Journal article

α,β → β,γ double bond migration in corallopyronin A biosynthesis


Authors listLohr, F; Jenniches, I; Frizler, M; Meehan, MJ; Sylvester, M; Schmitz, A; Gutschow, M; Dorrestein, PC; Konig, GM; Schaberle, TF

Publication year2013

Pages4175-4180

JournalChemical Science

Volume number4

Issue number11

ISSN2041-6520

DOI Linkhttps://doi.org/10.1039/c3sc51854j

PublisherRoyal Society of Chemistry


Abstract
In polyketide biosynthesis the reduction of beta-carbonyl groups to an alkene usually results in a alpha,beta double bond. However, in a few antibiotics the rare case of such a carbon-carbon double bond in beta,gamma position is observed. The in vivo active antibiotic corallopyronin A represents such a molecule, whereby a alpha,beta -> beta,gamma double bond migration takes place during the assembly of the molecule. Here we report the in vitro analysis of the enzyme domain responsible for this double bond isomerization. This "shift domain" was heterologously expressed and assayed with its acyl carrier protein bound substrate. To facilitate this analysis the biosynthetic corallopyronin A intermediate was chemically synthesized as a SNAC-derivative. Enzyme activity was analyzed by NMR and high-resolution MS measurements, the latter enabled by performing the assay in deuterated buffer. Mutated enzyme variants gave first experimental evidence for the essential amino acids involved in double bond migration. These results further support the proposed corallopyronin A biosynthesis.



Citation Styles

Harvard Citation styleLohr, F., Jenniches, I., Frizler, M., Meehan, M., Sylvester, M., Schmitz, A., et al. (2013) α,β → β,γ double bond migration in corallopyronin A biosynthesis, Chemical Science, 4(11), pp. 4175-4180. https://doi.org/10.1039/c3sc51854j

APA Citation styleLohr, F., Jenniches, I., Frizler, M., Meehan, M., Sylvester, M., Schmitz, A., Gutschow, M., Dorrestein, P., Konig, G., & Schaberle, T. (2013). α,β → β,γ double bond migration in corallopyronin A biosynthesis. Chemical Science. 4(11), 4175-4180. https://doi.org/10.1039/c3sc51854j


Last updated on 2025-21-05 at 16:19