Monobactam formation in sulfazecin by a nonribosomal peptide synthetase thioesterase.
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ABSTRACT: The N-sulfonated monocyclic ?-lactam ring characteristic of the monobactams confers resistance to zinc metallo-?-lactamases and affords the most effective class to combat carbapenem-resistant enterobacteria (CRE). Here we report unprecedented nonribosomal peptide synthetase activities, wherein an assembled tripeptide is N-sulfonated in trans before direct synthesis of the ?-lactam ring in a noncanonical, cysteine-containing thioesterase domain. This means of azetidinone synthesis is distinct from the three others known in nature.
SUBMITTER: Oliver RA
PROVIDER: S-EPMC5726899 | biostudies-literature | 2018 Jan
REPOSITORIES: biostudies-literature
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