ライフサイエンスコーパス: putida

1 whole human blood infected with Pseudomonas putida .

2 the dynamics of Cd(II) uptake by Pseudomonas putida.

3 m was initially misidentified as Pseudomonas putida.

4 ajectories of the soil bacterium Pseudomonas putida.

5 of the three CheR paralogues of Pseudomonas putida.

6 n growth competition assays with Pseudomonas putida.

7 ke processes in the genome-scale model of P. putida.

8 different samples with respect to that of P. putida.

9 lar metabolism and c-di-GMP signalling in P. putida.

10 naphthalene catabolic pathway of Pseudomonas putida.

11 amphor-hydroxylating system from Pseudomonas putida.

12 e cancer therapeutic cloned from Pseudomonas putida.

13 st step of camphor catabolism by Pseudomonas putida.

14 a coli was the donor compared to Pseudomonas putida.

15 genase cytochrome P450(cam) from Pseudomonas putida.

16 protease IV-negative Pseudomonas species, P. putida.

17 ared with planktonic cultures of Pseudomonas putida.

18 mma-lyase (MET) gene cloned from Pseudomonas putida.

19 expressed following initial attachment of P. putida.

20 to those of the same enzyme from Pseudomonas putida.

21 polyvalence enhanced PEf1 propagation in P. putida.

22 rmation regulation by the Rsm proteins in P. putida.

23 rates we observe competitive exclusion of P. putida.

24 mented in the platform bacterium Pseudomonas putida.

25 located on the EPS molecules produced by P. putida.

26 omatic compounds are intimately linked in P. putida.

27 e isolates in the P. fluorescens (57) and P. putida (19) groups.

28 llus sp. (5.1 x 10(-2) mM d(-1)) than for P. putida (2.32 mM d(-1)).

29 oline 2,4-dioxygenase (QDO) from Pseudomonas putida 33/1 are homologous cofactor-independent dioxygen

30 her concentrations by reproducing also in P. putida (7.2 +/- 0.4 vs 6.0 +/- 1.0 log10PFU/mL).

31 rable Hg(R) captured to the chromosome in P. putida A simple mathematical model suggests these differ

32 te lactonizing enzyme (MLE) from Pseudomonas putida, a member of a family that catalyzes the syn-cycl

33 In the presence of copper, Pseudomonas putida activates transcription of cinAQ via the two-comp

34 ia coli, Pseudomonas aeruginosa, Pseudomonas putida, Agrobacterium tumefaciens, and Acinetobacter cal

35 tions, alkane monooxygenase from Pseudomonas putida (alkB) is able to catalyze the difficult terminal

36 Homologous enzymes in P. putida and A. tumefaciens were identified based on a sim

37 cells detached from biofilm (over 70% for P. putida and approximately 40% for polysaccharide producin

38 oter with a consensus FNR-binding site in P. putida and E. coli strains expressing only one FNR prote

39 ng this protein can replicate in Pseudomonas putida and E. coli.

40 FFF and MALDI-TOF MS was demonstrated for P. putida and E. coli.

41 ndelate dehydrogenase (MDH) from Pseudomonas putida and of the substrate-reduced enzyme have been ana

42 Functional P. putida and P. aeruginosa transporters were identified, a

43 fprA expression in both P. putida and P. aeruginosa was found to be regulated by Fi

44 ver the course of growth of both Pseudomonas putida and P. aeruginosa, and compared the wild-type str

45 sing cocultures of two bacterial species, P. putida and P. veronii.

46 the DnaB replicative helicase of Pseudomonas putida and Pseudomonas aeruginosa and initiates the form

47 d morphogenesis genes encoded by Pseudomonas putida and Pseudomonas aeruginosa bacteriophages.

48 e replicative helicase, DnaB, of Pseudomonas putida and Pseudomonas aeruginosa were isolated and used

49 with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aeruginosa, yet revealed 1,159 ge

50 ly biofilm formation, HSLs extracted from P. putida and pure C(12)-HSL were added to 6-h planktonic c

51 ary for effective sulfate assimilation by P. putida and that the effect of finR mutation on PDTC prod

52 interaction between a strain of Pseudomonas putida and the fungus Saccharomyces cerevisiae was ident

53 ne hydrolase (rSAHH) cloned from Pseudomonas putida and Trichomonas vaginalis, respectively.

54 ncluding Pseudomonas aeruginosa, Pseudomonas putida and Yersinia pestis, and in the presence of a hel

55 nction and yielded the result P. fluorescens/putida) and Alcaligenes spp.

56 Biofilms with protein-based (Pseudomonas putida) and polysaccharide based EPS (Pseudomonas aerugi

57 g expression systems in P. aeruginosa and P. putida, and 'GFP-tagging' Y. pestis.

58 yields pyruvate, which supports growth of P. putida, and 3-sulfolactaldehyde (SLA), which is oxidized

59 ria, Pseudomonas fluorescens and Pseudomonas putida, and a mercury resistance (Hg(R)) plasmid, pQBR57

60 were added to 6-h planktonic cultures of P. putida, and cell extracts were analyzed by 2-D gel profi

61 such as Comamonas testosteroni, Pseudomonas putida, and Ochrobactrum anthropi were selectively enric

62 f genomic information for P. fluorescens, P. putida, and P. stutzeri suggests that the findings repor

63 generated from Escherichia coli, Pseudomonas putida, and Ralstonia eutropha.

64 re employed for EPS removal from Pseudomonas putida, and the measured sulfhydryl concentrations on ba

65 ologous to the TonB protein from Pseudomonas putida; and CjrC was homologous to a putative outer memb

66 P. putida arsH expressed in E. coli conferred resistance to

67 ndelate metabolic pathway permit Pseudomonas putida ATCC 12633 to utilize either or both enantiomers

68 sp. 1A, Arthrobacter sp. JS443, Pseudomonas putida B2) in the pH range 6.1-8.6 with resting cells an

69 ia coli, Salmonella enterica and Pseudomonas putida, based on single nucleotide differences in their

70 (S)-Mandelate dehydrogenase from Pseudomonas putida belongs to a FMN-dependent enzyme family that oxi

71 persistence in the middle section of the P. putida biofilm compared to the P. aeruginosa biofilms.

72 r between bulk and biofilm surface in the P. putida biofilm compared to those of P. aeruginosa biofil

73 However, Pseudomonas aeruginosa and P. putida biofilms remained insensitive to CCCP addition.

74 In Pseudomonas putida biofilms, nutrient starvation triggers c-di-GMP h

75 Here, exoproteomic analysis of Pseudomonas putida BIRD-1 (BIRD-1), Pseudomonas fluorescens SBW25 an

76 Pseudomonas putida bloodstream infections were reported in two prete

77 The rhizobacterium Pseudomonas putida BTP1 stimulates induced systemic resistance (ISR)

78 free linolenic acid accumulated faster in P. putida BTP1-treated plants than in control.

79 eased survival of desiccation not only by P. putida but also by Pseudomonas aeruginosa PAO1 and Pseud

80 he known stress tolerance traits known in P. putida but also recognizes the capacity of this bacteriu

81 nt for autonomous replication in Pseudomonas putida but not in Escherichia coli.

82 oots with a biocontrol strain of Pseudomonas putida, but not with a siderophore-deficient mutant, ind

83 , the strain was either P. fluorescens or P. putida, but the system did not make the distinction and

84 s lower intraspecific conjugation rate in P. putida By contrast, in two-species communities, both mod

85 t-associated terrestrial microbe Pseudomonas putida by Manuel Espinosa-Urgel's group that is reported

86 (5)-3-ketosteroid isomerase from Pseudomonas putida catalyzes a C-H bond cleavage and formation throu

87 caffeine degradation pathway of Pseudomonas putida CBB5 utilizes an unprecedented glutathione-S-tran

88 Pseudomonas putida CBB5 was isolated from soil by enrichment on caff

89 Some bacteria, such as Pseudomonas putida CBB5, utilize caffeine as a sole carbon and nitro

90 Pseudomonas putida CBB5, which grows on several purine alkaloids, me

91 These P. putida cell extracts produced a protein with the same mo

92 e attract significantly higher numbers of P. putida cells than roots of the DIMBOA-deficient bx1 muta

93 tal structure of the prokaryotic Pseudomonas putida CMLE (PpCMLE) at 2.6 A resolution.

94 The P450cam monooxygenase from Pseudomonas putida consists of three redox proteins: NADH-putidaredo

95 ol methylhydroxylase (PCMH) from Pseudomonas putida contains FAD covalently attached to Tyr384.

96 , Mycobacterium tuberculosis and Pseudomonas putida CRPs are considered in the context of the ecologi

97 P. putida cultivation in lignin-rich media is characterized

98 seudomonas aeruginosa and six in Pseudomonas putida, different transporters were predicted to functio

99 Escherichia coli or P.putida DnaB was active with either TrfA-33 or TrfA-44, w

100 performed a transposon screen of Pseudomonas putida DSM 3601 to identify genes necessary for PDTC pro

101 s, Sulfolobus acidocaldarius and Pseudomonas putida) enriched in (13) C, (15) N, (18) O, (2) H and/or

102 Like the P. putida enzyme, hh4-OT requires the amino-terminal prolin

103 The reaction with proteins in P. putida EPS multiplied both the time and the monochlorami

104 The N-DBP yield from P. putida EPS was two times higher than that of P. aerugino

105 Like other prokaryotic swimmers, P. putida exhibits a motion pattern dominated by persistent

106 P. putida expressing the cloned protease IV gene had signif

107 hydrocarbons such as toluene in Pseudomonas putida F1 (PpF1) occurs via lateral diffusion through Fa

108 P. putida F1 also responded weakly to cytidine, uridine, an

109 in mixtures with soil bacteria (Pseudomonas putida F1 and Bacillus subtilis 168).

110 /L nZVI induced a persistent phenotype of P. putida F1 as indicated by smaller colony morphology, a m

111 A screen of P. putida F1 mutants, each lacking one of the genes encodin

112 Exposure of Pseudomonas putida F1 to 0.1, 1.0, and 5.0 g/L of nZVI caused the re

113 of Pput2725 from the biodegrader Pseudomonas putida F1, a COG4313 channel of unknown function, using

114 hat do not serve as growth substrates for P. putida F1.

115 tructure of an OprB channel from Pseudomonas putida F1.

116 n in the solvent-tolerant strain Pseudomonas putida F1.

117 ay serve as chemoattractants for Pseudomonas putida F1.

118 erobic degradation of toluene by Pseudomonas putida F1.

119 the iron-sulfur clusters in the different P. putida FNR proteins influence their reactivity with O2,

120 changes of the plant saprophyte Pseudomonas putida following 6 h of attachment to a silicone surface

121 Naphthalene-degrading Pseudomonas putida G7 cells were exposed to glucose, salicylate, and

122 transport of the soil bacterium Pseudomonas putida G7 in saturated porous media.

123 ghtly motile, stationary-phase cells from P. putida G7 were mobilized effectively, but the actively m

124 vely motile, exponentially grown cells of P. putida G7 were not mobilized.

125 chemotactic to naphthalene, and Pseudomonas putida G7 Y1, a nonchemotactic mutant strain, were simul

126 a Mycobacterium gilvum VM552 and Pseudomonas putida G7, acting as representative nonflagellated and f

127 A 10 mL pulse of Pseudomonas putida G7, which is chemotactic to naphthalene, and Pseu

128 that of NahR-regulated genes in Pseudomonas putida G7.

129 naphthalene degradation genes in Pseudomonas putida G7.

130 but not in exponentially grown, cells of P. putida G7.

131 by the biofilm-forming bacterium Pseudomonas putida GB-1 and the white-rot fungus Coprinellus sp. The

132 mediated by the obligate aerobe Pseudomonas putida GB-1, was tested in a column of quartz sand fed w

133 Fractionation obtained with P. putida GPo1 was similar to acid hydrolysis and M. austro

134 Here we show that Pseudomonas putida graTA-encoded antitoxin GraA and toxin GraT diffe

135 otrophomonas maltophilia P21 and Pseudomonas putida H2.

136 ingle inoculations with R. irregularis or P. putida had differential growth effects on both cultivars

137 te dehydrogenase (MDH-GOX2) from Pseudomonas putida has been determined at 2.15 A resolution.

138 thioninase (rMETase) cloned from Pseudomonas putida has been found previously to be an effective anti

139 0cam (CYP101) from the bacterium Pseudomonas putida has been investigated by high-resolution solution

140 catabolite repression control in Pseudomonas putida has been investigated using the bkd operon, encod

141 Pseudomonas putida has two chromosomally encoded arsH genes and is h

142 hrome P450cam monooxygenase from Pseudomonas putida, has been determined to 1.90 A resolution.

143 how that nano-Se particles synthesized by P. putida have a size range of 100 to 500 nm and that they

144 camphor hydroxylation pathway of Pseudomonas putida have been investigated as a function of oxidation

145 trast, Shewanella oneidensis and Pseudomonas putida have high iron but low intracellular manganese co

146 450cam monooxygenase system from Pseudomonas putida, have been studied.

147 inosa helicase and significantly with the P. putida helicase, whereas deletion of amino acids 71-88 (

148 activity in vitro, particularly with the P. putida helicase.

149 ons were Pseudomonas fluorescens-Pseudomonas putida (i.e., the strain was either P. fluorescens or P.

150 Unsaturated biofilms of Pseudomonas putida, i.e., biofilms grown in humid air, were analyzed

151 Transcriptome analysis of DIMBOA-exposed P. putida identified increased transcription of genes contr

152 recovers the mean-square displacement of P. putida if the two distinct swimming speeds are taken int

153 OV) photoreceptor PpSB1-LOV from Pseudomonas putida in both the dark and light states.

154 investigated the in vitro persistence of P. putida in heparinized saline: even under refrigerated co

155 ed crystal structures of MurU of Pseudomonas putida in native and ligand-bound states at high resolut

156 Microbial growth rates of P. putida in subsurface environments can only be accurately

157 ep in the D-lysine catabolism of Pseudomonas putida in which 2OA is converted to D-2-hydroxyglutarate

158 ndelate dehydrogenase (MDH) from Pseudomonas putida is a flavin mononucleotide (FMN)-dependent enzyme

159 (S)-Mandelate dehydrogenase from Pseudomonas putida is a member of a FMN-dependent enzyme family that

160 Benzaldehyde lyase (BAL) from Pseudomonas putida is a thiamin diphosphate (ThDP)-dependent enzyme

161 Our results show that P. putida is able to reduce selenite aerobically, but not s

162 ucleotides and fluorosugars in engineered P. putida is demonstrated with mineral fluoride both as onl

163 e 3,4-dioxygenase (3,4-PCD) from Pseudomonas putida is ligated axially by Tyr447 and His462 and equat

164 ChrR of Pseudomonas putida is one such enzyme that has also been characteriz

165 P450cam from Pseudomonas putida is the best characterized member of the vast fami

166 GGDEF/EAL response regulator in Pseudomonas putida, is transcriptionally regulated by RpoS, ANR and

167 " X-ray crystallography data for Pseudomonas putida ketosteroid isomerase (KSI), and we obtained conf

168 deposition of bacterial strains Pseudomonas putida KT2440 and Pseudomonas fluorescens LP6a at varyin

169 As resistance arsRBC operons of Pseudomonas putida KT2440 are followed by a downstream gene called a

170 P. putida KT2440 catabolized the d-stereoisomers of lysine,

171 we demonstrate that a strain of Pseudomonas putida KT2440 endowed with chromosomal expression of the

172 ach of these amino acids was racemized by P. putida KT2440 enzymes.

173 ous to sequences present in the completed P. putida KT2440 genome sequence or plasmid pWWO sequence t

174 hemotaxis receptor (McpS-LBR) of Pseudomonas putida KT2440 in complex with different chemoattractants

175 ealed that the default metabolic state of P. putida KT2440 is characterized by a slight catabolic ove

176 The soil bacterium Pseudomonas putida KT2440 lacks a functional Embden-Meyerhof-Parnas

177 In the presence of copper, Pseudomonas putida KT2440 produces the CinA and CinQ proteins from a

178 a proof of principle, induced cultures of P. putida KT2440 producing an EGFP-fused model protein by m

179 The annotated proline racemase ProR of P. putida KT2440 showed negligible activity with either ste

180 1 and (to a lesser extent) arsH2 genes of P. putida KT2440 strengthened its tolerance to both inorgan

181 chnologically relevant bacterium Pseudomonas putida KT2440 that greatly expands computable prediction

182 nd rhizosphere-dwelling organism Pseudomonas putida KT2440 to elaborate on the genomics and enzymolog

183 cs, fluxomics, and proteomics in Pseudomonas putida KT2440 to investigate the constitutive metabolic

184 ed ability of the soil bacterium Pseudomonas putida KT2440 to synthesize nanoparticles of elemental s

185 ant increase in the copper sensitivity of P. putida KT2440 under the conditions tested.

186 e sequence of the soil bacterium Pseudomonas putida KT2440 was published in 2002 (Nelson et al., ) th

187 n non plasmid-harboring cells of Pseudomonas putida KT2440 were spiked with different dilutions of th

188 We genetically engineered the P. putida KT2440 with stable expression of an arsM-gfp fusi

189 ate in vivo syringol turnover in Pseudomonas putida KT2440 with the GcoA-F169A variant.

190 he interaction between maize and Pseudomonas putida KT2440, a competitive coloniser of the maize rhiz

191 idine, a sustainable pigment, in Pseudomonas putida KT2440, an emerging industrial microbe.

192 ringae pv. tomato strain DC3000, Pseudomonas putida KT2440, and Agrobacterium tumefaciens strain C58.

193 ous bacterial species, including Pseudomonas putida KT2440, Enterococcus faecalis ATCC 29212, Salmone

194 from a single bacterial species, Pseudomonas putida KT2440, have been analyzed.

195 n the plant-beneficial bacterium Pseudomonas putida KT2440, identifying L-arginine as the main one ca

196 among environmental pseudomonads such as P. putida KT2440, P. fluorescens PfO1 and P. fluorescens WC

197 the three species investigated (Pseudomonas putida KT2440, Pseudomonas protegens Pf-5, and Pseudomon

198 ree aromatic-catabolic bacteria: Pseudomonas putida KT2440, Rhodoccocus jostii RHA1, and Amycolatopsi

199 viors of five bacterial species, Pseudomonas putida KT2440, Salmonella Typhimurium ATCC 14028, Staphy

200 aromatic-catabolizing organism, Pseudomonas putida KT2440, to demonstrate that these aromatic metabo

201 rains, including E. coli K12 and Pseudomonas putida KT2440.

202 r efficient ethylene glycol metabolism in P. putida KT2440.

203 of ethylene glycol metabolism in Pseudomonas putida KT2440.

204 on that enables LA catabolism in Pseudomonas putida KT2440.

205 is and the rhizobacterial strain Pseudomonas putida KT2440.

206 transcriptional regulators from Pseudomonas putida KT2440.

207 romiscuous alanine racemase from Pseudomonas putida (KT2440) was coupled with that of PAM to increase

208 ith more competing soil bacteria species, P. putida lysis was less critical in mitigating interspecie

209 by higher PEf1 propagation was offset by P. putida lysis, which decreased stress from interspecies c

210 zyme in the mandelate pathway of Pseudomonas putida, mandelamide hydrolase (MAH), catalyzes the hydro

211 st flavocytochrome b2 (FCB2) and Pseudomonas putida mandelate dehydrogenase (MDH).

212 a 2-keto acid decarboxylase from Pseudomonas putida (mdlC) and native E. coli aldehyde reductase (adh

213 dye-decolorizing peroxidase from Pseudomonas putida MET94 (PpDyP) and three variants generated by dir

214 Here, we report that the Pseudomonas putida MPE protein is a manganese-dependent DNA endonucl

215 -dioxygenase system (BZDOS) from Pseudomonas putida mt-2 catalyzes the NADH-dependent oxidation of be

216 4-OT, from Pseudomonas putida mt-2, catalyzes the conversion of 2-oxo-4-hexened

217 4-OT, a homohexamer from Pseudomonas putida mt-2, is the most extensively studied 4-OT isozym

218 TOL catabolic plasmid pWW0 from Pseudomonas putida mt-2.

219 h hypothetical polypeptides from Pseudomonas putida, Mycobacterium tuberculosis, Rickettsia prowazaki

220 alene and 2-methylnaphthalene by Pseudomonas putida NCIB 9816 and Pseudomonas fluorescens ATCC 17483

221 a nicotine-degrading enzyme from Pseudomonas putida, NicA2, a flavin-containing protein.

222 nano-Se and the metabolic versatility of P. putida offer the opportunity to use this model organism

223 ingle inoculations with R. irregularis or P. putida, only the cultivar with high mycorrhizal compatib

224 naB helicase of P. aeruginosa or Pseudomonas putida onto the RK2 origin in vitro and did not support

225 en it expressed the five enzymes from the P. putida operon.

226 es from Pseudomonas fluorescens, Pseudomonas putida or Azotobacter vinelandii.

227 2-phosphonopropionate by either Pseudomonas putida or Escherichia coli cells.

228 sp. strain ADP1, P. aeruginosa PAO1, and P. putida P111.

229 observed to occur at high frequencies in P. putida PaW340.

230 t willow clones and a grass with Pseudomonas putida PD1 was found to promote root and shoot growth an

231 proximately 10(3) M for KSI from Pseudomonas putida (pKSI).

232 The root-colonizing pseudomonad Pseudomonas putida (Pp) appears to produce two subunits, alpha and b

233 ed E1beta structures from humans (HU) and P. putida (PP).

234 12 derivative introduced exogenously into P. putida PP3 via the suicide donor pAWT50 resulted in sile

235 enzoylformate decarboxylase from Pseudomonas putida (PpBFDC) is a thiamin diphosphate-dependent enzym

236 e Co-type nitrile hydratase from Pseudomonas putida (ppNHase) that may be important for catalysis.

237 P. putida producing protease IV, relative to P. putida with

238 endent monooxygenase system from Pseudomonas putida, putidaredoxin (Pdx) shuttles electrons between p

239 multiple copies, into the chromosome of a P. putida recipient.

240 porter homologous to proteins in Pseudomonas putida responsible for the extrusion of organic solvents

241 The structure of a QuiC1 enzyme from P. putida reveals that the protein is a fusion of two disti

242 an efficient D-xylose utilizing Pseudomonas putida S12 strain was obtained by introducing the D-xylo

243 Pseudomonas protegens Pf-5, and Pseudomonas putida S12), siderophore secretion is higher during grow

244 ic and detoxification pathway of Pseudomonas putida S12.

245 val, the measured sulfhydryl sites within P. putida samples was 34.9 +/- 9.5 mumol/g, and no sulfhydr

246 site concentrations for S. oneidensis and P. putida samples when grown in the TSB medium.

247 (iv) allowed mapping of its network to 82 P. putida sequenced strains revealing functional core that

248 GE P. putida showed high arsenic methylation and volatilizatio

249 reen Fluorescent Protein (GFP)-expressing P. putida showed that DIMBOA-producing roots of wild-type m

250 distant hosts: Escherichia coli, Pseudomonas putida, Sphingobium japonicum, and Cupriavidus necator.

251 The environmental isolate Pseudomonas putida SQ1 is also able to use SQ for growth, and excret

252 revealed the catabolic pathway for SQ in P. putida SQ1 through differential proteomics and transcrip

253 tidis, Enterobacter agglomerans, Pseudomonas putida, Staphylococcus aureus, and Bacillus subtilis was

254 ) extracted from an Hg-resistant Pseudomonas putida strain FB1.

255 to which alginate production by Pseudomonas putida strain mt-2 and by other fluorescent pseudomonads

256 Pseudomonas putida strain mt-2 unsaturated biofilm formation proceed

257 Pseudomonas putida strain PP3 produces two hydrolytic dehalogenases

258 s yield of the evolved D-xylose utilizing P. putida strain.

259 lary assay and demonstrated that Pseudomonas putida strains F1 and PRS2000 were attracted to cytosine

260 on the physiology and survival of certain P. putida strains throughout their natural history.

261 e clusters were found in genomes of other P. putida strains, in other gamma-Proteobacteria, and in be

262 scentus, Pseudomonas aeruginosa, Pseudomonas putida, Streptomyces coelicolor, and chromosome I of Vib

263 oxin of the CYP101A1 system from Pseudomonas putida supports substrate oxidation by CYP199A2 at appro

264 Pseudomonas palleroniana TCA16, Pseudomonas putida TCA23 and N7, and Pseudomonas stutzeri TRA27a wer

265 i-Tn5-'phoA to identify genes in Pseudomonas putida that are matric water stress controlled and to ge

266 7120, Pseudomonas aeruginosa and Pseudomonas putida that bind multiple zinc ions with high stability

267 portion of PcaK, a permease from Pseudomonas putida that transports 4-hydroxybenzoate (4-HBA), were r

268 amphor monooxygenase system from Pseudomonas putida, the [2Fe-2S]-containing putidaredoxin (Pdx) shut

269 Although cytochrome P450cam from Pseudomonas putida, the archetype for all heme monooxygenases, has l

270 has been described in other bacteria, in P. putida these proteins seem not to be directly responsibl

271 L-arginine influence biofilm formation by P. putida through changes in c-di-GMP content and altered e

272 architecture that affords adaptability of P. putida to divergent carbon substrates and highlight regu

273 ransport, and they were also required for P. putida to have a chemotactic response to 4-HBA.

274 n the nonocular pathogenic host, Pseudomonas putida, to elucidate the molecular properties and virule

275 of two outer membrane proteins, Pseudomonas putida TodX and Ralstonia pickettii TbuX, which have bee

276 Chemotaxis assays confirmed motility of P. putida towards DIMBOA.

277 te-type [2Fe-2S] ferredoxin from Pseudomonas putida, transfers electrons from NADH-putidaredoxin redu

278 e results presented here demonstrate that P. putida undergoes a global change in gene expression foll

279 , plasmid concentration of 0.8 ng/microl, P. putida UWC1 cell concentration of 2.5 x 10(9) CFU (colon

280 transfer plasmid pBBR1MCS2 into Pseudomonas putida UWC1, Escherichia coli DH5alpha and Pseudomonas f

281 fluorescens allowed pQBR57 to persist in P. putida via source-sink transfer dynamics.

282 artrate dehydrogenase (TDH) from Pseudomonas putida was carried out.

283 7 by nontransferable chromosomal Hg(R) in P. putida was slowed in coculture.

284 dr) and putidaredoxin (Pdx) from Pseudomonas putida was studied by molecular modeling, mutagenesis, a

285 s study, a genome-scale model of Pseudomonas putida was used to study the key issue of uncertainty ar

286 n donor to cytochrome P450cam in Pseudomonas putida, was improved by mutating non-ligating cysteine r

287 thologues from Pseudomonas aeruginosa and P. putida, we have determined that these operons encode enz

288 tat with cell retention (CCR) of Pseudomonas putida, we resolve this controversy and show that under

289 enetic tools and epistasis experiments in P. putida, we uncovered an 'upstream' cascade of three cons

290 (5)-3-ketosteroid isomerase from Pseudomonas putida were found to exhibit substantial variations in t

291 wo of which - Pseudomonas fluorescens and P. putida - were studied in depth.

292 expression of an arsM-gfp fusion gene (GE P. putida), which was inserted into the bacterial chromosom

293 ruction and new computable phenotypes for P. putida, which can be leveraged as a first step toward un

294 The flhF gene of Pseudomonas putida, which encodes a GTP-binding protein, is part of

295 of TtgABC, a key efflux pump in Pseudomonas putida, which is highly resistant to antibiotics, solven

296 overexpression of arsH1 and arsH2 endowed P. putida with a high tolerance to the oxidative stress cau

297 at was administered to the patients, grew P. putida with a pulsed-field gel electrophoresis (PFGE) pa

298 A derivative of P. putida with both arsH genes deleted is sensitive to MAs(

299 P101 (cytochrome P450(cam)) from Pseudomonas putida with the aim of generating novel systems for thei

300 putida producing protease IV, relative to P. putida with the vector alone, caused a threefold increas