ライフサイエンスコーパス: fluorescens

1 faecalis , Escherichia coli , or Pseudomonas fluorescens .

2 tudies of bacterial cells (i.e., Pseudomonas fluorescens).

3 ific phospholipase C (PC-PLC) of Pseudomonas fluorescens.

4 substrate activity with kynureninase from P. fluorescens.

5 adhesin regulating surface commitment by P. fluorescens.

6 ism impacts biofilm formation by Pseudomonas fluorescens.

7 calization and thus surface commitment by P. fluorescens.

8 dhesion required for biofilm formation by P. fluorescens.

9 ofilm formation by the bacterium Pseudomonas fluorescens.

10 ory populations of the bacterium Pseudomonas fluorescens.

11 ve trait of biofilm formation in Pseudomonas fluorescens.

12 ome c-type biogenesis protein of Pseudomonas fluorescens.

13 rse populations of the bacterium Pseudomonas fluorescens.

14 e and antifungal metabolite production in P. fluorescens.

15 control antibiotic production by Pseudomonas fluorescens.

16 to the root adhesin protein from Pseudomonas fluorescens.

17 tal structure of the enzyme from Pseudomonas fluorescens.

18 like P. aeruginosa and the less virulent P. fluorescens.

19 er jejuni, L. monocytogenes, and Pseudomonas fluorescens.

20 notably Escherichia species and Pseudomonas fluorescens.

21 ing to a proposal of a dynamical model of P. fluorescens 07A metalloprotease active and inactive conf

22 The molecular dynamics of the Pseudomonas fluorescens 07A metalloprotease in the presence of struc

23 f a clone of phzI in Escherichia coli and P. fluorescens 1855 resulted in the synthesis of all six ac

24 2-79 synthesizes 3-OH acyl-HSLs and that P. fluorescens 2-79 uses N-(3-hydroxy-hexanoyl)-HSL as its

25 The phz operon of Pseudomonas fluorescens 2-79, which produces phenazine-1-carboxylate

26 The Pseudomonas fluorescens 23F phosphonoacetate hydrolase gene (phnA) e

27 phosphonoacetate hydrolase, from Pseudomonas fluorescens 23F was cloned and expressed in Escherichia

28 fluences diverse physiological aspects of P. fluorescens 2P24 via the newly characterized AgtR.

29 nced the antibiotic tolerance of Pseudomonas fluorescens 2P24, a PGPR well known for its biocontrol c

30 c analyses classified the isolates in the P. fluorescens (57) and P. putida (19) groups.

31 P. fluorescens (a saprophyte) or hrp mutants defective in t

32 stigated the interaction between Pseudomonas fluorescens, a biofilm-forming bacterium, and polysulfon

33 Mannanase A (MANA) from Pseudomonas fluorescens, a member of glycosyl hydrolase family 26, w

34 duced by either the non-pathogen Pseudomonas fluorescens, a TTSS-deficient mutant of P. syringae pv.

35 ATCC 39167 and plant-deleterious Pseudomonas fluorescens A225 were grown in an iron-deficient culture

36 In case of pseudobactins from P. fluorescens A225, the octapeptide has the sequence Chr-S

37 riplasmic oxidoreductase PvdO of Pseudomonas fluorescens A506 is required for the final oxidation of

38 nist of E. amylovora (BlightBan, Pseudomonas fluorescens A506) can be included in antibiotic spray pr

39 etion, as well as the saprophyte Pseudomonas fluorescens A506, sensed water potentials of -0.3 to -0.

40 in a single radiating lineage of Pseudomonas fluorescens adapting to laboratory conditions.

41 store more biomass C per unit of N under P. fluorescens addition.

42 show that interspecific conjugation from P. fluorescens allowed pQBR57 to persist in P. putida via s

43 The enzymatic activity of Pseudomonas fluorescens alpha-amino-beta-carboxymuconic-epsilon-semi

44 Escherichia coli and probably in Pseudomonas fluorescens, although the permease from E. coli does not

45 is similar to that of HPPD from Pseudomonas fluorescens, although the position of the C-terminal alp

46 ate populations of the bacterium Pseudomonas fluorescens and a parasitic bacteriophage with parasite

47 s luteus, Brevibacterium linens, Pseudomonas fluorescens and Bacillus subtilis were found to be sensi

48 ing of LapA-mediated biofilm formation by P. fluorescens and discusses several emerging models for th

49 duced high levels of the autoinducer, the P. fluorescens and E. coli donors produced only trace amoun

50 The nonpathogenic bacteria Pseudomonas fluorescens and Escherichia coli can elicit a genotype-s

51 otic baths of surface symbionts, Pseudomonas fluorescens and Flavobacterium johnsoniae were administe

52 We experimentally evolved Pseudomonas fluorescens and its mercury resistance mega-plasmid, pQB

53 rmined the crystal structures of Pseudomonas fluorescens and Myxococcus xanthus lectins.

54 nt of measures to control the activity of P. fluorescens and other spoilage microorganism proteases.

55 acterial species, two of which - Pseudomonas fluorescens and P. putida - were studied in depth.

56 characterized ExoU homologs from Pseudomonas fluorescens and Photorhabdus asymbiotica also localized

57 hough both DKPs were absent from Pseudomonas fluorescens and Pseudomonas alcaligenes, we isolated, fr

58 nazine biosynthetic operons from Pseudomonas fluorescens and Pseudomonas aureofaciens.

59 species of common soil bacteria, Pseudomonas fluorescens and Pseudomonas putida, and a mercury resist

60 A mixed culture of Pseudomonas fluorescens and Pusillimonas noertemanii, obtained by so

61 We propose that the lipases produced by P. fluorescens and Serratia marcescens, which comprise a se

62 ression confers a surface-sensing mode on P. fluorescens and suggest this strategy may be broadly app

63 r and chemical dialogues between Pseudomonas fluorescens and the protist Naegleria americana.

64 a (Agrobacterium tumefaciens and Pseudomonas fluorescens) and a poorly crystalline manganese (Mn) oxi

65 benzoate hydroxylase (PHBH, from Pseudomonas fluorescens) and flavin-containing monooxygenases (FMOs,

66 3D) morphology of Gram-negative (Pseudomonas fluorescens) and Gram-positive (Bacillus thuringiensis)

67 cherichia coli, Vibrio cholerae, Pseudomonas fluorescens, and Pseudomonas aeruginosa result in defect

68 Nine patients became colonized with P. fluorescens, and six out of the nine developed febrile n

69 substrate for kynureninase from Pseudomonas fluorescens, and the rate-determining step changes from

70 aphylococcus aureus, followed by Pseudomonas fluorescens; and among these bacteria, the antibacterial

71 of 2 divergent large plasmids in Pseudomonas fluorescens are caused by inducing maladaptive expressio

72 The wrinkly spreader morph of Pseudomonas fluorescens arises repeatedly during experimental evolut

73 Using Pseudomonas fluorescens as a model biofilm-forming bacterium, we fin

74 and Southern analysis identified Pseudomonas fluorescens as the originating species of I2, with homol

75 i outer-membrane porin C and the Pseudomonas fluorescens-associated sequence I2, antisaccharomyces ce

76 ioquinolobactin siderophore from Pseudomonas fluorescens ATCC 17400 utilizes a variation of the sulfu

77 Pseudomonas putida NCIB 9816 and Pseudomonas fluorescens ATCC 17483 containing naphthalene dioxygenas

78 supported the growth of P. s. tabaci and P. fluorescens bacteria, both of which are nonpathogenic on

79 ed by the genetically engineered Pseudomonas fluorescens bacterial bioreporter 5RL.

80 sis seedlings overexpressing the Pseudomonas fluorescens beta-cyanoalanine nitrilase pinA were compar

81 t two decades, the mechanisms of Pseudomonas fluorescens biofilm formation and regulation have emerge

82 c model to explain regulation of Pseudomonas fluorescens biofilm formation by the environmentally rel

83 e on viability in single species Pseudomonas fluorescens biofilms were determined via dye staining me

84 duced by Pseudomonas aurantiaca (Pseudomonas fluorescens BL915).

85 r encoded by cosmid pHIR11 conferred upon P. fluorescens but not Escherichia coli the ability to secr

86 ode of action of pyoverdine from Pseudomonas fluorescens C7R12 on Arabidopsis (Arabidopsis thaliana)

87 In contrast to a P. fluorescens C7R12 strain impaired in apo-pyoverdine prod

88 ns strain WCS365, we have shown that: (i) P. fluorescens can form biofilms on an abiotic surface when

89 , we demonstrate that ACMSD from Pseudomonas fluorescens can self-assemble into homodimer, tetramer,

90 Pseudomonas fluorescens carrying a pHIR11 derivative lacking hrpH is

91 P. fluorescens carrying a pHIR11 derivative lacking shcA fa

92 ype III polyketide synthase from Pseudomonas fluorescens, catalyzes the synthesis of phloroglucinol f

93 sent here data for the spread of Pseudomonas fluorescens caused by a contaminated drinking water disp

94 ptor LapD as a central switch in Pseudomonas fluorescens cell adhesion.

95 Here we show that adhered Pseudomonas fluorescens cells under high permeate flux conditions ar

96 n in the plant beneficial strain Pseudomonas fluorescens CHA0.

97 LapG, a periplasmic cysteine protease of P. fluorescens, cleaves the N terminus of LapA, thus releas

98 There were no further cases of P. fluorescens colonization after the contaminated dispense

99 he wrinkly spreader phenotype of Pseudomonas fluorescens colonizes food/water sources and human tissu

100 e I polyketide synthase (PKS) in Pseudomonas fluorescens, consists of a mixture of mainly pseudomonic

101 ate that the P. aeruginosa homolog of the P. fluorescens DGC GcbA involved in promoting biofilm forma

102 Here, we show that the bacteria Pseudomonas fluorescens diversifies into defence specialists, when c

103 However, E. coli or P. fluorescens donors harboring the binary system did not t

104 persicum) or Arabidopsis through Pseudomonas fluorescens, engineered to express the type III secretio

105 ophores on bacteria inoculated ( Pseudomonas fluorescens) environments and (ii) hotspots of natural i

106 of 124 +/- 6 microM x min(-1), while the P. fluorescens enzyme had a Km for NG of 110 +/- 10 microM,

107 ons of the product distributions from the P. fluorescens enzyme showed that NG was denitrated with a

108 the crystal structure of the full-length P. fluorescens ExoU and found that it was similar to that o

109 y of biofilm present and the viability of P. fluorescens following electrochemical testing.

110 olating and identifying P. aeruginosa and P. fluorescens from tap water samples, which are both oppor

111 rved a sharp increase in the isolation of P. fluorescens from weekly pharyngeal surveillance swabs.

112 P. fluorescens GcbA was found to be functional in P. aerugi

113 The P. fluorescens gene, xenB, encodes a 37,441-Da monomeric, N

114 (4S)-muconolactone product (syn, Pseudomonas fluorescens, gi 70731221 ; anti, Mycobacterium smegmatis

115 Among the isolates in the P. fluorescens group, most (37) were classified in the P. k

116 investigate gene networks in the diverse P. fluorescens group.

117 Pseudomonas fluorescens grows at low temperature and produces thermo

118 Here, Pseudomonas fluorescens has been introduced to the system to underst

119 he reaction of kynureninase from Pseudomonas fluorescens have been determined.

120 d by wild-type P. syringae pv. tabaci and P. fluorescens heterologously expressing a P. syringae TTSS

121 yme families and analysis of the Pseudomonas fluorescens HPD crystal structure highlighted four resid

122 uctases, from Pseudomonas putida II-B and P. fluorescens I-C that removed nitrite from nitroglycerin

123 identified as Pseudomonas putida II-B and P. fluorescens I-C.

124 several site-directed mutants of Pseudomonas fluorescens ICH at resolutions ranging from 1.0 to 1.9 A

125 ol 2-dehydrogenase (54 kDa) from Pseudomonas fluorescens in a binary complex with NAD(+) and ternary

126 e cell level using the bacterium Pseudomonas fluorescens in an oligotrophic growth assay.

127 diversification of the bacterium Pseudomonas fluorescens in its natural environment, soil.

128 otype-specific HR was observed with avrB+ P. fluorescens in soybean and Arabidopsis plants carrying r

129 diversification of the bacterium Pseudomonas fluorescens in spatially structured microcosms.

130 These findings suggest roles for pfiT and P. fluorescens in the pathogenesis of Crohn's disease.

131 esidue, are required for LapG activity of P. fluorescens in vivo and in vitro.

132 advantage of the model bacterium Pseudomonas fluorescens in which the genotype-to-phenotype map deter

133 as used to inhibit the growth of Pseudomonas fluorescens in WPI-carrageenan gels during storage at 4

134 segnis, Gemella morbillorum, and Pseudomonas fluorescens) in lung samples that had not been reported

135 lant diseases by some strains of Pseudomonas fluorescens, including Pf-5.

136 In this experiment treatment with P. fluorescens increased apparent overwinter survival five-

137 dance spectroscopy it has been shown that P. fluorescens increases the rate of corrosion.

138 lis, Lactobacillus rhamnosus and Pseudomonas fluorescens induces C. elegans stress resistance.

139 Unlike eCO(2) effects, P. fluorescens inoculants did not change mass-specific micr

140 ioning by plant growth-promoting Pseudomonas fluorescens is a prospect for ecosystem management.

141 Pseudomonas fluorescens is a saprophytic bacterium commonly isolated

142 s revealed that a mucA mutant of Pseudomonas fluorescens is protected against T6SS attacks.

143 we examined the adaptation of a Pseudomonas fluorescens isolate (R124) from the nutrient-limited min

144 ness was cloned from a strain of Pseudomonas fluorescens isolated from copper-contaminated agricultur

145 nment of a silica cave in comparison with P. fluorescens isolates from surface soil and the rhizosphe

146 Molecular typing showed that all P. fluorescens isolates were identical by both random ampli

147 th with and without positive selection in P. fluorescens, it was lost or replaced by nontransferable

148 ons of a stable form of KMO from Pseudomonas fluorescens (KMO).

149 A structural superposition with the P. fluorescens kynureninase revealed that these two structu

150 molecular replacement using the Pseudomonas fluorescens kynureninase structure (PDB entry 1qz9) as t

151 Crystals of Pseudomonas fluorescens kynureninase were obtained, and the structur

152 The reaction of Pseudomonas fluorescens kynureninase with L-kynurenine and L-alanine

153 hat Lys-227 is the PLP-binding residue in P. fluorescens kynureninase.

154 mune priming toward the bacteria Pseudomonas fluorescens, Lactococcus lactis, and 4 strains of the en

155 Here, we identify a homolog of Pseudomonas fluorescens LapG as a dispersal factor that promotes cle

156 ns Pseudomonas putida KT2440 and Pseudomonas fluorescens LP6a at varying electrolyte concentrations a

157 we quantified the deposition of Pseudomonas fluorescens Lp6a in columns containing glass collectors

158 e the dispersal of PHE-degrading Pseudomonas fluorescens LP6a.

159 from the bioluminescent reporter Pseudomonas fluorescens M3A.

160 sults suggest that treatment of bats with P. fluorescens may substantially reduce WNS mortality, and,

161 ild-type mice, and germ-free and Pseudomonas fluorescens-monoassociated interleukin 10 -/- mice remai

162 Nitrate removal by ORR isolate Pseudomonas fluorescens N2A2 is virtually abolished by Fe/Al precipi

163 Cyanide oxygenase (CNO) from Pseudomonas fluorescens NCIMB 11764 catalyzes the pterin-dependent o

164 Biofilm formation by P. fluorescens occurs through the localization of an adhesi

165 ffects of plant growth-promoting Pseudomonas fluorescens on C and N cycling in the rhizosphere of a c

166 n of microfiltered milk with 9 strains of P. fluorescens on the stability of the corresponding UHT mi

167 th the farmer are two strains of Pseudomonas fluorescens, only one of which serves as a food source.

168 monas putida (i.e., the strain was either P. fluorescens or P. putida, but the system did not make th

169 cid, the non-pathogenic bacteria Pseudomonas fluorescens, or by the phytohormones jasmonic acid (JA)

170 ilica analysis of genomic information for P. fluorescens, P. putida, and P. stutzeri suggests that th

171 led that the three Legionella enzymes and P. fluorescens PC-PLC share conserved domains also present

172 analysis of the whole genome of Pseudomonas fluorescens Pf-5 and subsequently cloned and overexpress

173 Pseudomonas fluorescens Pf-5 is a plant commensal bacterium that inh

174 al evidence that the cofactor of Pseudomonas fluorescens Pf-5 UndA is actually a diiron cluster and s

175 The gacA gene of P. fluorescens Pf-5 was isolated, and the influence of gacS

176 together with other approaches, suggested P. fluorescens Pf-5's recent lateral acquisitions include s

177 domonas protegens Pf-5 (previously called P. fluorescens Pf-5) produces two siderophores, enantio-pyo

178 x known secondary metabolites produced by P. fluorescens Pf-5, three novel secondary metabolite biosy

179 rrolnitrin oxygenase (PrnD) from Pseudomonas fluorescens Pf-5.

180 ontribute to the biocontrol properties of P. fluorescens Pf-5.

181 within a 24-kb genomic region of Pseudomonas fluorescens Pf-5.

182 p., including the soil bacterium Pseudomonas fluorescens Pf-5.

183 MP controls biofilm formation by Pseudomonas fluorescens Pf0-1 by promoting the cell surface localiza

184 Biofilm formation by Pseudomonas fluorescens Pf0-1 requires the cell surface adhesin LapA

185 urface is a key step required by Pseudomonas fluorescens Pf0-1 to irreversibly attach to a surface an

186 cause reductions in biofilm formation by P. fluorescens Pf0-1 under the conditions tested.

187 enetic needs for the survival of Pseudomonas fluorescens Pf0-1, a gram-negative soil bacterium potent

188 For Pseudomonas fluorescens Pf0-1, c-di-GMP impacts the secretion and lo

189 ent for c-di-GMP for biofilm formation by P. fluorescens Pf0-1, no DGCs from this strain have been ch

190 ailability regulates biofilm formation by P. fluorescens Pf0-1.

191 the genome of the soil bacterium Pseudomonas fluorescens Pf0-1.

192 minate colonies of the bacterium Pseudomonas fluorescens Pf0-1.

193 ::inaZ transcriptional fusion in Pseudomonas fluorescens Pf5 showed that rulAB was rapidly induced af

194 PrnD from Pseudomonas fluorescens Pf5 was functionally expressed in Escherichi

195 o the metal center in ACMSD from Pseudomonas fluorescens (PfACMSD).

196 compared with that of CopC from Pseudomonas fluorescens (PfCopC) and with the LPMO-like protein Bim1

197 se produced with the enzyme from Pseudomonas fluorescens, PFL (57%).

198 of mannitol 2-dehydrogenase from Pseudomonas fluorescens (PfM2DH) is connected with bulk solvent thro

199 Here, we found mqsA in Pseudomonas fluorescens (PfmqsA) is acquired through horizontal gene

200 al pseudomonads such as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are abse

201 P. fluorescens (pHIR11 hrmA::TnphoA) mutants do not elicit

202 When expressed in Pseudomonas fluorescens, PrnB is red in color due to the fact that i

203 uch as Pseudomonas aeruginosa or Pseudomonas fluorescens produce pyoverdine siderophores that ensure

204 An isolate of Pseudomonas fluorescens produced five detectable species, three of w

205 s in experimental populations of Pseudomonas fluorescens propagated in a spatially heterogeneous envi

206 Strains of Pseudomonas fluorescens, Ps. poae and Chryseobacterium joostei, sele

207 -methylsuccinate by lipases from Pseudomonas fluorescens, Pseudomonas cepacia, and Candida rugosa.

208 , albeit not in the enzymes from Pseudomonas fluorescens, Pseudomonas putida or Azotobacter vinelandi

209 t common misidentifications were Pseudomonas fluorescens-Pseudomonas putida (i.e., the strain was eit

210 ke the distinction and yielded the result P. fluorescens/putida) and Alcaligenes spp.

211 Genes required for 2,4-DAPG synthesis by P. fluorescens Q2-87 are encoded by a 6.5-kb fragment of ge

212 Pseudomonas fluorescens Q8r1-96 represents a group of rhizosphere st

213 d pFRtra to Escherichia coli and Pseudomonas fluorescens recipients at frequencies similar to those o

214 r antibodies to oligomannan, the Pseudomonas fluorescens-related protein, Escherichia coli outer memb

215 overexpressed ACMSD enzyme from Pseudomonas fluorescens requires a divalent metal, such as Co(II), F

216 oli or in enzymes, pyocyanin-nonproducing P. fluorescens resulted in conversion of PCA to 1-hydroxyph

217 s of the expression and regulation of the P. fluorescens rsp pathway, both in the phytosphere and in

218 nd MGO against Listeria innocua, Pseudomonas fluorescens, Salmonella enterica and Bacillus cereus has

219 acteria (Pseudomonas aeruginosa, Pseudomonas fluorescens, Salmonella Enteritidis, Salmonella Typhimur

220 osphacta, Enterococcus faecalis, Pseudomonas fluorescens, Salmonella typhimurium, Staphylococcus aure

221 tal populations of the bacterium Pseudomonas fluorescens SBW25 and its viral parasite, phage Phi2, th

222 udomonas putida BIRD-1 (BIRD-1), Pseudomonas fluorescens SBW25 and Pseudomonas stutzeri DSM4166 was p

223 A complete physical map of the 6.63 Mbp P. fluorescens SBW25 chromosome was constructed using data

224 rinkly spreader (WS) genotype of Pseudomonas fluorescens SBW25 colonizes the air-liquid interface of

225 ich populations of the bacterium Pseudomonas fluorescens SBW25 evolved, de novo, the ability to switc

226 ects on competitive fitness of a Pseudomonas fluorescens SBW25 host, which was isolated at the same f

227 -promoting rhizobacterium (PGPR) Pseudomonas fluorescens SBW25 identified a homologue of the type III

228 Pseudomonas fluorescens SBW25 is a plant growth-promoting bacterium

229 The type III (Rsp) gene cluster in P. fluorescens SBW25 is flanked by a homologue of the P. sy

230 P. fluorescens SBW25 is non-pathogenic and does not elicit

231 In P. fluorescens SBW25 pinA is induced in the presence of bet

232 ance of the rhizosphere-expressed TTSS of P. fluorescens SBW25 remains unclear.

233 Deletion of mreB from Pseudomonas fluorescens SBW25 results in viable spherical cells of v

234 gnificant general role in the function of P. fluorescens SBW25 than previously appreciated.

235 ve plant-induced nitrilase gene (pinA) in P. fluorescens SBW25 that is expressed in the rhizosphere o

236 an atypical mode of motility in Pseudomonas fluorescens SBW25 that was revealed only after flagellum

237 The inability of wild-type P. fluorescens SBW25 to elicit a visible HR is therefore pa

238 pinA allows P. fluorescens SBW25 to use beta-cyano-L-alanine as a nitro

239 erred pBBR1MCS2 into E. coli DH5alpha and P. fluorescens SBW25 with efficiencies of 1.16 +/- 0.13 x 1

240 1, Escherichia coli DH5alpha and Pseudomonas fluorescens SBW25 with high efficiency.

241 Pseudomonas stutzeri DSM4166 and Pseudomonas fluorescens SBW25, respectively.

242 e presence of a focal bacterium, Pseudomonas fluorescens SBW25, that had been pre-adapted or not to t

243 ng pathway gene in the bacterium Pseudomonas fluorescens SBW25.

244 g proteins in the model organism Pseudomonas fluorescens SBW25.

245 aptive radiation - the bacterium Pseudomonas fluorescens SBW25.

246 tem for use in diverse strain isolates of P. fluorescens, SBW25, WH6 and Pf0-1.

247 alcohol binding pocket, L29P, in Pseudomonas fluorescens (SIK WI) aryl esterase (PFE) increased the s

248 Some strains within the P. fluorescens species complex produce phenazine derivative

249 stributed among four subgroups within the P. fluorescens species complex, the diversity of our collec

250 Compared to P. fluorescens spp., which require favorable conditions and

251 on and characterization of this enzyme in P. fluorescens strain A506.

252 ed from a previously unsequenced Pseudomonas fluorescens strain and performed structure-guided mutage

253 Pseudomonas fluorescens strain HK44 (DSM 6700) is a genetically engi

254 chemical analyses of individual Pseudomonas fluorescens strain NCIMB 11764 cells.

255 6.97-Mb draft genome sequence of Pseudomonas fluorescens strain NCIMB 11764, which is capable of grow

256 ogether with a derivative of the producer P. fluorescens strain NCIMB10586 lacking the mup cluster al

257 nome comparisons reveal similarities with P. fluorescens strain Pf-5, reveal the novelty of Wood1R, a

258 The plant-colonizing Pseudomonas fluorescens strain SBW25 harbors a gene cluster (rsp) wh

259 asmid failed to allow the closely related P. fluorescens strain SBW25 to convert PA-B to PA-A.

260 re, we show that root-colonizing Pseudomonas fluorescens strain SS101 (Pf.SS101) enhanced resistance

261 chment to an abiotic surface) by Pseudomonas fluorescens strain WCS365, we have shown that: (i) P. fl

262 reened a collection of 30 closely related P. fluorescens strains and detected the T3SS genes in all b

263 Pseudomonas fluorescens strains Wayne1R and Wood1R have proven capac

264 ntly, 318 rhizosphere-associated Pseudomonas fluorescens strains were isolated and characterized acro

265 clades distinct from currently recognized P. fluorescens subgroups, and probably represent new subgro

266 n, the enzyme processed the corresponding P. fluorescens substrate, indicating a common catalytic mec

267 acts from Pseudomonas putida and Pseudomonas fluorescens, suggesting a common mechanism of catabolite

268 is and define a broader cadre of genes in P. fluorescens than that described so far for its homolog,

269 dnA is a transcription factor in Pseudomonas fluorescens that affects flagellar synthesis, biofilm fo

270 mmotile strains of the bacterium Pseudomonas fluorescens that lack flagella due to deletion of the re

271 xperimentally with the bacterium Pseudomonas fluorescens, that cheats may be unable to invade patches

272 ginosa or plant growth-promoting Pseudomonas fluorescens The non-ribosomal peptide ferribactin underg

273 In Pseudomonas fluorescens, the regulatory cascade starts with the mast

274 In Pseudomonas fluorescens, this process is regulated by the Lap system

275 cteria like Escherichia coli and Pseudomonas fluorescens to elicit the HR in tobacco leaves.

276 t to direct Escherichia coli and Pseudomonas fluorescens to inject HopPsyA into tobacco cells, thereb

277 c response of the model organism Pseudomonas fluorescens to produced water exposure to provide a mech

278 using 10(7) and 10(8) CFU mL(-1) Pseudomonas fluorescens to study the effects of the electrochemicall

279 the capacity of stationary-phase cells of P. fluorescens to survive exposure to oxidative stress.

280 ficacy of a probiotic bacterium, Pseudomonas fluorescens, to reduce impacts of WNS in two simultaneou

281 ifference in survival between control and P. fluorescens-treated bats.

282 utrescine biosynthesis was upregulated in P. fluorescens upon predation.

283 P. fluorescens was cultured after the filtration of 100 ml

284 howed that destabilization of UHT milk by P. fluorescens was highly variable and strain-dependent.

285 -semialdehyde decarboxylase from Pseudomonas fluorescens was solved as a dimer, this enzyme is a mixt

286 TTSS-proficient P. fluorescens was used to test the ability of several P. s

287 The wild-type strain of P. fluorescens WCS365 and its lap mutant derivatives were a

288 P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are absent from pathogenic pseud

289 equired for biofilm formation by Pseudomonas fluorescens WCS365.

290 thamiana leaves infiltrated with Pseudomonas fluorescens, we identified and tested a set of 9 candida

291 ginosa strains tested as well as Pseudomonas fluorescens were found to produce OmlA.

292 crystal structure of ACMSD from Pseudomonas fluorescens which validates our previous predictions tha

293 described for the soil organism Pseudomonas fluorescens), which encodes a conserved global regulator

294 this theory using the bacterium Pseudomonas fluorescens, which diversifies into niche specialists wh

295 use the common aerobic bacterium Pseudomonas fluorescens, which evolves rapidly under novel environme

296 ecies and by Yersinia pestis and Pseudomonas fluorescens, which possess pgaABCD homologues.

297 was observed in control organism Pseudomonas fluorescens with a one-stage lifecycle.

298 th the root-associated bacterium Pseudomonas fluorescens, with consequences for plant fitness.

299 d substrate of kynureninase from Pseudomonas fluorescens, with k(cat) and k(cat)/K(m) values of 0.7 s

300 conducted with the P. putida xenA and the P. fluorescens xenB sequences demonstrated that these genes