glutaryl-7-aminocephalosporanic-acid and cytidylyl-(3--5-)-cytidine

Residue Phe375 of cephalosporin acylase has been identified as one of the residues that is involved in substrate specificity. A complete mutational analysis was performed by substituting Phe375 with the 19 other amino acids and characterising all purified mutant enzymes. Several mutations cause a substrate specificity shift from the preferred substrate of the enzyme, glutaryl-7-ACA, towards the desired substrate, adipyl-7-ADCA. The catalytic efficiency ( [Formula: see text] (cat)/ [Formula: see text] (m)) of mutant SY-77(F375C) towards adipyl-7-ADCA was increased 6-fold with respect to the wild-type enzyme, due to a strong decrease of [Formula: see text] (m). The [Formula: see text] (cat) of mutant SY-77(F375H) towards adipyl-7-ADCA was increased 2.4-fold. The mutational effects point at two possible mechanisms by which residue 375 accommodates the long side chain of adipyl-7-ADCA, either by a widening of a hydrophobic ring-like structure that positions the aliphatic part of the side chain of the substrate, or by hydrogen bonding to the carboxylate head of the side chain.

Topics: Adipates; Amino Acid Sequence; Cephalosporins; Dinucleoside Phosphates; Enzyme Activation; Hydrolysis; Molecular Sequence Data; Mutagenesis, Site-Directed; Penicillin Amidase; Protein Engineering; Protein Structure, Tertiary; Pseudomonas; Recombinant Proteins; Structure-Activity Relationship; Substrate Specificity