Issue 8, 2025

Comment on “Discovery of a polyketide carboxylate phytotoxin from a polyketide glycoside hybrid by β-glucosidase mediated ester bond hydrolysis” by X. Wang, D.-K. Kong, H.-R. Zhang, Y. Zou, Chem. Sci., 2024, 15, 17183

Abstract

We challenge the conclusion that the β-glucosidase in question directly catalyses hydrolysis of the substrate ester linkage. Rather we propose that this enzyme performs a normal glucoside hydrolysis and that the released aglycone undergoes rearrangement with formation of a quinone methide-like species through spontaneous cleavage of the ester.

Graphical abstract: Comment on “Discovery of a polyketide carboxylate phytotoxin from a polyketide glycoside hybrid by β-glucosidase mediated ester bond hydrolysis” by X. Wang, D.-K. Kong, H.-R. Zhang, Y. Zou, Chem. Sci., 2024, 15, 17183

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Article information

Article type
Comment
Submitted
14 nuve 2024
Accepted
16 ghje 2025
First published
28 ghje 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2025,16, 3755-3757

Comment on “Discovery of a polyketide carboxylate phytotoxin from a polyketide glycoside hybrid by β-glucosidase mediated ester bond hydrolysis” by X. Wang, D.-K. Kong, H.-R. Zhang, Y. Zou, Chem. Sci., 2024, 15, 17183

S. A. Nasseri, R. K. Bains, Y. Tian and S. G. Withers, Chem. Sci., 2025, 16, 3755 DOI: 10.1039/D4SC07749K

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