Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa
[Display omitted] •Isolated ceramides (1) from Cissus incisa leaves are new within genus.•Ceramides (1) were more active against carbapenems-resistant Acinetobacter baumannii.•Molecular docking showed that ceramides (1) target on Gram-negative cell membrane.•Biophysical assay shown that (1) disturb...
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Veröffentlicht in: | Bioorganic chemistry 2021-04, Vol.109, p.104745-104745, Article 104745 |
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creator | Nocedo-Mena, Deyani Arrasate, Sonia Garza-González, Elvira Rivas-Galindo, Verónica M. Romo-Mancillas, Antonio Munteanu, Cristian R. Sotomayor, Nuria Lete, Esther Barbolla, Iratxe Martín, César A. del Rayo Camacho-Corona, María |
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•Isolated ceramides (1) from Cissus incisa leaves are new within genus.•Ceramides (1) were more active against carbapenems-resistant Acinetobacter baumannii.•Molecular docking showed that ceramides (1) target on Gram-negative cell membrane.•Biophysical assay shown that (1) disturb membrane permeability without lithic action.•The set of obtained results allows to state a preliminary mechanism of action.
The developing of antibacterial resistance is becoming in crisis. In this sense, natural products play a fundamental role in the discovery of antibacterial agents with diverse mechanisms of action. Phytochemical investigation of Cissus incisa leaves led to isolation and characterization of the ceramides mixture (1): (8E)-2-(tritriacont-9-enoyl amino)-1,3,4-octadecanetriol-8-ene (1-I); (8E)-2-(2',3'-dihydroxyoctacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-II); (8E)-2-(2'-hydroxyheptacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-III); and (8E)-2-(-2'-hydroxynonacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-IV). Until now, this is the first report of the ceramides (1-I), (1-II), and (1-IV). The structures were elucidated using NMR and mass spectrometry analyses. Antibacterial activity of ceramides (1) and acetylated derivates (2) was evaluated against nine multidrug-resistant bacteria by Microdilution method. (1) showed the best results against Gram-negatives, mainly against carbapenems-resistant Acinetobacter baumannii with MIC = 50 μg/mL. Structure-activity analysis and molecular docking revealed interactions between plant ceramides with membrane proteins, and enzymes associated with biological membranes of Gram-negative bacteria, through hydrogen bonding of functional groups. Vesicular contents release assay showed the capacity of (1) to disturb membrane permeability detected by an increase of fluorescence probe over time. The membrane disruption is not caused for ceramides lytic action on cell membranes, according in vitro hemolyticactivity results. Combining SAR analysis, bioinformatics and biophysical techniques, and also experimental tests, it was possible to explain the antibacterial action of these natural ceramides. |
doi_str_mv | 10.1016/j.bioorg.2021.104745 |
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•Isolated ceramides (1) from Cissus incisa leaves are new within genus.•Ceramides (1) were more active against carbapenems-resistant Acinetobacter baumannii.•Molecular docking showed that ceramides (1) target on Gram-negative cell membrane.•Biophysical assay shown that (1) disturb membrane permeability without lithic action.•The set of obtained results allows to state a preliminary mechanism of action.
The developing of antibacterial resistance is becoming in crisis. In this sense, natural products play a fundamental role in the discovery of antibacterial agents with diverse mechanisms of action. Phytochemical investigation of Cissus incisa leaves led to isolation and characterization of the ceramides mixture (1): (8E)-2-(tritriacont-9-enoyl amino)-1,3,4-octadecanetriol-8-ene (1-I); (8E)-2-(2',3'-dihydroxyoctacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-II); (8E)-2-(2'-hydroxyheptacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-III); and (8E)-2-(-2'-hydroxynonacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-IV). Until now, this is the first report of the ceramides (1-I), (1-II), and (1-IV). The structures were elucidated using NMR and mass spectrometry analyses. Antibacterial activity of ceramides (1) and acetylated derivates (2) was evaluated against nine multidrug-resistant bacteria by Microdilution method. (1) showed the best results against Gram-negatives, mainly against carbapenems-resistant Acinetobacter baumannii with MIC = 50 μg/mL. Structure-activity analysis and molecular docking revealed interactions between plant ceramides with membrane proteins, and enzymes associated with biological membranes of Gram-negative bacteria, through hydrogen bonding of functional groups. Vesicular contents release assay showed the capacity of (1) to disturb membrane permeability detected by an increase of fluorescence probe over time. The membrane disruption is not caused for ceramides lytic action on cell membranes, according in vitro hemolyticactivity results. Combining SAR analysis, bioinformatics and biophysical techniques, and also experimental tests, it was possible to explain the antibacterial action of these natural ceramides.</description><identifier>ISSN: 0045-2068</identifier><identifier>EISSN: 1090-2120</identifier><identifier>DOI: 10.1016/j.bioorg.2021.104745</identifier><identifier>PMID: 33640629</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acinetobacter baumannii ; Cissus incisa ; Hemolysis ; Molecular docking ; Vesicular contents assay</subject><ispartof>Bioorganic chemistry, 2021-04, Vol.109, p.104745-104745, Article 104745</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-18d337ea7d6f599e3188cf8ebb0b6070ea0110c7cd4b8b920725f673919d315e3</citedby><cites>FETCH-LOGICAL-c408t-18d337ea7d6f599e3188cf8ebb0b6070ea0110c7cd4b8b920725f673919d315e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S004520682100122X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33640629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nocedo-Mena, Deyani</creatorcontrib><creatorcontrib>Arrasate, Sonia</creatorcontrib><creatorcontrib>Garza-González, Elvira</creatorcontrib><creatorcontrib>Rivas-Galindo, Verónica M.</creatorcontrib><creatorcontrib>Romo-Mancillas, Antonio</creatorcontrib><creatorcontrib>Munteanu, Cristian R.</creatorcontrib><creatorcontrib>Sotomayor, Nuria</creatorcontrib><creatorcontrib>Lete, Esther</creatorcontrib><creatorcontrib>Barbolla, Iratxe</creatorcontrib><creatorcontrib>Martín, César A.</creatorcontrib><creatorcontrib>del Rayo Camacho-Corona, María</creatorcontrib><title>Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa</title><title>Bioorganic chemistry</title><addtitle>Bioorg Chem</addtitle><description>[Display omitted]
•Isolated ceramides (1) from Cissus incisa leaves are new within genus.•Ceramides (1) were more active against carbapenems-resistant Acinetobacter baumannii.•Molecular docking showed that ceramides (1) target on Gram-negative cell membrane.•Biophysical assay shown that (1) disturb membrane permeability without lithic action.•The set of obtained results allows to state a preliminary mechanism of action.
The developing of antibacterial resistance is becoming in crisis. In this sense, natural products play a fundamental role in the discovery of antibacterial agents with diverse mechanisms of action. Phytochemical investigation of Cissus incisa leaves led to isolation and characterization of the ceramides mixture (1): (8E)-2-(tritriacont-9-enoyl amino)-1,3,4-octadecanetriol-8-ene (1-I); (8E)-2-(2',3'-dihydroxyoctacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-II); (8E)-2-(2'-hydroxyheptacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-III); and (8E)-2-(-2'-hydroxynonacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-IV). Until now, this is the first report of the ceramides (1-I), (1-II), and (1-IV). The structures were elucidated using NMR and mass spectrometry analyses. Antibacterial activity of ceramides (1) and acetylated derivates (2) was evaluated against nine multidrug-resistant bacteria by Microdilution method. (1) showed the best results against Gram-negatives, mainly against carbapenems-resistant Acinetobacter baumannii with MIC = 50 μg/mL. Structure-activity analysis and molecular docking revealed interactions between plant ceramides with membrane proteins, and enzymes associated with biological membranes of Gram-negative bacteria, through hydrogen bonding of functional groups. Vesicular contents release assay showed the capacity of (1) to disturb membrane permeability detected by an increase of fluorescence probe over time. The membrane disruption is not caused for ceramides lytic action on cell membranes, according in vitro hemolyticactivity results. Combining SAR analysis, bioinformatics and biophysical techniques, and also experimental tests, it was possible to explain the antibacterial action of these natural ceramides.</description><subject>Acinetobacter baumannii</subject><subject>Cissus incisa</subject><subject>Hemolysis</subject><subject>Molecular docking</subject><subject>Vesicular contents assay</subject><issn>0045-2068</issn><issn>1090-2120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9UU1v1DAQtRCILoV_gJCPHMgydpw4uSBVq_IhtUJq4Ww59qTrJYkX26m0f4LfjNMUjj3ZM_PePL15hLxlsGXA6o-Hbee8D3dbDpzllpCiekY2DFooOOPwnGwARFVwqJsz8irGAwBjQtYvyVlZ1gJq3m7In2s_oJkHHaj15peb7j7Q24sbqic9nKKL-WNpFjruc2X0QPXxGLw2e4zUTTTtkcY02xP1_UOhp-Q6bRIGt4BNcvcuPUwNBj06u_CiH3RCS_vgR7pzMc7LMuOifk1e9HqI-ObxPSc_P1_-2H0trr5_-ba7uCqMgCYVrLFlKVFLW_dV22LJmsb0DXYddDVIQJ2tgpHGiq7pWg6SV30ty5a1tmQVlufk_bo3m_k9Y0xqdNHgMOgJ_RwVF61opOTAMlSsUBN8jAF7dQxu1OGkGKglCXVQaxJqSUKtSWTau0eFuRvR_if9O30GfFoBmH3eOwwqGoeTQesCmqSsd08r_AXR0520</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Nocedo-Mena, Deyani</creator><creator>Arrasate, Sonia</creator><creator>Garza-González, Elvira</creator><creator>Rivas-Galindo, Verónica M.</creator><creator>Romo-Mancillas, Antonio</creator><creator>Munteanu, Cristian R.</creator><creator>Sotomayor, Nuria</creator><creator>Lete, Esther</creator><creator>Barbolla, Iratxe</creator><creator>Martín, César A.</creator><creator>del Rayo Camacho-Corona, María</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202104</creationdate><title>Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa</title><author>Nocedo-Mena, Deyani ; Arrasate, Sonia ; Garza-González, Elvira ; Rivas-Galindo, Verónica M. ; Romo-Mancillas, Antonio ; Munteanu, Cristian R. ; Sotomayor, Nuria ; Lete, Esther ; Barbolla, Iratxe ; Martín, César A. ; del Rayo Camacho-Corona, María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-18d337ea7d6f599e3188cf8ebb0b6070ea0110c7cd4b8b920725f673919d315e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acinetobacter baumannii</topic><topic>Cissus incisa</topic><topic>Hemolysis</topic><topic>Molecular docking</topic><topic>Vesicular contents assay</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nocedo-Mena, Deyani</creatorcontrib><creatorcontrib>Arrasate, Sonia</creatorcontrib><creatorcontrib>Garza-González, Elvira</creatorcontrib><creatorcontrib>Rivas-Galindo, Verónica M.</creatorcontrib><creatorcontrib>Romo-Mancillas, Antonio</creatorcontrib><creatorcontrib>Munteanu, Cristian R.</creatorcontrib><creatorcontrib>Sotomayor, Nuria</creatorcontrib><creatorcontrib>Lete, Esther</creatorcontrib><creatorcontrib>Barbolla, Iratxe</creatorcontrib><creatorcontrib>Martín, César A.</creatorcontrib><creatorcontrib>del Rayo Camacho-Corona, María</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nocedo-Mena, Deyani</au><au>Arrasate, Sonia</au><au>Garza-González, Elvira</au><au>Rivas-Galindo, Verónica M.</au><au>Romo-Mancillas, Antonio</au><au>Munteanu, Cristian R.</au><au>Sotomayor, Nuria</au><au>Lete, Esther</au><au>Barbolla, Iratxe</au><au>Martín, César A.</au><au>del Rayo Camacho-Corona, María</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa</atitle><jtitle>Bioorganic chemistry</jtitle><addtitle>Bioorg Chem</addtitle><date>2021-04</date><risdate>2021</risdate><volume>109</volume><spage>104745</spage><epage>104745</epage><pages>104745-104745</pages><artnum>104745</artnum><issn>0045-2068</issn><eissn>1090-2120</eissn><abstract>[Display omitted]
•Isolated ceramides (1) from Cissus incisa leaves are new within genus.•Ceramides (1) were more active against carbapenems-resistant Acinetobacter baumannii.•Molecular docking showed that ceramides (1) target on Gram-negative cell membrane.•Biophysical assay shown that (1) disturb membrane permeability without lithic action.•The set of obtained results allows to state a preliminary mechanism of action.
The developing of antibacterial resistance is becoming in crisis. In this sense, natural products play a fundamental role in the discovery of antibacterial agents with diverse mechanisms of action. Phytochemical investigation of Cissus incisa leaves led to isolation and characterization of the ceramides mixture (1): (8E)-2-(tritriacont-9-enoyl amino)-1,3,4-octadecanetriol-8-ene (1-I); (8E)-2-(2',3'-dihydroxyoctacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-II); (8E)-2-(2'-hydroxyheptacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-III); and (8E)-2-(-2'-hydroxynonacosanoyl amino)-1,3,4-octadecanetriol-8-ene (1-IV). Until now, this is the first report of the ceramides (1-I), (1-II), and (1-IV). The structures were elucidated using NMR and mass spectrometry analyses. Antibacterial activity of ceramides (1) and acetylated derivates (2) was evaluated against nine multidrug-resistant bacteria by Microdilution method. (1) showed the best results against Gram-negatives, mainly against carbapenems-resistant Acinetobacter baumannii with MIC = 50 μg/mL. Structure-activity analysis and molecular docking revealed interactions between plant ceramides with membrane proteins, and enzymes associated with biological membranes of Gram-negative bacteria, through hydrogen bonding of functional groups. Vesicular contents release assay showed the capacity of (1) to disturb membrane permeability detected by an increase of fluorescence probe over time. The membrane disruption is not caused for ceramides lytic action on cell membranes, according in vitro hemolyticactivity results. Combining SAR analysis, bioinformatics and biophysical techniques, and also experimental tests, it was possible to explain the antibacterial action of these natural ceramides.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33640629</pmid><doi>10.1016/j.bioorg.2021.104745</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acinetobacter baumannii Cissus incisa Hemolysis Molecular docking Vesicular contents assay |
title | Molecular docking, SAR analysis and biophysical approaches in the study of the antibacterial activity of ceramides isolated from Cissus incisa |
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