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Zymographic Characterization of Staphylococcus aureus Cell Wall
Susceptibilities of several preparations of Staphylococcus aureus cells to various peptidoglycan hydrolases with known bond specificity were analyzed by zymography. The substrates were intact S. aureus cells, cells boiled in the presence of SDS and cells treated with trichloroacetic acid after treat...
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Published in: | MICROBIOLOGY and IMMUNOLOGY 1998, Vol.42(3), pp.231-235 |
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creator | Ohta, Kouji Komatsuzawa, Hitoshi Sugai, Motoyuki Suginaka, Hidekazu |
description | Susceptibilities of several preparations of Staphylococcus aureus cells to various peptidoglycan hydrolases with known bond specificity were analyzed by zymography. The substrates were intact S. aureus cells, cells boiled in the presence of SDS and cells treated with trichloroacetic acid after treatment with boiling SDS solution (TCA-cells). Twofold dilution of lysostaphin (LS), lysozyme (LZ), S. aureus 51kDa glucosaminidase (GL) or S. aureus 62kDa amidase (AM) were electrophoresed, and the minimal enzyme dose showing a visible bacteriolytic band was defined as MBD (minimal bacteriolytic dose). Under the same experimental conditions, this method gave reproducible results. As the substrate for zymogram, TCA-cells were the most sensitive to LS, LZ and AM, whereas the three substrate were equally sensitive to GL. A zymographic analysis of methicillin-resistant S. aureus treated with methicillin together with previous studies suggest that this method can be used for the preliminary characterization of S. aureus cell wall peptidoglycan. |
doi_str_mv | 10.1111/j.1348-0421.1998.tb02276.x |
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The substrates were intact S. aureus cells, cells boiled in the presence of SDS and cells treated with trichloroacetic acid after treatment with boiling SDS solution (TCA-cells). Twofold dilution of lysostaphin (LS), lysozyme (LZ), S. aureus 51kDa glucosaminidase (GL) or S. aureus 62kDa amidase (AM) were electrophoresed, and the minimal enzyme dose showing a visible bacteriolytic band was defined as MBD (minimal bacteriolytic dose). Under the same experimental conditions, this method gave reproducible results. As the substrate for zymogram, TCA-cells were the most sensitive to LS, LZ and AM, whereas the three substrate were equally sensitive to GL. A zymographic analysis of methicillin-resistant S. aureus treated with methicillin together with previous studies suggest that this method can be used for the preliminary characterization of S. aureus cell wall peptidoglycan.</description><identifier>ISSN: 0385-5600</identifier><identifier>EISSN: 1348-0421</identifier><identifier>DOI: 10.1111/j.1348-0421.1998.tb02276.x</identifier><identifier>PMID: 9570289</identifier><identifier>CODEN: MIIMDV</identifier><language>eng</language><publisher>Tokyo: Blackwell Publishing Ltd</publisher><subject>Amidohydrolases - metabolism ; Anti-Bacterial Agents - pharmacology ; Autolysin ; Bacteriological methods and techniques used in bacteriology ; Bacteriology ; Bacteriolysis ; Biological and medical sciences ; Cell wall ; Cell Wall - chemistry ; Cell Wall - drug effects ; Cell Wall - metabolism ; Electrophoresis, Polyacrylamide Gel ; Fundamental and applied biological sciences. Psychology ; Hexosaminidases - metabolism ; Lysostaphin - metabolism ; MBD ; Microbiology ; Muramidase - metabolism ; Peptidoglycan - chemistry ; Peptidoglycan - drug effects ; Peptidoglycan - metabolism ; Staphylococcus aureus - chemistry ; Staphylococcus aureus - drug effects ; Zymography</subject><ispartof>MICROBIOLOGY and IMMUNOLOGY, 1998, Vol.42(3), pp.231-235</ispartof><rights>Center for Academic Publications Japan</rights><rights>owned by Center for Academic Publications Japan (Publisher)</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6816-bd57886b2c05dab3b5f5deb3241deae02cb5dbe6e5283acb2fcb4b55a54372763</citedby><cites>FETCH-LOGICAL-c6816-bd57886b2c05dab3b5f5deb3241deae02cb5dbe6e5283acb2fcb4b55a54372763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2299553$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9570289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohta, Kouji</creatorcontrib><creatorcontrib>Komatsuzawa, Hitoshi</creatorcontrib><creatorcontrib>Sugai, Motoyuki</creatorcontrib><creatorcontrib>Suginaka, Hidekazu</creatorcontrib><title>Zymographic Characterization of Staphylococcus aureus Cell Wall</title><title>MICROBIOLOGY and IMMUNOLOGY</title><addtitle>Microbiology and Immunology</addtitle><description>Susceptibilities of several preparations of Staphylococcus aureus cells to various peptidoglycan hydrolases with known bond specificity were analyzed by zymography. The substrates were intact S. aureus cells, cells boiled in the presence of SDS and cells treated with trichloroacetic acid after treatment with boiling SDS solution (TCA-cells). Twofold dilution of lysostaphin (LS), lysozyme (LZ), S. aureus 51kDa glucosaminidase (GL) or S. aureus 62kDa amidase (AM) were electrophoresed, and the minimal enzyme dose showing a visible bacteriolytic band was defined as MBD (minimal bacteriolytic dose). Under the same experimental conditions, this method gave reproducible results. As the substrate for zymogram, TCA-cells were the most sensitive to LS, LZ and AM, whereas the three substrate were equally sensitive to GL. A zymographic analysis of methicillin-resistant S. aureus treated with methicillin together with previous studies suggest that this method can be used for the preliminary characterization of S. aureus cell wall peptidoglycan.</description><subject>Amidohydrolases - metabolism</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Autolysin</subject><subject>Bacteriological methods and techniques used in bacteriology</subject><subject>Bacteriology</subject><subject>Bacteriolysis</subject><subject>Biological and medical sciences</subject><subject>Cell wall</subject><subject>Cell Wall - chemistry</subject><subject>Cell Wall - drug effects</subject><subject>Cell Wall - metabolism</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hexosaminidases - metabolism</subject><subject>Lysostaphin - metabolism</subject><subject>MBD</subject><subject>Microbiology</subject><subject>Muramidase - metabolism</subject><subject>Peptidoglycan - chemistry</subject><subject>Peptidoglycan - drug effects</subject><subject>Peptidoglycan - metabolism</subject><subject>Staphylococcus aureus - chemistry</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Zymography</subject><issn>0385-5600</issn><issn>1348-0421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqVkV9v0zAUxS0EGmXwEZAihHhL8J84tnkBVG1l0gYPK6rEy5XtOFtK0hQ7Ee0-_VwSRbwh_OBr6Rz_fO8xQm8Izkhc77cZYblMcU5JRpSSWW8wpaLIDk_QYpaeogVmkqe8wPg5ehHCFmMqqMzP0JniAlOpFujjj2Pb3Xm9v69tsrzXXtve-fpB93W3S7oque2jdmw621k7hEQP3sWydE2TbHTTvETPKt0E92qq5-j75cV6-SW9_ra6Wn6-Tm0hSZGakgspC0Mt5qU2zPCKl84wmpPSaYepNbw0rnCcSqatoZU1ueFc85yJOBk7R-9G7t53vwYXemjrYGMXeue6IYBQkioh838aSUElUYJH44fRaH0XgncV7H3dan8EguEUM2zhlCWcsoRTzDDFDId4-fX0ymBaV85Xp1yj_nbSdbC6qbze2TrMNkqV4pxF26fR9rtu3PE_GoCbq5s_x4i4GBHb0Os7NzO072vbOGj1rqzjwAJyCmzcKCOzbuOfg9tFTjpy6tC7w1-Yn1AIJjhsvq5AXK7ZSq1vYcMeAcfYwog</recordid><startdate>19980101</startdate><enddate>19980101</enddate><creator>Ohta, Kouji</creator><creator>Komatsuzawa, Hitoshi</creator><creator>Sugai, Motoyuki</creator><creator>Suginaka, Hidekazu</creator><general>Blackwell Publishing Ltd</general><general>Center For Academic Publications Japan</general><general>Center for Academic Publications Japan</general><scope>BSCLL</scope><scope>IQODW</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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19980101</creationdate><title>Zymographic Characterization of Staphylococcus aureus Cell Wall</title><author>Ohta, Kouji ; Komatsuzawa, Hitoshi ; Sugai, Motoyuki ; Suginaka, Hidekazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6816-bd57886b2c05dab3b5f5deb3241deae02cb5dbe6e5283acb2fcb4b55a54372763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amidohydrolases - metabolism</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Autolysin</topic><topic>Bacteriological methods and techniques used in bacteriology</topic><topic>Bacteriology</topic><topic>Bacteriolysis</topic><topic>Biological and medical sciences</topic><topic>Cell wall</topic><topic>Cell Wall - chemistry</topic><topic>Cell Wall - drug effects</topic><topic>Cell Wall - metabolism</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hexosaminidases - metabolism</topic><topic>Lysostaphin - metabolism</topic><topic>MBD</topic><topic>Microbiology</topic><topic>Muramidase - metabolism</topic><topic>Peptidoglycan - chemistry</topic><topic>Peptidoglycan - drug effects</topic><topic>Peptidoglycan - metabolism</topic><topic>Staphylococcus aureus - chemistry</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Zymography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohta, Kouji</creatorcontrib><creatorcontrib>Komatsuzawa, Hitoshi</creatorcontrib><creatorcontrib>Sugai, Motoyuki</creatorcontrib><creatorcontrib>Suginaka, Hidekazu</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>MICROBIOLOGY and IMMUNOLOGY</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohta, Kouji</au><au>Komatsuzawa, Hitoshi</au><au>Sugai, Motoyuki</au><au>Suginaka, Hidekazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Zymographic Characterization of Staphylococcus aureus Cell Wall</atitle><jtitle>MICROBIOLOGY and IMMUNOLOGY</jtitle><addtitle>Microbiology and Immunology</addtitle><date>1998-01-01</date><risdate>1998</risdate><volume>42</volume><issue>3</issue><spage>231</spage><epage>235</epage><pages>231-235</pages><issn>0385-5600</issn><eissn>1348-0421</eissn><coden>MIIMDV</coden><abstract>Susceptibilities of several preparations of Staphylococcus aureus cells to various peptidoglycan hydrolases with known bond specificity were analyzed by zymography. The substrates were intact S. aureus cells, cells boiled in the presence of SDS and cells treated with trichloroacetic acid after treatment with boiling SDS solution (TCA-cells). Twofold dilution of lysostaphin (LS), lysozyme (LZ), S. aureus 51kDa glucosaminidase (GL) or S. aureus 62kDa amidase (AM) were electrophoresed, and the minimal enzyme dose showing a visible bacteriolytic band was defined as MBD (minimal bacteriolytic dose). Under the same experimental conditions, this method gave reproducible results. As the substrate for zymogram, TCA-cells were the most sensitive to LS, LZ and AM, whereas the three substrate were equally sensitive to GL. A zymographic analysis of methicillin-resistant S. aureus treated with methicillin together with previous studies suggest that this method can be used for the preliminary characterization of S. aureus cell wall peptidoglycan.</abstract><cop>Tokyo</cop><pub>Blackwell Publishing Ltd</pub><pmid>9570289</pmid><doi>10.1111/j.1348-0421.1998.tb02276.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amidohydrolases - metabolism Anti-Bacterial Agents - pharmacology Autolysin Bacteriological methods and techniques used in bacteriology Bacteriology Bacteriolysis Biological and medical sciences Cell wall Cell Wall - chemistry Cell Wall - drug effects Cell Wall - metabolism Electrophoresis, Polyacrylamide Gel Fundamental and applied biological sciences. Psychology Hexosaminidases - metabolism Lysostaphin - metabolism MBD Microbiology Muramidase - metabolism Peptidoglycan - chemistry Peptidoglycan - drug effects Peptidoglycan - metabolism Staphylococcus aureus - chemistry Staphylococcus aureus - drug effects Zymography |
title | Zymographic Characterization of Staphylococcus aureus Cell Wall |
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