Biosynthesis of fluopsin C, a copper-containing antibiotic from Pseudomonas aeruginosa

Author:

Patteson Jon B.1ORCID,Putz Andrew T.1ORCID,Tao Lizhi2ORCID,Simke William C.1ORCID,Bryant L. Henry1ORCID,Britt R. David2ORCID,Li Bo12ORCID

Affiliation:

1. Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

2. Department of Chemistry, University of California, Davis, Davis, CA, USA.

Abstract

A copper-containing antibiotic Bacteria require transition metal ions for biological processes and must also protect themselves against excess metal, which is toxic. Patteson et al . explored how the environmental bacterium Pseudomonas aeruginosa uses a five-enzyme pathway to synthesize a small-molecule complex, fluopsin C, which is built from cysteine and contains a copper ion. The biosynthesis involves unusual enzymatic transformations that convert cysteine to a thiohydroximate, two of which chelate a copper ion in the final natural product. Fluopsin C protects P. aeruginosa from excess copper and also acts as a broad-spectrum antibiotic against other bacteria. —VV

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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