Li
Su
abc,
Yaouba
Souaibou
abd,
Laurence
Hôtel
b,
Christophe
Jacob
a,
Peter
Grün
c,
Yan-Ni
Shi
ce,
Alicia
Chateau
f,
Sophie
Pinel
f,
Helge B.
Bode
ceghi,
Bertrand
Aigle
*b and
Kira J.
Weissman
*a
aUniversité de Lorraine, CNRS, IMoPA, F-54000 Nancy, France. E-mail: kira.weissman@univ-lorraine.fr
bUniversité de Lorraine, INRAE, DynAMic, F-54000 Nancy, France. E-mail: bertrand.aigle@univ-lorraine.fr
cMax-Planck-Institute for Terrestrial Microbiology, Department of Natural Products in Organismic Interactions, 35043 Marburg, Germany
dIPHC, UMR 7178, CNRS, Université de Strasbourg, Equipe de Chimie Analytique des Molécules Bioactives et Pharmacognosie, Illkirch, France
eMolecular Biotechnology, Department of Biosciences, Goethe University Frankfurt, Frankfurt am Main, Germany
fUniversité de Lorraine, CNRS, CRAN, F-54000 Nancy, France
gChemical Biology, Department of Chemistry, Philipps University of Marburg, 35043 Marburg, Germany
hSenckenberg Gesellschaft für Naturforschung, 60325 Frankfurt am Main, Germany
iCenter for Synthetic Microbiology (SYNMIKRO), University of Marburg, 35043 Marburg, Germany
First published on 7th March 2025
Correction for ‘Exploiting the inherent promiscuity of the acyl transferase of the stambomycin polyketide synthase for the mutasynthesis of analogues’ by Li Su et al., Chem. Sci., 2025, https://doi.org/10.1039/d4sc06976e.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
This journal is © The Royal Society of Chemistry 2025 |