ライフサイエンスコーパス: Pseudomonas fluorescens

1 nterococcus faecalis , Escherichia coli , or Pseudomonas fluorescens .

2 g adhesion studies of bacterial cells (i.e., Pseudomonas fluorescens).

3 p4A) metabolism impacts biofilm formation by Pseudomonas fluorescens.

4 operative biofilm formation by the bacterium Pseudomonas fluorescens.

5 s in laboratory populations of the bacterium Pseudomonas fluorescens.

6 he cooperative trait of biofilm formation in Pseudomonas fluorescens.

7 to a cytochrome c-type biogenesis protein of Pseudomonas fluorescens.

8 nic and diverse populations of the bacterium Pseudomonas fluorescens.

9 re known to control antibiotic production by Pseudomonas fluorescens.

10 8% identity to the root adhesin protein from Pseudomonas fluorescens.

11 ing the crystal structure of the enzyme from Pseudomonas fluorescens.

12 microbiome and the evolution of one member, Pseudomonas fluorescens.

13 trans-AT Type I polyketide synthase (PKS) in Pseudomonas fluorescens.

14 Campylobacter jejuni, L. monocytogenes, and Pseudomonas fluorescens.

15 teobacteria, notably Escherichia species and Pseudomonas fluorescens.

16 choline-specific phospholipase C (PC-PLC) of Pseudomonas fluorescens.

17 s stutzeri (2.1% versus 1.0%, p = 0.024) and Pseudomonas fluorescens (0.9% versus 0.7%, p = 0.010), b

18 The molecular dynamics of the Pseudomonas fluorescens 07A metalloprotease in the prese

19 rationally avoid another pathogenic bacteria Pseudomonas fluorescens 15 (PF15).

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

21 The Pseudomonas fluorescens 23F phosphonoacetate hydrolase g

22 age enzyme, phosphonoacetate hydrolase, from Pseudomonas fluorescens 23F was cloned and expressed in

23 indole enhanced the antibiotic tolerance of Pseudomonas fluorescens 2P24, a PGPR well known for its

24 opy, we investigated the interaction between Pseudomonas fluorescens, a biofilm-forming bacterium, an

25 Mannanase A (MANA) from Pseudomonas fluorescens, a member of glycosyl hydrolase

26 tance was induced by either the non-pathogen Pseudomonas fluorescens, a TTSS-deficient mutant of P. s

27 onas putida ATCC 39167 and plant-deleterious Pseudomonas fluorescens A225 were grown in an iron-defic

28 putative periplasmic oxidoreductase PvdO of Pseudomonas fluorescens A506 is required for the final o

29 erial antagonist of E. amylovora (BlightBan, Pseudomonas fluorescens A506) can be included in antibio

30 ype III secretion, as well as the saprophyte Pseudomonas fluorescens A506, sensed water potentials of

31 rsification in a single radiating lineage of Pseudomonas fluorescens adapting to laboratory condition

32 The enzymatic activity of Pseudomonas fluorescens alpha-amino-beta-carboxymuconic-

33 so exist in Escherichia coli and probably in Pseudomonas fluorescens, although the permease from E. c

34 ry structure is similar to that of HPPD from Pseudomonas fluorescens, although the position of the C-

35 olved replicate populations of the bacterium Pseudomonas fluorescens and a parasitic bacteriophage wi

36 , Micrococcus luteus, Brevibacterium linens, Pseudomonas fluorescens and Bacillus subtilis were found

37 pable of taking global regulatory control in Pseudomonas fluorescens and causing a behavioural switch

38 The nonpathogenic bacteria Pseudomonas fluorescens and Escherichia coli can elicit

39 Probiotic baths of surface symbionts, Pseudomonas fluorescens and Flavobacterium johnsoniae we

40 We experimentally evolved Pseudomonas fluorescens and its mercury resistance mega-

41 AHs, we determined the crystal structures of Pseudomonas fluorescens and Myxococcus xanthus lectins.

42 ved for 13 bacterial species, two of which - Pseudomonas fluorescens and P. putida - were studied in

43 reviously uncharacterized ExoU homologs from Pseudomonas fluorescens and Photorhabdus asymbiotica als

44 Although both DKPs were absent from Pseudomonas fluorescens and Pseudomonas alcaligenes, we

45 studied phenazine biosynthetic operons from Pseudomonas fluorescens and Pseudomonas aureofaciens.

46 rimental invasions of two bacterial strains (Pseudomonas fluorescens and Pseudomonas putida) into lab

47 prising two species of common soil bacteria, Pseudomonas fluorescens and Pseudomonas putida, and a me

48 A mixed culture of Pseudomonas fluorescens and Pusillimonas noertemanii, ob

49 the molecular and chemical dialogues between Pseudomonas fluorescens and the protist Naegleria americ

50 soil bacteria (Agrobacterium tumefaciens and Pseudomonas fluorescens) and a poorly crystalline mangan

51 to p-hydroxybenzoate hydroxylase (PHBH, from Pseudomonas fluorescens) and flavin-containing monooxyge

52 imensional (3D) morphology of Gram-negative (Pseudomonas fluorescens) and Gram-positive (Bacillus thu

53 hologs of Escherichia coli, Vibrio cholerae, Pseudomonas fluorescens, and Pseudomonas aeruginosa resu

54 ampylobacter jejuni, Pseudomonas aeruginosa, Pseudomonas fluorescens, and Shewanella oneidensis.

55 wn to a good substrate for kynureninase from Pseudomonas fluorescens, and the rate-determining step c

56 y against Staphylococcus aureus, followed by Pseudomonas fluorescens; and among these bacteria, the a

57 homologous immotile variants of the bacteria Pseudomonas fluorescens, AR2 and Pf0-2x.

58 tness costs of 2 divergent large plasmids in Pseudomonas fluorescens are caused by inducing maladapti

59 The wrinkly spreader morph of Pseudomonas fluorescens arises repeatedly during experim

60 Using Pseudomonas fluorescens as a model biofilm-forming bacte

61 PCR and Southern analysis identified Pseudomonas fluorescens as the originating species of I2

62 herichia coli outer-membrane porin C and the Pseudomonas fluorescens-associated sequence I2, antisacc

63 accharomyces cerevisiae antibodies; and anti-Pseudomonas fluorescens-associated sequence).

64 The thioquinolobactin siderophore from Pseudomonas fluorescens ATCC 17400 utilizes a variation

65 hthalene by Pseudomonas putida NCIB 9816 and Pseudomonas fluorescens ATCC 17483 containing naphthalen

66 cence produced by the genetically engineered Pseudomonas fluorescens bacterial bioreporter 5RL.

67 re, Arabidopsis seedlings overexpressing the Pseudomonas fluorescens beta-cyanoalanine nitrilase pinA

68 Over the last two decades, the mechanisms of Pseudomonas fluorescens biofilm formation and regulation

69 a mechanistic model to explain regulation of Pseudomonas fluorescens biofilm formation by the environ

70 of Legionella pneumophila colonization of a Pseudomonas fluorescens biofilm, as information about th

71 gNP) exposure on viability in single species Pseudomonas fluorescens biofilms were determined via dye

72 orcinols produced by Pseudomonas aurantiaca (Pseudomonas fluorescens BL915).

73 sembles the biofilm-regulating Lap system of Pseudomonas fluorescens but is curiously missing the c-d

74 idence and mode of action of pyoverdine from Pseudomonas fluorescens C7R12 on Arabidopsis (Arabidopsi

75 Here, we demonstrate that ACMSD from Pseudomonas fluorescens can self-assemble into homodimer

76 Pseudomonas fluorescens carrying a pHIR11 derivative lac

77 PhlD, a type III polyketide synthase from Pseudomonas fluorescens, catalyzes the synthesis of phlo

78 We present here data for the spread of Pseudomonas fluorescens caused by a contaminated drinkin

79 taining receptor LapD as a central switch in Pseudomonas fluorescens cell adhesion.

80 n by RimK rapidly influenced the proteome of Pseudomonas fluorescens cells to facilitate colonisation

81 Here we show that adhered Pseudomonas fluorescens cells under high permeate flux c

82 de production in the plant beneficial strain Pseudomonas fluorescens CHA0.

83 r example, the wrinkly spreader phenotype of Pseudomonas fluorescens colonizes food/water sources and

84 arization (DNP) ssNMR to characterize native Pseudomonas fluorescens colony biofilms.

85 trans-AT Type I polyketide synthase (PKS) in Pseudomonas fluorescens, consists of a mixture of mainly

86 Here, we show that the bacteria Pseudomonas fluorescens diversifies into defence special

87 Solanum lycopersicum) or Arabidopsis through Pseudomonas fluorescens, engineered to express the type

88 ion of siderophores on bacteria inoculated ( Pseudomonas fluorescens) environments and (ii) hotspots

89 chemically cross-linked trimeric complex of Pseudomonas fluorescens Esterase (PFE), using nIM-MS to

90 unity context influences coevolution between Pseudomonas fluorescens (exploited) and Variovorax sp. (

91 the common (4S)-muconolactone product (syn, Pseudomonas fluorescens, gi 70731221 ; anti, Mycobacteri

92 tal gene transfer event with a member of the Pseudomonas fluorescens group.

93 Pseudomonas fluorescens grows at low temperature and pro

94 Here, Pseudomonas fluorescens has been introduced to the syste

95 solvent on the reaction of kynureninase from Pseudomonas fluorescens have been determined.

96 the HMS enzyme families and analysis of the Pseudomonas fluorescens HPD crystal structure highlighte

97 ld-type and several site-directed mutants of Pseudomonas fluorescens ICH at resolutions ranging from

98 chain mannitol 2-dehydrogenase (54 kDa) from Pseudomonas fluorescens in a binary complex with NAD(+)

99 nts at single cell level using the bacterium Pseudomonas fluorescens in an oligotrophic growth assay.

100 a series of crystal structures of MsuD from Pseudomonas fluorescens in different liganded states.

101 me adaptive diversification of the bacterium Pseudomonas fluorescens in its natural environment, soil

102 age) on the diversification of the bacterium Pseudomonas fluorescens in spatially structured microcos

103 ere we take advantage of the model bacterium Pseudomonas fluorescens in which the genotype-to-phenoty

104 acid film was used to inhibit the growth of Pseudomonas fluorescens in WPI-carrageenan gels during s

105 Haemophilus segnis, Gemella morbillorum, and Pseudomonas fluorescens) in lung samples that had not be

106 bacterial species, Staphylococcus aureus and Pseudomonas fluorescens, in well-characterized porous me

107 soilborne plant diseases by some strains of Pseudomonas fluorescens, including Pf-5.

108 cillus subtilis, Lactobacillus rhamnosus and Pseudomonas fluorescens induces C. elegans stress resist

109 robial functioning by plant growth-promoting Pseudomonas fluorescens is a prospect for ecosystem mana

110 Pseudomonas fluorescens is a saprophytic bacterium commo

111 stant mutants revealed that a mucA mutant of Pseudomonas fluorescens is protected against T6SS attack

112 this study, we examined the adaptation of a Pseudomonas fluorescens isolate (R124) from the nutrient

113 petitive fitness was cloned from a strain of Pseudomonas fluorescens isolated from copper-contaminate

114 half-reactions of a stable form of KMO from Pseudomonas fluorescens (KMO).

115 etermined by molecular replacement using the Pseudomonas fluorescens kynureninase structure (PDB entr

116 Crystals of Pseudomonas fluorescens kynureninase were obtained, and

117 The reaction of Pseudomonas fluorescens kynureninase with L-kynurenine a

118 nspecific immune priming toward the bacteria Pseudomonas fluorescens, Lactococcus lactis, and 4 strai

119 Here, we identify a homolog of Pseudomonas fluorescens LapG as a dispersal factor that

120 terial strains Pseudomonas putida KT2440 and Pseudomonas fluorescens LP6a at varying electrolyte conc

121 ng strengths we quantified the deposition of Pseudomonas fluorescens Lp6a in columns containing glass

122 rborne naphthalene (NAH) by surface-attached Pseudomonas fluorescens LP6a.

123 to facilitate the dispersal of PHE-degrading Pseudomonas fluorescens LP6a.

124 uminescence from the bioluminescent reporter Pseudomonas fluorescens M3A.

125 mmation in wild-type mice, and germ-free and Pseudomonas fluorescens-monoassociated interleukin 10 -/

126 rhabditis elegans and its microbiota isolate Pseudomonas fluorescens MYb115 that is known to protect

127 Nitrate removal by ORR isolate Pseudomonas fluorescens N2A2 is virtually abolished by F

128 clinically important antibiotic produced by Pseudomonas fluorescens NCIMB 10586 that is assembled by

129 ure of pseudomonic acids (PAs) isolated from Pseudomonas fluorescens NCIMB 10586, presents significan

130 Cyanide oxygenase (CNO) from Pseudomonas fluorescens NCIMB 11764 catalyzes the pterin

131 amined the effects of plant growth-promoting Pseudomonas fluorescens on C and N cycling in the rhizos

132 ssociated with the farmer are two strains of Pseudomonas fluorescens, only one of which serves as a f

133 no butyric acid, the non-pathogenic bacteria Pseudomonas fluorescens, or by the phytohormones jasmoni

134 ) oils was tested with Candida rugosa (CRL), Pseudomonas fluorescens, or Pancreatic porcine lipases.

135 via sequence analysis of the whole genome of Pseudomonas fluorescens Pf-5 and subsequently cloned and

136 Pseudomonas fluorescens Pf-5 is a plant commensal bacter

137 nd biochemical evidence that the cofactor of Pseudomonas fluorescens Pf-5 UndA is actually a diiron c

138 y of aminopyrrolnitrin oxygenase (PrnD) from Pseudomonas fluorescens Pf-5.

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

140 eudomonas spp., including the soil bacterium Pseudomonas fluorescens Pf-5.

141 c-di-GMP controls biofilm formation by Pseudomonas fluorescens Pf0-1 by promoting the cell surf

142 Biofilm formation by Pseudomonas fluorescens Pf0-1 requires the cell surface

143 o the cell surface is a key step required by Pseudomonas fluorescens Pf0-1 to irreversibly attach to

144 ermine the genetic needs for the survival of Pseudomonas fluorescens Pf0-1, a gram-negative soil bact

145 For Pseudomonas fluorescens Pf0-1, c-di-GMP impacts the secr

146 gae 61 into the genome of the soil bacterium Pseudomonas fluorescens Pf0-1.

147 face, and dominate colonies of the bacterium Pseudomonas fluorescens Pf0-1.

148 sing a rulAB::inaZ transcriptional fusion in Pseudomonas fluorescens Pf5 showed that rulAB was rapidl

149 PrnD from Pseudomonas fluorescens Pf5 was functionally expressed i

150 e adjacent to the metal center in ACMSD from Pseudomonas fluorescens (PfACMSD).

151 (TaAA9A) is compared with that of CopC from Pseudomonas fluorescens (PfCopC) and with the LPMO-like

152 y of lipases from porcine pancreas (PPL) and Pseudomonas fluorescens (PFL) using nine TGs differing i

153 2%), and those produced with the enzyme from Pseudomonas fluorescens, PFL (57%).

154 active site of mannitol 2-dehydrogenase from Pseudomonas fluorescens (PfM2DH) is connected with bulk

155 Here, we found mqsA in Pseudomonas fluorescens (PfmqsA) is acquired through hor

156 etically and phenotypically characterize the Pseudomonas fluorescens population in a commercial potat

157 In our previous work, we found Pseudomonas fluorescens PpR24 can orally infect and kill

158 When expressed in Pseudomonas fluorescens, PrnB is red in color due to the

159 eudomonads such as Pseudomonas aeruginosa or Pseudomonas fluorescens produce pyoverdine siderophores

160 An isolate of Pseudomonas fluorescens produced five detectable species

161 n that occurs in experimental populations of Pseudomonas fluorescens propagated in a spatially hetero

162 Strains of Pseudomonas fluorescens, Ps. poae and Chryseobacterium j

163 and dimethyl-methylsuccinate by lipases from Pseudomonas fluorescens, Pseudomonas cepacia, and Candid

164 s campestris, albeit not in the enzymes from Pseudomonas fluorescens, Pseudomonas putida or Azotobact

165 Most common misidentifications were Pseudomonas fluorescens-Pseudomonas putida (i.e., the st

166 Pseudomonas fluorescens Q8r1-96 represents a group of rh

167 lso mobilized pFRtra to Escherichia coli and Pseudomonas fluorescens recipients at frequencies simila

168 re tested for antibodies to oligomannan, the Pseudomonas fluorescens-related protein, Escherichia col

169 ort that the overexpressed ACMSD enzyme from Pseudomonas fluorescens requires a divalent metal, such

170 vity of GO and MGO against Listeria innocua, Pseudomonas fluorescens, Salmonella enterica and Bacillu

171 m-negative bacteria (Pseudomonas aeruginosa, Pseudomonas fluorescens, Salmonella Enteritidis, Salmone

172 othrix thermosphacta, Enterococcus faecalis, Pseudomonas fluorescens, Salmonella typhimurium, Staphyl

173 t arose during evolution experiments between Pseudomonas fluorescens SBW25 and its sympatric mercury

174 ng experimental populations of the bacterium Pseudomonas fluorescens SBW25 and its viral parasite, ph

175 lysis of Pseudomonas putida BIRD-1 (BIRD-1), Pseudomonas fluorescens SBW25 and Pseudomonas stutzeri D

176 The wrinkly spreader (WS) genotype of Pseudomonas fluorescens SBW25 colonizes the air-liquid i

177 riment in which populations of the bacterium Pseudomonas fluorescens SBW25 evolved, de novo, the abil

178 ed their effects on competitive fitness of a Pseudomonas fluorescens SBW25 host, which was isolated a

179 plant growth-promoting rhizobacterium (PGPR) Pseudomonas fluorescens SBW25 identified a homologue of

180 Pseudomonas fluorescens SBW25 is a plant growth-promotin

181 Deletion of mreB from Pseudomonas fluorescens SBW25 results in viable spherica

182 investigate an atypical mode of motility in Pseudomonas fluorescens SBW25 that was revealed only aft

183 s putida UWC1, Escherichia coli DH5alpha and Pseudomonas fluorescens SBW25 with high efficiency.

184 Here, we cultured the bacterium Pseudomonas fluorescens SBW25 with sterile filtrate obta

185 I, found in Pseudomonas stutzeri DSM4166 and Pseudomonas fluorescens SBW25, respectively.

186 result of the presence of a focal bacterium, Pseudomonas fluorescens SBW25, that had been pre-adapted

187 of a signaling pathway gene in the bacterium Pseudomonas fluorescens SBW25.

188 malathion in the underutilized host organism Pseudomonas fluorescens SBW25.

189 r cdG binding proteins in the model organism Pseudomonas fluorescens SBW25.

190 ystem for adaptive radiation - the bacterium Pseudomonas fluorescens SBW25.

191 tion in the alcohol binding pocket, L29P, in Pseudomonas fluorescens (SIK WI) aryl esterase (PFE) inc

192 e by KN65.2 in the presence of a competitor (Pseudomonas fluorescens sp. P17).

193 rotein derived from a previously unsequenced Pseudomonas fluorescens strain and performed structure-g

194 Pseudomonas fluorescens strain HK44 (DSM 6700) is a gene

195 qualitative chemical analyses of individual Pseudomonas fluorescens strain NCIMB 11764 cells.

196 rt here the 6.97-Mb draft genome sequence of Pseudomonas fluorescens strain NCIMB 11764, which is cap

197 The plant-colonizing Pseudomonas fluorescens strain SBW25 harbors a gene clus

198 Here, we show that root-colonizing Pseudomonas fluorescens strain SS101 (Pf.SS101) enhanced

199 n (e.g. attachment to an abiotic surface) by Pseudomonas fluorescens strain WCS365, we have shown tha

200 While Pseudomonas fluorescens strains have demonstrated biocon

201 Pseudomonas fluorescens strains Wayne1R and Wood1R have

202 Consequently, 318 rhizosphere-associated Pseudomonas fluorescens strains were isolated and charac

203 n crude extracts from Pseudomonas putida and Pseudomonas fluorescens, suggesting a common mechanism o

204 AdnA is a transcription factor in Pseudomonas fluorescens that affects flagellar synthesis

205 engineered immotile strains of the bacterium Pseudomonas fluorescens that lack flagella due to deleti

206 cally, and experimentally with the bacterium Pseudomonas fluorescens, that cheats may be unable to in

207 domonas aeruginosa or plant growth-promoting Pseudomonas fluorescens The non-ribosomal peptide ferrib

208 In Pseudomonas fluorescens, the regulatory cascade starts w

209 In Pseudomonas fluorescens, this process is regulated by th

210 prophytic bacteria like Escherichia coli and Pseudomonas fluorescens to elicit the HR in tobacco leav

211 is sufficient to direct Escherichia coli and Pseudomonas fluorescens to inject HopPsyA into tobacco c

212 e the genetic response of the model organism Pseudomonas fluorescens to produced water exposure to pr

213 carried out using 10(7) and 10(8) CFU mL(-1) Pseudomonas fluorescens to study the effects of the elec

214 ested the efficacy of a probiotic bacterium, Pseudomonas fluorescens, to reduce impacts of WNS in two

215 nate-epsilon-semialdehyde decarboxylase from Pseudomonas fluorescens was solved as a dimer, this enzy

216 n that are required for biofilm formation by Pseudomonas fluorescens WCS365.

217 from N. benthamiana leaves infiltrated with Pseudomonas fluorescens, we identified and tested a set

218 crobial model system with the soil bacterium Pseudomonas fluorescens, we reveal a hierarchy among tra

219 es cerevisiae, Levilactobacillus brevis, and Pseudomonas fluorescens were exemplarily used as model o

220 All P. aeruginosa strains tested as well as Pseudomonas fluorescens were found to produce OmlA.

221 h-resolution crystal structure of ACMSD from Pseudomonas fluorescens which validates our previous pre

222 (originally described for the soil organism Pseudomonas fluorescens), which encodes a conserved glob

223 We tested this theory using the bacterium Pseudomonas fluorescens, which diversifies into niche sp

224 We use the common aerobic bacterium Pseudomonas fluorescens, which evolves rapidly under nov

225 by these species and by Yersinia pestis and Pseudomonas fluorescens, which possess pgaABCD homologue

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

227 associate with the root-associated bacterium Pseudomonas fluorescens, with consequences for plant fit

228 ine is a good substrate of kynureninase from Pseudomonas fluorescens, with k(cat) and k(cat)/K(m) val