده , , Allen M. and Nagpal، نويسنده , , Akanksha and Valley، نويسنده , , Michael P.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
9
From page :
157
To page :
165
Abstract :
While several flavoproteins will oxidize nitroalkanes in addition to their physiological substrates, nitroalkane oxidase (NAO) is the only one which does not require the anionic nitroalkane. This, in addition to the induction of NAO by nitroethane seen in Fusarium oxysporum, suggests that oxidation of a nitroaliphatic species is the physiological role of the enzyme. Mechanistic studies of the reaction with nitroethane as substrate have established many of the details of the enzymatic reaction. The enzyme is unique in being the only flavoprotein to date for which a carbanion is definitively established as an intermediate in catalysis. Recent structural analyses show that NAO is homologous to the acyl-CoA dehydrogenase and acyl-CoA oxidase families of enzymes. In NAO, the glutamate which acts as the active site base in the latter enzymes is replaced by an aspartate.
Keywords :
flavoprotein , Acyl-CoA dehydrogenase , nitroalkane oxidase , Acyl-CoA oxidase , structure , Mechanism
Journal title :
Archives of Biochemistry and Biophysics
Serial Year :
2005
Journal title :
Archives of Biochemistry and Biophysics
Record number :
1626714
Link To Document :
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