1996
DOI: 10.1016/s0008-6215(96)90797-1
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Structure of stewartan, the capsular exopolysaccharide from the corn pathogen Erwinia stewartii

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Cited by 27 publications
(34 citation statements)
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“…For example, P. stewartii is note to produce “stewartan” a heteropolymer of glucose and galactose [54]. P. agglomerans KFS-9 produces a heteropolymer constituted by arabinose, glucose galactose and gulcuronic acid with a molecular weight of 760 kDa [55].…”
Section: Resultsmentioning
confidence: 99%
“…For example, P. stewartii is note to produce “stewartan” a heteropolymer of glucose and galactose [54]. P. agglomerans KFS-9 produces a heteropolymer constituted by arabinose, glucose galactose and gulcuronic acid with a molecular weight of 760 kDa [55].…”
Section: Resultsmentioning
confidence: 99%
“…Cells of overnight cultures were streaked on a cellophane disk placed on CPG or MM2C agar [10,19]. After 3 d incubation at 28 • C, the cell cultures were suspended in 2 ml water and gently vortexed.…”
Section: Preparation Of Epsmentioning
confidence: 99%
“…Amylovoran consists of five different sugar residues and a glucose residue in a second side chain [9]. Pyrifolan, produced by E. pyrifoliae, and stewartan are related to amylovoran, but the glucose of the second side chain is absent in pyrifolan and a galactose residue in the backbone of stewartan is substituted by glucose [10]. Also the main side chain of stewartan terminates in glucose rather than pyruvate.…”
Section: Introductionmentioning
confidence: 99%
“…stewartii uses the EsaI/EsaR QS circuitry to regulate stewartan EPS production, necessary for biofilm formation, plant colonization, and virulence. Stewartan EPS is a well-characterized acidic polymer of glucose, galactose and glucuronic acid that enmeshes bacteria in mature biofilms [41,42]. At low cell density and low AHL concentrations, the EsaR QS regulator represses transcription of the stewartan EPS biosynthetic genes and bacteria are competent for attachment to abiotic surfaces [32,43].…”
Section: Epssmentioning
confidence: 99%
“…Furthermore, QS as target for the eradication of biofilms is also discussed. [22,45,47,58,59,[65][66][67] Burkholderia cenocepacia C6-HSL, C8-HSL, BDSF unknown defective in late stages [23,27] Aeromonas hydrophila C4-HSL unknown defective in late stages [9] Pseudomonas putida 3-oxo-C10-HSL, 3-oxo-C12-HSL putisolvin I and II structured biofilm (QS as biofilm repressor) [25,56] Serratia marcescens C4-HSL EPS thin and nonstructured [26,30] Pantoea stewartii 3-oxo-C6-HSL stewartan EPS flat and uniform [32,42,43] Xanthomonas campestris DSF unknown no development or no dispersal [34,35] Xylella fastidiosa DSF unknown no development [17] transcriptional and post-transcriptional level [11]. This highly sophisticated regulatory network, which integrates various environmental parameters, may explain why the influence of QS on biofilm structures was found to be highly dependent on experimental conditions.…”
Section: Introductionmentioning
confidence: 99%