Isopenicillin N synthase (IPNS), a non-haem iron-dependent oxidase, catalys
es the biosynthesis of isopenicillin N (IPN), the precursor of all penicill
ins and cephalosporins'. The key steps in this reaction are the two iron-di
oxygen-mediated ring closures of the tripeptide delta-(L-alpha-aminoadipoyl
)-L-cysteinyl-D-valin (ACV). It has been proposed that the four-membered be
ta-lactam ring forms initially, associated with a highly oxidized iron(rv)-
oxo (ferryl) moiety, which subsequently mediates closure of the five-member
ed thiazolidine ring(2). Here we describe observation of the IPNS reaction
in crystals by X-ray crystallography. IPNS.Fe2+.substrate crystals were gro
wn anaerobically(3,4), exposed to high pressures of oxygen to promote react
ion and frozen, and their structures were elucidated by X-ray diffraction.
Using the natural substrate ACV, this resulted in the IPNS.Fe2+.IPN product
complex. With the substrate analogue, delta-(L-alpha-aminoadipoyl)-L-cyste
inyl-L-S-methyl-cysteine (ACmC) in the crystal, the reaction cycle was inte
rrupted at the monocyclic stage. These mono- and bicyclic structures suppor
t our hypothesis of a two-stage reaction sequence leading to penicillin. Fu
rthermore, the formation of a monocyclic sulphoxide product from ACmC is mo
st simply explained by the interception of a high-valency iron-ore species.