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Correction: Molecular basis of sulfolactate synthesis by sulfolactaldehyde dehydrogenase from Rhizobium leguminosarum

Jinling Li a, Mahima Sharma b, Richard Meek b, Amani Alhifthi ac, Zachary Armstrong a, Niccolay Madiedo Soler d, Mihwa Lee a, Ethan D. Goddard-Borger de, James N. Blaza b, Gideon J. Davies *b and Spencer J. Williams *a
aSchool of Chemistry and Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville, Victoria 3010, Australia. E-mail: sjwill@unimelb.edu.au
bYork Structural Biology Laboratory, Department of Chemistry, University of York, York YO10 5DD, UK. E-mail: gideon.davies@york.ac.uk
cChemistry Department, Faculty of Science (Female Section), Jazan University, Jazan 82621, Saudi Arabia
dACRF Chemical Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3010, Australia
eDepartment of Medical Biology, University of Melbourne, Parkville, Victoria 3010, Australia

Received 30th November 2023 , Accepted 30th November 2023

First published on 12th December 2023


Abstract

Correction for ‘Molecular basis of sulfolactate synthesis by sulfolactaldehyde dehydrogenase from Rhizobium leguminosarum’ by Jinling Li et al., Chem. Sci., 2023, 14, 11429–11440, https://doi.org/10.1039/D3SC01594G.


The authors note that the stereochemistry of several compounds in Fig. 1 were incorrectly drawn. The corrected Fig. 1 and amended figure legend are provided here.
image file: d3sc90238b-f1.tif
Fig. 1 (a) Formation of S-sulfolactate (S-SL) and S-dihydroxypropanesulfonate (S-DHPS) through the pathways of sulfoglycolysis from sulfoquinovose (SQ). (b) Formation and degradation of S-SL by catabolism of DHPS.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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