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1                                              P. fluorescens (a saprophyte) or hrp mutants defective i
2                                              P. fluorescens (pHIR11 hrmA::TnphoA) mutants do not elic
3                                              P. fluorescens carrying a pHIR11 derivative lacking shcA
4                                              P. fluorescens GcbA was found to be functional in P. aer
5                                              P. fluorescens SBW25 is non-pathogenic and does not elic
6                                              P. fluorescens was cultured after the filtration of 100
7 onstituted its predicted SRB Lap system in a P. fluorescens strain lacking its native Lap regulatory
8                             In contrast to a P. fluorescens C7R12 strain impaired in apo-pyoverdine p
9             Molecular typing showed that all P. fluorescens isolates were identical by both random am
10                                  pinA allows P. fluorescens SBW25 to use beta-cyano-L-alanine as a ni
11  isolating and identifying P. aeruginosa and P. fluorescens from tap water samples, which are both op
12 reductases, from Pseudomonas putida II-B and P. fluorescens I-C that removed nitrite from nitroglycer
13 nd identified as Pseudomonas putida II-B and P. fluorescens I-C.
14 n of a clone of phzI in Escherichia coli and P. fluorescens 1855 resulted in the synthesis of all six
15 o difference in survival between control and P. fluorescens-treated bats.
16 nsferred pBBR1MCS2 into E. coli DH5alpha and P. fluorescens SBW25 with efficiencies of 1.16 +/- 0.13
17 vealed that the three Legionella enzymes and P. fluorescens PC-PLC share conserved domains also prese
18    These findings suggest roles for pfiT and P. fluorescens in the pathogenesis of Crohn's disease.
19 as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are absent from pathogenic ps
20 lso supported the growth of P. s. tabaci and P. fluorescens bacteria, both of which are nonpathogenic
21 ssed by wild-type P. syringae pv. tabaci and P. fluorescens heterologously expressing a P. syringae T
22 genotype-specific HR was observed with avrB+ P. fluorescens in soybean and Arabidopsis plants carryin
23 jor adhesin regulating surface commitment by P. fluorescens.
24  localization and thus surface commitment by P. fluorescens.
25 anding of LapA-mediated biofilm formation by P. fluorescens and discusses several emerging models for
26                         Biofilm formation by P. fluorescens occurs through the localization of an adh
27 t 4 cause reductions in biofilm formation by P. fluorescens Pf0-1 under the conditions tested.
28 rement for c-di-GMP for biofilm formation by P. fluorescens Pf0-1, no DGCs from this strain have been
29  availability regulates biofilm formation by P. fluorescens Pf0-1.
30 e adhesion required for biofilm formation by P. fluorescens.
31 y showed that destabilization of UHT milk by P. fluorescens was highly variable and strain-dependent.
32      We propose that the lipases produced by P. fluorescens and Serratia marcescens, which comprise a
33  six known secondary metabolites produced by P. fluorescens Pf-5, three novel secondary metabolite bi
34     Genes required for 2,4-DAPG synthesis by P. fluorescens Q2-87 are encoded by a 6.5-kb fragment of
35 seudomonas protegens Pf-5 (previously called P. fluorescens Pf-5) produces two siderophores, enantio-
36 nown, the enzyme processed the corresponding P. fluorescens substrate, indicating a common catalytic
37  to investigate gene networks in the diverse P. fluorescens group.
38                       Unlike eCO(2) effects, P. fluorescens inoculants did not change mass-specific m
39 udomonas putida (i.e., the strain was either P. fluorescens or P. putida, but the system did not make
40              The microbiome and non-evolving P. fluorescens together promote host fitness, whereas th
41 n silica analysis of genomic information for P. fluorescens, P. putida, and P. stutzeri suggests that
42 nts show that interspecific conjugation from P. fluorescens allowed pQBR57 to persist in P. putida vi
43 or substrate activity with kynureninase from P. fluorescens.
44                In case of pseudobactins from P. fluorescens A225, the octapeptide has the sequence Ch
45 ied the C-terminal soluble form of WssI from P. fluorescens and Achromobacter insuavis and demonstrat
46 scens strain WCS365, we have shown that: (i) P. fluorescens can form biofilms on an abiotic surface w
47                                           In P. fluorescens SBW25 pinA is induced in the presence of
48           The type III (Rsp) gene cluster in P. fluorescens SBW25 is flanked by a homologue of the P.
49 ation and characterization of this enzyme in P. fluorescens strain A506.
50 hesis and define a broader cadre of genes in P. fluorescens than that described so far for its homolo
51 ative plant-induced nitrilase gene (pinA) in P. fluorescens SBW25 that is expressed in the rhizospher
52 onse and antifungal metabolite production in P. fluorescens.
53 t that Lys-227 is the PLP-binding residue in P. fluorescens kynureninase.
54  both with and without positive selection in P. fluorescens, it was lost or replaced by nontransferab
55 o putrescine biosynthesis was upregulated in P. fluorescens upon predation.
56 ental pseudomonads such as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are a
57 ned the crystal structure of the full-length P. fluorescens ExoU and found that it was similar to tha
58      A complete physical map of the 6.63 Mbp P. fluorescens SBW25 chromosome was constructed using da
59 a coli or in enzymes, pyocyanin-nonproducing P. fluorescens resulted in conversion of PCA to 1-hydrox
60 pment of measures to control the activity of P. fluorescens and other spoilage microorganism protease
61 e residue, are required for LapG activity of P. fluorescens in vivo and in vitro.
62  influences diverse physiological aspects of P. fluorescens 2P24 via the newly characterized AgtR.
63               There were no further cases of P. fluorescens colonization after the contaminated dispe
64 es the capacity of stationary-phase cells of P. fluorescens to survive exposure to oxidative stress.
65  stabilization may control the deposition of P. fluorescens.
66  significant general role in the function of P. fluorescens SBW25 than previously appreciated.
67                             The gacA gene of P. fluorescens Pf-5 was isolated, and the influence of g
68 system for use in diverse strain isolates of P. fluorescens, SBW25, WH6 and Pf0-1.
69 bserved a sharp increase in the isolation of P. fluorescens from weekly pharyngeal surveillance swabs
70 eading to a proposal of a dynamical model of P. fluorescens 07A metalloprotease active and inactive c
71 y contribute to the biocontrol properties of P. fluorescens Pf-5.
72 hat LapG, a periplasmic cysteine protease of P. fluorescens, cleaves the N terminus of LapA, thus rel
73                      The wild-type strain of P. fluorescens WCS365 and its lap mutant derivatives wer
74 tion of microfiltered milk with 9 strains of P. fluorescens on the stability of the corresponding UHT
75 ficance of the rhizosphere-expressed TTSS of P. fluorescens SBW25 remains unclear.
76 ency of biofilm present and the viability of P. fluorescens following electrochemical testing.
77  colonized to a greater extent the 3-day-old P. fluorescens biofilms, presumably entering in VBNC sta
78 expression confers a surface-sensing mode on P. fluorescens and suggest this strategy may be broadly
79                          However, E. coli or P. fluorescens donors harboring the binary system did no
80                     Using the model organism P. fluorescens, we show that PvdM is anchored to the per
81 E together with a derivative of the producer P. fluorescens strain NCIMB10586 lacking the mup cluster
82                              TTSS-proficient P. fluorescens was used to test the ability of several P
83                 Microbiome presence promotes P. fluorescens' rapid evolution to form biofilm, which r
84 subclades distinct from currently recognized P. fluorescens subgroups, and probably represent new sub
85  plasmid failed to allow the closely related P. fluorescens strain SBW25 to convert PA-B to PA-A.
86  screened a collection of 30 closely related P. fluorescens strains and detected the T3SS genes in al
87  make the distinction and yielded the result P. fluorescens/putida) and Alcaligenes spp.
88 t, together with other approaches, suggested P. fluorescens Pf-5's recent lateral acquisitions includ
89 ain 2-79 synthesizes 3-OH acyl-HSLs and that P. fluorescens 2-79 uses N-(3-hydroxy-hexanoyl)-HSL as i
90                          Results showed that P. fluorescens structure did not significantly change up
91 mpedance spectroscopy it has been shown that P. fluorescens increases the rate of corrosion.
92                                          The P. fluorescens gene, xenB, encodes a 37,441-Da monomeric
93 es conducted with the P. putida xenA and the P. fluorescens xenB sequences demonstrated that these ge
94 produced high levels of the autoinducer, the P. fluorescens and E. coli donors produced only trace am
95 ations of the product distributions from the P. fluorescens enzyme showed that NG was denitrated with
96 etic analyses classified the isolates in the P. fluorescens (57) and P. putida (19) groups.
97                    Among the isolates in the P. fluorescens group, most (37) were classified in the P
98 strate that the P. aeruginosa homolog of the P. fluorescens DGC GcbA involved in promoting biofilm fo
99 ysis of the expression and regulation of the P. fluorescens rsp pathway, both in the phytosphere and
100 max of 124 +/- 6 microM x min(-1), while the P. fluorescens enzyme had a Km for NG of 110 +/- 10 micr
101          A structural superposition with the P. fluorescens kynureninase revealed that these two stru
102  oxidized FMN to enzymes involved within the P. fluorescens enzymatic pathway responsible for convert
103                      Some strains within the P. fluorescens species complex produce phenazine derivat
104  Distributed among four subgroups within the P. fluorescens species complex, the diversity of our col
105                                  Compared to P. fluorescens spp., which require favorable conditions
106                   The inability of wild-type P. fluorescens SBW25 to elicit a visible HR is therefore
107  to store more biomass C per unit of N under P. fluorescens addition.
108 ster encoded by cosmid pHIR11 conferred upon P. fluorescens but not Escherichia coli the ability to s
109 ens like P. aeruginosa and the less virulent P. fluorescens.
110  theory, and humic acid concentration, while P. fluorescens EVs deviated from DLVO predictions, sugge
111  results suggest that treatment of bats with P. fluorescens may substantially reduce WNS mortality, a
112          Nine patients became colonized with P. fluorescens, and six out of the nine developed febril
113 ironment of a silica cave in comparison with P. fluorescens isolates from surface soil and the rhizos
114 te host fitness, whereas the microbiome with P. fluorescens that evolves biofilm reduces the benefici
115  Genome comparisons reveal similarities with P. fluorescens strain Pf-5, reveal the novelty of Wood1R
116            In this experiment treatment with P. fluorescens increased apparent overwinter survival fi

 
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