Isopenicillin N synthase (IPNS) is a non-heme iron oxidase central to the biosynthesis of β-lactam antibiotics. IPNS converts the tripeptide δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine (ACV) to isopenicillin N while reducing molecular oxygen to water. The substrate analogue δ-(L-α-aminoadipoyl)-L-cysteinyl-O-methyl-D-threonine (ACmT) is not turned over by IPNS. Epimeric δ-(L-α-aminoadipoyl)-L-cysteinyl-O-methyl-D-allo-threonine (ACmaT) is converted to a bioactive penam product. ACmT and ACmaT differ from each other only in the stereochemistry at the β-carbon atom of their third residue. These substrates both contain a methyl ether in place of the isopropyl group of ACV. We report an X-ray crystal structure for the anaerobic IPNS:Fe(II):ACmT complex. This structure reveals an additional water molecule bound to the active site metal, held by hydrogen-bonding to the ether oxygen atom of the substrate analogue.
Keywords: AC-; AC-O-methyl-d-allo-threonine; AC-O-methyl-d-threonine; AC-d-allo-isoleucine; AC-d-isoleucine; AC-d-thio-allo-isoleucine; AC-d-thioisoleucine; AC-d-valine; ACI; ACV; ACaI; ACmT; ACmaT; ACtI; ACtaI; Antibiotic; Biosynthesis; IPN; IPNS; Metalloenzyme; Non-heme iron oxidase; Penicillin; Protein crystallography; isopenicillin N; isopenicillin N synthase; δ-l-α-aminoadipoyl-l-cysteinyl-.
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