Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin
Terreic acid is a metabolite with antibiotic properties produced by the fungus Aspergillus terreus, but its cellular target remains unknown. We recently reported that terreic acid inactivates the bacterial cell wall biosynthetic enzyme MurA in vitro by covalent reaction with residue Cys115 in a simi...
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Veröffentlicht in: | Journal of basic microbiology 2014-04, Vol.54 (4), p.322-326 |
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description | Terreic acid is a metabolite with antibiotic properties produced by the fungus Aspergillus terreus, but its cellular target remains unknown. We recently reported that terreic acid inactivates the bacterial cell wall biosynthetic enzyme MurA in vitro by covalent reaction with residue Cys115 in a similar manner as the MurA‐specific antibiotic fosfomycin. To address if terreic acid also targets MurA in vivo, we conducted antibacterial studies using selected E. coli strains in parallel with fosfomycin. While overexpression of MurA conferred resistance to fosfomycin, it did not protect cells treated with terreic acid. Furthermore, flow cytometry revealed that the antibiotic action of terreic acid appears to be primarily bacteriostatic, as opposed to the bactericidal action observed for fosfomycin. Combined, the data suggest that MurA is not the molecular target of terreic acid and that the antibiotic activity of terreic acid proceeds through a different mechanism of action. The methodology applied here provides a reliable and convenient tool to rapidly assess the potential of newly discovered in vitro inhibitors to target residue Cys115 of MurA in the cell. |
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We recently reported that terreic acid inactivates the bacterial cell wall biosynthetic enzyme MurA in vitro by covalent reaction with residue Cys115 in a similar manner as the MurA‐specific antibiotic fosfomycin. To address if terreic acid also targets MurA in vivo, we conducted antibacterial studies using selected E. coli strains in parallel with fosfomycin. While overexpression of MurA conferred resistance to fosfomycin, it did not protect cells treated with terreic acid. Furthermore, flow cytometry revealed that the antibiotic action of terreic acid appears to be primarily bacteriostatic, as opposed to the bactericidal action observed for fosfomycin. Combined, the data suggest that MurA is not the molecular target of terreic acid and that the antibiotic activity of terreic acid proceeds through a different mechanism of action. The methodology applied here provides a reliable and convenient tool to rapidly assess the potential of newly discovered in vitro inhibitors to target residue Cys115 of MurA in the cell.</description><identifier>ISSN: 0233-111X</identifier><identifier>EISSN: 1521-4028</identifier><identifier>DOI: 10.1002/jobm.201200617</identifier><identifier>PMID: 23686727</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Alkyl and Aryl Transferases - antagonists & inhibitors ; Anti-Bacterial Agents - pharmacology ; antibacterial properties ; Antibiotics ; Aspergillus ; Aspergillus terreus ; bacteria ; Cell Proliferation - drug effects ; cell walls ; Drug discovery ; Drug Resistance, Bacterial ; Escherichia coli ; Escherichia coli - cytology ; Escherichia coli - drug effects ; Escherichia coli - enzymology ; Escherichia coli - genetics ; Flow cytometry ; fosfomycin ; Fosfomycin - pharmacology ; fungi ; mechanism of action ; metabolites ; Mutation ; Natural products ; Quinones - pharmacology ; Terreic acid</subject><ispartof>Journal of basic microbiology, 2014-04, Vol.54 (4), p.322-326</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5447-6a87cc6833b258f7af27ae7aacc977f6609cb7a91ff201111cffde596a441b643</citedby><cites>FETCH-LOGICAL-c5447-6a87cc6833b258f7af27ae7aacc977f6609cb7a91ff201111cffde596a441b643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjobm.201200617$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjobm.201200617$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23686727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Olesen, Sanne H.</creatorcontrib><creatorcontrib>Ingles, Donna J.</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Schönbrunn, Ernst</creatorcontrib><title>Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin</title><title>Journal of basic microbiology</title><addtitle>J. Basic Microbiol</addtitle><description>Terreic acid is a metabolite with antibiotic properties produced by the fungus Aspergillus terreus, but its cellular target remains unknown. We recently reported that terreic acid inactivates the bacterial cell wall biosynthetic enzyme MurA in vitro by covalent reaction with residue Cys115 in a similar manner as the MurA‐specific antibiotic fosfomycin. To address if terreic acid also targets MurA in vivo, we conducted antibacterial studies using selected E. coli strains in parallel with fosfomycin. While overexpression of MurA conferred resistance to fosfomycin, it did not protect cells treated with terreic acid. Furthermore, flow cytometry revealed that the antibiotic action of terreic acid appears to be primarily bacteriostatic, as opposed to the bactericidal action observed for fosfomycin. Combined, the data suggest that MurA is not the molecular target of terreic acid and that the antibiotic activity of terreic acid proceeds through a different mechanism of action. The methodology applied here provides a reliable and convenient tool to rapidly assess the potential of newly discovered in vitro inhibitors to target residue Cys115 of MurA in the cell.</description><subject>Alkyl and Aryl Transferases - antagonists & inhibitors</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibacterial properties</subject><subject>Antibiotics</subject><subject>Aspergillus</subject><subject>Aspergillus terreus</subject><subject>bacteria</subject><subject>Cell Proliferation - drug effects</subject><subject>cell walls</subject><subject>Drug discovery</subject><subject>Drug Resistance, Bacterial</subject><subject>Escherichia coli</subject><subject>Escherichia coli - cytology</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - enzymology</subject><subject>Escherichia coli - genetics</subject><subject>Flow cytometry</subject><subject>fosfomycin</subject><subject>Fosfomycin - pharmacology</subject><subject>fungi</subject><subject>mechanism of action</subject><subject>metabolites</subject><subject>Mutation</subject><subject>Natural products</subject><subject>Quinones - pharmacology</subject><subject>Terreic acid</subject><issn>0233-111X</issn><issn>1521-4028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtvEzEUhS0EoqGwZYlmyWaC3x5vkEpLU1BKWfDIzvI418RlZpzaE2j-PY5SorIq3lxZ9ztH9-gg9JLgKcGYvrmObT-lmFCMJVGP0IQISmqOafMYTTBlrCaELI7Qs5yvMcZaU_0UHVEmG6momqDFWfAeEgxjsF1ly2itGyHtfusU15DGALmKvhpXUF1u0kkVhlVowxhTrgqYILjKurAs4mXlY_ax37owPEdPvO0yvLibx-jr-fsvpxf1_Gr24fRkXjvBuaqlbZRzsmGspaLxynqqLChrndNKeSmxdq2ymnhfUpbnvF-C0NJyTlrJ2TF6u_ddb9oelq4kSbYz6xR6m7Ym2mD-3QxhZX7EX4ZLgploisHrO4MUbzaQR9OH7KDr7ABxkw1RXDJBNGcPo4Ji1pTj_sNVEM6pZHSXYLpHXYo5J_CH4wk2u5LNrmRzKLkIXt2PfMD_tloAvQd-hw62D9iZj1fvLu-b13ttyCPcHrQ2_TRSMSXM908zMz87__ZZLGYGsz971sRY</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Olesen, Sanne H.</creator><creator>Ingles, Donna J.</creator><creator>Yang, Yan</creator><creator>Schönbrunn, Ernst</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>201404</creationdate><title>Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin</title><author>Olesen, Sanne H. ; Ingles, Donna J. ; Yang, Yan ; Schönbrunn, Ernst</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5447-6a87cc6833b258f7af27ae7aacc977f6609cb7a91ff201111cffde596a441b643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Alkyl and Aryl Transferases - antagonists & inhibitors</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antibacterial properties</topic><topic>Antibiotics</topic><topic>Aspergillus</topic><topic>Aspergillus terreus</topic><topic>bacteria</topic><topic>Cell Proliferation - drug effects</topic><topic>cell walls</topic><topic>Drug discovery</topic><topic>Drug Resistance, Bacterial</topic><topic>Escherichia coli</topic><topic>Escherichia coli - cytology</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - enzymology</topic><topic>Escherichia coli - genetics</topic><topic>Flow cytometry</topic><topic>fosfomycin</topic><topic>Fosfomycin - pharmacology</topic><topic>fungi</topic><topic>mechanism of action</topic><topic>metabolites</topic><topic>Mutation</topic><topic>Natural products</topic><topic>Quinones - pharmacology</topic><topic>Terreic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olesen, Sanne H.</creatorcontrib><creatorcontrib>Ingles, Donna J.</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Schönbrunn, Ernst</creatorcontrib><collection>Istex</collection><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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of basic microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olesen, Sanne H.</au><au>Ingles, Donna J.</au><au>Yang, Yan</au><au>Schönbrunn, Ernst</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin</atitle><jtitle>Journal of basic microbiology</jtitle><addtitle>J. Basic Microbiol</addtitle><date>2014-04</date><risdate>2014</risdate><volume>54</volume><issue>4</issue><spage>322</spage><epage>326</epage><pages>322-326</pages><issn>0233-111X</issn><eissn>1521-4028</eissn><abstract>Terreic acid is a metabolite with antibiotic properties produced by the fungus Aspergillus terreus, but its cellular target remains unknown. We recently reported that terreic acid inactivates the bacterial cell wall biosynthetic enzyme MurA in vitro by covalent reaction with residue Cys115 in a similar manner as the MurA‐specific antibiotic fosfomycin. To address if terreic acid also targets MurA in vivo, we conducted antibacterial studies using selected E. coli strains in parallel with fosfomycin. While overexpression of MurA conferred resistance to fosfomycin, it did not protect cells treated with terreic acid. Furthermore, flow cytometry revealed that the antibiotic action of terreic acid appears to be primarily bacteriostatic, as opposed to the bactericidal action observed for fosfomycin. Combined, the data suggest that MurA is not the molecular target of terreic acid and that the antibiotic activity of terreic acid proceeds through a different mechanism of action. The methodology applied here provides a reliable and convenient tool to rapidly assess the potential of newly discovered in vitro inhibitors to target residue Cys115 of MurA in the cell.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>23686727</pmid><doi>10.1002/jobm.201200617</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkyl and Aryl Transferases - antagonists & inhibitors Anti-Bacterial Agents - pharmacology antibacterial properties Antibiotics Aspergillus Aspergillus terreus bacteria Cell Proliferation - drug effects cell walls Drug discovery Drug Resistance, Bacterial Escherichia coli Escherichia coli - cytology Escherichia coli - drug effects Escherichia coli - enzymology Escherichia coli - genetics Flow cytometry fosfomycin Fosfomycin - pharmacology fungi mechanism of action metabolites Mutation Natural products Quinones - pharmacology Terreic acid |
title | Differential antibacterial properties of the MurA inhibitors terreic acid and fosfomycin |
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