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Pyran formation by an atypical CYP-mediated four-electron oxygenation-cyclization cascade in an engineered aureothin
Martin Richter1, Benjamin Busch, Keishi Ishida
1Dept. Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology, HKI, Beutenbergstrasse 11a, 07745 Jena, Germany.
Chembiochem : a European Journal of Chemical Biology
|September 11, 2012
Abstract:
Small changes, big effect: A new aureothin derivative, aureopyran, which features an unusual pyran backbone, was generated by simply altering the enzymatic methylation topology. The α-pyrone ring hampers the correct placement of the polyketide backbone in the multifunctional cytochrome P450 monooxygenase AurH. Instead of a tetrahydrofuran ring, an oxo intermediate is formed that readily undergoes a rare electrocyclization reaction.