Flavoenzyme‐Catalyzed Formation of Disulfide Bonds in Natural Products1. Issue 8 (20th January 2014)

• Record Type: Journal Article
• Authors: Scharf, Daniel H.; Groll, Michael; Habel, Andreas; Heinekamp, Thorsten; Hertweck, Christian; Brakhage, Axel A.; Huber, Eva M.
• Is Part Of: Angewandte Chemie international edition. Volume 53:Issue 8(2014)
• Page Start: 2221
• Page End: 2224
• Publication Date: 2014-01-20
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201309302
• Languages: English
• ISSNs: 1433-7851

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Nature provides a rich source of compounds with diverse chemical structures and biological activities, among them, sulfur‐containing metabolites from bacteria and fungi. Some of these compounds bear a disulfide moiety that is indispensable for their bioactivity. Specialized oxidoreductases such as GliT, HlmI, and DepH catalyze the formation of this disulfide bridge in the virulence factor gliotoxin, the antibiotic holomycin, and the anticancer drug romidepsin, respectively. We have examined all three enzymes by X‐ray crystallography and activity assays. Despite their differently sized substrate binding clefts and hence, their diverse substrate preferences, a unifying reaction mechanism is proposed based on the obtained crystal structures and further supported by mutagenesis experiments.</p> </abstract>