ライフサイエンスコーパス: P. fluorescens

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

8 Molecular typing showed that all P. fluorescens isolates were identical by both random am

9 pinA allows P. fluorescens SBW25 to use beta-cyano-L-alanine as a ni

10 isolating and identifying P. aeruginosa and P. fluorescens from tap water samples, which are both op

11 reductases, from Pseudomonas putida II-B and P. fluorescens I-C that removed nitrite from nitroglycer

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

13 n of a clone of phzI in Escherichia coli and P. fluorescens 1855 resulted in the synthesis of all six

14 nsferred pBBR1MCS2 into E. coli DH5alpha and P. fluorescens SBW25 with efficiencies of 1.16 +/- 0.13

15 vealed that the three Legionella enzymes and P. fluorescens PC-PLC share conserved domains also prese

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

17 as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are absent from pathogenic ps

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

19 ssed by wild-type P. syringae pv. tabaci and P. fluorescens heterologously expressing a P. syringae T

20 genotype-specific HR was observed with avrB+ P. fluorescens in soybean and Arabidopsis plants carryin

21 jor adhesin regulating surface commitment by P. fluorescens.

22 localization and thus surface commitment by P. fluorescens.

23 t 4 cause reductions in biofilm formation by P. fluorescens Pf0-1 under the conditions tested.

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

25 availability regulates biofilm formation by P. fluorescens Pf0-1.

26 e adhesion required for biofilm formation by P. fluorescens.

27 y showed that destabilization of UHT milk by P. fluorescens was highly variable and strain-dependent.

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

29 six known secondary metabolites produced by P. fluorescens Pf-5, three novel secondary metabolite bi

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

31 seudomonas protegens Pf-5 (previously called P. fluorescens Pf-5) produces two siderophores, enantio-

32 nown, the enzyme processed the corresponding P. fluorescens substrate, indicating a common catalytic

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

34 udomonas putida (i.e., the strain was either P. fluorescens or P. putida, but the system did not make

35 n silica analysis of genomic information for P. fluorescens, P. putida, and P. stutzeri suggests that

36 nts show that interspecific conjugation from P. fluorescens allowed pQBR57 to persist in P. putida vi

37 or substrate activity with kynureninase from P. fluorescens.

38 In case of pseudobactins from P. fluorescens A225, the octapeptide has the sequence Ch

39 scens strain WCS365, we have shown that: (i) P. fluorescens can form biofilms on an abiotic surface w

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

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

42 ation and characterization of this enzyme in P. fluorescens strain A506.

43 hesis and define a broader cadre of genes in P. fluorescens than that described so far for its homolo

44 ative plant-induced nitrilase gene (pinA) in P. fluorescens SBW25 that is expressed in the rhizospher

45 onse and antifungal metabolite production in P. fluorescens.

46 t that Lys-227 is the PLP-binding residue in P. fluorescens kynureninase.

47 both with and without positive selection in P. fluorescens, it was lost or replaced by nontransferab

48 o putrescine biosynthesis was upregulated in P. fluorescens upon predation.

49 ental pseudomonads such as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WCS365, but are a

50 ned the crystal structure of the full-length P. fluorescens ExoU and found that it was similar to tha

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

52 a coli or in enzymes, pyocyanin-nonproducing P. fluorescens resulted in conversion of PCA to 1-hydrox

53 e residue, are required for LapG activity of P. fluorescens in vivo and in vitro.

54 There were no further cases of P. fluorescens colonization after the contaminated dispe

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

56 significant general role in the function of P. fluorescens SBW25 than previously appreciated.

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

58 bserved a sharp increase in the isolation of P. fluorescens from weekly pharyngeal surveillance swabs

59 y contribute to the biocontrol properties of P. fluorescens Pf-5.

60 hat LapG, a periplasmic cysteine protease of P. fluorescens, cleaves the N terminus of LapA, thus rel

61 The wild-type strain of P. fluorescens WCS365 and its lap mutant derivatives wer

62 tion of microfiltered milk with 9 strains of P. fluorescens on the stability of the corresponding UHT

63 ficance of the rhizosphere-expressed TTSS of P. fluorescens SBW25 remains unclear.

64 ency of biofilm present and the viability of P. fluorescens following electrochemical testing.

65 expression confers a surface-sensing mode on P. fluorescens and suggest this strategy may be broadly

66 However, E. coli or P. fluorescens donors harboring the binary system did no

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

68 subclades distinct from currently recognized P. fluorescens subgroups, and probably represent new sub

69 screened a collection of 30 closely related P. fluorescens strains and detected the T3SS genes in al

70 make the distinction and yielded the result P. fluorescens/putida) and Alcaligenes spp.

71 t, together with other approaches, suggested P. fluorescens Pf-5's recent lateral acquisitions includ

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

73 mpedance spectroscopy it has been shown that P. fluorescens increases the rate of corrosion.

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

75 es conducted with the P. putida xenA and the P. fluorescens xenB sequences demonstrated that these ge

76 produced high levels of the autoinducer, the P. fluorescens and E. coli donors produced only trace am

77 ations of the product distributions from the P. fluorescens enzyme showed that NG was denitrated with

78 etic analyses classified the isolates in the P. fluorescens (57) and P. putida (19) groups.

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

80 strate that the P. aeruginosa homolog of the P. fluorescens DGC GcbA involved in promoting biofilm fo

81 ysis of the expression and regulation of the P. fluorescens rsp pathway, both in the phytosphere and

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

83 A structural superposition with the P. fluorescens kynureninase revealed that these two stru

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

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

86 ster encoded by cosmid pHIR11 conferred upon P. fluorescens but not Escherichia coli the ability to s

87 ens like P. aeruginosa and the less virulent P. fluorescens.

88 Nine patients became colonized with P. fluorescens, and six out of the nine developed febril

89 ironment of a silica cave in comparison with P. fluorescens isolates from surface soil and the rhizos

90 Genome comparisons reveal similarities with P. fluorescens strain Pf-5, reveal the novelty of Wood1R