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Antimicrobial activity of synthetic all- d mastoparan M
Mastoparan M, a tetradecapeptide toxin (INKAIAALAKKLL-NH2) from hornet venom and its d-form mastoparan M were synthesized chemically. All d- and l-mastoparan M forms were found to adopt 28% α-helical structures in a 30% trifluroethanol solution as shown by the circular dichroism spectrum. All- d mas...
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Published in: | International journal of antimicrobial agents 2000, Vol.13 (3), p.203-208 |
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creator | Li, Ming-Liang Liao, Ru-Wen Qiu, Jian-Wen Wang, Zhi-Jian Wu, Tzong-Ming |
description | Mastoparan M, a tetradecapeptide toxin (INKAIAALAKKLL-NH2) from hornet venom and its
d-form mastoparan M were synthesized chemically. All
d- and
l-mastoparan M forms were found to adopt 28% α-helical structures in a 30% trifluroethanol solution as shown by the circular dichroism spectrum. All-
d mastoparan M caused
3H-thymidine release from labeled bacterial cells after incubation for 1 h and complete cell lysis by 4 h. Both
l- and
d-mastoparan M showed strong activity against Gram-positive and Gram-negative bacteria. All-
d mastoparan M showed 2-fold higher antibacterial activity than
l-mastoparan M. The effects of all-
d mastoparan M on the surface morphology of
Staphylococcus
aureus (ATCC29213) and
Escherichia coli (ATCC25922) were studied by scanning-beam electron microscopy. Blast-like bleb extrusions on the surface of some
S. aureus and swellings on the end of
E. coli were seen after culture with all-
d mastoparan M. These findings indicated the all-
d mastoparan M could kill bacteria by disrupting cells. |
doi_str_mv | 10.1016/S0924-8579(99)00127-2 |
format | article |
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d-form mastoparan M were synthesized chemically. All
d- and
l-mastoparan M forms were found to adopt 28% α-helical structures in a 30% trifluroethanol solution as shown by the circular dichroism spectrum. All-
d mastoparan M caused
3H-thymidine release from labeled bacterial cells after incubation for 1 h and complete cell lysis by 4 h. Both
l- and
d-mastoparan M showed strong activity against Gram-positive and Gram-negative bacteria. All-
d mastoparan M showed 2-fold higher antibacterial activity than
l-mastoparan M. The effects of all-
d mastoparan M on the surface morphology of
Staphylococcus
aureus (ATCC29213) and
Escherichia coli (ATCC25922) were studied by scanning-beam electron microscopy. Blast-like bleb extrusions on the surface of some
S. aureus and swellings on the end of
E. coli were seen after culture with all-
d mastoparan M. These findings indicated the all-
d mastoparan M could kill bacteria by disrupting cells.</description><identifier>ISSN: 0924-8579</identifier><identifier>EISSN: 1872-7913</identifier><identifier>DOI: 10.1016/S0924-8579(99)00127-2</identifier><identifier>PMID: 10724025</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anti-Bacterial Agents - chemical synthesis ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Antimicrobial ; Bacteria ; Circular Dichroism ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli - growth & development ; Escherichia coli - ultrastructure ; Mastoparan M ; Microscopy, Electron, Scanning ; Peptides - chemical synthesis ; Peptides - chemistry ; Peptides - pharmacology ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Staphylococcus aureus - growth & development ; Staphylococcus aureus - ultrastructure ; Stereoisomerism ; Wasp Venoms - chemical synthesis ; Wasp Venoms - chemistry ; Wasp Venoms - pharmacology</subject><ispartof>International journal of antimicrobial agents, 2000, Vol.13 (3), p.203-208</ispartof><rights>2000 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-e571565c9c84276d1a2caee4a3ec9d2c201ba47402895b77df616ef3cb62c53d3</citedby><cites>FETCH-LOGICAL-c458t-e571565c9c84276d1a2caee4a3ec9d2c201ba47402895b77df616ef3cb62c53d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4022,27922,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10724025$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ming-Liang</creatorcontrib><creatorcontrib>Liao, Ru-Wen</creatorcontrib><creatorcontrib>Qiu, Jian-Wen</creatorcontrib><creatorcontrib>Wang, Zhi-Jian</creatorcontrib><creatorcontrib>Wu, Tzong-Ming</creatorcontrib><title>Antimicrobial activity of synthetic all- d mastoparan M</title><title>International journal of antimicrobial agents</title><addtitle>Int J Antimicrob Agents</addtitle><description>Mastoparan M, a tetradecapeptide toxin (INKAIAALAKKLL-NH2) from hornet venom and its
d-form mastoparan M were synthesized chemically. All
d- and
l-mastoparan M forms were found to adopt 28% α-helical structures in a 30% trifluroethanol solution as shown by the circular dichroism spectrum. All-
d mastoparan M caused
3H-thymidine release from labeled bacterial cells after incubation for 1 h and complete cell lysis by 4 h. Both
l- and
d-mastoparan M showed strong activity against Gram-positive and Gram-negative bacteria. All-
d mastoparan M showed 2-fold higher antibacterial activity than
l-mastoparan M. The effects of all-
d mastoparan M on the surface morphology of
Staphylococcus
aureus (ATCC29213) and
Escherichia coli (ATCC25922) were studied by scanning-beam electron microscopy. Blast-like bleb extrusions on the surface of some
S. aureus and swellings on the end of
E. coli were seen after culture with all-
d mastoparan M. These findings indicated the all-
d mastoparan M could kill bacteria by disrupting cells.</description><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antimicrobial</subject><subject>Bacteria</subject><subject>Circular Dichroism</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - growth & development</subject><subject>Escherichia coli - ultrastructure</subject><subject>Mastoparan M</subject><subject>Microscopy, Electron, Scanning</subject><subject>Peptides - chemical synthesis</subject><subject>Peptides - chemistry</subject><subject>Peptides - pharmacology</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - growth & development</subject><subject>Staphylococcus aureus - ultrastructure</subject><subject>Stereoisomerism</subject><subject>Wasp Venoms - chemical synthesis</subject><subject>Wasp Venoms - chemistry</subject><subject>Wasp Venoms - pharmacology</subject><issn>0924-8579</issn><issn>1872-7913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkMtKAzEUhoMotlYfQZmV6GI018lkJaV4g4oLdR0yyRmMzKUmaaFv7_SCuHN1Nt9__nM-hM4JviGYFLdvWFGel0KqK6WuMSZU5vQAjUkpaS4VYYdo_IuM0EmMXwMkGBfHaESwpBxTMUZy2iXfehv6ypsmMzb5lU_rrK-zuO7SJyRvM9M0eeay1sTUL0wwXfZyio5q00Q4288J-ni4f5895fPXx-fZdJ5bLsqUg5BEFMIqW3IqC0cMtQaAGwZWOWopJpXhcrilVKKS0tUFKaBmtiqoFcyxCbrc7V2E_nsJMenWRwtNYzrol1FLrKTARP4LEsk5Y3IDih04_BxjgFovgm9NWGuC9Uat3qrVG29aKb1Vq-mQu9gXLKsW3J_UzuUA3O0AGHysPAQdrYfOgvMBbNKu9_9U_AAv2IeF</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Li, Ming-Liang</creator><creator>Liao, Ru-Wen</creator><creator>Qiu, Jian-Wen</creator><creator>Wang, Zhi-Jian</creator><creator>Wu, Tzong-Ming</creator><general>Elsevier B.V</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>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>2000</creationdate><title>Antimicrobial activity of synthetic all- d mastoparan M</title><author>Li, Ming-Liang ; Liao, Ru-Wen ; Qiu, Jian-Wen ; Wang, Zhi-Jian ; Wu, Tzong-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-e571565c9c84276d1a2caee4a3ec9d2c201ba47402895b77df616ef3cb62c53d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antimicrobial</topic><topic>Bacteria</topic><topic>Circular Dichroism</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli - ultrastructure</topic><topic>Mastoparan M</topic><topic>Microscopy, Electron, Scanning</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>Peptides - pharmacology</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus - growth & development</topic><topic>Staphylococcus aureus - ultrastructure</topic><topic>Stereoisomerism</topic><topic>Wasp Venoms - chemical synthesis</topic><topic>Wasp Venoms - chemistry</topic><topic>Wasp Venoms - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ming-Liang</creatorcontrib><creatorcontrib>Liao, Ru-Wen</creatorcontrib><creatorcontrib>Qiu, Jian-Wen</creatorcontrib><creatorcontrib>Wang, Zhi-Jian</creatorcontrib><creatorcontrib>Wu, Tzong-Ming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>MEDLINE - Academic</collection><jtitle>International journal of antimicrobial agents</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ming-Liang</au><au>Liao, Ru-Wen</au><au>Qiu, Jian-Wen</au><au>Wang, Zhi-Jian</au><au>Wu, Tzong-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial activity of synthetic all- d mastoparan M</atitle><jtitle>International journal of antimicrobial agents</jtitle><addtitle>Int J Antimicrob Agents</addtitle><date>2000</date><risdate>2000</risdate><volume>13</volume><issue>3</issue><spage>203</spage><epage>208</epage><pages>203-208</pages><issn>0924-8579</issn><eissn>1872-7913</eissn><abstract>Mastoparan M, a tetradecapeptide toxin (INKAIAALAKKLL-NH2) from hornet venom and its
d-form mastoparan M were synthesized chemically. All
d- and
l-mastoparan M forms were found to adopt 28% α-helical structures in a 30% trifluroethanol solution as shown by the circular dichroism spectrum. All-
d mastoparan M caused
3H-thymidine release from labeled bacterial cells after incubation for 1 h and complete cell lysis by 4 h. Both
l- and
d-mastoparan M showed strong activity against Gram-positive and Gram-negative bacteria. All-
d mastoparan M showed 2-fold higher antibacterial activity than
l-mastoparan M. The effects of all-
d mastoparan M on the surface morphology of
Staphylococcus
aureus (ATCC29213) and
Escherichia coli (ATCC25922) were studied by scanning-beam electron microscopy. Blast-like bleb extrusions on the surface of some
S. aureus and swellings on the end of
E. coli were seen after culture with all-
d mastoparan M. These findings indicated the all-
d mastoparan M could kill bacteria by disrupting cells.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>10724025</pmid><doi>10.1016/S0924-8579(99)00127-2</doi><tpages>6</tpages></addata></record> |
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source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Anti-Bacterial Agents - chemical synthesis Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Antimicrobial Bacteria Circular Dichroism Escherichia coli Escherichia coli - drug effects Escherichia coli - growth & development Escherichia coli - ultrastructure Mastoparan M Microscopy, Electron, Scanning Peptides - chemical synthesis Peptides - chemistry Peptides - pharmacology Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus - growth & development Staphylococcus aureus - ultrastructure Stereoisomerism Wasp Venoms - chemical synthesis Wasp Venoms - chemistry Wasp Venoms - pharmacology |
title | Antimicrobial activity of synthetic all- d mastoparan M |
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