Isopenicillin N synthase
Class of enzymes
From Wikipedia, the free encyclopedia
Isopenicillin N synthase (IPNS) is a non-heme iron protein. This enzyme catalyzes the formation of isopenicillin N from δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine (LLD-ACV).[1] IPNS occupies an early and key role in the biosynthetic pathway of all of the penicillins and cephalosporins, which are types of β-lactam antibiotics. This class of antibiotics is the most widely used. They act by inhibiting the synthesis of the peptidoglycan layer of bacterial cell walls, which is especially important in Gram-positive organisms.
- N-[(5S)-5-amino-5-carboxypentanoyl]-L-cysteinyl-D-valine + O2 isopenicillin N + 2 H2O
| isopenicillin N synthase | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||
| EC no. | 1.21.3.1 | ||||||||
| CAS no. | 78642-31-6 | ||||||||
| Databases | |||||||||
| BRENDA | enzyme data | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | enzyme entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| Rhea | reactions | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / QuickGO | ||||||||
| |||||||||
This reaction is a step in the biosynthesis of penicillin and cephalosporin antibiotics.[1]
The active sites of most isopenicillin N synthases contain an iron ion. This enzyme is also called isopenicillin N synthetase.
Mechanism
The active site features Fe(II) bound to at least two histidine residues, an aspartate residue, a glutamine residue, and two water molecules. The two histidine residues and one aspartic acid residue are conserved. Concomitant with deprotonation of the thiol, ACV binds the active site, displacing Gln330 and one water molecule.[1]
The linear tripeptide δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine (LLD-ACV) must first be assembled from its component amino acids by N-(5-amino-5-carboxypentanoyl)-L-cysteinyl-D-valine synthase (ACV synthase).[2]
The ligation of ACV decreases the Fe(II)/Fe(III) redox potential, which is known in model systems.[3][4] The electron-rich Fe(II) center binds dioxygen. An intramolecular hydrogen atom transfer from FeSCH2 to the Fe-O2 group converts the Fe(III) back to the Fe(II). The Fe(II)-OOH then deprotonates the amide, which then closes the β-lactam ring by a nucleophilic attack at the thioaldehyde carbon.This causes the hydrogen atom at the C-3 of the valine residue to come closer to the iron(IV) oxo ligand which is highly electrophilic. A second hydrogen transfer occurs, most likely producing an isopropyl radical which closes the thiazolidine ring by attacking the thiolate sulfur atom.[1]
Role in Antibiotic Formation
Following the IPNS pathway, further enzymes are responsible for the epimerization of isopenicillin N to penicillin N, the derivitazation to other penicillins, and the ring expansion that eventually leads to the various cephalosporins.[5]
Structural studies
Many structures have been solved for this class of enzymes, with PDB accession codes PDB: 1ODM, PDB: 1UZW, PDB: 1W03, PDB: 1W04, PDB: 1W05, PDB: 1W06, PDB: 1W3V, PDB: 1W3X, PDB: 2BJS, PDB: 2BU9, PDB: 2IVI, PDB: 2IVJ, 2JB4, 1QJE, 1ODN, 1HB1, 1HB2, 1HB3, 1HB4, 1QIQ, 1QJF, 1BK0, 1BLZ, 1OBN, 1OC1, 1IPS
Further reading
- Roach PL, Clifton IJ, Hensgens CM, Shibata N, Schofield CJ, Hajdu J, Baldwin JE (June 1997). "Structure of isopenicillin N synthase complexed with substrate and the mechanism of penicillin formation". Nature. 387 (6635): 827–30. Bibcode:1997Natur.387..827R. doi:10.1038/42990. PMID 9194566. S2CID 205032251.
- Borovok I, Landman O, Kreisberg-Zakarin R, Aharonowitz Y, Cohen G (February 1996). "Ferrous active site of isopenicillin N synthase: genetic and sequence analysis of the endogenous ligands". Biochemistry. 35 (6): 1981–7. doi:10.1021/bi951534t. PMID 8639682.
- Miller FD, Chapman JL, Queener SW (1992). "Substrate specificity of isopenicillin N synthase". J. Med. Chem. 35 (10): 1897–914. doi:10.1021/jm00088a028. PMID 1588566.
- Andersson I, Schofield CJ, Baldwin JE (1995). "Crystal structure of isopenicillin N synthase is the first from a new structural family of enzymes". Nature. 375 (6533): 700–4. Bibcode:1995Natur.375..700R. doi:10.1038/375700a0. PMID 7791906. S2CID 22804064.
