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 |
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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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•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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c271t-fa3afe7de9509682f45a11980e7b2829b07446e5ad2aef217aa035ae945dffd83</citedby><cites>FETCH-LOGICAL-c271t-fa3afe7de9509682f45a11980e7b2829b07446e5ad2aef217aa035ae945dffd83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X23006617$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37245294$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei, Liangwan</creatorcontrib><creatorcontrib>Wang, Zhe</creatorcontrib><creatorcontrib>Chu, Yindi</creatorcontrib><creatorcontrib>Cai, Kun</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Huang, Piying</creatorcontrib><creatorcontrib>Qin, Youcai</creatorcontrib><creatorcontrib>Liu, Dailin</creatorcontrib><creatorcontrib>Zhuang, Xiaocui</creatorcontrib><creatorcontrib>Guo, Mingquan</creatorcontrib><creatorcontrib>Song, Xinbo</creatorcontrib><creatorcontrib>Fan, Enguo</creatorcontrib><title>Licochalcone A inhibits the assembly function of β-barrel assembly machinery in Escherichia coli</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>Antimicrobial resistance</subject><subject>Assembly function</subject><subject>Bacterial Outer Membrane Proteins - metabolism</subject><subject>Chalcones - pharmacology</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Licochalcone A</subject><subject>Protein Folding</subject><subject>The outer membrane permeability</subject><subject>β-barrel assembly machinery</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LJDEQhsPi4oyuf2APkqOXbivpz4AXEb9gYC-7sLdQna7QGbo7mvQI87f8If4me5hRb54Kqp73hXoY-y0gFSDKy3XaNMGkEmSWQpFCnf1gSwEKEikgP2JLACgTqcT_BTuJcQ0gRF6qY7bIKpkXUuVLhitnvOmwN34kfs3d2LnGTZFPHXGMkYam33K7Gc3k_Mi95W-vSYMhUP91HtB0bqSwneP8NpqOgps3yI3v3S_202If6ewwT9m_u9u_Nw_J6s_94831KjGyElNiMUNLVUuqAFXW0uYFCqFqoKqRtVQNVHleUoGtRLJSVIiQFUgqL1pr2zo7ZRf73qfgnzcUJz24aKjvcSS_iXougSyrlJIzKveoCT7GQFY_BTdg2GoBeqdWr_VOrd6p1VDoWe0cOj_0b5qB2s_Ih8sZuNoDNH_54ijoaByNhloXyEy69e67_ncmBovv</recordid><startdate>20230806</startdate><enddate>20230806</enddate><creator>Wei, Liangwan</creator><creator>Wang, Zhe</creator><creator>Chu, Yindi</creator><creator>Cai, Kun</creator><creator>Li, Wei</creator><creator>Huang, Piying</creator><creator>Qin, Youcai</creator><creator>Liu, Dailin</creator><creator>Zhuang, Xiaocui</creator><creator>Guo, Mingquan</creator><creator>Song, Xinbo</creator><creator>Fan, Enguo</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20230806</creationdate><title>Licochalcone A inhibits the assembly function of β-barrel assembly machinery in Escherichia coli</title><author>Wei, Liangwan ; Wang, Zhe ; Chu, Yindi ; Cai, Kun ; Li, Wei ; Huang, Piying ; Qin, Youcai ; Liu, Dailin ; Zhuang, Xiaocui ; Guo, Mingquan ; Song, Xinbo ; Fan, Enguo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c271t-fa3afe7de9509682f45a11980e7b2829b07446e5ad2aef217aa035ae945dffd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antimicrobial resistance</topic><topic>Assembly function</topic><topic>Bacterial Outer Membrane Proteins - metabolism</topic><topic>Chalcones - pharmacology</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>Licochalcone A</topic><topic>Protein Folding</topic><topic>The outer membrane permeability</topic><topic>β-barrel assembly machinery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Liangwan</creatorcontrib><creatorcontrib>Wang, Zhe</creatorcontrib><creatorcontrib>Chu, Yindi</creatorcontrib><creatorcontrib>Cai, Kun</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Huang, Piying</creatorcontrib><creatorcontrib>Qin, Youcai</creatorcontrib><creatorcontrib>Liu, Dailin</creatorcontrib><creatorcontrib>Zhuang, Xiaocui</creatorcontrib><creatorcontrib>Guo, Mingquan</creatorcontrib><creatorcontrib>Song, Xinbo</creatorcontrib><creatorcontrib>Fan, Enguo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Liangwan</au><au>Wang, Zhe</au><au>Chu, Yindi</au><au>Cai, Kun</au><au>Li, Wei</au><au>Huang, Piying</au><au>Qin, Youcai</au><au>Liu, Dailin</au><au>Zhuang, Xiaocui</au><au>Guo, Mingquan</au><au>Song, Xinbo</au><au>Fan, Enguo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Licochalcone A inhibits the assembly function of β-barrel assembly machinery in Escherichia coli</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2023-08-06</date><risdate>2023</risdate><volume>668</volume><spage>90</spage><epage>95</epage><pages>90-95</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><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.
•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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37245294</pmid><doi>10.1016/j.bbrc.2023.05.083</doi><tpages>6</tpages></addata></record> |
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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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