Document Type

Article

Publication Date

9-12-2023

Abstract

Chlorogenic acid esterases (ChlEs) are a useful class of enzymes that hydrolyze chlorogenic acid (CGA) into caffeic and quinic acid. ChlEs can break down CGA in foods to improve their sensory properties and release caffeic acid in the digestive system to improve the absorption of bioactive compounds. This work presents the structure, molecular dynamics, and biochemical characterization of a ChlE from Lactobacillus helveticus (Lh). Molecular dynamics simulations suggest that substrate access to the active site of LhChlE is modulated by two hairpin loops above the active site. Docking simulations and mutational analysis suggest that two residues within the loops, Gln145 and Lys164, are important for CGA binding. Lys164 provides a slight substrate preference for CGA, whereas Gln145 is required for efficient turnover. This work is the first to examine the dynamics of a bacterial ChlE and provides insights on the substrate binding preference and turnover in this type of enzyme.

Comments

This is the accepted version of the following article:

Omori, K.K., Drucker, C.T., Okumura, T.L.S., Carl, N.B., Dinn, B.T., Ly, D., Sacapano, K.N., Tajii, A. and Owens, C.P. (2023), The structure of a Lactobacillus helveticus chlorogenic acid esterase and the dynamics of its insertion domain provide insights into substrate binding. FEBS Lett. "https://doi.org/10.1002/1873-3468.14731

which has been published in final form at https://doi.org/10.1002/1873-3468.14731. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.

feb214731-sup-0001-supinfo.docx (9057 kB)
Supporting information

Copyright

Wiley

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