ライフサイエンスコーパス: fluorescens

1 faecalis , Escherichia coli , or Pseudomonas fluorescens .

2 substrate activity with kynureninase from P. fluorescens.

3 adhesin regulating surface commitment by P. fluorescens.

4 ism impacts biofilm formation by Pseudomonas fluorescens.

5 calization and thus surface commitment by P. fluorescens.

6 dhesion required for biofilm formation by P. fluorescens.

7 ofilm formation by the bacterium Pseudomonas fluorescens.

8 ory populations of the bacterium Pseudomonas fluorescens.

9 ve trait of biofilm formation in Pseudomonas fluorescens.

10 ome c-type biogenesis protein of Pseudomonas fluorescens.

11 rse populations of the bacterium Pseudomonas fluorescens.

12 e and antifungal metabolite production in P. fluorescens.

13 control antibiotic production by Pseudomonas fluorescens.

14 to the root adhesin protein from Pseudomonas fluorescens.

15 tal structure of the enzyme from Pseudomonas fluorescens.

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

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

18 notably Escherichia species and Pseudomonas fluorescens.

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

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

21 2-79 synthesizes 3-OH acyl-HSLs and that P. fluorescens 2-79 uses N-(3-hydroxy-hexanoyl)-HSL as its

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 nazine biosynthetic operons from Pseudomonas fluorescens and Pseudomonas aureofaciens.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 duced by Pseudomonas aurantiaca (Pseudomonas fluorescens BL915).

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

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

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

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

78 Pseudomonas fluorescens carrying a pHIR11 derivative lacking hrpH is

79 P. fluorescens carrying a pHIR11 derivative lacking shcA fa

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

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

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

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

84 n in the plant beneficial strain Pseudomonas fluorescens CHA0.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 (4S)-muconolactone product (syn, Pseudomonas fluorescens, gi 70731221 ; anti, Mycobacterium smegmatis

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

102 Pseudomonas fluorescens grows at low temperature and produces thermo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 Pseudomonas fluorescens is a saprophytic bacterium commonly isolated

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

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

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

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

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

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

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

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

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

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

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

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

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

137 from the bioluminescent reporter Pseudomonas fluorescens M3A.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

168 PrnD from Pseudomonas fluorescens Pf5 was functionally expressed in Escherichi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

195 Pseudomonas fluorescens SBW25 is a plant growth-promoting bacterium

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

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

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

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

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

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

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

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

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

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

206 1, Escherichia coli DH5alpha and Pseudomonas fluorescens SBW25 with high efficiency.

207 Pseudomonas stutzeri DSM4166 and Pseudomonas fluorescens SBW25, respectively.

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

209 ng pathway gene in the bacterium Pseudomonas fluorescens SBW25.

210 g proteins in the model organism Pseudomonas fluorescens SBW25.

211 aptive radiation - the bacterium Pseudomonas fluorescens SBW25.

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

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

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

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

216 6.97-Mb draft genome sequence of Pseudomonas fluorescens strain NCIMB 11764, which is capable of grow

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

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

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

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

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

222 Pseudomonas fluorescens strains Wayne1R and Wood1R have proven capac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 equired for biofilm formation by Pseudomonas fluorescens WCS365.

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

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

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

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

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

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

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

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

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

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