ライフサイエンスコーパス: exopolysaccharide

1 e first step in the assembly of colanic acid exopolysaccharide.

2 ly proteins, and glycanases that cleave host exopolysaccharide.

3 ents biofilm formation by condensing biofilm exopolysaccharide.

4 are cocultured with cells expressing either exopolysaccharide.

5 ce of sugars for the synthesis of the matrix exopolysaccharide.

6 g the utility of having a redundant scaffold exopolysaccharide.

7 tracellular matrix consisting of protein and exopolysaccharide.

8 ine interacts directly and specifically with exopolysaccharide.

9 hich encodes synthesis of the biofilm matrix exopolysaccharide.

10 y of producing a net-like matrix of secreted exopolysaccharide.

11 active low-molecular-weight fraction of this exopolysaccharide.

12 ires an abundant matrix protein, TasA and an exopolysaccharide.

13 hat Psl is a galactose-rich and mannose-rich exopolysaccharide.

14 n and to influence the production of the Pel exopolysaccharide.

15 required for synthesis of the biofilm matrix exopolysaccharide.

16 fied within the biosynthetic pathway of each exopolysaccharide.

17 enomenon was attributed to expression of Psl exopolysaccharide.

18 biofilms, despite being able to bind to the exopolysaccharide.

19 and redundant roles for two distinct biofilm exopolysaccharides.

20 eins necessary for secreting biofilm-forming exopolysaccharides.

21 light-organ colonization by inducing the Syp exopolysaccharide, a mediator of biofilm formation durin

22 prM fluorescent substrate) and extracellular exopolysaccharide abundance (contributing to a mucoid ph

23 lts is that appropriate symbiotically active exopolysaccharides act as signals to plant hosts to init

24 ient availability for production of pili and exopolysaccharide adhesion structures.

25 suggests a potential protective function of exopolysaccharides against H2O2 during early symbiosis.

26 enicol challenge and in T. maritima bound in exopolysaccharide aggregates during methanogenic cocultu

27 These include the overproduction of the exopolysaccharide alginate and the loss of complete lipo

28 Overproduction of the exopolysaccharide alginate causes mucoid conversion in P

29 portunistic human pathogen that secretes the exopolysaccharide alginate during infection of the respi

30 bacteria, copious quantities of the biofilm exopolysaccharide alginate slightly promoted dissolution

31 The exopolysaccharide alginate, produced by mucoid Pseudomon

32 f the biofilm during these infections is the exopolysaccharide alginate, which is synthesized at the

33 n of genes involved in the production of the exopolysaccharides alginate and levan.

34 t was hypermotile, produced higher amount of exopolysaccharide amylovoran, and had increased expressi

35 The biofilm matrix is composed of an exopolysaccharide and an amyloid fiber-forming protein,

36 ratitis, is facilitated by the bacterial Psl exopolysaccharide and associated with heightened virulen

37 The all2Delta mutant shed a less viscous exopolysaccharide and exhibited higher sensitivity to hy

38 gically similar to heterocysts that produced exopolysaccharide and glycolipids specific to heterocyst

39 capsulated within an extracellular matrix of exopolysaccharide and protein, requires the polyamine sp

40 sulfide ore also affected the production of exopolysaccharide and protein.

41 tivating transcription of the biofilm matrix exopolysaccharide and TasA operons through the regulator

42 ression of the operons for production of the exopolysaccharide and TasA protein biofilm matrix compon

43 her in bundles by an extracellular matrix of exopolysaccharide and the protein TasA.

44 uction of poly-beta(1-6)-N-acetylglucosamine exopolysaccharide and virulence in worms.

45 pathogen Pseudomonas aeruginosa, Psl and Pel exopolysaccharides and extracellular DNA (eDNA) serve as

46 contrast, espH and hag mutants, defective in exopolysaccharides and flagellum production, respectivel

47 nts show that Delta hprK mutants overproduce exopolysaccharides and form nodules that do not fix nitr

48 tinct from that of other known P. aeruginosa exopolysaccharides and is instrumental in its ability to

49 us secondary metabolites, an uncharacterized exopolysaccharide, and a predicted chitin-binding protei

50 ular matrix typically consisting of protein, exopolysaccharide, and often DNA.

51 acellular matrix comprised of nucleic acids, exopolysaccharides, and adhesion proteins.

52 the bacterial synthesis of oligosaccharides, exopolysaccharides, and capsular polysaccharides.

53 ion of the extracytoplasmic stress response, exopolysaccharides, and the virulence of V. vulnificus.

54 The type 3 secretion protein PcrV and Psl exopolysaccharide are promising therapeutic antibody tar

55 dies have shown that the protein TasA and an exopolysaccharide are the main components of the matrix.

56 Exopolysaccharides are key structural components of this

57 Exopolysaccharides are required for the development and

58 Finally, exopolysaccharide as a potential nutrient source for spe

59 bacteria, including the presence of secreted exopolysaccharides as core components of the extracellul

60 es a foundation for the synthesis of biofilm exopolysaccharides, as well as its activation by cyclic-

61 our current understanding of fungal biofilm exopolysaccharides, as well as the parallels that can be

62 f c-di-GMP receptors that appear to regulate exopolysaccharide assembly at the protein level through

63 uishes compatible and incompatible rhizobial exopolysaccharides at the epidermis.

64 The Pel exopolysaccharide (biofilm matrix component) and cyclic

65 eQ regulates the expression of flagellar and exopolysaccharide biosynthesis genes in response to cell

66 pecific structural genes (flagella, pili and exopolysaccharide biosynthesis) and regulatory processes

67 se encoding proteins required for virulence, exopolysaccharide biosynthesis, and flagellum production

68 n previously unidentified putative bacterial exopolysaccharide biosynthetic operons and in other fung

69 Mutants of strain R7A affected in early exopolysaccharide biosynthetic steps form nitrogen-fixin

70 These exopolysaccharides both contain 1,4-linked N-acetyl-d-ga

71 s well as hyaluronic acid (HA) and B. cereus exopolysaccharide (BPS) capsules.

72 Exopolysaccharide-C47 product (molecular weight: 7.3 x 1

73 The rheological properties of exopolysaccharide-C47 product are influenced by the salt

74 The apparent viscosity of exopolysaccharide-C47 product decreased with the increas

75 r and alpha-amylase inhibitory activities of exopolysaccharide-C47 product reached up to 67.52, 59.35

76 (EPS) produced by Lactococcus garvieae-C47 (exopolysaccharide-C47 product), a potential probiotic ba

77 Overproduction of the exopolysaccharide called alginate provides P. aeruginosa

78 regulate the expression of a putative novel exopolysaccharide called Psl.

79 Sinorhizobium meliloti produces an exopolysaccharide called succinoglycan that plays a crit

80 e mechanisms, including the production of an exopolysaccharide capsule and the secretion of a myriad

81 The exopolysaccharide capsule of Streptococcus pneumoniae is

82 ed alterations in cell wall chitosan and the exopolysaccharide capsule, a primary cryptococcal virule

83 an effective survival factor, the sialylated exopolysaccharide capsule.

84 gradation of the terminal sialic acid on its exopolysaccharide capsule.

85 y phenotype due to production of UPP and the exopolysaccharide cellulose, when A. tumefaciens is incu

86 tion of microbially excreted organics (e.g., exopolysaccharides) coating Feppt in our microscopic ana

87 The presence of the exopolysaccharide component of the matrix causes an incr

88 tedly found that Pel is a positively charged exopolysaccharide composed of partially acetylated 1-->4

89 ormation of biofilm, which contained a novel exopolysaccharide consisting of an amylose-like glucan.

90 ccharides in the assembled capsule, isolated exopolysaccharides contained reducing ends.

91 Exopolysaccharides contribute significantly to attachmen

92 r binding, followed by lipopolysaccharide or exopolysaccharide degradation.

93 l pathogen Vibrio cholerae synthesizes a VPS exopolysaccharide-dependent biofilm matrix that allows i

94 Exopolysaccharide-depolymerization products (EDP) varyin

95 To determine the requirement of exopolysaccharide during in vivo biofilm infections, we

96 ram to form biofilms that are independent of exopolysaccharides during CAUTI.

97 rature [25 degrees C]) results in measurable exopolysaccharide (EPS) accumulation and biofilm formati

98 Total exopolysaccharide (EPS) and alginate production increase

99 Both BPS and exopolysaccharide (EPS) are produced by dedicated Wzx/Wz

100 of flagellar reversals and production of an exopolysaccharide (EPS) as factors in the establishment

101 In Bacillus subtilis, secretion of the exopolysaccharide (EPS) component of the extracellular m

102 o-transcriptional regulation is required for exopolysaccharide (eps) expression.

103 We previously identified exopolysaccharide (EPS) from a probiotic, Bacillus subti

104 hage (PhiAB6TSP) that digests Pse-containing exopolysaccharide (EPS) from Acinetobacter baumannii str

105 Exopolysaccharide (EPS) from the probiotic Bacillus subt

106 A single dose of exopolysaccharide (EPS) from the probiotic spore-forming

107 The presence of capsular exopolysaccharide (EPS) in Mollicutes has been inferred

108 c-di-GMP activate biosynthesis of an unknown exopolysaccharide (EPS) in the food-borne pathogen Liste

109 We report that the Bacillus subtilis exopolysaccharide (EPS) is a signaling molecule that con

110 he corn pathogen P. stewartii, production of exopolysaccharide (EPS) is repressed by EsaR at low cell

111 estigated a multitargeted approach combining exopolysaccharide (EPS) matrix-degrading glucanohydrolas

112 lso exhibits lytic activity towards capsular exopolysaccharide (EPS) of the multiresistant clinical s

113 rain R7A and Lotus japonicus Gifu, rhizobial exopolysaccharide (EPS) plays an important role in infec

114 activities and rheological properties of the exopolysaccharide (EPS) produced by Lactococcus garvieae

115 Stewartan and amylovoran exopolysaccharide (EPS) produced by the plant pathogenic

116 ations VitC impaired quorum sensing (QS) and exopolysaccharide (EPS) production and induced sugar and

117 ate (c-di-GMP) supress motility and activate exopolysaccharide (EPS) production in a variety of bacte

118 (MCP)-like sensory transducer that regulates exopolysaccharide (EPS) production in Myxococcus xanthus

119 e DifE histidine kinase in the regulation of exopolysaccharide (EPS) production in the Gram-negative

120 A strain with high exopolysaccharide (EPS) production was isolated from soi

121 The main aim of the work was to increase the exopolysaccharide (EPS) production where customised milk

122 he mutant also showed moderate impairment in exopolysaccharide (EPS) production, but comparison with

123 ncluding the eps operon encoding enzymes for exopolysaccharide (EPS) production, were decreased in ex

124 teria (LAB) are well known for homopolymeric exopolysaccharide (EPS) production.

125 ity requires the type IV pilus (T4P) and the exopolysaccharide (EPS) to function.

126 M. xanthus exopolysaccharide (EPS) was shown to be an extracellular

127 fective in the synthesis of Nod Factor (NF), exopolysaccharide (EPS), or lipopolysaccharide (LPS), we

128 e UCC2003 produces a cell surface-associated exopolysaccharide (EPS), the biosynthesis of which is di

129 Additionally, exopolysaccharide (EPS), the major constituent of bacter

130 No protection was observed when an exopolysaccharide (EPS)-deficient mutant of B. subtilis

131 Anthrone method and exopolysaccharide (EPS):bacteria volume ratio measured b

132 In the legume-rhizobium symbiosis, bacterial exopolysaccharides (EPS) are essential for the developme

133 s have focused on high molecular weight (Mw) exopolysaccharides (EPS) as a source of potentially bioa

134 ling mechanisms, such as the biosynthesis of exopolysaccharides (EPS) by S. meliloti.

135 ed by type IV pili, requires the presence of exopolysaccharides (EPS) on the cell surface.

136 of type IV pili and requires the presence of exopolysaccharides (EPS) produced by neighboring cells.

137 hydrogen cyanide (HCN), ammonia (NH(3)), and exopolysaccharides (EPS) production.

138 ethod for quantitative analysis of bacterial exopolysaccharides (EPS) was developed.

139 ntly shown to produce phosphonate-containing exopolysaccharides (EPS), also known as phosphonoglycans

140 TFP are known to bind to secreted exopolysaccharides (EPS), but it is unclear how M. xanth

141 udomonas aeruginosa biofilms are composed of exopolysaccharides (EPS), exogenous DNA, and proteins th

142 ce of C. albicans augments the production of exopolysaccharides (EPS), such that cospecies biofilms a

143 Here we show that exopolysaccharides (EPS), the major extracellular compon

144 Streptococcus mutans can produce exopolysaccharides (EPS)-matrix and assemble microcoloni

145 solid surfaces, which requires both TFP and exopolysaccharides (EPS).

146 L. johnsonii FI9785 can produce two types of exopolysaccharide: EPS-1 is a branched dextran with the

147 Microbial exopolysaccharides (EPSs) exhibit diverse functionalitie

148 RapA2 interacts specifically with the acidic exopolysaccharides (EPSs) produced by R. leguminosarum i

149 antibodies (mAbs) targeting the Psl biofilm exopolysaccharide exhibit protective activity against pl

150 The exopolysaccharides formed through interactions between s

151 tructure of both high and low molecular mass exopolysaccharide from R7A.

152 -like kinase, EPR3, binds low molecular mass exopolysaccharide from strain R7A to regulate bacterial

153 Research involving exopolysaccharides from extremophiles is only recently g

154 n capsular polysaccharides and extracellular exopolysaccharides from Gram-negative bacteria.

155 accharides from Pleurotus eryngii (PEPS) and exopolysaccharides from Streptococcus thermophilus ASCC

156 The exopolysaccharide galactosaminogalactan (GAG) contribute

157 The exopolysaccharide galactosaminogalactan (GAG) is an impo

158 glycoconjugates are related to fragments of exopolysaccharide galactosaminogalactan (GG) found in As

159 EAR increases expression of exopolysaccharide genes and biofilm formation, and appea

160 serve the capacity to produce a biofilm when exopolysaccharide genes are subjected to mutation.

161 aeruginosa derepresses the expression of Pel exopolysaccharide genes required for biofilm formation w

162 d to biofilm formation and pathogenesis, the exopolysaccharides have been well characterized for only

163 ss responses, the synthesis and transport of exopolysaccharides, heat shock response proteins, enzyme

164 in mediating this process is succinoglycan (exopolysaccharide I [EPSI]), a polysaccharide composed o

165 exopolysaccharides such as succinoglycan and exopolysaccharide II (EPS II) enables the bacterium to i

166 gulate the biosynthesis of succinoglycan, an exopolysaccharide important for host invasion.

167 sitively regulates the secretion of the main exopolysaccharide in E. amylovora, amylovoran, leading t

168 ossible role of the non-polar domains of the exopolysaccharide in facilitating the diffusion of aliph

169 ace and production of flagellar proteins and exopolysaccharide in response to light.

170 apsule to study the function of the alginate exopolysaccharide in the interaction of Pseudomonas aeru

171 In addition, insight into the role of exopolysaccharides in biofilms is highlighted through th

172 Sinorhizobium meliloti requires exopolysaccharides in order to form a successful nitroge

173 lanktonic growth and biofilm formation in an exopolysaccharide-independent manner.

174 This exopolysaccharide is important for P. aeruginosa attachm

175 esterol biofilms but that expression of this exopolysaccharide is not necessary for binding to glass

176 The Bps exopolysaccharide is one of the critical determinants fo

177 The exopolysaccharide is produced by enzymes encoded by the

178 Because the alginate exopolysaccharide is surface-exposed, levels of SP-A may

179 , yet little is known about how this biofilm exopolysaccharide is synthesized and exported from the c

180 f capsular polysaccharides (CPS) or secreted exopolysaccharides is ubiquitous in bacteria, and the Wz

181 a high molecular weight acidic heteropolymer exopolysaccharide, is a virulent factor of E. amylovora.

182 for the production of a glucose-rich matrix exopolysaccharide, is shown to be greatly reduced in las

183 to changing environments and can secrete an exopolysaccharide known as alginate as a protection resp

184 Mucoidy, or overproduction of the exopolysaccharide known as alginate, in Pseudomonas aeru

185 iosynthesis of the environmentally regulated exopolysaccharide known as colanic acid, whereas in othe

186 Bordetella species produce an exopolysaccharide, known as the Bordetella polysaccharid

187 growth defects, and changes in cell size and exopolysaccharide levels, among others.

188 olysaccharide, the double mutants had higher exopolysaccharide levels.

189 duction, indicating that AlgL operates as an exopolysaccharide lyase.

190 oncerning spatio-temporal development of the exopolysaccharide matrix and its essential role in the p

191 Specific proteins associated with exopolysaccharide matrix assembly, metabolic and stress

192 These observations provide an example of how exopolysaccharide matrix biosynthesis by a community of

193 t mucoid strains of bacteria that produce an exopolysaccharide matrix do not induce NPR-1-dependent b

194 In staphylococci, this exopolysaccharide matrix is composed of polysaccharide i

195 acteria commonly encapsulated by an adhesive exopolysaccharide matrix.

196 Each of these structures involves exopolysaccharide-mediated cell-cell interactions, which

197 Studies with exopolysaccharide mutants, which are defective in aggreg

198 data suggest the presence of an unidentified exopolysaccharide necessary for mature biofilm developme

199 G is a heterogeneous linear alpha-1,4-linked exopolysaccharide of galactose and GalNAc that is partia

200 s review, we present the current research on exopolysaccharides of oral microbes regarding their bios

201 Studies on the exopolysaccharides of other oral organisms, however, are

202 ocolonies in biofilms, (ii) the influence of exopolysaccharides on formation of microcolonies, and (i

203 trating mechanism, and chemical reactions in exopolysaccharide or proteinaceous surface layers are as

204 ed for the synthesis of galactose-containing exopolysaccharides or galactose metabolism.

205 aride fragment of the Pseudomonas aeruginosa exopolysaccharide Pel was assembled using a [2 + 2 + 2]

206 Pseudomonas aeruginosa produces the cationic exopolysaccharide Pel, which protects bacteria from amin

207 egradation of phytate, antioxidant capacity, exopolysaccharides, phenolic compound content and in vit

208 e a biofilm matrix composed primarily of the exopolysaccharide phosphoethanolamine (pEtN) cellulose.

209 Exopolysaccharides play an important structural and func

210 Capsular polysaccharides and exopolysaccharides play critical roles in bacterial surv

211 The exopolysaccharide poly-beta-(1->6)-N-acetylglucosamine (

212 aphylococci, partial de-N-acetylation of the exopolysaccharide poly-beta-1,6-N-acetyl-d-glucosamine (

213 richia coli, partial de-N-acetylation of the exopolysaccharide poly-beta-1,6-N-acetyl-D-glucosamine (

214 ion of the ica operon coding for the biofilm exopolysaccharide polysaccharide intercellular adhesin (

215 single nucleotide substitution (19%) in the exopolysaccharide priming-glycosyl transferase (p-gtf).

216 results suggest that the level of symbiotic exopolysaccharide produced by a rhizobial species is one

217 beta-1,6-N-acetyl-D-glucosamine (PNAG) is an exopolysaccharide produced by a wide variety of medicall

218 ation into the hydrophobic properties of the exopolysaccharide produced by Burkholderia multivorans s

219 unit of the immunogenic beta-Kdo-containing exopolysaccharide produced by Burkholderia pseudomallei

220 ins showed reduced levan production, another exopolysaccharide produced by E. amylovora.

221 The identification of an exopolysaccharide produced by H. somni prompted us to ev

222 Colanic acid (CA) or M-antigen is an exopolysaccharide produced by many enterobacteria, inclu

223 Colanic acid (CA) is a common exopolysaccharide produced by many genera in the Enterob

224 The low molecular mass exopolysaccharide produced by R7A is a monomer unit of t

225 er analysis suggested that the nature of the exopolysaccharide produced, rather than the amount, may

226 nto the biosynthesis and structures of novel exopolysaccharides produced by L. johnsonii FI9785, whic

227 Exopolysaccharides produced by lactic acid bacteria are

228 For example, at least one of two exopolysaccharides produced by S. meliloti (succinoglyca

229 A key component is currently undefined exopolysaccharides produced from proteins encoded by gen

230 An exopolysaccharide, produced during the late stage of sta

231 he oral cavity contains a rich consortium of exopolysaccharide-producing microbes.

232 The exopolysaccharide product produced by L. garvieae C47 po

233 tration of c-di-GMP, which in turn decreased exopolysaccharide production and biofilm formation.

234 onent of the matrix but had little effect on exopolysaccharide production and localization within the

235 P gene in P. aeruginosa PAK led to increased exopolysaccharide production and upregulation of the typ

236 antly decreased motility, biofilm formation, exopolysaccharide production and virulence to crustacean

237 ld be a widespread feature of the control of exopolysaccharide production in bacteria.

238 ns to modulate virulence gene expression and exopolysaccharide production in response to changes in o

239 Exopolysaccharide production is downregulated by Ltp1 th

240 RSCV traits such as increased exopolysaccharide production leading to antibiotic toler

241 attenuate the QS-dependent factors, such as exopolysaccharide production, alginate production, swimm

242 cycle, while PtsN controls nitrogen uptake, exopolysaccharide production, and potassium homeostasis,

243 t AmyR plays an important role in regulating exopolysaccharide production, and thus virulence in E. a

244 exerts pleiotropic regulation of amylovoran exopolysaccharide production, biofilm formation, motilit

245 of podJ1 interferes with flagellar motility, exopolysaccharide production, cell envelope integrity, c

246 The fusA1 mutant also displayed elevated exopolysaccharide production, dysregulated siderophore p

247 For example, exopolysaccharide production, which has been shown to pl

248 Cl) reestablishes QS-dependent repression of exopolysaccharide production.

249 ction and that EPR3 perception of compatible exopolysaccharide promotes an intracellular cortical inf

250 olecule Pseudomonas quinolone signal and the exopolysaccharide Psl, is regulated not only through the

251 omonas aeruginosa is the biosynthesis of the exopolysaccharide Psl.

252 bgsBA transcription is dependent on the exopolysaccharide/quorum sensing ExpR/SinI regulatory sy

253 the structure of the Lotus japonicus (Lotus) exopolysaccharide receptor 3 (EPR3) ectodomain.

254 These results suggest that exopolysaccharide recognition is reiterated during the p

255 se in colony corrugation and accumulation of exopolysaccharides relative to the rugose variant.

256 erlying pEtN derivatization of the cellulose exopolysaccharide remains elusive.

257 ar substance of the aggregates for potential exopolysaccharides revealed the existence of both sulfat

258 abolic activity of microbes embedded in this exopolysaccharide-rich and diffusion-limiting matrix lea

259 mechanism of the Pel apparatus, a widespread exopolysaccharide secretion system found in environmenta

260 nse variation in capsular polysaccharide and exopolysaccharide structures, patterns are evident in st

261 S. meliloti unable to produce the exopolysaccharide succinoglycan are unable to establish

262 Production of the exopolysaccharide succinoglycan by the nitrogen-fixing b

263 Overproduction of the exopolysaccharide succinoglycan is a dramatic phenotype

264 ed production of the symbiotically important exopolysaccharide succinoglycan.

265 nts of Rm1021 that are unable to produce the exopolysaccharide succinoglycan.

266 nvolved in the biosynthesis of the symbiotic exopolysaccharide succinoglycan.

267 Levels of production of the exopolysaccharides succinoglycan (EPS-I) and galactogluc

268 The production of biofilms and exopolysaccharides such as capsular polysaccharides and

269 In Sinorhizobium meliloti, the production of exopolysaccharides such as succinoglycan and exopolysacc

270 haride synthases), ftf (encoding the fructan exopolysaccharide synthase), and the scrAB pathway (suga

271 types indicated that gtfBCD (encoding glucan exopolysaccharide synthases), ftf (encoding the fructan

272 Biofilm formation is dependent on exopolysaccharide synthesis and is controlled by the int

273 luence of c-di-GMP beyond that of regulating exopolysaccharide synthesis and motility.

274 Biochemical studies of exopolysaccharide synthesis are hampered by difficulties

275 Bacterial exopolysaccharide synthesis is a prevalent and indispens

276 volved in the cold-shock response and in Psl exopolysaccharide synthesis respectively.

277 vI is a key regulator of gene expression for exopolysaccharide synthesis, biofilm formation, motility

278 hed in glycosyltransferase genes involved in exopolysaccharide synthesis.

279 ority of research to date has focused on the exopolysaccharide systems of biofilm-forming bacteria, r

280 the matrix proteins Bap1, RbmA, and RbmC, an exopolysaccharide termed Vibrio polysaccharide, and DNA.

281 The exopolysaccharide that is most efficient in mediating th

282 enveloping the cell and/or take the form of exopolysaccharides that are mostly secreted into the imm

283 bium meliloti 1021 produces acidic symbiotic exopolysaccharides that enable it to initiate and mainta

284 like PHB synthesis mutants that have reduced exopolysaccharide, the double mutants had higher exopoly

285 A decreased the binding of purified alginate exopolysaccharide to AEC.

286 With sucrose, S. mutans produces exopolysaccharides to enhance bacterial adhesion on the

287 In contrast, extracellular secretion of the exopolysaccharide VPS, an essential component of the bio

288 Vibrio exopolysaccharides (VPS) and the matrix proteins RbmA, B

289 and calcium-regulated, biofilm-promoting brp exopolysaccharide was IamA-dependent.

290 A greater incidence (P < 0.05) of Pel exopolysaccharide was present in samples fixed with Boui

291 oduction of water-insoluble, adhesive glucan exopolysaccharides, was down-regulated in cells growing

292 Exopolysaccharides were isolated and purified from Lacto

293 thesis locus (psl) is predicted to encode an exopolysaccharide which is critical for biofilm formatio

294 Bacillus subtilis, the matrix consists of an exopolysaccharide, which is specified by the epsA-O oper

295 is known that P. aeruginosa secretes the Psl exopolysaccharide, which promotes surface attachment by

296 s and Actinomyces naeslundii steadily formed exopolysaccharides, which allowed the initial clustering

297 The exopolysaccharides, which are mostly glucans synthesized

298 ng and microcolony assembly are dependent on exopolysaccharides, while population growth dynamics and

299 mmercial production of curdlan, an important exopolysaccharide with food and medical applications.

300 in the secretion of a shorter, more viscous exopolysaccharide with less branching and structural com