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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Sprache:eng
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Zusammenfassung: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.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2023.05.083