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Biosci Biotechnol Biochem ; 66(6): 1256-61, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12162546

ABSTRACT

The gene encoding the fructosyl-amino acid oxidase (fructosyl-alpha-L-amino acid: oxygen oxidoreductase (defructosylating); EC 1.5.3) of Corynebacterium sp. 2-4-1 was cloned and expressed in Escherichia coli. The gene consists of 1,116 nucleotides and encodes a protein of 372 amino acids with a predicted molecular mass of 39,042. The open reading frame was confirmed as the gene of the fructosyl-amino acid oxidase by comparison with the N-terminal amino acid sequence of the purified fructosyl-amino acid oxidase from Corynebacterium sp. 2-4-1. The sequence of the AMP-binding motif, GXGXXG, was found in the deduced N-terminal region. The amino acid sequence of the fructosyl-amino acid oxidase showed no similarity to that of fungal fructosyl-amino acid oxidases. In addition, substrate specificities of this fructosyl-amino acid oxidase were different from those of other fructosyl-amino acid oxidases. The fructosyl-amino acid oxidase of Corynebacterium sp. 2-4-1 is an enzyme that has unique substrate specificity and primary structure in comparison with fungal fructosyl-amino acid oxidases.


Subject(s)
Amino Acid Oxidoreductases/genetics , Corynebacterium/enzymology , Corynebacterium/genetics , Escherichia coli/genetics , Amino Acid Motifs , Amino Acid Oxidoreductases/chemistry , Amino Acid Oxidoreductases/isolation & purification , Amino Acid Oxidoreductases/metabolism , Amino Acid Sequence , Base Sequence , Cloning, Molecular , Fungi/enzymology , Molecular Sequence Data , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Substrate Specificity
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