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

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 sh...

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Veröffentlicht in:Biochemical and biophysical research communications 2023-08, Vol.668, p.90-95
Hauptverfasser: Wei, Liangwan, Wang, Zhe, Chu, Yindi, Cai, Kun, Li, Wei, Huang, Piying, Qin, Youcai, Liu, Dailin, Zhuang, Xiaocui, Guo, Mingquan, Song, Xinbo, Fan, Enguo
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container_issue
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container_title Biochemical and biophysical research communications
container_volume 668
creator Wei, Liangwan
Wang, Zhe
Chu, Yindi
Cai, Kun
Li, Wei
Huang, Piying
Qin, Youcai
Liu, Dailin
Zhuang, Xiaocui
Guo, Mingquan
Song, Xinbo
Fan, Enguo
description 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. •Licochalcone A from licorice interacts with BamA and BamD, the core components of BAM.•Licochalcone A reduces the outer membrane protein A integration efficiency.•Licochalcone A holds a great potential to be used as a sensitizer to combat AMR.
doi_str_mv 10.1016/j.bbrc.2023.05.083
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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. •Licochalcone A from licorice interacts with BamA and BamD, the core components of BAM.•Licochalcone A reduces the outer membrane protein A integration efficiency.•Licochalcone A holds a great potential to be used as a sensitizer to combat AMR.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2023.05.083</identifier><identifier>PMID: 37245294</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antimicrobial resistance ; Assembly function ; Bacterial Outer Membrane Proteins - metabolism ; Chalcones - pharmacology ; Escherichia coli - metabolism ; Escherichia coli Proteins - metabolism ; Licochalcone A ; Protein Folding ; The outer membrane permeability ; β-barrel assembly machinery</subject><ispartof>Biochemical and biophysical research communications, 2023-08, Vol.668, p.90-95</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023 Elsevier Inc. 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subjects Antimicrobial resistance
Assembly function
Bacterial Outer Membrane Proteins - metabolism
Chalcones - pharmacology
Escherichia coli - metabolism
Escherichia coli Proteins - metabolism
Licochalcone A
Protein Folding
The outer membrane permeability
β-barrel assembly machinery
title Licochalcone A inhibits the assembly function of β-barrel assembly machinery in Escherichia coli
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