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Structure and Mechanism of the Lantibiotic Cyclase Involved in Nisin Biosynthesis

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Journal Science
Specialty Science
Date 2006 Mar 11
PMID 16527981
Citations 135
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Abstract

Nisin is a posttranslationally modified antimicrobial peptide that is widely used as a food preservative. It contains five cyclic thioethers of varying sizes that are installed by a single enzyme, NisC. Reported here are the in vitro reconstitution of the cyclization process and the x-ray crystal structure of the NisC enzyme. The structure reveals similarities in fold and substrate activation with mammalian farnesyl transferases, suggesting that human homologs of NisC posttranslationally modify a cysteine of a protein substrate.

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