{"title":"Purification and composition of lipopolysaccharides from Pseudomonas syringae pv. glycinea","authors":"P.A. Barton-Willis , M.C. Wang, M.J. Holliday , M.R. Long, N.T. Keen","doi":"10.1016/0048-4059(84)90045-6","DOIUrl":null,"url":null,"abstract":"<div><p>Purified lipopolysaccharides (LPS) from four races of <em>Pseudomonas syringae</em> pv. <em>glycinea</em> were assayed for phytoalexin elicitor activity in soybean cotyledons, and isolated O-chain fractions were chemically characterized. The LPS were weak elicitors of glyceollin accumulation, but no race specificity was noted. SDS-Polyacrylamide gel electrophoresis showed considerable size heterogeneity in the LPS but only slight differences were noted between preparations from the various races. The major components of the O-chain fractions from all races were rhamnose and N-acetylglucosamine. The ratio of these components in preparations from race 4 differed significantly from those of races 1, 5 and 6.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 387-398"},"PeriodicalIF":0.0000,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90045-6","citationCount":"30","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological Plant Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0048405984900456","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 30
Abstract
Purified lipopolysaccharides (LPS) from four races of Pseudomonas syringae pv. glycinea were assayed for phytoalexin elicitor activity in soybean cotyledons, and isolated O-chain fractions were chemically characterized. The LPS were weak elicitors of glyceollin accumulation, but no race specificity was noted. SDS-Polyacrylamide gel electrophoresis showed considerable size heterogeneity in the LPS but only slight differences were noted between preparations from the various races. The major components of the O-chain fractions from all races were rhamnose and N-acetylglucosamine. The ratio of these components in preparations from race 4 differed significantly from those of races 1, 5 and 6.