ライフサイエンスコーパス: Pseudomonas fluorescens

1 nterococcus faecalis , Escherichia coli , or Pseudomonas fluorescens .

2 he cooperative trait of biofilm formation in Pseudomonas fluorescens.

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

4 nic and diverse populations of the bacterium Pseudomonas fluorescens.

5 re known to control antibiotic production by Pseudomonas fluorescens.

6 8% identity to the root adhesin protein from Pseudomonas fluorescens.

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

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

9 teobacteria, notably Escherichia species and Pseudomonas fluorescens.

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

11 p4A) metabolism impacts biofilm formation by Pseudomonas fluorescens.

12 operative biofilm formation by the bacterium Pseudomonas fluorescens.

13 s in laboratory populations of the bacterium Pseudomonas fluorescens.

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

15 The Pseudomonas fluorescens 23F phosphonoacetate hydrolase g

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 The nonpathogenic bacteria Pseudomonas fluorescens and Escherichia coli can elicit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 Using Pseudomonas fluorescens as a model biofilm-forming bacte

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

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

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

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

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

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

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

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

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

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

57 Pseudomonas fluorescens carrying a pHIR11 derivative lac

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

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

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

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

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

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

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

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

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

67 Pseudomonas fluorescens grows at low temperature and pro

68 Here, Pseudomonas fluorescens has been introduced to the syste

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

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

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

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

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

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

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

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

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

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

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

80 Pseudomonas fluorescens is a saprophytic bacterium commo

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

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

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

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

85 Crystals of Pseudomonas fluorescens kynureninase were obtained, and

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

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

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

89 uminescence from the bioluminescent reporter Pseudomonas fluorescens M3A.

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

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

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

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

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

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

96 Pseudomonas fluorescens Pf-5 is a plant commensal bacter

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

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

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

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

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

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

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

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

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

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

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

108 PrnD from Pseudomonas fluorescens Pf5 was functionally expressed i

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

110 2%), and those produced with the enzyme from Pseudomonas fluorescens, PFL (57%).

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

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

113 An isolate of Pseudomonas fluorescens produced five detectable species

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

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

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

117 Pseudomonas fluorescens Q8r1-96 represents a group of rh

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

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

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

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

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

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

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

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

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

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

128 Pseudomonas fluorescens SBW25 is a plant growth-promotin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 Pseudomonas fluorescens strains Wayne1R and Wood1R have

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

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

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

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

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

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

150 In Pseudomonas fluorescens, this process is regulated by th

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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