ライフサイエンスコーパス: putida

1 whole human blood infected with Pseudomonas putida .

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

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

4 naphthalene catabolic pathway of Pseudomonas putida.

5 amphor-hydroxylating system from Pseudomonas putida.

6 e cancer therapeutic cloned from Pseudomonas putida.

7 polyvalence enhanced PEf1 propagation in P. putida.

8 st step of camphor catabolism by Pseudomonas putida.

9 a coli was the donor compared to Pseudomonas putida.

10 genase cytochrome P450(cam) from Pseudomonas putida.

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

12 ared with planktonic cultures of Pseudomonas putida.

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

14 expressed following initial attachment of P. putida.

15 to those of the same enzyme from Pseudomonas putida.

16 sion control has been studied in Pseudomonas putida.

17 ve a role in polar flagellar placement in P. putida.

18 drogenase multienzyme complex of Pseudomonas putida.

19 as the source of the ion near m/z 7684 in P. putida.

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

21 omatic compounds are intimately linked in P. putida.

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

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

24 m was initially misidentified as Pseudomonas putida.

25 ajectories of the soil bacterium Pseudomonas putida.

26 of the three CheR paralogues of Pseudomonas putida.

27 n growth competition assays with Pseudomonas putida.

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

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

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

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

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

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

34 ndelate dehydrogenase (MDH) from Pseudomonas putida, a member of the flavin mononucleotide-dependent

35 (S)-Mandelate dehydrogenase from Pseudomonas putida, a member of the flavin mononucleotide-dependent

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

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

38 In P. putida, all these genes (with the exception of pcaH,G )

39 (S)-Mandelate dehydrogenase from Pseudomonas putida, an FMN-dependent alpha-hydroxy acid dehydrogenas

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

41 crystal structures of PcaHG from Pseudomonas putida and Acinetobacter sp. as well as of residues in o

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

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

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

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

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

47 The bkd operons of P. putida and P. aeruginosa encode the inducible multienzym

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 proteins from Escherichia coli, Pseudomonas putida, and Pseudomonas aeruginosa bind to the DnaA boxe

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

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

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

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

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

74 catechol) was developed based on Pseudomonas putida bacteria harboring the plasmid pSMM50R-B'.

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

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

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

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

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

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

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

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

83 Pseudomonas putida bloodstream infections were reported in two prete

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

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

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

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

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

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

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

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

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

93 (5)-3-ketosteroid isomerase from Pseudomonas putida catalyzes a C-H bond cleavage and formation throu

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

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

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

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

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

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

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

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

102 Pseudomonas putida converts benzoate to catechol using two enzymes t

103 13-kb cloned DNA fragment containing the P. putida crc gene region was sequenced.

104 BkdR levels were elevated in a P. putida crc mutant, but bkdR transcript levels were the s

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

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

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

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

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

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

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

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

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

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

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

116 toea agglomerans ATCC 33243, and Pseudomonas putida F1 are collected and form a reference library.

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

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

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

120 s-dihydrodiol dehydrogenase from Pseudomonas putida F1 was used to produce enantiomerically pure (-)-

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

122 tructure of an OprB channel from Pseudomonas putida F1.

123 ay serve as chemoattractants for Pseudomonas putida F1.

124 erobic degradation of toluene by Pseudomonas putida F1.

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

126 ike PchF obtained from PCMH purified from P. putida, FAD was bound noncovalently.

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

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

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

130 Pseudomonas putida G7 exhibits chemotaxis to naphthalene, but the mo

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

132 A P. putida G7 nahY mutant grew on naphthalene but was not ch

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

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

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

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

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

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

139 naphthalene degradation genes in Pseudomonas putida G7.

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

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

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

143 The P. putida gene, xenA, encodes a 39,702-Da monomeric, NAD(P)

144 ctive sites of human, yeast, and Pseudomonas putida glyoxalase I, as the log K(i) values for these me

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

146 otrophomonas maltophilia P21 and Pseudomonas putida H2.

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

148 ransport and chemotaxis demonstrates that P. putida has a chemoreceptor that differs from the classic

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

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

151 0cam (CYP101) from the bacterium Pseudomonas putida has been investigated by high-resolution solution

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

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

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

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

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

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

158 450cam monooxygenase system from Pseudomonas putida, have been studied.

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

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

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

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

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

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

165 ated xenobiotic reductases, from Pseudomonas putida II-B and P. fluorescens I-C that removed nitrite

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

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

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

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

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

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

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

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

174 egradation of protocatechuate in Pseudomonas putida is accomplished by the products of the pca genes

175 (S)-Mandelate dehydrogenase from Pseudomonas putida is an FMN-dependent alpha-hydroxy acid dehydrogen

176 ol methylhydroxylase (PCMH) from Pseudomonas putida is composed of a flavoprotein homodimer (alpha(2)

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

178 cid 4-hydroxybenzoate (4-HBA) by Pseudomonas putida is mediated by PcaK, a membrane-bound protein tha

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

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

181 Cytochrome P450cam (CYP101) from Pseudomonas putida is unusual among P450 enzymes in that it exhibits

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 on that enables LA catabolism in Pseudomonas putida KT2440.

207 is and the rhizobacterial strain Pseudomonas putida KT2440.

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

209 transcriptional regulators from Pseudomonas putida KT2440.

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

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

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

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

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

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

216 ed an adenoviral vector inserted with the P. putida methioninase (MET) gene (rAd-MET).

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

218 nylpyruvate hydratase (VPH) from Pseudomonas putida mt-2 form a complex that converts 2-oxo-3-hexened

219 4-OT, from Pseudomonas putida mt-2, catalyzes the conversion of 2-oxo-4-hexened

220 4-OT, a homohexamer from Pseudomonas putida mt-2, is the most extensively studied 4-OT isozym

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

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

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

224 th the corresponding subunits in Pseudomonas putida NCIB 9816-4, for which the tertiary structure has

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

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

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

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

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

230 2-phosphonopropionate by either Pseudomonas putida or Escherichia coli cells.

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

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

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

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

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

236 Genes from Pseudomonas putida (Pp), sodA, encoding manganese-superoxide dismuta

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

238 12 derivative introduced exogenously into P. putida PP3 via the suicide donor pAWT50 resulted in sile

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

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

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

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

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

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

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

246 sigma(54) protein encoded by the Pseudomonas putida rpoN gene.

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

248 ic and detoxification pathway of Pseudomonas putida S12.

249 ia coli: Pseudomonas aeruginosa, Pseudomonas putida, Salmonella enterica serovar Typhimurium, and Rho

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

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

252 GE P. putida showed high arsenic methylation and volatilizatio

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

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

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

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

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

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

259 Pseudomonas putida strain mt-2 unsaturated biofilm formation proceed

260 Pseudomonas putida strain PP3 produces two hydrolytic dehalogenases

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

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

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

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

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

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

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

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

269 7120, Pseudomonas aeruginosa and Pseudomonas putida that bind multiple zinc ions with high stability

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

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

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

273 ected evolution of the P450 from Pseudomonas putida to create mutants that hydroxylate naphthalene in

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

275 inally, benzoate represses the ability of P. putida to transport 4-hydroxybenzoate (4-HBA) by prevent

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

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

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

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

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

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

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

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

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

285 7 by nontransferable chromosomal Hg(R) in P. putida was slowed in coculture.

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

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

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

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

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

291 (5)-3-ketosteroid isomerase from Pseudomonas putida were found to exhibit substantial variations in t

292 bacter may also be applicable to Pseudomonas putida, where the PcaK permease has an additional role i

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

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

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

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

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

300 BLAST analyses conducted with the P. putida xenA and the P. fluorescens xenB sequences demons