Diverging Mechanisms: Cytochrome-P450-Catalyzed Demethylation and γ-Lactone Formation in Bacterial Gibberellin Biosynthesis.

Angew Chem Int Ed Engl

Roy J. Carver Dep. of Biochem., Biophys. & Mol. Biol., Iowa State University, Ames, IA, 50011, USA.

Published: May 2018

Biosynthesis of the gibberellin (GA) plant hormones evolved independently in plants and microbes, but the pathways proceed by similar transformations. The combined demethylation and γ-lactone ring forming transformation is of significant mechanistic interest, yet remains unclear. The relevant CYP112 from bacteria was probed by activity assays and O -labeling experiments. Notably, the ability of tert-butyl hydroperoxide to drive this transformation indicates use of the ferryl-oxo (Compound I) from the CYP catalytic cycle for this reaction. Together with the confirmed loss of C20 as CO , this necessitates two catalytic cycles for carbon-carbon bond scission and γ-lactone formation. The ability of CYP112 to hydroxylate the δ-lactone form of GA , shown by the labeling studies, is consistent with the implied use of a further oxygenated heterocycle in the final conversion of GA into GA , with the partial labeling of GA , thus demonstrating that CYP112 partitions its reactants between two diverging mechanisms.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020689PMC
http://dx.doi.org/10.1002/anie.201713403DOI Listing

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