{"title":"聚类法测定变酵素诱导的化脓性放线菌的裂解","authors":"Ch. Lämmler , Ch. Frede","doi":"10.1016/S0176-6724(88)80066-X","DOIUrl":null,"url":null,"abstract":"<div><p>The lytic activity of mutanolysin from <em>Streptomyces globisporus</em> on 42 cultures of <em>Actinomyces pyogenes</em> could be effectively analyzed in an aggregometer. It was expressed as increase of transmittance at 546 nm after 20 min and 2 h at 37°C. The <em>A. pyogenes</em> cultures revealed no uniform lysis pattern. Most of the cultures were lyzed within 20 to 40 min at 37°C, others were lyzed only moderately or weakly within 2 h of incubation. The lytic activity was optimal at low (0.01 mol/1) molarity of the lysis buffer between pH 5.7 and 7 and could be inhibited by HgCl<sub>2</sub>. <em>A. pyogenes</em> was not lyzed by lysostaphin or lysozyme.</p></div>","PeriodicalId":101291,"journal":{"name":"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology","volume":"269 4","pages":"Pages 447-453"},"PeriodicalIF":0.0000,"publicationDate":"1988-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0176-6724(88)80066-X","citationCount":"4","resultStr":"{\"title\":\"Mutanolysin-induced lysis of actinomyces pyogenes determined by aggregometry\",\"authors\":\"Ch. Lämmler , Ch. Frede\",\"doi\":\"10.1016/S0176-6724(88)80066-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The lytic activity of mutanolysin from <em>Streptomyces globisporus</em> on 42 cultures of <em>Actinomyces pyogenes</em> could be effectively analyzed in an aggregometer. It was expressed as increase of transmittance at 546 nm after 20 min and 2 h at 37°C. The <em>A. pyogenes</em> cultures revealed no uniform lysis pattern. Most of the cultures were lyzed within 20 to 40 min at 37°C, others were lyzed only moderately or weakly within 2 h of incubation. The lytic activity was optimal at low (0.01 mol/1) molarity of the lysis buffer between pH 5.7 and 7 and could be inhibited by HgCl<sub>2</sub>. <em>A. pyogenes</em> was not lyzed by lysostaphin or lysozyme.</p></div>\",\"PeriodicalId\":101291,\"journal\":{\"name\":\"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology\",\"volume\":\"269 4\",\"pages\":\"Pages 447-453\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1988-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0176-6724(88)80066-X\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S017667248880066X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S017667248880066X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mutanolysin-induced lysis of actinomyces pyogenes determined by aggregometry
The lytic activity of mutanolysin from Streptomyces globisporus on 42 cultures of Actinomyces pyogenes could be effectively analyzed in an aggregometer. It was expressed as increase of transmittance at 546 nm after 20 min and 2 h at 37°C. The A. pyogenes cultures revealed no uniform lysis pattern. Most of the cultures were lyzed within 20 to 40 min at 37°C, others were lyzed only moderately or weakly within 2 h of incubation. The lytic activity was optimal at low (0.01 mol/1) molarity of the lysis buffer between pH 5.7 and 7 and could be inhibited by HgCl2. A. pyogenes was not lyzed by lysostaphin or lysozyme.