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Biocomputational Assessment of Natural Compounds as a Potent Inhibitor to Quorum Sensors in Ralstonia solanacearum
is among the most damaging bacterial phytopathogens with a wide number of hosts and a broad geographic distribution worldwide. The pathway of phenotype conversion (Phc) is operated by quorum-sensing signals and modulated through the (R)-methyl 3-hydroxypalmitate (3-OH PAME) in . However, the molecul...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2022-05, Vol.27 (9), p.3034 |
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creator | Kumar, Sunil Ahmad, Khurshid Behera, Santosh Kumar Nagrale, Dipak T Chaurasia, Anurag Yadav, Manoj Kumar Murmu, Sneha Jha, Yachana Rajawat, Mahendra Vikram Singh Malviya, Deepti Singh, Udai B Shankar, Raja Tripathy, Minaketan Singh, Harsh Vardhan |
description | is among the most damaging bacterial phytopathogens with a wide number of hosts and a broad geographic distribution worldwide. The pathway of phenotype conversion (Phc) is operated by quorum-sensing signals and modulated through the (R)-methyl 3-hydroxypalmitate (3-OH PAME) in
. However, the molecular structures of the Phc pathway components are not yet established, and the structural consequences of 3-OH PAME on quorum sensing are not well studied. In this study, 3D structures of quorum-sensing proteins of the Phc pathway (PhcA and PhcR) were computationally modeled, followed by the virtual screening of the natural compounds library against the predicted active site residues of PhcA and PhcR proteins that could be employed in limiting signaling through 3-OH PAME. Two of the best scoring common ligands ZINC000014762512 and ZINC000011865192 for PhcA and PhcR were further analyzed utilizing orbital energies such as HOMO and LUMO, followed by molecular dynamics simulations of the complexes for 100 ns to determine the ligands binding stability. The findings indicate that ZINC000014762512 and ZINC000011865192 may be capable of inhibiting both PhcA and PhcR. We believe that, after further validation, these compounds may have the potential to disrupt bacterial quorum sensing and thus control this devastating phytopathogenic bacterial pathogen. |
doi_str_mv | 10.3390/molecules27093034 |
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. However, the molecular structures of the Phc pathway components are not yet established, and the structural consequences of 3-OH PAME on quorum sensing are not well studied. In this study, 3D structures of quorum-sensing proteins of the Phc pathway (PhcA and PhcR) were computationally modeled, followed by the virtual screening of the natural compounds library against the predicted active site residues of PhcA and PhcR proteins that could be employed in limiting signaling through 3-OH PAME. Two of the best scoring common ligands ZINC000014762512 and ZINC000011865192 for PhcA and PhcR were further analyzed utilizing orbital energies such as HOMO and LUMO, followed by molecular dynamics simulations of the complexes for 100 ns to determine the ligands binding stability. The findings indicate that ZINC000014762512 and ZINC000011865192 may be capable of inhibiting both PhcA and PhcR. We believe that, after further validation, these compounds may have the potential to disrupt bacterial quorum sensing and thus control this devastating phytopathogenic bacterial pathogen.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules27093034</identifier><identifier>PMID: 35566383</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Bacteria ; Bacterial Proteins - metabolism ; Binding sites ; Energy ; Gene expression ; Gene Expression Regulation, Bacterial ; Geographical distribution ; Ligands ; Metabolites ; molecular docking ; Molecular dynamics ; Molecular orbitals ; Molecular structure ; natural compounds ; Pathogens ; PhcA and PhcR ; Phenotypes ; Proteins ; Quorum sensing ; Quorum Sensing - genetics ; Ralstonia solanacearum ; Simulation ; Virulence</subject><ispartof>Molecules (Basel, Switzerland), 2022-05, Vol.27 (9), p.3034</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-d81d9c6ff6426240a9c7bd39f10a71cdb65f1654c9550f83b54f8ab04b979e9c3</citedby><cites>FETCH-LOGICAL-c493t-d81d9c6ff6426240a9c7bd39f10a71cdb65f1654c9550f83b54f8ab04b979e9c3</cites><orcidid>0000-0002-1095-8445 ; 0000-0002-3834-6686 ; 0000-0003-3219-0171</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2663049879/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2663049879?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35566383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, Sunil</creatorcontrib><creatorcontrib>Ahmad, Khurshid</creatorcontrib><creatorcontrib>Behera, Santosh Kumar</creatorcontrib><creatorcontrib>Nagrale, Dipak T</creatorcontrib><creatorcontrib>Chaurasia, Anurag</creatorcontrib><creatorcontrib>Yadav, Manoj Kumar</creatorcontrib><creatorcontrib>Murmu, Sneha</creatorcontrib><creatorcontrib>Jha, Yachana</creatorcontrib><creatorcontrib>Rajawat, Mahendra Vikram Singh</creatorcontrib><creatorcontrib>Malviya, Deepti</creatorcontrib><creatorcontrib>Singh, Udai B</creatorcontrib><creatorcontrib>Shankar, Raja</creatorcontrib><creatorcontrib>Tripathy, Minaketan</creatorcontrib><creatorcontrib>Singh, Harsh Vardhan</creatorcontrib><title>Biocomputational Assessment of Natural Compounds as a Potent Inhibitor to Quorum Sensors in Ralstonia solanacearum</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>is among the most damaging bacterial phytopathogens with a wide number of hosts and a broad geographic distribution worldwide. The pathway of phenotype conversion (Phc) is operated by quorum-sensing signals and modulated through the (R)-methyl 3-hydroxypalmitate (3-OH PAME) in
. However, the molecular structures of the Phc pathway components are not yet established, and the structural consequences of 3-OH PAME on quorum sensing are not well studied. In this study, 3D structures of quorum-sensing proteins of the Phc pathway (PhcA and PhcR) were computationally modeled, followed by the virtual screening of the natural compounds library against the predicted active site residues of PhcA and PhcR proteins that could be employed in limiting signaling through 3-OH PAME. Two of the best scoring common ligands ZINC000014762512 and ZINC000011865192 for PhcA and PhcR were further analyzed utilizing orbital energies such as HOMO and LUMO, followed by molecular dynamics simulations of the complexes for 100 ns to determine the ligands binding stability. The findings indicate that ZINC000014762512 and ZINC000011865192 may be capable of inhibiting both PhcA and PhcR. We believe that, after further validation, these compounds may have the potential to disrupt bacterial quorum sensing and thus control this devastating phytopathogenic bacterial pathogen.</description><subject>Bacteria</subject><subject>Bacterial Proteins - metabolism</subject><subject>Binding sites</subject><subject>Energy</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Geographical distribution</subject><subject>Ligands</subject><subject>Metabolites</subject><subject>molecular docking</subject><subject>Molecular dynamics</subject><subject>Molecular orbitals</subject><subject>Molecular structure</subject><subject>natural compounds</subject><subject>Pathogens</subject><subject>PhcA and PhcR</subject><subject>Phenotypes</subject><subject>Proteins</subject><subject>Quorum sensing</subject><subject>Quorum Sensing - genetics</subject><subject>Ralstonia solanacearum</subject><subject>Simulation</subject><subject>Virulence</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkltvFCEUxydGY2v1A_hiSHzxZRUGhoEXk7qxuknj3WcCDLRsZjgrFxO_fdlubVpNSCDn_M7_cC5d95zg15RK_GaB2dk6u9yPWFJM2YPumLAeryhm8uGd91H3JOctxj1hZHjcHdFh4JwKetyldwEsLLtadAkQ9YxOc3Y5Ly4WBB590qWmZl03BmqcMtLtoC9Q9sAmXgYTCiRUAH2tkOqCvruYIWUUIvqm51wgBo0yzDpq63QjnnaPfHO4Zzf3Sffz7P2P9cfV-ecPm_Xp-coySctqEmSSlnvPWc97hrW0o5mo9ATrkdjJ8METPjArhwF7Qc3AvNAGMyNH6aSlJ93moDuB3qpdCotOfxTooK4NkC6UTiXY2SlviKBcCDPKkcnRmJbOUekIF9I62TettwetXTWLm2wrvnXlnuh9TwyX6gJ-K0lwz_le4NWNQIJf1eWilpCtm1tbHNSsGsQEJrzHDX35D7qFmtporqn9OMUoG0UOlE2Qc3L-9jMEq_12qP-2o8W8uFvFbcTfdaBXgoa6Dg</recordid><startdate>20220509</startdate><enddate>20220509</enddate><creator>Kumar, Sunil</creator><creator>Ahmad, Khurshid</creator><creator>Behera, Santosh Kumar</creator><creator>Nagrale, Dipak T</creator><creator>Chaurasia, Anurag</creator><creator>Yadav, Manoj Kumar</creator><creator>Murmu, Sneha</creator><creator>Jha, Yachana</creator><creator>Rajawat, Mahendra Vikram Singh</creator><creator>Malviya, Deepti</creator><creator>Singh, Udai B</creator><creator>Shankar, Raja</creator><creator>Tripathy, Minaketan</creator><creator>Singh, Harsh Vardhan</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1095-8445</orcidid><orcidid>https://orcid.org/0000-0002-3834-6686</orcidid><orcidid>https://orcid.org/0000-0003-3219-0171</orcidid></search><sort><creationdate>20220509</creationdate><title>Biocomputational Assessment of Natural Compounds as a Potent Inhibitor to Quorum Sensors in Ralstonia solanacearum</title><author>Kumar, Sunil ; Ahmad, Khurshid ; Behera, Santosh Kumar ; Nagrale, Dipak T ; Chaurasia, Anurag ; Yadav, Manoj Kumar ; Murmu, Sneha ; Jha, Yachana ; Rajawat, Mahendra Vikram Singh ; Malviya, Deepti ; Singh, Udai B ; Shankar, Raja ; Tripathy, Minaketan ; Singh, Harsh Vardhan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-d81d9c6ff6426240a9c7bd39f10a71cdb65f1654c9550f83b54f8ab04b979e9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bacteria</topic><topic>Bacterial Proteins - metabolism</topic><topic>Binding sites</topic><topic>Energy</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Geographical distribution</topic><topic>Ligands</topic><topic>Metabolites</topic><topic>molecular docking</topic><topic>Molecular dynamics</topic><topic>Molecular orbitals</topic><topic>Molecular structure</topic><topic>natural compounds</topic><topic>Pathogens</topic><topic>PhcA and PhcR</topic><topic>Phenotypes</topic><topic>Proteins</topic><topic>Quorum sensing</topic><topic>Quorum Sensing - genetics</topic><topic>Ralstonia solanacearum</topic><topic>Simulation</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Sunil</creatorcontrib><creatorcontrib>Ahmad, Khurshid</creatorcontrib><creatorcontrib>Behera, Santosh Kumar</creatorcontrib><creatorcontrib>Nagrale, Dipak T</creatorcontrib><creatorcontrib>Chaurasia, Anurag</creatorcontrib><creatorcontrib>Yadav, Manoj Kumar</creatorcontrib><creatorcontrib>Murmu, Sneha</creatorcontrib><creatorcontrib>Jha, Yachana</creatorcontrib><creatorcontrib>Rajawat, Mahendra Vikram Singh</creatorcontrib><creatorcontrib>Malviya, Deepti</creatorcontrib><creatorcontrib>Singh, Udai B</creatorcontrib><creatorcontrib>Shankar, Raja</creatorcontrib><creatorcontrib>Tripathy, Minaketan</creatorcontrib><creatorcontrib>Singh, Harsh Vardhan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Sunil</au><au>Ahmad, Khurshid</au><au>Behera, Santosh Kumar</au><au>Nagrale, Dipak T</au><au>Chaurasia, Anurag</au><au>Yadav, Manoj Kumar</au><au>Murmu, Sneha</au><au>Jha, Yachana</au><au>Rajawat, Mahendra Vikram Singh</au><au>Malviya, Deepti</au><au>Singh, Udai B</au><au>Shankar, Raja</au><au>Tripathy, Minaketan</au><au>Singh, Harsh Vardhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biocomputational Assessment of Natural Compounds as a Potent Inhibitor to Quorum Sensors in Ralstonia solanacearum</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2022-05-09</date><risdate>2022</risdate><volume>27</volume><issue>9</issue><spage>3034</spage><pages>3034-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>is among the most damaging bacterial phytopathogens with a wide number of hosts and a broad geographic distribution worldwide. The pathway of phenotype conversion (Phc) is operated by quorum-sensing signals and modulated through the (R)-methyl 3-hydroxypalmitate (3-OH PAME) in
. However, the molecular structures of the Phc pathway components are not yet established, and the structural consequences of 3-OH PAME on quorum sensing are not well studied. In this study, 3D structures of quorum-sensing proteins of the Phc pathway (PhcA and PhcR) were computationally modeled, followed by the virtual screening of the natural compounds library against the predicted active site residues of PhcA and PhcR proteins that could be employed in limiting signaling through 3-OH PAME. Two of the best scoring common ligands ZINC000014762512 and ZINC000011865192 for PhcA and PhcR were further analyzed utilizing orbital energies such as HOMO and LUMO, followed by molecular dynamics simulations of the complexes for 100 ns to determine the ligands binding stability. The findings indicate that ZINC000014762512 and ZINC000011865192 may be capable of inhibiting both PhcA and PhcR. We believe that, after further validation, these compounds may have the potential to disrupt bacterial quorum sensing and thus control this devastating phytopathogenic bacterial pathogen.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35566383</pmid><doi>10.3390/molecules27093034</doi><orcidid>https://orcid.org/0000-0002-1095-8445</orcidid><orcidid>https://orcid.org/0000-0002-3834-6686</orcidid><orcidid>https://orcid.org/0000-0003-3219-0171</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Bacterial Proteins - metabolism Binding sites Energy Gene expression Gene Expression Regulation, Bacterial Geographical distribution Ligands Metabolites molecular docking Molecular dynamics Molecular orbitals Molecular structure natural compounds Pathogens PhcA and PhcR Phenotypes Proteins Quorum sensing Quorum Sensing - genetics Ralstonia solanacearum Simulation Virulence |
title | Biocomputational Assessment of Natural Compounds as a Potent Inhibitor to Quorum Sensors in Ralstonia solanacearum |
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