Licochalcone A inhibits the assembly function of β-barrel assembly machinery in Escherichia coli

Biochem Biophys Res Commun. 2023 Aug 6:668:90-95. doi: 10.1016/j.bbrc.2023.05.083. Epub 2023 May 22.

Abstract

Antimicrobial resistance (AMR) crisis urges the development of new antibiotics. In the present work, we for the first time used bio-affinity ultrafiltration combined with HPLC-MS (UF-HPLC-MS) to examine the interaction between the outer membrane β-barrel proteins and natural products. Our results showed that natural product licochalcone A from licorice interacts with BamA and BamD with the enrichment factor of 6.38 ± 1.46 and 4.80 ± 1.23, respectively. The interaction was further confirmed by use of biacore analysis, which demonstrated that the Kd value between BamA/D and licochalcone was 6.63/28.27 μM, suggesting a good affinity. To examine the effect of licochalcone A on BamA/D function, the developed versatile in vitro reconstitution assay was used and the results showed that 128 μg/mL licochalcone A could reduce the outer membrane protein A integration efficiency to 20%. Although licochalcone A alone can not inhibit the growth of E. coli, but it can affect the membrane permeability, suggesting that licochalcone A holds the potential to be used as a sensitizer to combat AMR.

Keywords: Antimicrobial resistance; Assembly function; Licochalcone A; The outer membrane permeability; β-barrel assembly machinery.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Outer Membrane Proteins / metabolism
  • Chalcones* / pharmacology
  • Escherichia coli / metabolism
  • Escherichia coli Proteins* / metabolism
  • Protein Folding

Substances

  • Escherichia coli Proteins
  • licochalcone A
  • Chalcones
  • Bacterial Outer Membrane Proteins
  • BamA protein, E coli